Gábor Zsurka
Gábor Zsurka
Department of Epileptology, University of Bonn
Verified email at ukb.uni-bonn.de
Cited by
Cited by
Mrs2p is an essential component of the major electrophoretic Mg2+ influx system in mitochondria
M Kolisek, G Zsurka, J Samaj, J Weghuber, RJ Schweyen, M Schweigel
The EMBO journal 22 (6), 1235-1244, 2003
The LETM1/YOL027 gene family encodes a factor of the mitochondrial K+ homeostasis with a potential role in the Wolf-Hirschhorn syndrome
K Nowikovsky, EM Froschauer, G Zsurka, J Samaj, S Reipert, M Kolisek, ...
Journal of Biological Chemistry 279 (29), 30307-30315, 2004
Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease
C Kornblum, TJ Nicholls, TB Haack, S Schöler, V Peeva, K Danhauser, ...
Nature genetics 45 (2), 214, 2013
Mitochondrial involvement in temporal lobe epilepsy
AP Kudin, G Zsurka, CE Elger, WS Kunz
Experimental neurology 218 (2), 326-332, 2009
Mitochondrial dysfunction and seizures: the neuronal energy crisis
G Zsurka, WS Kunz
The Lancet Neurology 14 (9), 956-966, 2015
The human mitochondrial Mrs2 protein functionally substitutes for its yeast homologue, a candidate magnesium transporter
G Zsurka, J Gregáň, RJ Schweyen
Genomics 72 (2), 158-168, 2001
Mitochondrial DNA damage and the aging process–facts and imaginations
RJ Wiesner, G Zsurka, WS Kunz, RJ Wiesner, G Zsurka, WS Kunz
Free radical research 40 (12), 1284-1294, 2006
Recombination of mitochondrial DNA in skeletal muscle of individuals with multiple mitochondrial DNA heteroplasmy
G Zsurka, Y Kraytsberg, T Kudina, C Kornblum, CE Elger, K Khrapko, ...
Nature genetics 37 (8), 873-877, 2005
The mitochondrial inner membrane protein Lpe10p, a homologue of Mrs2p, is essential for magnesium homeostasis and group II intron splicing in yeast
J Gregan, DM Bui, R Pillich, M Fink, G Zsurka, RJ Schweyen
Molecular and General Genetics MGG 264 (6), 773-781, 2001
Mitofusin 2 mutations affect mitochondrial function by mitochondrial DNA depletion
S Vielhaber, G Debska-Vielhaber, V Peeva, S Schoeler, AP Kudin, I Minin, ...
Acta neuropathologica 125 (2), 245-256, 2013
Conditional knockdown of hMRS2 results in loss of mitochondrial Mg + uptake and cell death
M Piskacek, L Zotova, G Zsurka, RJ Schweyen
Journal of cellular and molecular medicine 13 (4), 693-700, 2009
Linear mitochondrial DNA is rapidly degraded by components of the replication machinery
V Peeva, D Blei, G Trombly, S Corsi, MJ Szukszto, P Rebelo-Guiomar, ...
Nature communications 9 (1), 1-11, 2018
Repeats, longevity and the sources of mtDNA deletions: evidence from ‘deletional spectra’
X Guo, KY Popadin, N Markuzon, YL Orlov, Y Kraytsberg, KJ Krishnan, ...
Trends in genetics 26 (8), 340-343, 2010
A homozygous splice-site mutation in CARS2 is associated with progressive myoclonic epilepsy
K Hallmann, G Zsurka, S Moskau-Hartmann, J Kirschner, R Korinthenberg, ...
Neurology 83 (23), 2183-2187, 2014
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals
YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ...
The American Journal of Human Genetics 105 (2), 267-282, 2019
Linear mtDNA fragments and unusual mtDNA rearrangements associated with pathological deficiency of MGME1 exonuclease
TJ Nicholls, G Zsurka, V Peeva, S Schöler, RJ Szczesny, D Cysewski, ...
Human molecular genetics 23 (23), 6147-6162, 2014
Clonally expanded mitochondrial DNA mutations in epileptic individuals with mutated DNA polymerase γ
G Zsurka, M Baron, JD Stewart, C Kornblum, M Bös, R Sassen, RW Taylor, ...
Journal of Neuropathology & Experimental Neurology 67 (9), 857-866, 2008
Mosaic deficiency in mitochondrial oxidative metabolism promotes cardiac arrhythmia during aging
OR Baris, S Ederer, JFG Neuhaus, JC von Kleist-Retzow, CM Wunderlich, ...
Cell metabolism 21 (5), 667-677, 2015
Mitochondrial dysfunction in neurological disorders with epileptic phenotypes
G Zsurka, WS Kunz
Journal of bioenergetics and biomembranes 42 (6), 443-448, 2010
Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNAPhe gene
G Zsurka, KG Hampel, I Nelson, C Jardel, SR Mirandola, R Sassen, ...
Neurology 74 (6), 507-512, 2010
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