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Wolfram S Kunz

Title['Prof.']
InstitutionUniversity of Bonn
DepartmentExperimental Epileptology and Cognition Research
AddressBonn 53127
Phone+492286885290
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Gellerich FN, Szibor M, Gizatullina Z, Lessmann V, Schwarzer M, Doenst T, Vielhaber S, Kunz WS. Reply to Rutter et al.: The roles of cytosolic and intramitochondrial Ca2+ and the mitochondrial Ca2+-uniporter (MCU) in the stimulation of mammalian oxidative phosphorylation. J Biol Chem. 2020 Jul 24; 295(30):10507. PMID: 32709761.
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    2. Rotko D, Kunz WS, Szewczyk A, Kulawiak B. Signaling pathways targeting mitochondrial potassium channels. Int J Biochem Cell Biol. 2020 Aug; 125:105792. PMID: 32574707.
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    3. Rotko D, Bednarczyk P, Koprowski P, Kunz WS, Szewczyk A, Kulawiak B. Heme is required for carbon monoxide activation of mitochondrial BKCa channel. Eur J Pharmacol. 2020 Aug 15; 881:173191. PMID: 32422186.
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    4. Wolking S, Schulz H, Nies AT, McCormack M, Schaeffeler E, Auce P, Avbersek A, Becker F, Klein KM, Krenn M, Møller RS, Nikanorova M, Weckhuysen S, Consortium E, Cavalleri GL, Delanty N, Depondt C, Johnson MR, Koeleman BP, Kunz WS, Marson AG, Sander JW, Sills GJ, Striano P, Zara F, Zimprich F, Weber YG, Krause R, Sisodiya S, Schwab M, Sander T, Lerche H. Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study. Pharmacogenomics. 2020 Apr; 21(5):325-335. PMID: 32308125.
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    5. Wolking S, Moreau C, Nies AT, Schaeffeler E, McCormack M, Auce P, Avbersek A, Becker F, Krenn M, Møller RS, Nikanorova M, Weber YG, Weckhuysen S, Cavalleri GL, Delanty N, Depondt C, Johnson MR, Koeleman BPC, Kunz WS, Marson AG, Sander JW, Sills GJ, Striano P, Zara F, Zimprich F, Schwab M, Krause R, Sisodiya SM, Cossette P, Girard SL, Lerche H. Testing association of rare genetic variants with resistance to three common antiseizure medications. Epilepsia. 2020 Apr; 61(4):657-666. PMID: 32141622.
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    6. Stöckigt F, Eichhorn L, Beiert T, Knappe V, Radecke T, Steinmetz M, Nickenig G, Peeva V, Kudin AP, Kunz WS, Berwanger C, Kamm L, Schultheis D, Schlötzer-Schrehardt U, Clemen CS, Schröder R, Schrickel JW. Heart failure after pressure overload in autosomal-dominant desminopathies: Lessons from heterozygous DES-p.R349P knock-in mice. PLoS One. 2020; 15(3):e0228913. PMID: 32126091.
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    7. Szibor M, Gizatullina Z, Gainutdinov T, Endres T, Debska-Vielhaber G, Kunz M, Karavasili N, Hallmann K, Schreiber F, Bamberger A, Schwarzer M, Doenst T, Heinze HJ, Lessmann V, Vielhaber S, Kunz WS, Gellerich FN. Cytosolic, but not matrix, calcium is essential for adjustment of mitochondrial pyruvate supply. J Biol Chem. 2020 04 03; 295(14):4383-4397. PMID: 32094224.
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    8. Subhash S, Kalmbach N, Wegner F, Petri S, Glomb T, Dittrich-Breiholz O, Huang C, Bali KK, Kunz WS, Samii A, Bertalanffy H, Kanduri C, Kar S. Transcriptome-wide Profiling of Cerebral Cavernous Malformations Patients Reveal Important Long noncoding RNA molecular signatures. Sci Rep. 2019 12 03; 9(1):18203. PMID: 31796831.
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    9. Brenner D, Baumgartner T, von Spiczak S, Lewerenz J, Weis R, Grimmer A, Gaspirova P, Wurster CD, Kunz WS, Wagner J, Minassian BA, Elger CE, Ludolph AC, Biskup S, Döcker D. Genotypes and phenotypes of patients with Lafora disease living in Germany. Neurol Res Pract. 2019; 1. PMID: 32587944.
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    10. Heavin SB, McCormack M, Wolking S, Slattery L, Walley N, Avbersek A, Novy J, Sinha SR, Radtke R, Doherty C, Auce P, Craig J, Johnson MR, Koeleman BPC, Krause R, Kunz WS, Marson AG, O'Brien TJ, Sander JW, Sills GJ, Stefansson H, Striano P, Zara F, Depondt C, Sisodiya S, Goldstein D, Lerche H, Cavalleri GL, Delanty N. Genomic and clinical predictors of lacosamide response in refractory epilepsies. Epilepsia Open. 2019 Dec; 4(4):563-571. PMID: 31819912.
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    11. Annis S, Fleischmann Z, Khrapko M, Franco M, Wasko K, Woods D, Kunz WS, Ellis P, Khrapko K. Quasi-Mendelian paternal inheritance of mitochondrial DNA: A notorious artifact, or anticipated behavior? Proc Natl Acad Sci U S A. 2019 07 23; 116(30):14797-14798. PMID: 31311874.
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    12. Silvennoinen K, de Lange N, Zagaglia S, Balestrini S, Androsova G, Wassenaar M, Auce P, Avbersek A, Becker F, Berghuis B, Campbell E, Coppola A, Francis B, Wolking S, Cavalleri GL, Craig J, Delanty N, Johnson MR, Koeleman BPC, Kunz WS, Lerche H, Marson AG, O'Brien TJ, Sander JW, Sills GJ, Striano P, Zara F, van der Palen J, Krause R, Depondt C, Sisodiya SM. Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy. Epilepsia Open. 2019 Sep; 4(3):420-430. PMID: 31440723.
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    13. Torregrosa-Muñumer R, Hangas A, Goffart S, Blei D, Zsurka G, Griffith J, Kunz WS, Pohjoismäki JLO. Replication fork rescue in mammalian mitochondria. Sci Rep. 2019 06 19; 9(1):8785. PMID: 31217442.
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    14. Schlapakow E, Peeva V, Zsurka G, Jeub M, Wabbels B, Kornblum C, Kunz WS. Distinct segregation of the pathogenic m.5667G>A mitochondrial tRNAAsn mutation in extraocular and skeletal muscle in chronic progressive external ophthalmoplegia. Neuromuscul Disord. 2019 05; 29(5):358-367. PMID: 30962064.
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    15. Schulz H, Ruppert AK, Zara F, Madia F, Iacomino M, S Vari M, Balagura G, Minetti C, Striano P, Bianchi A, Marini C, Guerrini R, Weber YG, Becker F, Lerche H, Kapser C, Schankin CJ, Kunz WS, Møller RS, Oliver KL, Bellows ST, Mullen SA, Berkovic SF, Scheffer IE, Caglayan H, Ozbek U, Hoffmann P, Schramm S, Tsortouktzidis D, Becker AJ, Sander T. No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsy. Epilepsia. 2019 05; 60(5):e31-e36. PMID: 30719712.
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    16. Nass RD, Hansen N, Quesada C, Rüber T, Kornblum C, Zsurka G, Hermann P, Becker A, Gärtner F, Hattingen E, Block W, Steidl E, Elger CE, Surges R, Kunz WS. Retinoencephalopathy with occipital lobe epilepsy in an OPA-1 mutation carrier. Seizure. 2019 Mar; 66:1-3. PMID: 30738307.
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    17. Berghuis B, Stapleton C, Sonsma ACM, Hulst J, de Haan GJ, Lindhout D, Demurtas R, Krause R, Depondt C, Kunz WS, Zara F, Striano P, Craig J, Auce P, Marson AG, Stefansson H, O'Brien TJ, Johnson MR, Sills GJ, Wolking S, Lerche H, Sisodiya SM, Sander JW, Cavalleri GL, Koeleman BPC, McCormack M. A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. Epilepsia Open. 2019 Mar; 4(1):102-109. PMID: 30868120.
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    18. May P, Girard S, Harrer M, Bobbili DR, Schubert J, Wolking S, Becker F, Lachance-Touchette P, Meloche C, Gravel M, Niturad CE, Knaus J, De Kovel C, Toliat M, Polvi A, Iacomino M, Guerrero-López R, Baulac S, Marini C, Thiele H, Altmüller J, Jabbari K, Ruppert AK, Jurkowski W, Lal D, Rusconi R, Cestèle S, Terragni B, Coombs ID, Reid CA, Striano P, Caglayan H, Siren A, Everett K, Møller RS, Hjalgrim H, Muhle H, Helbig I, Kunz WS, Weber YG, Weckhuysen S, Jonghe P, Sisodiya SM, Nabbout R, Franceschetti S, Coppola A, Vari MS, Kasteleijn-Nolst Trenité D, Baykan B, Ozbek U, Bebek N, Klein KM, Rosenow F, Nguyen DK, Dubeau F, Carmant L, Lortie A, Desbiens R, Clément JF, Cieuta-Walti C, Sills GJ, Auce P, Francis B, Johnson MR, Marson AG, Berghuis B, Sander JW, Avbersek A, McCormack M, Cavalleri GL, Delanty N, Depondt C, Krenn M, Zimprich F, Peter S, Nikanorova M, Kraaij R, van Rooij J, Balling R, Ikram MA, Uitterlinden AG, Avanzini G, Schorge S, Petrou S, Mantegazza M, Sander T, LeGuern E, Serratosa JM, Koeleman BPC, Palotie A, Lehesjoki AE, Nothnagel M, Nürnberg P, Maljevic S, Zara F, Cossette P, Krause R, Lerche H. Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study. Lancet Neurol. 2018 08; 17(8):699-708. PMID: 30033060.
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    19. Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, Lee PH, Turley P, Grenier-Boley B, Chouraki V, Kamatani Y, Berr C, Letenneur L, Hannequin D, Amouyel P, Boland A, Deleuze JF, Duron E, Vardarajan BN, Reitz C, Goate AM, Huentelman MJ, Kamboh MI, Larson EB, Rogaeva E, St George-Hyslop P, Hakonarson H, Kukull WA, Farrer LA, Barnes LL, Beach TG, Demirci FY, Head E, Hulette CM, Jicha GA, Kauwe JSK, Kaye JA, Leverenz JB, Levey AI, Lieberman AP, Pankratz VS, Poon WW, Quinn JF, Saykin AJ, Schneider LS, Smith AG, Sonnen JA, Stern RA, Van Deerlin VM, Van Eldik LJ, Harold D, Russo G, Rubinsztein DC, Bayer A, Tsolaki M, Proitsi P, Fox NC, Hampel H, Owen MJ, Mead S, Passmore P, Morgan K, Nöthen MM, Rossor M, Lupton MK, Hoffmann P, Kornhuber J, Lawlor B, McQuillin A, Al-Chalabi A, Bis JC, Ruiz A, Boada M, Seshadri S, Beiser A, Rice K, van der Lee SJ, De Jager PL, Geschwind DH, Riemenschneider M, Riedel-Heller S, Rotter JI, Ransmayr G, Hyman BT, Cruchaga C, Alegret M, Winsvold B, Palta P, Farh KH, Cuenca-Leon E, Furlotte N, Kurth T, Ligthart L, Terwindt GM, Freilinger T, Ran C, Gordon SD, Borck G, Adams HHH, Lehtimäki T, Wedenoja J, Buring JE, Schürks M, Hrafnsdottir M, Hottenga JJ, Penninx B, Artto V, Kaunisto M, Vepsäläinen S, Martin NG, Montgomery GW, Kurki MI, Hämäläinen E, Huang H, Huang J, Sandor C, Webber C, Muller-Myhsok B, Schreiber S, Salomaa V, Loehrer E, Göbel H, Macaya A, Pozo-Rosich P, Hansen T, Werge T, Kaprio J, Metspalu A, Kubisch C, Ferrari MD, Belin AC, van den Maagdenberg AMJM, Zwart JA, Boomsma D, Eriksson N, Olesen J, Chasman DI, Nyholt DR, Avbersek A, Baum L, Berkovic S, Bradfield J, Buono RJ, Catarino CB, Cossette P, De Jonghe P, Depondt C, Dlugos D, Ferraro TN, French J, Hjalgrim H, Jamnadas-Khoda J, Kälviäinen R, Kunz WS, Lerche H, Leu C, Lindhout D, Lo W, Lowenstein D, McCormack M, Møller RS, Molloy A, Ng PW, Oliver K, Privitera M, Radtke R, Ruppert AK, Sander T, Schachter S, Schankin C, Scheffer I, Schoch S, Sisodiya SM, Smith P, Sperling M, Striano P, Surges R, Thomas GN, Visscher F, Whelan CD, Zara F, Heinzen EL, Marson A, Becker F, Stroink H, Zimprich F, Gasser T, Gibbs R, Heutink P, Martinez M, Morris HR, Sharma M, Ryten M, Mok KY, Pulit S, Bevan S, Holliday E, Attia J, Battey T, Boncoraglio G, Thijs V, Chen WM, Mitchell B, Rothwell P, Sharma P, Sudlow C, Vicente A, Markus H, Kourkoulis C, Pera J, Raffeld M, Silliman S, Boraska Perica V, Thornton LM, Huckins LM, William Rayner N, Lewis CM, Gratacos M, Rybakowski F, Keski-Rahkonen A, Raevuori A, Hudson JI, Reichborn-Kjennerud T, Monteleone P, Karwautz A, Mannik K, Baker JH, O'Toole JK, Trace SE, Davis OSP, Helder SG, Ehrlich S, Herpertz-Dahlmann B, Danner UN, van Elburg AA, Clementi M, Forzan M, Docampo E, Lissowska J, Hauser J, Tortorella A, Maj M, Gonidakis F, Tziouvas K, Papezova H, Yilmaz Z, Wagner G, Cohen-Woods S, Herms S, Julià A, Rabionet R, Dick DM, Ripatti S, Andreassen OA, Espeseth T, Lundervold AJ, Steen VM, Pinto D, Scherer SW, Aschauer H, Schosser A, Alfredsson L, Padyukov L, Halmi KA, Mitchell J, Strober M, Bergen AW, Kaye W, Szatkiewicz JP, Cormand B, Ramos-Quiroga JA, Sánchez-Mora C, Ribasés M, Casas M, Hervas A, Arranz MJ, Haavik J, Zayats T, Johansson S, Williams N, Dempfle A, Rothenberger A, Kuntsi J, Oades RD, Banaschewski T, Franke B, Buitelaar JK, Arias Vasquez A, Doyle AE, Reif A, Lesch KP, Freitag C, Rivero O, Palmason H, Romanos M, Langley K, Rietschel M, Witt SH, Dalsgaard S, Børglum AD, Waldman I, Wilmot B, Molly N, Bau CHD, Crosbie J, Schachar R, Loo SK, McGough JJ, Grevet EH, Medland SE, Robinson E, Weiss LA, Bacchelli E, Bailey A, Bal V, Battaglia A, Betancur C, Bolton P, Cantor R, Celestino-Soper P, Dawson G, De Rubeis S, Duque F, Green A, Klauck SM, Leboyer M, Levitt P, Maestrini E, Mane S, De-Luca DM, Parr J, Regan R, Reichenberg A, Sandin S, Vorstman J, Wassink T, Wijsman E, Cook E, Santangelo S, Delorme R, et al. Analysis of shared heritability in common disorders of the brain. Science. 2018 06 22; 360(6395). PMID: 29930110.
