Kunz WS - Search Results

1

Is there mitochondrial dysfunction in amyotrophic lateral sclerosis skeletal muscle?

Vielhaber S, Kudin A, Winkler K, Wiedemann F, Schröder R, Feistner H, Heinze HJ, Elger CE, Kunz WS. Vielhaber S, et al. Among authors: kunz ws. Ann Neurol. 2003 May;53(5):686-7; author reply 687-8. doi: 10.1002/ana.10564. Ann Neurol. 2003. PMID: 12731009 No abstract available.

2

Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophies--a comment.

Vielhaber S, Kornblum C, Heinze HJ, Elger CE, Kunz WS. Vielhaber S, et al. Among authors: kunz ws. Brain. 2005 Dec;128(Pt 12):E38. doi: 10.1093/brain/awh652. Brain. 2005. PMID: 16311266 No abstract available.

3

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

4

Mitochondrial dysfunction in myofibrillar myopathy.

Reimann J, Kunz WS, Vielhaber S, Kappes-Horn K, Schröder R. Reimann J, et al. Among authors: kunz ws. Neuropathol Appl Neurobiol. 2003 Feb;29(1):45-51. doi: 10.1046/j.1365-2990.2003.00428.x. Neuropathol Appl Neurobiol. 2003. PMID: 12581339

5

Functional imaging of mitochondrial redox state.

Kunz D, Winkler K, Elger CE, Kunz WS. Kunz D, et al. Among authors: kunz ws. Methods Enzymol. 2002;352:135-50. doi: 10.1016/s0076-6879(02)52014-0. Methods Enzymol. 2002. PMID: 12125342 No abstract available.

6

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.

Niessen HG, Angenstein F, Sander K, Kunz WS, Teuchert M, Ludolph AC, Heinze HJ, Scheich H, Vielhaber S. Niessen HG, et al. Among authors: kunz ws. Exp Neurol. 2006 Oct;201(2):293-300. doi: 10.1016/j.expneurol.2006.04.007. Epub 2006 Jun 5. Exp Neurol. 2006. PMID: 16740261

7

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.

Kudin A, Vielhaber S, Elger CE, Kunz WS. Kudin A, et al. Among authors: kunz ws. Mol Biol Rep. 2002;29(1-2):89-92. doi: 10.1023/a:1020374924550. Mol Biol Rep. 2002. PMID: 12241082

8

Metabolic progression markers of neurodegeneration in the transgenic G93A-SOD1 mouse model of amyotrophic lateral sclerosis.

Niessen HG, Debska-Vielhaber G, Sander K, Angenstein F, Ludolph AC, Hilfert L, Willker W, Leibfritz D, Heinze HJ, Kunz WS, Vielhaber S. Niessen HG, et al. Among authors: kunz ws. Eur J Neurosci. 2007 Mar;25(6):1669-77. doi: 10.1111/j.1460-9568.2007.05415.x. Eur J Neurosci. 2007. PMID: 17432958

9

Disorganization of the desmin cytoskeleton and mitochondrial dysfunction in plectin-related epidermolysis bullosa simplex with muscular dystrophy.

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. Schröder R, et al. Among authors: kunz ws. J Neuropathol Exp Neurol. 2002 Jun;61(6):520-30. doi: 10.1093/jnen/61.6.520. J Neuropathol Exp Neurol. 2002. PMID: 12071635

10

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.

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