Kunz WS - Search Results

1

Mitochondrial diseases--an expanding spectrum of disorders and affected genes.

von Kleist-Retzow JC, Schauseil-Zipf U, Michalk DV, Kunz WS. von Kleist-Retzow JC, et al. Among authors: kunz ws. Exp Physiol. 2003 Jan;88(1):155-66. doi: 10.1113/eph8802509. Exp Physiol. 2003. PMID: 12525864 Free article. Review.

2

Complete failure of insulin-transmitted signaling, but not obesity-induced insulin resistance, impairs respiratory chain function in muscle.

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. Franko A, et al. Among authors: kunz ws. J Mol Med (Berl). 2012 Oct;90(10):1145-60. doi: 10.1007/s00109-012-0887-y. Epub 2012 Mar 13. J Mol Med (Berl). 2012. PMID: 22411022

3

Different metabolic properties of mitochondrial oxidative phosphorylation in different cell types--important implications for mitochondrial cytopathies.

Kunz WS. Kunz WS. Exp Physiol. 2003 Jan;88(1):149-54. doi: 10.1113/eph8802512. Exp Physiol. 2003. PMID: 12525863 Free article. Review.

4

Human epidermal keratinocytes accumulate superoxide due to low activity of Mn-SOD, leading to mitochondrial functional impairment.

Hornig-Do HT, von Kleist-Retzow JC, Lanz K, Wickenhauser C, Kudin AP, Kunz WS, Wiesner RJ, Schauen M. Hornig-Do HT, et al. Among authors: kunz ws. J Invest Dermatol. 2007 May;127(5):1084-93. doi: 10.1038/sj.jid.5700666. Epub 2006 Dec 21. J Invest Dermatol. 2007. PMID: 17185981 Free article.

5

Mitochondrial DNA damage and the aging process: facts and imaginations.

Wiesner RJ, Zsurka G, Kunz WS. Wiesner RJ, et al. Among authors: kunz ws. Free Radic Res. 2006 Dec;40(12):1284-94. doi: 10.1080/10715760600913168. Free Radic Res. 2006. PMID: 17090418 Review.

6

Expression pattern of mitochondrial respiratory chain enzymes in skeletal muscle of patients harboring the A3243G point mutation or large-scale deletions of mitochondrial DNA.

Vielhaber S, Varlamov DA, Kudina TA, Schröder R, Kappes-Horn K, Elger CE, Seibel M, Seibel P, Kunz WS. Vielhaber S, et al. Among authors: kunz ws. J Neuropathol Exp Neurol. 2002 Oct;61(10):885-95. doi: 10.1093/jnen/61.10.885. J Neuropathol Exp Neurol. 2002. PMID: 12387454

7

Recombination of mitochondrial DNA in skeletal muscle of individuals with multiple mitochondrial DNA heteroplasmy.

Zsurka G, Kraytsberg Y, Kudina T, Kornblum C, Elger CE, Khrapko K, Kunz WS. Zsurka G, et al. Among authors: kunz ws. Nat Genet. 2005 Aug;37(8):873-7. doi: 10.1038/ng1606. Epub 2005 Jul 17. Nat Genet. 2005. PMID: 16025113 Free PMC article.

8

Diagnostic value of mitochondrial DNA mutation analysis in juvenile unilateral ptosis.

Okulla T, Kunz WS, Klockgether T, Schröder R, Kornblum C. Okulla T, et al. Among authors: kunz ws. Graefes Arch Clin Exp Ophthalmol. 2005 Apr;243(4):380-2. doi: 10.1007/s00417-004-1000-1. Epub 2004 Oct 13. Graefes Arch Clin Exp Ophthalmol. 2005. PMID: 15864628

9

Clonally expanded mitochondrial DNA mutations in epileptic individuals with mutated DNA polymerase gamma.

Zsurka G, Baron M, Stewart JD, Kornblum C, Bös M, Sassen R, Taylor RW, Elger CE, Chinnery PF, Kunz WS. Zsurka G, et al. Among authors: kunz ws. J Neuropathol Exp Neurol. 2008 Sep;67(9):857-66. doi: 10.1097/NEN.0b013e3181839b2d. J Neuropathol Exp Neurol. 2008. PMID: 18716558

10

Seizure-dependent modulation of mitochondrial oxidative phosphorylation in rat hippocampus.

Kudin AP, Kudina TA, Seyfried J, Vielhaber S, Beck H, Elger CE, Kunz WS. Kudin AP, et al. Among authors: kunz ws. Eur J Neurosci. 2002 Apr;15(7):1105-14. doi: 10.1046/j.1460-9568.2002.01947.x. Eur J Neurosci. 2002. PMID: 11982622

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