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    20. Peeva V, Blei D, Trombly G, Corsi S, Szukszto MJ, Rebelo-Guiomar P, Gammage PA, Kudin AP, Becker C, Altmüller J, Minczuk M, Zsurka G, Kunz WS. Linear mitochondrial DNA is rapidly degraded by components of the replication machinery. Nat Commun. 2018 04 30; 9(1):1727. PMID: 29712893.
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    21. Zsurka G, Peeva V, Kotlyar A, Kunz WS. Is There Still Any Role for Oxidative Stress in Mitochondrial DNA-Dependent Aging? Genes (Basel). 2018 Mar 21; 9(4). PMID: 29561808.
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    22. Augustynek B, Koprowski P, Rotko D, Kunz WS, Szewczyk A, Kulawiak B. Mitochondrial BK Channel Openers CGS7181 and CGS7184 Exhibit Cytotoxic Properties. Int J Mol Sci. 2018 Jan 25; 19(2). PMID: 29370072.
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    23. McCormack M, Gui H, Ingason A, Speed D, Wright GEB, Zhang EJ, Secolin R, Yasuda C, Kwok M, Wolking S, Becker F, Rau S, Avbersek A, Heggeli K, Leu C, Depondt C, Sills GJ, Marson AG, Auce P, Brodie MJ, Francis B, Johnson MR, Koeleman BPC, Striano P, Coppola A, Zara F, Kunz WS, Sander JW, Lerche H, Klein KM, Weckhuysen S, Krenn M, Gudmundsson LJ, Stefánsson K, Krause R, Shear N, Ross CJD, Delanty N, Pirmohamed M, Carleton BC, Cendes F, Lopes-Cendes I, Liao WP, O'Brien TJ, Sisodiya SM, Cherny S, Kwan P, Baum L, Cavalleri GL. Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients. Neurology. 2018 01 23; 90(4):e332-e341. PMID: 29288229.
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    24. Kovács R, Kunz WS. Metabolic Epilepsies-Commemorative Issue in Honor of Professor Uwe Heinemann. Int J Mol Sci. 2017 Nov 22; 18(11). PMID: 29165369.
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    25. Kudin AP, Mawasi H, Eisenkraft A, Elger CE, Bialer M, Kunz WS. Mitochondrial Liver Toxicity of Valproic Acid and Its Acid Derivatives Is Related to Inhibition of α-Lipoamide Dehydrogenase. Int J Mol Sci. 2017 Sep 06; 18(9). PMID: 28878165.
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    26. Androsova G, Krause R, Borghei M, Wassenaar M, Auce P, Avbersek A, Becker F, Berghuis B, Campbell E, Coppola A, Francis B, Wolking S, Cavalleri GL, Craig J, Delanty N, Koeleman BPC, Kunz WS, Lerche H, Marson AG, Sander JW, Sills GJ, Striano P, Zara F, Sisodiya SM, Depondt C. Comparative effectiveness of antiepileptic drugs in patients with mesial temporal lobe epilepsy with hippocampal sclerosis. Epilepsia. 2017 10; 58(10):1734-1741. PMID: 28857179.
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    27. Becker F, Reid CA, Hallmann K, Tae HS, Phillips AM, Teodorescu G, Weber YG, Kleefuss-Lie A, Elger C, Perez-Reyes E, Petrou S, Kunz WS, Lerche H, Maljevic S. Functional variants in HCN4 and CACNA1H may contribute to genetic generalized epilepsy. Epilepsia Open. 2017 09; 2(3):334-342. PMID: 29588962.
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    28. Schreiber S, Debska-Vielhaber G, Abdulla S, Machts J, Schreiber F, Kropf S, KÖrtvelyessy P, KÖrner S, Kollewe K, Petri S, Dengler R, Kunz WS, Nestor PJ, Vielhaber S. Peripheral nerve atrophy together with higher cerebrospinal fluid progranulin indicate axonal damage in amyotrophic lateral sclerosis. Muscle Nerve. 2018 02; 57(2):273-278. PMID: 28472860.
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    29. Reimann J, Lehmann D, Hardy SA, Falkous G, Knowles CV, Jones RL, Kunz WS, Taylor RW, Kornblum C. Camptocormia and shuffling gait due to a novel MT-TV mutation: Diagnostic pitfalls. Neurol Genet. 2017 Jun; 3(3):e147. PMID: 28396884.
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    30. Kudin AP, Baron G, Zsurka G, Hampel KG, Elger CE, Grote A, Weber Y, Lerche H, Thiele H, Nürnberg P, Schulz H, Ruppert AK, Sander T, Cheng Q, Arnér ES, Schomburg L, Seeher S, Fradejas-Villar N, Schweizer U, Kunz WS. Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsy. Free Radic Biol Med. 2017 05; 106:270-277. PMID: 28232204.
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    31. Augustynek B, Kunz WS, Szewczyk A. Guide to the Pharmacology of Mitochondrial Potassium Channels. Handb Exp Pharmacol. 2017; 240:103-127. PMID: 27838853.
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    32. Hansen N, Widman G, Hattingen E, Elger CE, Kunz WS. Mesial temporal lobe epilepsy associated with KCNT1 mutation. Seizure. 2017 Feb; 45:181-183. PMID: 28081520.
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    33. Winter L, Wittig I, Peeva V, Eggers B, Heidler J, Chevessier F, Kley RA, Barkovits K, Strecker V, Berwanger C, Herrmann H, Marcus K, Kornblum C, Kunz WS, Schröder R, Clemen CS. Mutant desmin substantially perturbs mitochondrial morphology, function and maintenance in skeletal muscle tissue. Acta Neuropathol. 2016 09; 132(3):453-73. PMID: 27393313.
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    34. Lenk GM, Szymanska K, Debska-Vielhaber G, Rydzanicz M, Walczak A, Bekiesinska-Figatowska M, Vielhaber S, Hallmann K, Stawinski P, Buehring S, Hsu DA, Kunz WS, Meisler MH, Ploski R. Biallelic Mutations of VAC14 in Pediatric-Onset Neurological Disease. Am J Hum Genet. 2016 Jul 07; 99(1):188-94. PMID: 27292112.
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    35. Lal D, Reinthaler EM, Dejanovic B, May P, Thiele H, Lehesjoki AE, Schwarz G, Riesch E, Ikram MA, van Duijn CM, Uitterlinden AG, Hofman A, Steinböck H, Gruber-Sedlmayr U, Neophytou B, Zara F, Hahn A, Gormley P, Becker F, Weber YG, Cilio MR, Kunz WS, Krause R, Zimprich F, Lemke JR, Nürnberg P, Sander T, Lerche H, Neubauer BA. Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes. PLoS One. 2016; 11(3):e0150426. PMID: 26990884.
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    36. Volmering E, Niehusmann P, Peeva V, Grote A, Zsurka G, Altmüller J, Nürnberg P, Becker AJ, Schoch S, Elger CE, Kunz WS. Neuropathological signs of inflammation correlate with mitochondrial DNA deletions in mesial temporal lobe epilepsy. Acta Neuropathol. 2016 08; 132(2):277-288. PMID: 26993140.
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    37. Hallmann K, Kudin AP, Zsurka G, Kornblum C, Reimann J, Stüve B, Waltz S, Hattingen E, Thiele H, Nürnberg P, Rüb C, Voos W, Kopatz J, Neumann H, Kunz WS. Loss of the smallest subunit of cytochrome c oxidase, COX8A, causes Leigh-like syndrome and epilepsy. Brain. 2016 Feb; 139(Pt 2):338-45. PMID: 26685157.
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    38. Zsurka G, Kunz WS. Mitochondrial dysfunction and seizures: the neuronal energy crisis. Lancet Neurol. 2015 Sep; 14(9):956-66. PMID: 26293567.
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    39. Lal D, Pernhorst K, Klein KM, Reif P, Tozzi R, Toliat MR, Winterer G, Neubauer B, Nürnberg P, Rosenow F, Becker F, Lerche H, Kunz WS, Kurki MI, Hoffmann P, Becker AJ, Perucca E, Zara F, Sander T, Weber YG. Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy. Epilepsia. 2015 Sep; 56(9):e129-33. PMID: 26174448.
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    40. Lal D, Ruppert AK, Trucks H, Schulz H, de Kovel CG, Kasteleijn-Nolst Trenité D, Sonsma AC, Koeleman BP, Lindhout D, Weber YG, Lerche H, Kapser C, Schankin CJ, Kunz WS, Surges R, Elger CE, Gaus V, Schmitz B, Helbig I, Muhle H, Stephani U, Klein KM, Rosenow F, Neubauer BA, Reinthaler EM, Zimprich F, Feucht M, Møller RS, Hjalgrim H, De Jonghe P, Suls A, Lieb W, Franke A, Strauch K, Gieger C, Schurmann C, Schminke U, Nürnberg P, Sander T. Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies. PLoS Genet. 2015 May; 11(5):e1005226. PMID: 25950944.
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    41. Baris OR, Ederer S, Neuhaus JF, von Kleist-Retzow JC, Wunderlich CM, Pal M, Wunderlich FT, Peeva V, Zsurka G, Kunz WS, Hickethier T, Bunck AC, Stöckigt F, Schrickel JW, Wiesner RJ. Mosaic Deficiency in Mitochondrial Oxidative Metabolism Promotes Cardiac Arrhythmia during Aging. Cell Metab. 2015 May 05; 21(5):667-77. PMID: 25955204.
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    42. Becker F, Schubert J, Weckhuysen S, Suls A, Grüninger S, Korn-Merker E, Hofmann-Peters A, Sperner J, Cross H, Hallmann K, Elger CE, Kunz WS, Madeleyen R, Lerche H, Weber YG. Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet? Epilepsy Res. 2015 Aug; 114:47-51. PMID: 26088884.
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    43. Müller-Höcker J, Schäfer S, Krebs S, Blum H, Zsurka G, Kunz WS, Prokisch H, Seibel P, Jung A. Oxyphil cell metaplasia in the parathyroids is characterized by somatic mitochondrial DNA mutations in NADH dehydrogenase genes and cytochrome c oxidase activity-impairing genes. Am J Pathol. 2014 Nov; 184(11):2922-35. PMID: 25418474.
