Kunz WS - Search Results

1

Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsy.

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. Kudin AP, et al. Among authors: kunz ws. Free Radic Biol Med. 2017 May;106:270-277. doi: 10.1016/j.freeradbiomed.2017.02.040. Epub 2017 Feb 21. Free Radic Biol Med. 2017. PMID: 28232204

2

Metabolic consequences of the cytochrome c oxidase deficiency in brain of copper-deficient Mo(vbr) mice.

Kunz WS, Kuznetsov AV, Clark JF, Tracey I, Elger CE. Kunz WS, et al. J Neurochem. 1999 Apr;72(4):1580-5. doi: 10.1046/j.1471-4159.1999.721580.x. J Neurochem. 1999. PMID: 10098864 Free article.

3

Altered mitochondrial oxidative phosphorylation in hippocampal slices of kainate-treated rats.

Kunz WS, Goussakov IV, Beck H, Elger CE. Kunz WS, et al. Brain Res. 1999 May 1;826(2):236-42. doi: 10.1016/s0006-8993(99)01279-2. Brain Res. 1999. PMID: 10224301

4

Visualization of defective mitochondrial function in skeletal muscle fibers of patients with sporadic amyotrophic lateral sclerosis.

Vielhaber S, Winkler K, Kirches E, Kunz D, Büchner M, Feistner H, Elger CE, Ludolph AC, Riepe MW, Kunz WS. Vielhaber S, et al. Among authors: kunz d, kunz ws. J Neurol Sci. 1999 Oct 31;169(1-2):133-9. doi: 10.1016/s0022-510x(99)00236-1. J Neurol Sci. 1999. PMID: 10540022

5

Quantitative investigation of mitochondrial function in single rat hippocampal slices: a novel application of high-resolution respirometry and laser-excited fluorescence spectroscopy.

Kudin A, Vielhaber S, Beck H, Elger CE, Kunz WS. Kudin A, et al. Among authors: kunz ws. Brain Res Brain Res Protoc. 1999 Dec;4(3):329-34. doi: 10.1016/s1385-299x(99)00037-9. Brain Res Brain Res Protoc. 1999. PMID: 10592342

6

Evaluation of methods for the determination of mitochondrial respiratory chain enzyme activities in human skeletal muscle samples.

Wiedemann FR, Vielhaber S, Schröder R, Elger CE, Kunz WS. Wiedemann FR, et al. Among authors: kunz ws. Anal Biochem. 2000 Mar 1;279(1):55-60. doi: 10.1006/abio.1999.4434. Anal Biochem. 2000. PMID: 10683230

7

Muscle fibres: applications for the study of the metabolic consequences of enzyme deficiencies in skeletal muscle.

Vielhaber S, Kudin A, Schröder R, Elger CE, Kunz WS. Vielhaber S, et al. Among authors: kunz ws. Biochem Soc Trans. 2000 Feb;28(2):159-64. doi: 10.1042/bst0280159. Biochem Soc Trans. 2000. PMID: 10816119

8

Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis.

Vielhaber S, Kunz D, Winkler K, Wiedemann FR, Kirches E, Feistner H, Heinze HJ, Elger CE, Schubert W, Kunz WS. Vielhaber S, et al. Among authors: kunz d, kunz ws. Brain. 2000 Jul;123 ( Pt 7):1339-48. doi: 10.1093/brain/123.7.1339. Brain. 2000. PMID: 10869047 Clinical Trial.

9

Flux control of cytochrome c oxidase in human skeletal muscle.

Kunz WS, Kudin A, Vielhaber S, Elger CE, Attardi G, Villani G. Kunz WS, et al. J Biol Chem. 2000 Sep 8;275(36):27741-5. doi: 10.1074/jbc.M004833200. J Biol Chem. 2000. PMID: 10869362 Free article.

10

New insights into the metabolic consequences of large-scale mtDNA deletions: a quantitative analysis of biochemical, morphological, and genetic findings in human skeletal muscle.

Schröder R, Vielhaber S, Wiedemann FR, Kornblum C, Papassotiropoulos A, Broich P, Zierz S, Elger CE, Reichmann H, Seibel P, Klockgether T, Kunz WS. Schröder R, et al. Among authors: kunz ws. J Neuropathol Exp Neurol. 2000 May;59(5):353-60. doi: 10.1093/jnen/59.5.353. J Neuropathol Exp Neurol. 2000. PMID: 10888364

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

295 results

Search Page