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Viktoriya Peeva
Viktoriya Peeva
Bestätigte E-Mail-Adresse bei ukb.uni-bonn.de
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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), 214-219, 2013
2582013
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), 1727, 2018
1832018
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, 245-256, 2013
942013
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
852015
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
842014
Mutant desmin substantially perturbs mitochondrial morphology, function and maintenance in skeletal muscle tissue
L Winter, I Wittig, V Peeva, B Eggers, J Heidler, F Chevessier, RA Kley, ...
Acta neuropathologica 132, 453-473, 2016
632016
Is there still any role for oxidative stress in mitochondrial DNA-dependent aging?
G Zsurka, V Peeva, A Kotlyar, WS Kunz
Genes 9 (4), 175, 2018
602018
Neuropathological signs of inflammation correlate with mitochondrial DNA deletions in mesial temporal lobe epilepsy
E Volmering, P Niehusmann, V Peeva, A Grote, G Zsurka, J Altmüller, ...
Acta neuropathologica 132, 277-288, 2016
422016
Distinct patterns of mitochondrial genome diversity in bonobos (Pan paniscus) and humans
G Zsurka, T Kudina, V Peeva, K Hallmann, CE Elger, K Khrapko, WS Kunz
BMC evolutionary biology 10, 1-11, 2010
302010
Impairment of mitochondrial oxidative phosphorylation in skin fibroblasts of SALS and FALS patients is rescued by in vitro treatment with ROS scavengers
G Debska-Vielhaber, I Miller, V Peeva, W Zuschratter, J Walczak, ...
Experimental neurology 339, 113620, 2021
182021
Desmin knock-out cardiomyopathy: A heart on the verge of metabolic crisis
B Elsnicova, D Hornikova, V Tibenska, D Kolar, T Tlapakova, B Schmid, ...
International Journal of Molecular Sciences 23 (19), 12020, 2022
132022
Birth asphyxia as the most frequent perinatal complication
V Peeva, O Golubnitschaja
Predictive diagnostics and personalized treatment: dream or reality, 499-507, 2009
132009
Chromium-picolinate therapy in diabetes care: molecular and subcellular profiling revealed a necessity for individual outcome prediction, personalised treatment algorithms …
K Yeghiazaryan, V Peeva, A Shenoy, H H Schild, O Golubnitschaja
Infectious Disorders-Drug Targets (Formerly Current Drug Targets-Infectious …, 2011
122011
Distinct segregation of the pathogenic m. 5667G> A mitochondrial tRNAAsn mutation in extraocular and skeletal muscle in chronic progressive external ophthalmoplegia
E Schlapakow, V Peeva, G Zsurka, M Jeub, B Wabbels, C Kornblum, ...
Neuromuscular Disorders 29 (5), 358-367, 2019
112019
Potential targets for early diagnosis and neuroprotection in asphyxiated newborns
K Yeghiazaryan, V Peeva, O Golubnitschaja, M Morelli, ...
Predictive diagnostics and personalized treatment: dream or reality, 509-526, 2009
102009
A preliminary characterization of a novel bacteriocin-like substance from Enterococcus durum M-3
V Peeva, P Ivanova, N Harizanova, S Dimov
Biotechnology & Biotechnological Equipment 20 (3), 120-127, 2006
62006
Heart failure after pressure overload in autosomal-dominant desminopathies: Lessons from heterozygous DES-p.R349P knock-in mice
F Stöckigt, L Eichhorn, T Beiert, V Knappe, T Radecke, M Steinmetz, ...
PLoS One 15 (3), e0228913, 2020
52020
Novel pathogenic sequence variation m. 5789T> C causes NARP syndrome and promotes formation of deletions of the mitochondrial genome
M Hippen, G Zsurka, V Peeva, J Machts, K Schwiecker, ...
Neurology: Genetics 8 (2), e660, 2021
42021
O. 24 Loss of function of MGME1, a novel player in mitochondrial DNA replication, causes a distinct autosomal recessive mitochondrial disorder
C Kornblum, T Nicholls, TB Haack, S Schoeler, V Peeva, K Danhauser, ...
Neuromuscular Disorders 23 (9-10), 852, 2013
22013
The fate of oxidative strand breaks in mitochondrial DNA
G Trombly, AM Said, AP Kudin, V Peeva, J Altmüller, K Becker, K Köhrer, ...
Antioxidants 12 (5), 1087, 2023
12023
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