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    44. Hallmann K, Zsurka G, Moskau-Hartmann S, Kirschner J, Korinthenberg R, Ruppert AK, Ozdemir O, Weber Y, Becker F, Lerche H, Elger CE, Thiele H, Nürnberg P, Sander T, Kunz WS. A homozygous splice-site mutation in CARS2 is associated with progressive myoclonic epilepsy. Neurology. 2014 Dec 02; 83(23):2183-7. PMID: 25361775.
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    45. Salar S, Maslarova A, Lippmann K, Nichtweiss J, Weissberg I, Sheintuch L, Kunz WS, Shorer Z, Friedman A, Heinemann U. Blood-brain barrier dysfunction can contribute to pharmacoresistance of seizures. Epilepsia. 2014 Aug; 55(8):1255-63. PMID: 24995798.
      Citations:    
    46. Nicholls TJ, Zsurka G, Peeva V, Schöler S, Szczesny RJ, Cysewski D, Reyes A, Kornblum C, Sciacco M, Moggio M, Dziembowski A, Kunz WS, Minczuk M. Linear mtDNA fragments and unusual mtDNA rearrangements associated with pathological deficiency of MGME1 exonuclease. Hum Mol Genet. 2014 Dec 01; 23(23):6147-62. PMID: 24986917.
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    47. Kukat A, Dogan SA, Edgar D, Mourier A, Jacoby C, Maiti P, Mauer J, Becker C, Senft K, Wibom R, Kudin AP, Hultenby K, Flögel U, Rosenkranz S, Ricquier D, Kunz WS, Trifunovic A. Loss of UCP2 attenuates mitochondrial dysfunction without altering ROS production and uncoupling activity. PLoS Genet. 2014 Jun; 10(6):e1004385. PMID: 24945157.
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    48. Augustynek B, Kudin AP, Bednarczyk P, Szewczyk A, Kunz WS. Hemin inhibits the large conductance potassium channel in brain mitochondria: a putative novel mechanism of neurodegeneration. Exp Neurol. 2014 Jul; 257:70-5. PMID: 24792919.
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    49. Dejanovic B, Lal D, Catarino CB, Arjune S, Belaidi AA, Trucks H, Vollmar C, Surges R, Kunz WS, Motameny S, Altmüller J, Köhler A, Neubauer BA, Nürnberg P, Noachtar S, Schwarz G, Sander T. Exonic microdeletions of the gephyrin gene impair GABAergic synaptic inhibition in patients with idiopathic generalized epilepsy. Neurobiol Dis. 2014 Jul; 67:88-96. PMID: 24561070.
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    50. Otáhal J, Folbergrová J, Kovacs R, Kunz WS, Maggio N. Epileptic focus and alteration of metabolism. Int Rev Neurobiol. 2014; 114:209-43. PMID: 25078504.
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    51. Claude J, Linnartz-Gerlach B, Kudin AP, Kunz WS, Neumann H. Microglial CD33-related Siglec-E inhibits neurotoxicity by preventing the phagocytosis-associated oxidative burst. J Neurosci. 2013 Nov 13; 33(46):18270-6. PMID: 24227736.
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    52. Kasperaviciute D, Catarino CB, Matarin M, Leu C, Novy J, Tostevin A, Leal B, Hessel EV, Hallmann K, Hildebrand MS, Dahl HH, Ryten M, Trabzuni D, Ramasamy A, Alhusaini S, Doherty CP, Dorn T, Hansen J, Krämer G, Steinhoff BJ, Zumsteg D, Duncan S, Kälviäinen RK, Eriksson KJ, Kantanen AM, Pandolfo M, Gruber-Sedlmayr U, Schlachter K, Reinthaler EM, Stogmann E, Zimprich F, Théâtre E, Smith C, O'Brien TJ, Meng Tan K, Petrovski S, Robbiano A, Paravidino R, Zara F, Striano P, Sperling MR, Buono RJ, Hakonarson H, Chaves J, Costa PP, Silva BM, da Silva AM, de Graan PN, Koeleman BP, Becker A, Schoch S, von Lehe M, Reif PS, Rosenow F, Becker F, Weber Y, Lerche H, Rössler K, Buchfelder M, Hamer HM, Kobow K, Coras R, Blumcke I, Scheffer IE, Berkovic SF, Weale ME, Delanty N, Depondt C, Cavalleri GL, Kunz WS, Sisodiya SM. Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A. Brain. 2013 Oct; 136(Pt 10):3140-50. PMID: 24014518.
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    53. Schorlemmer K, Bauer S, Belke M, Hermsen A, Klein KM, Reif PS, Oertel WH, Kunz WS, Knake S, Rosenow F, Strzelczyk A. Sustained seizure remission on perampanel in progressive myoclonic epilepsy (Lafora disease). Epilepsy Behav Case Rep. 2013; 1:118-21. PMID: 25667843.
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    54. Zsurka G, Becker F, Heinen M, Gdynia HJ, Lerche H, Kunz WS, Weber YG. Mutation in the mitochondrial tRNA(Ile) gene causes progressive myoclonus epilepsy. Seizure. 2013 Jul; 22(6):483-6. PMID: 23601850.
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    55. Schreiber S, Oldag A, Kornblum C, Kollewe K, Kropf S, Schoenfeld A, Feistner H, Jakubiczka S, Kunz WS, Scherlach C, Tempelmann C, Mawrin C, Dengler R, Schreiber F, Goertler M, Vielhaber S. Sonography of the median nerve in CMT1A, CMT2A, CMTX, and HNPP. Muscle Nerve. 2013 Mar; 47(3):385-95. PMID: 23381770.
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    56. Lal D, Trucks H, Møller RS, Hjalgrim H, Koeleman BP, de Kovel CG, Visscher F, Weber YG, Lerche H, Becker F, Schankin CJ, Neubauer BA, Surges R, Kunz WS, Zimprich F, Franke A, Illig T, Ried JS, Leu C, Nürnberg P, Sander T. Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy. Epilepsia. 2013 Feb; 54(2):265-71. PMID: 23350840.
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    57. Zsurka G, Kunz WS. Mitochondrial involvement in neurodegenerative diseases. IUBMB Life. 2013 Mar; 65(3):263-72. PMID: 23341346.
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    58. Kornblum C, Nicholls TJ, Haack TB, Schöler S, Peeva V, Danhauser K, Hallmann K, Zsurka G, Rorbach J, Iuso A, Wieland T, Sciacco M, Ronchi D, Comi GP, Moggio M, Quinzii CM, DiMauro S, Calvo SE, Mootha VK, Klopstock T, Strom TM, Meitinger T, Minczuk M, Kunz WS, Prokisch H. Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease. Nat Genet. 2013 Feb; 45(2):214-9. PMID: 23313956.
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    59. Møller RS, Weber YG, Klitten LL, Trucks H, Muhle H, Kunz WS, Mefford HC, Franke A, Kautza M, Wolf P, Dennig D, Schreiber S, Rückert IM, Wichmann HE, Ernst JP, Schurmann C, Grabe HJ, Tommerup N, Stephani U, Lerche H, Hjalgrim H, Helbig I, Sander T. Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy. Epilepsia. 2013 Feb; 54(2):256-64. PMID: 23294455.
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    60. Tschampa HJ, Urbach H, Greschus S, Kunz WS, Kornblum C. Neuroimaging characteristics in mitochondrial encephalopathies associated with the m.3243A>G MTTL1 mutation. J Neurol. 2013 Apr; 260(4):1071-80. PMID: 23196335.
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    61. Steffens M, Leu C, Ruppert AK, Zara F, Striano P, Robbiano A, Capovilla G, Tinuper P, Gambardella A, Bianchi A, La Neve A, Crichiutti G, de Kovel CG, Kasteleijn-Nolst Trenité D, de Haan GJ, Lindhout D, Gaus V, Schmitz B, Janz D, Weber YG, Becker F, Lerche H, Steinhoff BJ, Kleefuß-Lie AA, Kunz WS, Surges R, Elger CE, Muhle H, von Spiczak S, Ostertag P, Helbig I, Stephani U, Møller RS, Hjalgrim H, Dibbens LM, Bellows S, Oliver K, Mullen S, Scheffer IE, Berkovic SF, Everett KV, Gardiner MR, Marini C, Guerrini R, Lehesjoki AE, Siren A, Guipponi M, Malafosse A, Thomas P, Nabbout R, Baulac S, Leguern E, Guerrero R, Serratosa JM, Reif PS, Rosenow F, Mörzinger M, Feucht M, Zimprich F, Kapser C, Schankin CJ, Suls A, Smets K, De Jonghe P, Jordanova A, Caglayan H, Yapici Z, Yalcin DA, Baykan B, Bebek N, Ozbek U, Gieger C, Wichmann HE, Balschun T, Ellinghaus D, Franke A, Meesters C, Becker T, Wienker TF, Hempelmann A, Schulz H, Rüschendorf F, Leber M, Pauck SM, Trucks H, Toliat MR, Nürnberg P, Avanzini G, Koeleman BP, Sander T. Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. Hum Mol Genet. 2012 Dec 15; 21(24):5359-72. PMID: 22949513.
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    62. Vielhaber S, Debska-Vielhaber G, Peeva V, Schoeler S, Kudin AP, Minin I, Schreiber S, Dengler R, Kollewe K, Zuschratter W, Kornblum C, Zsurka G, Kunz WS. Mitofusin 2 mutations affect mitochondrial function by mitochondrial DNA depletion. Acta Neuropathol. 2013 Feb; 125(2):245-56. PMID: 22926664.
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    63. Jennissen K, Siegel F, Liebig-Gonglach M, Hermann MR, Kipschull S, van Dooren S, Kunz WS, Fässler R, Pfeifer A. A VASP-Rac-soluble guanylyl cyclase pathway controls cGMP production in adipocytes. Sci Signal. 2012 Aug 28; 5(239):ra62. PMID: 22932701.
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    64. Helmstaedter C, Mihov Y, Toliat MR, Thiele H, Nuernberg P, Schoch S, Surges R, Elger CE, Kunz WS, Hurlemann R. Genetic variation in dopaminergic activity is associated with the risk for psychiatric side effects of levetiracetam. Epilepsia. 2013 Jan; 54(1):36-44. PMID: 22881836.
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    65. Franko A, von Kleist-Retzow JC, Böse M, Sanchez-Lasheras C, Brodesser S, Krut O, Kunz WS, Wiedermann D, Hoehn M, Stöhr O, Moll L, Freude S, Krone W, Schubert M, Wiesner RJ. Complete failure of insulin-transmitted signaling, but not obesity-induced insulin resistance, impairs respiratory chain function in muscle. J Mol Med (Berl). 2012 Oct; 90(10):1145-60. PMID: 22411022.
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    66. Kudin AP, Augustynek B, Lehmann AK, Kovács R, Kunz WS. The contribution of thioredoxin-2 reductase and glutathione peroxidase to H(2)O(2) detoxification of rat brain mitochondria. Biochim Biophys Acta. 2012 Oct; 1817(10):1901-6. PMID: 22398128.
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    67. Auburger G, Klinkenberg M, Drost J, Marcus K, Morales-Gordo B, Kunz WS, Brandt U, Broccoli V, Reichmann H, Gispert S, Jendrach M. Primary skin fibroblasts as a model of Parkinson's disease. Mol Neurobiol. 2012 Aug; 46(1):20-7. PMID: 22350618.
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    68. Leu C, de Kovel CG, Zara F, Striano P, Pezzella M, Robbiano A, Bianchi A, Bisulli F, Coppola A, Giallonardo AT, Beccaria F, Trenité DK, Lindhout D, Gaus V, Schmitz B, Janz D, Weber YG, Becker F, Lerche H, Kleefuss-Lie AA, Hallman K, Kunz WS, Elger CE, Muhle H, Stephani U, Møller RS, Hjalgrim H, Mullen S, Scheffer IE, Berkovic SF, Everett KV, Gardiner MR, Marini C, Guerrini R, Lehesjoki AE, Siren A, Nabbout R, Baulac S, Leguern E, Serratosa JM, Rosenow F, Feucht M, Unterberger I, Covanis A, Suls A, Weckhuysen S, Kaneva R, Caglayan H, Turkdogan D, Baykan B, Bebek N, Ozbek U, Hempelmann A, Schulz H, Rüschendorf F, Trucks H, Nürnberg P, Avanzini G, Koeleman BP, Sander T. Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies. Epilepsia. 2012 Feb; 53(2):308-18. PMID: 22242659.
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    69. Becker B, Mihov Y, Scheele D, Kendrick KM, Feinstein JS, Matusch A, Aydin M, Reich H, Urbach H, Oros-Peusquens AM, Shah NJ, Kunz WS, Schlaepfer TE, Zilles K, Maier W, Hurlemann R. Fear processing and social networking in the absence of a functional amygdala. Biol Psychiatry. 2012 Jul 01; 72(1):70-7. PMID: 22218285.
