Wolfram S Kunz
Wolfram S Kunz
Professor of Neurochemistry, University Bonn
Email verificata su ukb.uni-bonn.de - Home page
TitoloCitata daAnno
Analysis of mitochondrial function in situ in permeabilized muscle fibers, tissues and cells
AV Kuznetsov, V Veksler, FN Gellerich, V Saks, R Margreiter, WS Kunz
Nature protocols 3 (6), 965, 2008
Characterization of superoxide-producing sites in isolated brain mitochondria
AP Kudin, NYB Bimpong-Buta, S Vielhaber, CE Elger, WS Kunz
Journal of Biological Chemistry 279 (6), 4127-4135, 2004
Permeabilized cell and skinned fiber techniques in studies of mitochondrial function in vivo
VA Saks, VI Veksler, AV Kuznetsov, L Kay, P Sikk, T Tiivel, L Tranqui, ...
Bioenergetics of the cell: quantitative aspects, 81-100, 1998
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), eaap8757, 2018
Recombination of human mitochondrial DNA
Y Kraytsberg, M Schwartz, TA Brown, K Ebralidse, WS Kunz, DA Clayton, ...
Science 304 (5673), 981-981, 2004
Parkinson phenotype in aged PINK1-deficient mice is accompanied by progressive mitochondrial dysfunction in absence of neurodegeneration
S Gispert, F Ricciardi, A Kurz, M Azizov, HH Hoepken, D Becker, W Voos, ...
PloS one 4 (6), 2009
Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis
S Vielhaber, D Kunz, K Winkler, FR Wiedemann, E Kirches, H Feistner, ...
Brain 123 (7), 1339-1348, 2000
Neurobehavioral outcome prediction after cardiac surgery: role of neurobiochemical markers of damage to neuronal and glial brain tissue
M Herrmann, AD Ebert, I Galazky, MT Wunderlich, WS Kunz, C Huth
Stroke 31 (3), 645-650, 2000
Impairment of mitochondrial function in skeletal muscle of patients with amyotrophic lateral sclerosis
FR Wiedemann, K Winkler, AV Kuznetsov, C Bartels, S Vielhaber, ...
Journal of the neurological sciences 156 (1), 65-72, 1998
Mitochondrial dysfunction, peroxidation damage and changes in glutathione metabolism in PARK6
HH Hoepken, S Gispert, B Morales, O Wingerter, D Del Turco, A Mlsch, ...
Neurobiology of disease 25 (2), 401-411, 2007
Mitochondrial complex I deficiency in the epileptic focus of patients with temporal lobe epilepsy
WS Kunz, AP Kudin, S Vielhaber, I Blmcke, W Zuschratter, J Schramm, ...
Annals of neurology 48 (5), 766-773, 2000
The mechanism of neuroprotection by topiramate in an animal model of epilepsy
AP Kudin, G Debska‐Vielhaber, S Vielhaber, CE Elger, WS Kunz
Epilepsia 45 (12), 1478-1487, 2004
Seizure‐dependent modulation of mitochondrial oxidative phosphorylation in rat hippocampus
AP Kudin, TA Kudina, J Seyfried, S Vielhaber, H Beck, CE Elger, WS Kunz
European Journal of Neuroscience 15 (7), 1105-1114, 2002
Impaired mitochondrial oxidative phosphorylation in skeletal muscle of the dystrophin-deficient mdx mouse
AV Kuznetsov, K Winkler, F Wiedemann, P von Bossanyi, K Dietzmann, ...
Molecular and cellular biochemistry 183 (1-2), 87-96, 1998
Mitochondrial potassium channels
A Szewczyk, W Jarmuszkiewicz, WS Kunz
IUBMB life 61 (2), 134-143, 2009
Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease
C Kornblum, TJ Nicholls, TB Haack, S Schler, V Peeva, K Danhauser, ...
Nature genetics 45 (2), 214, 2013
The role of mitochondria in epileptogenesis
WS Kunz
Current opinion in neurology 15 (2), 179-184, 2002
Myofiber integrity depends on desmin network targeting to Z-disks and costameres via distinct plectin isoforms
P Konieczny, P Fuchs, S Reipert, WS Kunz, A Zeöld, I Fischer, D Paulin, ...
The Journal of cell biology 181 (4), 667-681, 2008
Contribution of different enzymes to flavoprotein fluorescence of isolated rat liver mitochondria
WS Kunz, W Kunz
Biochimica et Biophysica Acta (BBA)-General Subjects 841 (3), 237-246, 1985
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16. 1, 2q22. 3 and 17q21. 32
Epicure Consortium, EMINet Consortium, M Steffens, C Leu, AK Ruppert, ...
Human molecular genetics 21 (24), 5359-5372, 2012
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
Articoli 1–20