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    70. Hopfner F, Schormair B, Knauf F, Berthele A, Tölle TR, Baron R, Maier C, Treede RD, Binder A, Sommer C, Maihöfner C, Kunz W, Zimprich F, Heemann U, Pfeufer A, Näbauer M, Kääb S, Nowak B, Gieger C, Lichtner P, Trenkwalder C, Oexle K, Winkelmann J. Novel SCARB2 mutation in action myoclonus-renal failure syndrome and evaluation of SCARB2 mutations in isolated AMRF features. BMC Neurol. 2011 Oct 27; 11:134. PMID: 22032306.
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    71. Malinska D, Kudin AP, Bejtka M, Kunz WS. Changes in mitochondrial reactive oxygen species synthesis during differentiation of skeletal muscle cells. Mitochondrion. 2012 Jan; 12(1):144-8. PMID: 21782978.
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    72. Otte DM, Sommersberg B, Kudin A, Guerrero C, Albayram O, Filiou MD, Frisch P, Yilmaz O, Drews E, Turck CW, Bilkei-Gorzó A, Kunz WS, Beck H, Zimmer A. N-acetyl cysteine treatment rescues cognitive deficits induced by mitochondrial dysfunction in G72/G30 transgenic mice. Neuropsychopharmacology. 2011 Oct; 36(11):2233-43. PMID: 21716263.
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    73. Folbergrová J, Kunz WS. Mitochondrial dysfunction in epilepsy. Mitochondrion. 2012 Jan; 12(1):35-40. PMID: 21530687.
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    74. Niehusmann P, Surges R, von Wrede RD, Elger CE, Wellmer J, Reimann J, Urbach H, Vielhaber S, Bien CG, Kunz WS. Mitochondrial dysfunction due to Leber's hereditary optic neuropathy as a cause of visual loss during assessment for epilepsy surgery. Epilepsy Behav. 2011 Jan; 20(1):38-43. PMID: 21145289.
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    75. Stewart JD, Schoeler S, Sitarz KS, Horvath R, Hallmann K, Pyle A, Yu-Wai-Man P, Taylor RW, Samuels DC, Kunz WS, Chinnery PF. POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblasts. Biochim Biophys Acta. 2011 Mar; 1812(3):321-5. PMID: 21138766.
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    76. Zsurka G, Kunz WS. Mitochondrial dysfunction in neurological disorders with epileptic phenotypes. J Bioenerg Biomembr. 2010 Dec; 42(6):443-8. PMID: 21069442.
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    77. Zsurka G, Kudina T, Peeva V, Hallmann K, Elger CE, Khrapko K, Kunz WS. Distinct patterns of mitochondrial genome diversity in bonobos (Pan paniscus) and humans. BMC Evol Biol. 2010 Sep 02; 10:270. PMID: 20813043.
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    78. Malinska D, Kulawiak B, Wrzosek A, Kunz WS, Szewczyk A. The cytoprotective action of the potassium channel opener BMS-191095 in C2C12 myoblasts is related to the modulation of calcium homeostasis. Cell Physiol Biochem. 2010; 26(2):235-46. PMID: 20798507.
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    79. Guo X, Popadin KY, Markuzon N, Orlov YL, Kraytsberg Y, Krishnan KJ, Zsurka G, Turnbull DM, Kunz WS, Khrapko K. Repeats, longevity and the sources of mtDNA deletions: evidence from 'deletional spectra'. Trends Genet. 2010 Aug; 26(8):340-3. PMID: 20591530.
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    80. Malinska D, Kulawiak B, Kudin AP, Kovacs R, Huchzermeyer C, Kann O, Szewczyk A, Kunz WS. Complex III-dependent superoxide production of brain mitochondria contributes to seizure-related ROS formation. Biochim Biophys Acta. 2010 Jun-Jul; 1797(6-7):1163-70. PMID: 20211146.
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    81. Zsurka G, Hampel KG, Nelson I, Jardel C, Mirandola SR, Sassen R, Kornblum C, Marcorelles P, Lavoué S, Lombès A, Kunz WS. Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNA(Phe) gene. Neurology. 2010 Feb 09; 74(6):507-12. PMID: 20142618.
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    82. Malinska D, Mirandola SR, Kunz WS. Mitochondrial potassium channels and reactive oxygen species. FEBS Lett. 2010 May 17; 584(10):2043-8. PMID: 20080090.
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    83. Debska-Vielhaber G, Godlewski MM, Kicinska A, Skalska J, Kulawiak B, Piwonska M, Zablocki K, Kunz WS, Szewczyk A, Motyl T. Large-conductance K+ channel openers induce death of human glioma cells. J Physiol Pharmacol. 2009 Dec; 60(4):27-36. PMID: 20065494.
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    84. Choma K, Bednarczyk P, Koszela-Piotrowska I, Kulawiak B, Kudin A, Kunz WS, Dolowy K, Szewczyk A. Single channel studies of the ATP-regulated potassium channel in brain mitochondria. J Bioenerg Biomembr. 2009 Aug; 41(4):323-34. PMID: 19821034.
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    85. Gispert S, Ricciardi F, Kurz A, Azizov M, Hoepken HH, Becker D, Voos W, Leuner K, Müller WE, Kudin AP, Kunz WS, Zimmermann A, Roeper J, Wenzel D, Jendrach M, García-Arencíbia M, Fernández-Ruiz J, Huber L, Rohrer H, Barrera M, Reichert AS, Rüb U, Chen A, Nussbaum RL, Auburger G. Parkinson phenotype in aged PINK1-deficient mice is accompanied by progressive mitochondrial dysfunction in absence of neurodegeneration. PLoS One. 2009 Jun 03; 4(6):e5777. PMID: 19492057.
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    86. Skalska J, Bednarczyk P, Piwonska M, Kulawiak B, Wilczynski G, Dolowy K, Kudin AP, Kunz WS, Szewczyk A. Calcium ions regulate K? uptake into brain mitochondria: the evidence for a novel potassium channel. Int J Mol Sci. 2009 Mar; 10(3):1104-20. PMID: 19399240.
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    87. Kudin AP, Zsurka G, Elger CE, Kunz WS. Mitochondrial involvement in temporal lobe epilepsy. Exp Neurol. 2009 Aug; 218(2):326-32. PMID: 19268667.
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    88. Szewczyk A, Jarmuszkiewicz W, Kunz WS. Mitochondrial potassium channels. IUBMB Life. 2009 Feb; 61(2):134-43. PMID: 19165895.
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    89. Otte DM, Bilkei-Gorzó A, Filiou MD, Turck CW, Yilmaz O, Holst MI, Schilling K, Abou-Jamra R, Schumacher J, Benzel I, Kunz WS, Beck H, Zimmer A. Behavioral changes in G72/G30 transgenic mice. Eur Neuropsychopharmacol. 2009 May; 19(5):339-48. PMID: 19189879.
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    90. Frisch C, Hüsch K, Angenstein F, Kudin A, Kunz W, Elger CE, Helmstaedter C. Dose-dependent memory effects and cerebral volume changes after in utero exposure to valproate in the rat. Epilepsia. 2009 Jun; 50(6):1432-41. PMID: 19374658.
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    91. Malinska D, Kudin AP, Debska-Vielhaber G, Vielhaber S, Kunz WS. Chapter 23 Quantification of superoxide production by mouse brain and skeletal muscle mitochondria. Methods Enzymol. 2009; 456:419-37. PMID: 19348902.
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    92. Gekeler J, Zsurka G, Kunz WS, Preuss SF, Klussmann JP, Guntinas-Lichius O, Wiesner RJ. Clonal expansion of different mtDNA variants without selective advantage in solid tumors. Mutat Res. 2009 Mar 09; 662(1-2):28-32. PMID: 19114048.
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    93. Boes M, Bauer J, Urbach H, Elger CE, Frank S, Baron M, Zsurka G, Kunz WS, Kornblum C. Proof of progression over time: finally fulminant brain, muscle, and liver affection in Alpers syndrome associated with the A467T POLG1 mutation. Seizure. 2009 Apr; 18(3):232-4. PMID: 18783964.
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    94. Zsurka G, Baron M, Stewart JD, Kornblum C, Bös M, Sassen R, Taylor RW, Elger CE, Chinnery PF, Kunz WS. Clonally expanded mitochondrial DNA mutations in epileptic individuals with mutated DNA polymerase gamma. J Neuropathol Exp Neurol. 2008 Sep; 67(9):857-66. PMID: 18716558.
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    95. Paus S, Zsurka G, Baron M, Deschauer M, Bamberg C, Klockgether T, Kunz WS, Kornblum C. Apraxia of lid opening mimicking ptosis in compound heterozygosity for A467T and W748S POLG1 mutations. Mov Disord. 2008 Jul 15; 23(9):1286-8. PMID: 18546343.
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    96. Wabbels B, Ali N, Kunz WS, Roggenkämper P, Kornblum C. [Chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome : interdisciplinary diagnosis and therapy]. Ophthalmologe. 2008 Jun; 105(6):550-6. PMID: 18373100.
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    97. Mueller CF, Wassmann K, Widder JD, Wassmann S, Chen CH, Keuler B, Kudin A, Kunz WS, Nickenig G. Multidrug resistance protein-1 affects oxidative stress, endothelial dysfunction, and atherogenesis via leukotriene C4 export. Circulation. 2008 Jun 03; 117(22):2912-8. PMID: 18506003.
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    98. Kudin AP, Malinska D, Kunz WS. Sites of generation of reactive oxygen species in homogenates of brain tissue determined with the use of respiratory substrates and inhibitors. Biochim Biophys Acta. 2008 Jul-Aug; 1777(7-8):689-95. PMID: 18510942.
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    99. Skalska J, Piwonska M, Wyroba E, Surmacz L, Wieczorek R, Koszela-Piotrowska I, Zielinska J, Bednarczyk P, Dolowy K, Wilczynski GM, Szewczyk A, Kunz WS. A novel potassium channel in skeletal muscle mitochondria. Biochim Biophys Acta. 2008 Jul-Aug; 1777(7-8):651-9. PMID: 18515063.
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    100. Kulawiak B, Kudin AP, Szewczyk A, Kunz WS. BK channel openers inhibit ROS production of isolated rat brain mitochondria. Exp Neurol. 2008 Aug; 212(2):543-7. PMID: 18572168.
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    101. Konieczny P, Fuchs P, Reipert S, Kunz WS, Zeöld A, Fischer I, Paulin D, Schröder R, Wiche G. Myofiber integrity depends on desmin network targeting to Z-disks and costameres via distinct plectin isoforms. J Cell Biol. 2008 May 19; 181(4):667-81. PMID: 18490514.
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    102. Kornblum C, Zsurka G, Wiesner RJ, Schröder R, Kunz WS. Concerted action of two novel tRNA mtDNA point mutations in chronic progressive external ophthalmoplegia. Biosci Rep. 2008 Apr; 28(2):89-96. PMID: 18384291.
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    103. Kuznetsov AV, Veksler V, Gellerich FN, Saks V, Margreiter R, Kunz WS. Analysis of mitochondrial function in situ in permeabilized muscle fibers, tissues and cells. Nat Protoc. 2008; 3(6):965-76. PMID: 18536644.
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    104. Baron M, Kudin AP, Kunz WS. Mitochondrial dysfunction in neurodegenerative disorders. Biochem Soc Trans. 2007 Nov; 35(Pt 5):1228-31. PMID: 17956319.
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    105. Vielhaber S, Niessen HG, Debska-Vielhaber G, Kudin AP, Wellmer J, Kaufmann J, Schönfeld MA, Fendrich R, Willker W, Leibfritz D, Schramm J, Elger CE, Heinze HJ, Kunz WS. Subfield-specific loss of hippocampal N-acetyl aspartate in temporal lobe epilepsy. Epilepsia. 2008 Jan; 49(1):40-50. PMID: 17822430.
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    106. Koszela-Piotrowska I, Choma K, Bednarczyk P, Dolowy K, Szewczyk A, Kunz WS, Malekova L, Kominkova V, Ondrias K. Stilbene derivatives inhibit the activity of the inner mitochondrial membrane chloride channels. Cell Mol Biol Lett. 2007; 12(4):493-508. PMID: 17457523.
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    107. Niessen HG, Debska-Vielhaber G, Sander K, Angenstein F, Ludolph AC, Hilfert L, Willker W, Leibfritz D, Heinze HJ, Kunz WS, Vielhaber S. Metabolic progression markers of neurodegeneration in the transgenic G93A-SOD1 mouse model of amyotrophic lateral sclerosis. Eur J Neurosci. 2007 Mar; 25(6):1669-77. PMID: 17432958.
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    108. Zsurka G, Hampel KG, Kudina T, Kornblum C, Kraytsberg Y, Elger CE, Khrapko K, Kunz WS. Inheritance of mitochondrial DNA recombinants in double-heteroplasmic families: potential implications for phylogenetic analysis. Am J Hum Genet. 2007 Feb; 80(2):298-305. PMID: 17236134.
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    109. Hornig-Do HT, von Kleist-Retzow JC, Lanz K, Wickenhauser C, Kudin AP, Kunz WS, Wiesner RJ, Schauen M. Human epidermal keratinocytes accumulate superoxide due to low activity of Mn-SOD, leading to mitochondrial functional impairment. J Invest Dermatol. 2007 May; 127(5):1084-93. PMID: 17185981.
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    110. Wiesner RJ, Zsurka G, Kunz WS. Mitochondrial DNA damage and the aging process: facts and imaginations. Free Radic Res. 2006 Dec; 40(12):1284-94. PMID: 17090418.
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    111. Hoepken HH, Gispert S, Morales B, Wingerter O, Del Turco D, Mülsch A, Nussbaum RL, Müller K, Dröse S, Brandt U, Deller T, Wirth B, Kudin AP, Kunz WS, Auburger G. Mitochondrial dysfunction, peroxidation damage and changes in glutathione metabolism in PARK6. Neurobiol Dis. 2007 Feb; 25(2):401-11. PMID: 17141510.
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    112. Frisch C, Kudin AP, Elger CE, Kunz WS, Helmstaedter C. Amelioration of water maze performance deficits by topiramate applied during pilocarpine-induced status epilepticus is negatively dose-dependent. Epilepsy Res. 2007 Feb; 73(2):173-80. PMID: 17084066.
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    113. Linnebank M, Lutz H, Jarre E, Vielhaber S, Noelker C, Struys E, Jakobs C, Klockgether T, Evert BO, Kunz WS, Wüllner U. Binding of copper is a mechanism of homocysteine toxicity leading to COX deficiency and apoptosis in primary neurons, PC12 and SHSY-5Y cells. Neurobiol Dis. 2006 Sep; 23(3):725-30. PMID: 16876425.
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    114. Niessen HG, Angenstein F, Sander K, Kunz WS, Teuchert M, Ludolph AC, Heinze HJ, Scheich H, Vielhaber S. In vivo quantification of spinal and bulbar motor neuron degeneration in the G93A-SOD1 transgenic mouse model of ALS by T2 relaxation time and apparent diffusion coefficient. Exp Neurol. 2006 Oct; 201(2):293-300. PMID: 16740261.
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    115. Szewczyk A, Skalska J, Glab M, Kulawiak B, Malinska D, Koszela-Piotrowska I, Kunz WS. Mitochondrial potassium channels: from pharmacology to function. Biochim Biophys Acta. 2006 May-Jun; 1757(5-6):715-20. PMID: 16787636.
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    116. Vielhaber S, Kornblum C, Heinze HJ, Elger CE, Kunz WS. Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophies--a comment. Brain. 2005 Dec; 128(Pt 12):E38. PMID: 16311266.
      Citations:    
    117. Zsurka G, Kraytsberg Y, Kudina T, Kornblum C, Elger CE, Khrapko K, Kunz WS. Recombination of mitochondrial DNA in skeletal muscle of individuals with multiple mitochondrial DNA heteroplasmy. Nat Genet. 2005 Aug; 37(8):873-7. PMID: 16025113.
      Citations:    
    118. Niessen HG, Angenstein F, Vielhaber S, Frisch C, Kudin A, Elger CE, Heinze HJ, Scheich H, Kunz WS. Volumetric magnetic resonance imaging of functionally relevant structural alterations in chronic epilepsy after pilocarpine-induced status epilepticus in rats. Epilepsia. 2005 Jul; 46(7):1021-6. PMID: 16026554.
      Citations:    
    119. Skalska J, Debska G, Kunz WS, Szewczyk A. Antidiabetic sulphonylureas activate mitochondrial permeability transition in rat skeletal muscle. Br J Pharmacol. 2005 Jul; 145(6):785-91. PMID: 15895111.
      Citations:    
    120. Kudin AP, Debska-Vielhaber G, Kunz WS. Characterization of superoxide production sites in isolated rat brain and skeletal muscle mitochondria. Biomed Pharmacother. 2005 May; 59(4):163-8. PMID: 15862710.
      Citations:    
    121. Minnerop M, Kornblum C, Joe AY, Tatsch K, Kunz WS, Klockgether T, Wüllner U, Reinhardt MJ. Dopamine transporter SPECT in patients with mitochondrial disorders. J Neurol Neurosurg Psychiatry. 2005 Jan; 76(1):118-20. PMID: 15608010.
      Citations:    
    122. Kudin AP, Debska-Vielhaber G, Vielhaber S, Elger CE, Kunz WS. The mechanism of neuroprotection by topiramate in an animal model of epilepsy. Epilepsia. 2004 Dec; 45(12):1478-87. PMID: 15571505.
      Citations:    
    123. Zsurka G, Schröder R, Kornblum C, Rudolph J, Wiesner RJ, Elger CE, Kunz WS. Tissue dependent co-segregation of the novel pathogenic G12276A mitochondrial tRNALeu(CUN) mutation with the A185G D-loop polymorphism. J Med Genet. 2004 Dec; 41(12):e124. PMID: 15591266.
      Citations:    
    124. Kornblum C, Kunz WS, Klockgether T, Roggenkämper P, Schröder R. [Diagnostic value of mitochondrial DNA analysis in chronic progressive external ophthalmoplegia (CPEO)]. Klin Monbl Augenheilkd. 2004 Dec; 221(12):1057-61. PMID: 15599814.
      Citations:    
    125. Vielhaber S, Feistner H, Weis J, Kreuder J, Sailer M, Schröder JM, Kunz WS. Primary carnitine deficiency: adult onset lipid storage myopathy with a mild clinical course. J Clin Neurosci. 2004 Nov; 11(8):919-24. PMID: 15519880.
      Citations:    
    126. Okulla T, Kunz WS, Klockgether T, Schröder R, Kornblum C. Diagnostic value of mitochondrial DNA mutation analysis in juvenile unilateral ptosis. Graefes Arch Clin Exp Ophthalmol. 2005 Apr; 243(4):380-2. PMID: 15864628.
      Citations:    
    127. Winkler-Stuck K, Kirches E, Mawrin C, Dietzmann K, Lins H, Wallesch CW, Kunz WS, Wiedemann FR. Re-evaluation of the dysfunction of mitochondrial respiratory chain in skeletal muscle of patients with Parkinson's disease. J Neural Transm (Vienna). 2005 Apr; 112(4):499-518. PMID: 15340872.
      Citations:    
    128. Winkler-Stuck K, Wiedemann FR, Wallesch CW, Kunz WS. Effect of coenzyme Q10 on the mitochondrial function of skin fibroblasts from Parkinson patients. J Neurol Sci. 2004 May 15; 220(1-2):41-8. PMID: 15140604.
      Citations:    
    129. Kraytsberg Y, Schwartz M, Brown TA, Ebralidse K, Kunz WS, Clayton DA, Vissing J, Khrapko K. Recombination of human mitochondrial DNA. Science. 2004 May 14; 304(5673):981. PMID: 15143273.
      Citations:    
    130. Kunz WS, Bimpong-Buta NY, Kudin AP, Elger CE. The role of mitochondria in epilepsy: implications for neurodegenerative diseases. Toxicol Mech Methods. 2004; 14(1-2):19-23. PMID: 20021117.
      Citations:    
    131. Michel A, Knobloch J, Kunz W. P19: a female and tissue specifically expressed gene in Schistosoma mansoni, regulated by pairing with the male. Parasitology. 2003 Dec; 127(Pt 6):519-24. PMID: 14700187.
      Citations:    
    132. Kudin AP, Bimpong-Buta NY, Vielhaber S, Elger CE, Kunz WS. Characterization of superoxide-producing sites in isolated brain mitochondria. J Biol Chem. 2004 Feb 06; 279(6):4127-35. PMID: 14625276.
      Citations:    
    133. Vielhaber S, Kudin AP, Kudina TA, Stiller D, Scheich H, Schoenfeld A, Feistner H, Heinze HJ, Elger CE, Kunz WS. Hippocampal N-acetyl aspartate levels do not mirror neuronal cell densities in creatine-supplemented epileptic rats. Eur J Neurosci. 2003 Oct; 18(8):2292-300. PMID: 14622190.
      Citations:    
    134. Kuznetsov AV, Kunz WS, Saks V, Usson Y, Mazat JP, Letellier T, Gellerich FN, Margreiter R. Cryopreservation of mitochondria and mitochondrial function in cardiac and skeletal muscle fibers. Anal Biochem. 2003 Aug 15; 319(2):296-303. PMID: 12871725.
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    135. Vielhaber S, Kudin A, Winkler K, Wiedemann F, Schröder R, Feistner H, Heinze HJ, Elger CE, Kunz WS. Is there mitochondrial dysfunction in amyotrophic lateral sclerosis skeletal muscle? Ann Neurol. 2003 May; 53(5):686-7; author reply 687-8. PMID: 12731009.
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    136. Schröder R, Goudeau B, Simon MC, Fischer D, Eggermann T, Clemen CS, Li Z, Reimann J, Xue Z, Rudnik-Schöneborn S, Zerres K, van der Ven PF, Fürst DO, Kunz WS, Vicart P. On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondria. Hum Mol Genet. 2003 Mar 15; 12(6):657-69. PMID: 12620971.
      Citations:    
    137. Vielhaber S, Von Oertzen JH, Kudin AF, Schoenfeld A, Menzel C, Biersack HJ, Kral T, Elger CE, Kunz WS. Correlation of hippocampal glucose oxidation capacity and interictal FDG-PET in temporal lobe epilepsy. Epilepsia. 2003 Feb; 44(2):193-9. PMID: 12558573.
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    138. Reimann J, Kunz WS, Vielhaber S, Kappes-Horn K, Schröder R. Mitochondrial dysfunction in myofibrillar myopathy. Neuropathol Appl Neurobiol. 2003 Feb; 29(1):45-51. PMID: 12581339.
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    139. Khrapko K, Nekhaeva E, Kraytsberg Y, Kunz W. Clonal expansions of mitochondrial genomes: implications for in vivo mutational spectra. Mutat Res. 2003 Jan 28; 522(1-2):13-9. PMID: 12517407.
      Citations:    
    140. Kunz WS. Different metabolic properties of mitochondrial oxidative phosphorylation in different cell types--important implications for mitochondrial cytopathies. Exp Physiol. 2003 Jan; 88(1):149-54. PMID: 12525863.
      Citations:    
    141. von Kleist-Retzow JC, Schauseil-Zipf U, Michalk DV, Kunz WS. Mitochondrial diseases--an expanding spectrum of disorders and affected genes. Exp Physiol. 2003 Jan; 88(1):155-66. PMID: 12525864.
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    142. Debska G, Kicinska A, Skalska J, Szewczyk A, May R, Elger CE, Kunz WS. Opening of potassium channels modulates mitochondrial function in rat skeletal muscle. Biochim Biophys Acta. 2002 Dec 02; 1556(2-3):97-105. PMID: 12460666.
      Citations:    
    143. Vielhaber S, Varlamov DA, Kudina TA, Schröder R, Kappes-Horn K, Elger CE, Seibel M, Seibel P, Kunz WS. Expression pattern of mitochondrial respiratory chain enzymes in skeletal muscle of patients harboring the A3243G point mutation or large-scale deletions of mitochondrial DNA. J Neuropathol Exp Neurol. 2002 Oct; 61(10):885-95. PMID: 12387454.
      Citations:    
    144. Varlamov DA, Kudin AP, Vielhaber S, Schröder R, Sassen R, Becker A, Kunz D, Haug K, Rebstock J, Heils A, Elger CE, Kunz WS. Metabolic consequences of a novel missense mutation of the mtDNA CO I gene. Hum Mol Genet. 2002 Aug 01; 11(16):1797-805. PMID: 12140182.
      Citations:    
    145. Schröder R, Kunz WS, Rouan F, Pfendner E, Tolksdorf K, Kappes-Horn K, Altenschmidt-Mehring M, Knoblich R, van der Ven PF, Reimann J, Fürst DO, Blümcke I, Vielhaber S, Zillikens D, Eming S, Klockgether T, Uitto J, Wiche G, Rolfs A. Disorganization of the desmin cytoskeleton and mitochondrial dysfunction in plectin-related epidermolysis bullosa simplex with muscular dystrophy. J Neuropathol Exp Neurol. 2002 Jun; 61(6):520-30. PMID: 12071635.
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    146. Kudin AP, Kudina TA, Seyfried J, Vielhaber S, Beck H, Elger CE, Kunz WS. Seizure-dependent modulation of mitochondrial oxidative phosphorylation in rat hippocampus. Eur J Neurosci. 2002 Apr; 15(7):1105-14. PMID: 11982622.
      Citations:    
    147. Kunz WS. The role of mitochondria in epileptogenesis. Curr Opin Neurol. 2002 Apr; 15(2):179-84. PMID: 11923632.
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    148. Kudin A, Vielhaber S, Elger CE, Kunz WS. Differences in flux control and reserve capacity of cytochrome c oxidase (COX) in human skeletal muscle and brain suggest different metabolic effects of mild COX deficiencies. Mol Biol Rep. 2002; 29(1-2):89-92. PMID: 12241082.
      Citations:    
    149. Kunz D, Winkler K, Elger CE, Kunz WS. Functional imaging of mitochondrial redox state. Methods Enzymol. 2002; 352:135-50. PMID: 12125342.
      Citations:    
    150. Vielhaber S, Kaufmann J, Kanowski M, Sailer M, Feistner H, Tempelmann C, Elger CE, Heinze HJ, Kunz WS. Effect of creatine supplementation on metabolite levels in ALS motor cortices. Exp Neurol. 2001 Dec; 172(2):377-82. PMID: 11716561.
      Citations:    
    151. Schechtman D, Winnen R, Tarrab-Hazdai R, Ram D, Shinder V, Grevelding CG, Kunz W, Arnon R. Expression and immunolocalization of the 14-3-3 protein of Schistosoma mansoni. Parasitology. 2001 Dec; 123(Pt 6):573-82. PMID: 11814044.
      Citations:    
    152. Vielhaber S, Schröder R, Winkler K, Weis S, Sailer M, Feistner H, Heinze HJ, Schröder JM, Kunz WS. Defective mitochondrial oxidative phosphorylation in myopathies with tubular aggregates originating from sarcoplasmic reticulum. J Neuropathol Exp Neurol. 2001 Nov; 60(11):1032-40. PMID: 11706933.
      Citations:    
    153. Kunz WS. Control of oxidative phosphorylation in skeletal muscle. Biochim Biophys Acta. 2001 Mar 01; 1504(1):12-9. PMID: 11239481.
      Citations:    
    154. Kunz D, Kunz WS, Scott CS, Gressner AM. Automated CD61 immunoplatelet analysis of thrombocytopenic samples. Br J Haematol. 2001 Mar; 112(3):584-92. PMID: 11260058.
      Citations:    
    155. Kapp K, Schüssler P, Kunz W, Grevelding CG. Identification, isolation and characterization of a Fyn-like tyrosine kinase from Schistosoma mansoni. Parasitology. 2001 Mar; 122(Pt 3):317-27. PMID: 11289068.
      Citations:    
    156. Debska G, May R, Kicinska A, Szewczyk A, Elger CE, Kunz WS. Potassium channel openers depolarize hippocampal mitochondria. Brain Res. 2001 Feb 16; 892(1):42-50. PMID: 11172747.
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    157. Schwarz CS, Evert BO, Seyfried J, Schaupp M, Kunz WS, Vielhaber S, Klockgether T, Wüllner U. Overexpression of bcl-2 results in reduction of cytochrome c content and inhibition of complex I activity. Biochem Biophys Res Commun. 2001 Feb 02; 280(4):1021-7. PMID: 11162629.
      Citations:    
    158. Böhm P, Kunz W, Horny HP, Einsele H. Adult Gaucher disease in association with primary malignant bone tumors. Cancer. 2001 Feb 01; 91(3):457-62. PMID: 11169926.
      Citations:    
    159. Heils A, Haug K, Kunz WS, Fernandez G, Horvath S, Rebstock J, Propping P, Elger CE. Interleukin-1beta gene polymorphism and susceptibility to temporal lobe epilepsy with hippocampal sclerosis. Ann Neurol. 2000 Dec; 48(6):948-50. PMID: 11117556.
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    160. Kunz WS, Kudin AP, Vielhaber S, Blümcke I, Zuschratter W, Schramm J, Beck H, Elger CE. Mitochondrial complex I deficiency in the epileptic focus of patients with temporal lobe epilepsy. Ann Neurol. 2000 Nov; 48(5):766-73. PMID: 11079540.
      Citations:    
    161. Kunz D, Höffkes H, Kunz WS, Gressner AM. Standardized flow cytometric method for the accurate determination of platelet counts in patients with severe thrombocytopenia. Cytometry. 2000 Oct 15; 42(5):284-9. PMID: 11025486.
      Citations:    
    162. Kunz WS, Kudin A, Vielhaber S, Elger CE, Attardi G, Villani G. Flux control of cytochrome c oxidase in human skeletal muscle. J Biol Chem. 2000 Sep 08; 275(36):27741-5. PMID: 10869362.
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    163. Vielhaber S, Kunz D, Winkler K, Wiedemann FR, Kirches E, Feistner H, Heinze HJ, Elger CE, Schubert W, Kunz WS. Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis. Brain. 2000 Jul; 123 ( Pt 7):1339-48. PMID: 10869047.
      Citations:    
    164. Schröder R, Vielhaber S, Wiedemann FR, Kornblum C, Papassotiropoulos A, Broich P, Zierz S, Elger CE, Reichmann H, Seibel P, Klockgether T, Kunz WS. New insights into the metabolic consequences of large-scale mtDNA deletions: a quantitative analysis of biochemical, morphological, and genetic findings in human skeletal muscle. J Neuropathol Exp Neurol. 2000 May; 59(5):353-60. PMID: 10888364.
      Citations:    
    165. Seyfried J, Soldner F, Kunz WS, Schulz JB, Klockgether T, Kovar KA, Wüllner U. Effect of 1-methyl-4-phenylpyridinium on glutathione in rat pheochromocytoma PC 12 cells. Neurochem Int. 2000 May; 36(6):489-97. PMID: 10762085.
      Citations:    
    166. Herrmann M, Ebert AD, Galazky I, Wunderlich MT, Kunz WS, Huth C. Neurobehavioral outcome prediction after cardiac surgery: role of neurobiochemical markers of damage to neuronal and glial brain tissue. Stroke. 2000 Mar; 31(3):645-50. PMID: 10700498.
      Citations:    
    167. Wiedemann FR, Vielhaber S, Schröder R, Elger CE, Kunz WS. Evaluation of methods for the determination of mitochondrial respiratory chain enzyme activities in human skeletal muscle samples. Anal Biochem. 2000 Mar 01; 279(1):55-60. PMID: 10683230.
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    168. Vielhaber S, Kudin A, Schröder R, Elger CE, Kunz WS. Muscle fibres: applications for the study of the metabolic consequences of enzyme deficiencies in skeletal muscle. Biochem Soc Trans. 2000 Feb; 28(2):159-64. PMID: 10816119.
      Citations:    
    169. Vielhaber S, Feistner H, Schneider W, Weis J, Kunz WS. Mitochondrial complex I deficiency in a female with multiplex arthrogryposis congenita. Pediatr Neurol. 2000 Jan; 22(1):53-6. PMID: 10669207.
      Citations:    
    170. Kicinska A, D bska G, Kunz W, Szewczyk A. Mitochondrial potassium and chloride channels. Acta Biochim Pol. 2000; 47(3):541-51. PMID: 11310958.
      Citations:    
    171. Kudin A, Vielhaber S, Beck H, Elger CE, Kunz WS. Quantitative investigation of mitochondrial function in single rat hippocampal slices: a novel application of high-resolution respirometry and laser-excited fluorescence spectroscopy. Brain Res Brain Res Protoc. 1999 Dec; 4(3):329-34. PMID: 10592342.
      Citations:    
    172. Vielhaber S, Winkler K, Kirches E, Kunz D, Büchner M, Feistner H, Elger CE, Ludolph AC, Riepe MW, Kunz WS. Visualization of defective mitochondrial function in skeletal muscle fibers of patients with sporadic amyotrophic lateral sclerosis. J Neurol Sci. 1999 Oct 31; 169(1-2):133-9. PMID: 10540022.
      Citations:    
    173. Kirches E, Winkler K, Vielhaber S, Michael M, Warich-Kirches M, von Bossanyi P, Plate I, Kunz WS, Szibor R, Feistner H, Dietzmann K. Mitochondrial tRNA(Cys) mutation A5823G in a patient with motor neuron disease and temporal lobe epilepsy. Pathobiology. 1999 Jul-Aug; 67(4):214-8. PMID: 10738184.
      Citations:    
    174. Kunz WS, Goussakov IV, Beck H, Elger CE. Altered mitochondrial oxidative phosphorylation in hippocampal slices of kainate-treated rats. Brain Res. 1999 May 01; 826(2):236-42. PMID: 10224301.
      Citations:    
    175. Kunz WS, Kuznetsov AV, Clark JF, Tracey I, Elger CE. Metabolic consequences of the cytochrome c oxidase deficiency in brain of copper-deficient Mo(vbr) mice. J Neurochem. 1999 Apr; 72(4):1580-5. PMID: 10098864.
      Citations:    
    176. Kampkötter A, Ridgers I, Johnston DA, Rollinson D, Kunz W, Grevelding CG. Schistosoma mansoni: cloning and characterization of the Ras homologue. Exp Parasitol. 1999 Mar; 91(3):280-3. PMID: 10072330.
      Citations:    
    177. Wiedemann FR, Winkler K, Lins H, Wallesch CW, Kunz WS. Detection of respiratory chain defects in cultivated skin fibroblasts and skeletal muscle of patients with Parkinson's disease. Ann N Y Acad Sci. 1999; 893:426-9. PMID: 10672282.
      Citations:    
    178. Saks VA, Veksler VI, Kuznetsov AV, Kay L, Sikk P, Tiivel T, Tranqui L, Olivares J, Winkler K, Wiedemann F, Kunz WS. Permeabilized cell and skinned fiber techniques in studies of mitochondrial function in vivo. Mol Cell Biochem. 1998 Jul; 184(1-2):81-100. PMID: 9746314.
      Citations:    
    179. Quack T, Doenhoff M, Kunz W, Grevelding CG. Schistosoma mansoni: the varying occurrence of repetitive elements in different strains shows sex-specific polymorphisms. Exp Parasitol. 1998 Jun; 89(2):222-7. PMID: 9635446.
      Citations:    
    180. Kuznetsov AV, Winkler K, Wiedemann FR, von Bossanyi P, Dietzmann K, Kunz WS. Impaired mitochondrial oxidative phosphorylation in skeletal muscle of the dystrophin-deficient mdx mouse. Mol Cell Biochem. 1998 Jun; 183(1-2):87-96. PMID: 9655182.
      Citations:    
    181. Kirches EJ, Winkler K, Warich-Kirches M, Szibor R, Wien F, Kunz WS, von Bossanyi P, Bajaj PK, Dietzmann K. mtDNA depletion and impairment of mitochondrial function in a case of a multisystem disorder including severe myopathy. J Inherit Metab Dis. 1998 Jun; 21(4):400-8. PMID: 9700597.
      Citations:    
    182. Kuznetsov AV, Mayboroda O, Kunz D, Winkler K, Schubert W, Kunz WS. Functional imaging of mitochondria in saponin-permeabilized mice muscle fibers. J Cell Biol. 1998 Mar 09; 140(5):1091-9. PMID: 9490722.
      Citations:    
    183. Schüssler P, Köhrer K, Finken-Eigen M, Michel A, Grevelding CG, Kunz W. A female-specific cDNA sequence of Schistosoma mansoni encoding an amidase that is expressed in the gastrodermis. Parasitology. 1998 Feb; 116 ( Pt 2):131-7. PMID: 9509022.
      Citations:    
    184. Wiedemann FR, Kunz WS. Oxygen dependence of flux control of cytochrome c oxidase -- implications for mitochondrial diseases. FEBS Lett. 1998 Jan 23; 422(1):33-5. PMID: 9475164.
      Citations:    
    185. Wiedemann FR, Winkler K, Kuznetsov AV, Bartels C, Vielhaber S, Feistner H, Kunz WS. Impairment of mitochondrial function in skeletal muscle of patients with amyotrophic lateral sclerosis. J Neurol Sci. 1998; 156(1):65-72. PMID: 9559989.
      Citations:    
    186. Kuznetsov AV, Wiedemann FR, Winkler K, Kunz WS. Use of saponin-permeabilized muscle fibers for the diagnosis of mitochondrial diseases. Biofactors. 1998; 7(3):221-3. PMID: 9568252.
      Citations:    
    187. Kunz WS, Winkler K, Kuznetsov AV, Lins H, Kirches E, Wallesch CW. Detection of mitochondrial defects by laser fluorimetry. Mol Cell Biochem. 1997 Sep; 174(1-2):97-100. PMID: 9309672.
      Citations:    
    188. Finken-Eigen M, Kunz W. Schistosoma mansoni: gene structure and localization of a homologue to cysteine protease ER 60. Exp Parasitol. 1997 May; 86(1):1-7. PMID: 9149235.
      Citations:    
    189. Kuznetsov AV, Winkler K, Kirches E, Lins H, Feistner H, Kunz WS. Application of inhibitor titrations for the detection of oxidative phosphorylation defects in saponin-skinned muscle fibers of patients with mitochondrial diseases. Biochim Biophys Acta. 1997 Apr 12; 1360(2):142-50. PMID: 9128179.
      Citations:    
    190. Kunz D, Luley C, Winkler K, Lins H, Kunz WS. Flow cytometric detection of mitochondrial dysfunction in subpopulations of human mononuclear cells. Anal Biochem. 1997 Mar 15; 246(2):218-24. PMID: 9073359.
      Citations:    
    191. Schüssler P, Grevelding CG, Kunz W. Cloning and characterization of elongation factor 1-alpha of Schistosoma mansoni. Parasitol Res. 1997; 83(2):206-8. PMID: 9039706.
      Citations:    
    192. Kuznetsov AV, Clark JF, Winkler K, Kunz WS. Increase of flux control of cytochrome c oxidase in copper-deficient mottled brindled mice. J Biol Chem. 1996 Jan 05; 271(1):283-8. PMID: 8550574.
      Citations:    
    193. Winkler K, Kuznetsov AV, Lins H, Kirches E, von Bossanyi P, Dietzmann K, Frank B, Feistner H, Kunz WS. Laser-excited fluorescence studies of mitochondrial function in saponin-skinned skeletal muscle fibers of patients with chronic progressive external ophthalmoplegia. Biochim Biophys Acta. 1995 Dec 12; 1272(3):181-4. PMID: 8541350.
      Citations:    
    194. Menrath M, Michel A, Kunz W. A female-specific cDNA sequence of Schistosoma mansoni encoding a mucin-like protein that is expressed in the epithelial cells of the reproductive duct. Parasitology. 1995 Nov; 111 ( Pt 4):477-83. PMID: 11023412.
      Citations:    
    195. Schüssler P, Gohr LG, Sommer G, Kunz W, Grevelding CG. Combined isolation of nucleic acids and protein from small amounts of tissue. Trends Genet. 1995 Oct; 11(10):378-9. PMID: 7482759.
      Citations:    
    196. Michel A, Ghoneim H, Resto M, Klinkert MQ, Kunz W. Sequence, characterization and localization of a cysteine proteinase cathepsin L in Schistosoma mansoni. Mol Biochem Parasitol. 1995 Jul; 73(1-2):7-18. PMID: 8577349.
      Citations:    
    197. Wisniewski E, Gellerich FN, Kunz WS. Distribution of flux control among the enzymes of mitochondrial oxidative phosphorylation in calcium-activated saponin-skinned rat musculus soleus fibers. Eur J Biochem. 1995 Jun 01; 230(2):549-54. PMID: 7607228.
      Citations:    
    198. Kunz D, Luley C, Fritz S, Bohnensack R, Winkler K, Kunz WS, Wallesch CW. Oxygraphic evaluation of mitochondrial function in digitonin-permeabilized mononuclear cells and cultured skin fibroblasts of patients with chronic progressive external ophthalmoplegia. Biochem Mol Med. 1995 Apr; 54(2):105-11. PMID: 8581354.
      Citations:    
    199. Khuchua Z, Belikova Y, Kuznetsov AV, Gellerich FN, Schild L, Neumann HW, Kunz WS. Caffeine and Ca2+ stimulate mitochondrial oxidative phosphorylation in saponin-skinned human skeletal muscle fibers due to activation of actomyosin ATPase. Biochim Biophys Acta. 1994 Dec 30; 1188(3):373-9. PMID: 7803452.
      Citations:    
    200. Kunz W, Gellerich FN, Schild L. Contribution to control of mitochondrial oxidative phosphorylation by supplement of reducing equivalents. Biochem Med Metab Biol. 1994 Jun; 52(1):65-75. PMID: 7917469.
      Citations:    
    201. Gellerich FN, Ulrich J, Kunz W. Unusual properties of mitochondria from the human term placenta are caused by alkaline phosphatase. Placenta. 1994 Apr; 15(3):299-310. PMID: 8066053.
      Citations:    
    202. Gellerich FN, Kapischke M, Kunz W, Neumann W, Kuznetsov A, Brdiczka D, Nicolay K. The influence of the cytosolic oncotic pressure on the permeability of the mitochondrial outer membrane for ADP: implications for the kinetic properties of mitochondrial creatine kinase and for ADP channelling into the intermembrane space. Mol Cell Biochem. 1994 Apr-May; 133-134:85-104. PMID: 7808467.
      Citations:    
    203. Finken M, Sobek A, Symmons P, Kunz W. Characterization of the complete protein disulfide isomerase gene of Schistosoma mansoni and identification of the tissues of its expression. Mol Biochem Parasitol. 1994 Mar; 64(1):135-44. PMID: 8078516.
      Citations:    
    204. Kunz WS, Kuznetsov AV, Winkler K, Gellerich FN, Neuhof S, Neumann HW. Measurement of fluorescence changes of NAD(P)H and of fluorescent flavoproteins in saponin-skinned human skeletal muscle fibers. Anal Biochem. 1994 Feb 01; 216(2):322-7. PMID: 8179187.
      Citations:    
    205. Kunz WS, Kuznetsov AV, Schulze W, Eichhorn K, Schild L, Striggow F, Bohnensack R, Neuhof S, Grasshoff H, Neumann HW, Gellerich FN. Functional characterization of mitochondrial oxidative phosphorylation in saponin-skinned human muscle fibers. Biochim Biophys Acta. 1993 Aug 16; 1144(1):46-53. PMID: 8347661.
      Citations:    
    206. Kunz WS, Gellerich FN. Quantification of the content of fluorescent flavoproteins in mitochondria from liver, kidney cortex, skeletal muscle, and brain. Biochem Med Metab Biol. 1993 Aug; 50(1):103-10. PMID: 8373630.
      Citations:    
    207. Kunz WS, Kuznetsov AV, Gellerich FN. Mitochondrial oxidative phosphorylation in saponin-skinned human muscle fibers is stimulated by caffeine. FEBS Lett. 1993 May 24; 323(1-2):188-90. PMID: 8495738.
      Citations:    
    208. Wisniewski E, Kunz WS, Gellerich FN. Phosphate affects the distribution of flux control among the enzymes of oxidative phosphorylation in rat skeletal muscle mitochondria. J Biol Chem. 1993 May 05; 268(13):9343-6. PMID: 8486629.
      Citations:    
    209. Weston D, Schmitz J, Kemp WM, Kunz W. Cloning and sequencing of a complete myosin heavy chain cDNA from Schistosoma mansoni. Mol Biochem Parasitol. 1993 Mar; 58(1):161-4. PMID: 8459827.
      Citations:    
    210. Hoeltke HJ, Ettl I, Finken M, West S, Kunz W. Multiple nucleic acid labeling and rainbow detection. Anal Biochem. 1992 Nov 15; 207(1):24-31. PMID: 1489097.
      Citations:    
    211. Kunz WS, Krinelke L, Gellerich FN. Glutamine affects glutamate metabolism in isolated rat kidney cortex mitochondria. Biochim Biophys Acta. 1992 Jun 19; 1100(3):329-31. PMID: 1351747.
      Citations:    
    212. Noack H, Kunz WS, Augustin W. Evaluation of a procedure for the simultaneous determination of oxidized and reduced pyridine nucleotides and adenylates in organic phenol extracts from mitochondria. Anal Biochem. 1992 Apr; 202(1):162-5. PMID: 1621979.
      Citations:    
    213. Dietzel J, Hirzmann J, Preis D, Symmons P, Kunz W. Ferritins of Schistosoma mansoni: sequence comparison and expression in female and male worms. Mol Biochem Parasitol. 1992 Feb; 50(2):245-54. PMID: 1741011.
      Citations:    
    214. Halangk W, Kunz WS. Use of NAD(P)H and flavoprotein fluorescence signals to characterize the redox state of pyridine nucleotides in epididymal bull spermatozoa. Biochim Biophys Acta. 1991 Feb 08; 1056(3):273-8. PMID: 2001381.
      Citations:    
    215. Scholz W, Wolf A, Kunz W, Willenbrock R, Steffen C. Effect of orotic acid on the generation of reactive oxygen and on lipid peroxidation in rat liver. Toxicology. 1991 Feb; 66(2):197-212. PMID: 2014518.
      Citations:    
    216. Kunz WS, Davis EJ. Control of reversible intracellular transfer of reducing potential. Arch Biochem Biophys. 1991 Jan; 284(1):40-6. PMID: 1824912.
      Citations:    
    217. Kunz WS. Application of the theory of steady-state flux control to mitochondrial beta-oxidation. Biomed Biochim Acta. 1991; 50(12):1143-57. PMID: 1668635.
      Citations:    
    218. Gellerich FN, Kunz WS, Bohnensack R. Estimation of flux control coefficients from inhibitor titrations by non-linear regression. FEBS Lett. 1990 Nov 12; 274(1-2):167-70. PMID: 2253770.
      Citations:    
    219. West S, Schröder J, Kunz W. A multiple-staining procedure for the detection of different DNA fragments on a single blot. Anal Biochem. 1990 Nov 01; 190(2):254-8. PMID: 1705397.
      Citations:    
    220. Bohnensack R, Gellerich FN, Schild L, Kunz W. The function of the adenine nucleotide translocator in the control of oxidative phosphorylation. Biochim Biophys Acta. 1990 Jul 25; 1018(2-3):182-4. PMID: 2168208.
      Citations:    
    221. Krinelke L, Kunz WS. [Characterization of surface fluorescence signals of isolated perfused rat kidney]. Biomed Biochim Acta. 1990; 49(11):1119-30. PMID: 2094217.
      Citations:    
    222. Schönfeld P, Schild L, Kunz W. Long-chain fatty acids act as protonophoric uncouplers of oxidative phosphorylation in rat liver mitochondria. Biochim Biophys Acta. 1989 Dec 07; 977(3):266-72. PMID: 2556180.
      Citations:    
    223. Schönfeld P, Wojtczak AB, Geelen MJ, Kunz W, Wojtczak L. On the mechanism of the so-called uncoupling effect of medium- and short-chain fatty acids. Biochim Biophys Acta. 1988 Dec 07; 936(3):280-8. PMID: 3196710.
      Citations:    
    224. Kunz W, Gellerich FN, Schild L, Schönfeld P. Kinetic limitations in the overall reaction of mitochondrial oxidative phosphorylation accounting for flux-dependent changes in the apparent delta GexP/delta mu H+ ratio. FEBS Lett. 1988 Jun 06; 233(1):17-21. PMID: 2898384.
      Citations:    
    225. Kunz WS. Evaluation of electron-transfer flavoprotein and alpha-lipoamide dehydrogenase redox states by two-channel fluorimetry and its application to the investigation of beta-oxidation. Biochim Biophys Acta. 1988 Jan 20; 932(1):8-16. PMID: 3337800.
      Citations:    
    226. Halangk W, Dietz H, Bohnensack R, Kunz W. Regulation of oxidative phosphorylation in mitochondria of epididymal bull spermatozoa. Biochim Biophys Acta. 1987 Aug 12; 893(1):100-8. PMID: 3607041.
      Citations:    
    227. Gellerich FN, Schlame M, Bohnensack R, Kunz W. Dynamic compartmentation of adenine nucleotides in the mitochondrial intermembrane space of rat-heart mitochondria. Biochim Biophys Acta. 1987 Feb 11; 890(2):117-26. PMID: 3801462.
      Citations:    
    228. Wustmann C, Petzold D, Kunz W, Fischer HD. Respiratory function of rat brain mitochondria after hypobaric hypoxia and piracetam treatment. Biomed Biochim Acta. 1987; 46(7):635-8. PMID: 3426574.
      Citations:    
    229. Gellerich FN, Kunz W. Cause and consequences of dynamic compartmentation of adenine nucleotides in the mitochondrial intermembrane space in respect to exchange of energy rich phosphates between cytosol and mitochondria. Biomed Biochim Acta. 1987; 46(8-9):S545-8. PMID: 3435511.
      Citations:    
    230. Wustmann C, Petzold D, Fischer HD, Kunz W. [ATP-metabolizing enzymes in suspensions of isolated coupled rat brain mitochondria]. Biomed Biochim Acta. 1987; 46(5):331-40. PMID: 3663204.
      Citations:    
    231. Kunz WS. Spectral properties of fluorescent flavoproteins of isolated rat liver mitochondria. FEBS Lett. 1986 Jan 20; 195(1-2):92-6. PMID: 3753688.
      Citations:    
    232. Kunz WS, Kunz W. Contribution of different enzymes to flavoprotein fluorescence of isolated rat liver mitochondria. Biochim Biophys Acta. 1985 Sep 06; 841(3):237-46. PMID: 4027266.
      Citations:    
    233. Halangk W, Bohnensack R, Kunz W. Interdependence of mitochondrial ATP production and extramitochondrial ATP utilization in intact spermatozoa. Biochim Biophys Acta. 1985 Jul 17; 808(2):316-22. PMID: 3848331.
      Citations:    
    234. Buchmann A, Kuhlmann W, Schwarz M, Kunz W, Wolf CR, Moll E, Friedberg T, Oesch F. Regulation and expression of four cytochrome P-450 isoenzymes, NADPH-cytochrome P-450 reductase, the glutathione transferases B and C and microsomal epoxide hydrolase in preneoplastic and neoplastic lesions in rat liver. Carcinogenesis. 1985 Apr; 6(4):513-21. PMID: 3921270.
      Citations:    
    235. Kamensky Y, Konstantinov AA, Kunz WS, Surkov S. Effects of bc1-site electron transfer inhibitors on the absorption spectra of mitochondrial cytochromes b. FEBS Lett. 1985 Feb 11; 181(1):95-9. PMID: 2982656.
      Citations:    
    236. Halangk W, Bohnensack R, Frank K, Kunz W. Effect of various substrates on mitochondrial and cellular energy state of intact spermatozoa. Biomed Biochim Acta. 1985; 44(3):411-20. PMID: 4004841.
      Citations:    
    237. Hartung KJ, Jung K, Minda R, Kunz W. Mitochondrial respiratory function as indicator of the ischemic injury of the rat kidney. Biomed Biochim Acta. 1985; 44(10):1435-43. PMID: 4084249.
      Citations:    
    238. Kunz WS, Konstantinov A. Cytochrome b reduction by hexaammineruthenium in mitochondria and submitochondrial particles. Evidence for heme b-562 localization at the M-side of the mitochondrial membrane. FEBS Lett. 1984 Sep 17; 175(1):100-4. PMID: 6479328.
      Citations:    
    239. Kunz WS, Konstantinov A, Tsofina L, Liberman EA. Localization of a ferricyanide-reactive site of cytochrome b-c1 complex, possibly of cytochrome b or ubisemiquinone, at the outer face of submitochondrial particles. FEBS Lett. 1984 Jul 09; 172(2):261-6. PMID: 6086391.
      Citations:    
    240. Schönfeld P, Petzold D, Kunz W. Influence of octanoate on the rate of oxidative phosphorylation and the associated extramitochondrial ATP/ADP ratios studied with isolated rat liver mitochondria oxidizing pyruvate. Biomed Biochim Acta. 1984; 43(10):1055-65. PMID: 6525184.
      Citations:    
    241. Kunz WS, Konstantinov AA. Effect of b-c1-site inhibitors on the midpoint potentials of mitochondrial cytochromes b. FEBS Lett. 1983 May 08; 155(2):237-40. PMID: 6303845.
      Citations:    
    242. Gellerich FN, Bohnensack R, Kunz W. Control of mitochondrial respiration. The contribution of the adenine nucleotide translocator depends on the ATP- and ADP-consuming enzymes. Biochim Biophys Acta. 1983 Feb 17; 722(2):381-91. PMID: 6301555.
      Citations:    
    243. Kunz WS, Konstantinov A. Energy-linked spectral shift of ferrocytochrome b in beef heart submitochondrial particles. FEBS Lett. 1983 Feb 07; 152(1):53-6. PMID: 6840277.
      Citations:    
    244. Tager JM, Wanders RJ, Groen AK, Kunz W, Bohnensack R, Küster U, Letko G, Böhme G, Duszynski J, Wojtczak L. Control of mitochondrial respiration. FEBS Lett. 1983 Jan 10; 151(1):1-9. PMID: 6337871.
      Citations:    
    245. Schönfeld P, Bohnensack R, Böhme G, Kunz W. Influence of the beta-hydroxybutyrate/acetoacetate ratio on the redox states of mitochondrial NAD(P) and cytochrome c systems, extramitochondrial ATP/ADP ratio and the respiration of isolated liver mitochondria in the resting state. Biomed Biochim Acta. 1983; 42(1):3-13. PMID: 6309158.
      Citations:    
    246. Hartung KJ, Böhme G, Kunz W. Involvement of intramitochondrial adenine nucleotides and inorganic phosphate in oxidative phosphorylation of extramitochondrially added adenosine-5'-diphosphate. Biomed Biochim Acta. 1983; 42(1):15-26. PMID: 6224484.
      Citations:    
    247. Markefski M, Kunz W, Zinchenko VP. Role of substrates in Sr2+-induced oscillations of ionic fluxes in rat liver mitochondria. Biochim Biophys Acta. 1982 Mar 16; 679(3):444-51. PMID: 7066310.
      Citations:    
    248. Letko G, Küster U, Bohnensack R, Böhme G, Pohl K, Kunz W. Interrelationship between oxidative energy transformation and energy consumption at mitochondrial and cellular levels. Acta Biol Med Ger. 1982; 41(9):735-50. PMID: 6299035.
      Citations:    
    249. Böhme G, Schönfeld P, Bohnensack R, Küster U, Kunz W. Interrelationships between hydrogen-supplying reactions, respiration rate and extramitochondrial adenine nucleotide pattern. Physiol Bohemoslov. 1982; 31(2):159-68. PMID: 6212956.
      Citations:    
    250. Duszynski J, Bogucka K, Letko G, Küster U, Kunz W, Wojtczak L. Relationship between the energy cost of ATP transport and ATP synthesis in mitochondria. Biochim Biophys Acta. 1981 Sep 14; 637(2):217-23. PMID: 7295709.
      Citations:    
    251. Küster U, Letko G, Kunz W, Duszynsky J, Bogucka K, Wojtczak L. Influence of different energy drains on the interrelationship between the rate of respiration, proton-motive force and adenine nucleotide patterns in isolated mitochondria. Biochim Biophys Acta. 1981 Jun 12; 636(1):32-8. PMID: 7284343.
      Citations:    
    252. Kunz W, Bohnensack R, Böhme G, Küster U, Letko G, Schönfeld P. Relations between extramitochondrial and intramitochondrial adenine nucleotide systems. Arch Biochem Biophys. 1981 Jun; 209(1):219-29. PMID: 6456693.
      Citations:    
    253. Kuhlmann WD, Krischan R, Kunz W, Guenthner TM, Oesch F. Focal elevation of liver microsomal epoxide hydrolase in early preneoplastic stages and its behaviour in the further course of hepatocarcinogenesis. Biochem Biophys Res Commun. 1981 Jan 30; 98(2):417-23. PMID: 6111998.
      Citations:    
    254. Kitta D, Schwarz M, Tennekes HA, Uehleke H, Kunz W. Covalent binding of CCl4-intermediates to reduced pyridine nucleotides in mouse liver. Adv Exp Med Biol. 1981; 136 Pt A:769-77. PMID: 7344492.
      Citations:    
    255. Letko G, Küster U, Duszynski J, Kunz W. Investigation of the dependence of the intramitochondrial [ATP]/[ADP] ratio on the respiration rate. Biochim Biophys Acta. 1980 Dec 03; 593(2):196-203. PMID: 7236631.
      Citations:    
    256. Böhme G, Schönfeld P, Küster U, Kunz W, Lyr H. The multifunctional actions of beta-thujaplicin on the oxidative energy transformations as a consequence of its lipophilic and chelating properties. Acta Biol Med Ger. 1980; 39(11-12):1153-63. PMID: 6787824.
      Citations:    
    257. Laib RJ, Stöckle G, Bolt HM, Kunz W. Vinyl chloride and trichloroethylene: comparison of alkylating effects of metabolites and induction of preneoplastic enzyme deficiencies in rat liver. J Cancer Res Clin Oncol. 1979 Jun 08; 94(2):139-47. PMID: 157359.
      Citations:    
    258. Appel KE, Ruf HH, Mahr B, Schwarz M, Rickart R, Kunz W. Binding of nitrosamines to cytochrome P-450 of liver microsomes. Chem Biol Interact. 1979; 28(1):17-33. PMID: 227615.
      Citations:    
    259. Schaller H, Letko G, Kunz W. Influence of Mg2+-ions on the properties of rat heart mitochondria in dependence on the preparation. Acta Biol Med Ger. 1978; 37(1):31-8. PMID: 706927.
      Citations:    
    260. Bohnensack R, Kunz W. Mathematical model of regulation of oxidative phosphorylation in intact mitochondria. Acta Biol Med Ger. 1978; 37(1):97-112. PMID: 706931.
      Citations:    
    261. Reichert M, Schaller H, Kunz W, Gerber G. The dependence on the extramitochondrial ATP/ADP-ratio of the oxidative phosphorylation in mitochondria isolated by a new procedure from rat skeletal muscle. Acta Biol Med Ger. 1978; 37(8):1167-76. PMID: 749453.
      Citations:    
    262. Küster U, Bohnensack R, Kunz W. Control of oxidative phosphorylation by the extra-mitochondrial ATP/ADP ratio. Biochim Biophys Acta. 1976 Aug 13; 440(2):391-402. PMID: 952975.
      Citations:    
    263. Lenartowicz E, Winter C, Kunz W, Wojtczak AB. The inhibition of isocitrate oxidation by palmitoyl-l-carnitine and palmitoyl-C0 A in rat liver mitochondria. Eur J Biochem. 1976 Aug 01; 67(1):137-44. PMID: 183951.
      Citations:    
    264. Schewe T, Rapoport S, Böhme G, Kunz W. [Action site of the systemic fungicide carboxin in the respiratory chain]. Acta Biol Med Ger. 1973; 31(1):73-86. PMID: 4774673.
      Citations:    
    265. Lutze G, Liese W, Kunz W. FEBS Lett. 1972 Aug 01; 24(2):189-192. PMID: 11946669.
      Citations:    
    266. Steinbrecht I, Kunz W. [Determination of oxydated and reduced pyridine nucleotides in human and rabbit blood using the polarographic cycling method]. Acta Biol Med Ger. 1972; 29(4):495-507. PMID: 4405795.
      Citations:    
    267. Mücke D, Kranz D, Kunz W, Gmyrek D. [Role of the liver in mucoviscidosis (cystic fibrosis). Results of clinical and biopsy studies]. Dtsch Gesundheitsw. 1971 Dec 16; 26(51):2418-24. PMID: 5148594.
      Citations:    
    268. Bohnensack R, Kunz W. [Investigation of the penetration of oxaloacetate into rat liver mitochondria]. Biochim Biophys Acta. 1971 Jan 12; 226(1):33-41. PMID: 4323696.
      Citations:    
    269. Liese W, Jung K, Kunz W, David H. [Enzyme and electron microscopy studies on the preparation of membranes from rat liver mitochondria]. Acta Biol Med Ger. 1971; 27(3):477-98. PMID: 4336793.
      Citations:    
    270. Lutze G, Liese W, Kunz W. FEBS Lett. 1970 Oct 05; 10(3):133-135. PMID: 11945376.
      Citations:    
    271. Lutze G, Liese W, Kunz W. FEBS Lett. 1970 Jun 08; 8(4):210-212. PMID: 11947573.
      Citations:    
    272. Steinbrecht I, Kunz W. [Use of "cycling" technic for random quantitative determination of the degree of reduction of NAD and NADP system in rat liver mitochondria with continuous recording of the measurements]. Acta Biol Med Ger. 1970; 25(5):731-47. PMID: 4399840.
      Citations:    
    273. Kunz W, Böhme G. [A simple registering single beam fluorometer for recording of redox changes in mitochondrial pyridine nucleotides]. Acta Biol Med Ger. 1969; 22(3):643-51. PMID: 4391413.
      Citations:    
    274. Kunz W. [Short time regulation of breathing systems]. Folia Haematol Int Mag Klin Morphol Blutforsch. 1968; 89(2):165-70. PMID: 4174946.
      Citations:    
    275. Kunz W, Klossek P. [On the energy-linked ion translocation through the mitochondrial membrane]. Acta Biol Med Ger. 1967; 19(5):766-79. PMID: 5589680.
      Citations:    
    276. KUNZ W, BOEHME G. [STUDIES ON COMPARTMENTATION OF ATP IN THE MITOCHONDRIA FROM THE RAT LIVER AND ASCITES TUMOR CELLS]. Acta Biol Med Ger. 1965; 14:250-8. PMID: 14315561.
      Citations:    
    277. KUNZ W, BOEHME G. [ON THE PREPARATION AND FUNCTIONAL PROPERTIES OF MITOCHONDRIA OF EHRLICH ASCITES CARCINOMA IN THE MOUSE]. Acta Biol Med Ger. 1964; 13:865-82. PMID: 14335765.
      Citations:    
    278. KUNZ W. [POLAROGRAPHIC STUDIES ON THE EFFECT OF OXALOACETATE ON SUCCINATE OXIDATION BY INTACT LIVER MITOCHONDRIA]. Hoppe Seylers Z Physiol Chem. 1963; 334:128-40. PMID: 14136703.
      Citations:    
    279. KUNZ W. [On the kinetics of choline oxidation by isolated liver mitochondria]. Acta Biol Med Ger. 1962; 9:674-81. PMID: 13927399.
      Citations:    
    280. KUNZ W, KAISER G. [On the interaction of oleic acid, serum albumin and calcium ions with liver mitochondria]. Hoppe Seylers Z Physiol Chem. 1961 Oct 25; 326:17-24. PMID: 14460633.
      Citations:    
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