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1

Apraxia of lid opening mimicking ptosis in compound heterozygosity for A467T and W748S POLG1 mutations

Sebastian Paus, Gabor Zsurka, Miriam Baron, Marcus Deschauer, Christian Bamberg, Thomas Klockgether, Wolfram S. Kunz, Cornelia Kornblum

Journal:

Movement Disorders

Year:

2008

Language:

english

File:

PDF, 749 KB

english, 2008

2

Mitochondrial mutation as a probable causative factor in familial progressive tubulointerstitial nephritis

Gábor Zsurka, Jenö Ormos, Béla Iványi, Sándor Túri, Emöke Endreffy, Márta Magyari, Sándor Sonkodi, P. Venetianer

Journal:

Year:

1997

Language:

english

File:

PDF, 533 KB

english, 1997

3

Mitochondrial dysfunction in neurological disorders with epileptic phenotypes

Gábor Zsurka, Wolfram S. Kunz

Journal:

Journal of Bioenergetics and Biomembranes

Year:

2010

Language:

english

File:

PDF, 131 KB

english, 2010

4

Recombination of mitochondrial DNA in skeletal muscle of individuals with multiple mitochondrial DNA heteroplasmy

Zsurka, Gábor, Kraytsberg, Yevgenia, Kudina, Tatiana, Kornblum, Cornelia, Elger, Christian E, Khrapko, Konstantin, Kunz, Wolfram S

Journal:

Nature Genetics

Year:

2005

Language:

english

File:

PDF, 289 KB

english, 2005

5

Analysis of mitochondrial DNA deletions in epileptic hippocampus

Viktoriya M. Peeva, Gábor Zsurka, Wolfram S. Kunz

Journal:

Biochimica et Biophysica Acta (BBA) - Bioenergetics

Year:

2010

Language:

english

File:

PDF, 52 KB

english, 2010

6

Clonal expansion of different mtDNA variants without selective advantage in solid tumors

Julia Gekeler, Gábor Zsurka, Wolfram S. Kunz, Simon F. Preuss, Jens Peter Klussmann, Orlando Guntinas-Lichius, Rudolf J. Wiesner

Journal:

Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis

Year:

2009

Language:

english

File:

PDF, 842 KB

english, 2009

7

Repeats, longevity and the sources of mtDNA deletions: evidence from ‘deletional spectra’

Xinhong Guo, Konstantin Yu. Popadin, Natalya Markuzon, Yuriy L. Orlov, Yevgenya Kraytsberg, Kim J. Krishnan, Gábor Zsurka, Douglas M. Turnbull, Wolfram S. Kunz, Konstantin Khrapko

Journal:

Trends in Genetics

Year:

2010

Language:

english

File:

PDF, 787 KB

english, 2010

8

Conditional knockdown of hMRS2 results in loss of mitochondrial Mg + uptake and cell death

Martin Piskacek, Ludmila Zotova, Gábor Zsurka, Rudolf J. Schweyen

Journal:

Journal of Cellular and Molecular Medicine

Year:

2009

Language:

english

File:

PDF, 4.06 MB

english, 2009

9

Distinct patterns of mitochondrial genome diversity in bonobos (Pan paniscus) and humans

Gábor Zsurka, Tatiana Kudina, Viktoriya Peeva, Kerstin Hallmann, Christian E Elger, Konstantin Khrapko, Wolfram S Kunz

Journal:

BMC Evolutionary Biology

Year:

2010

Language:

english

File:

PDF, 944 KB

english, 2010

10

The Human Mitochondrial Mrs2 Protein Functionally Substitutes for Its Yeast Homologue, A Candidate Magnesium Transporter

Gábor Zsurka, Juraj Gregáň, Rudolf J. Schweyen

Journal:

Year:

2001

Language:

english

File:

PDF, 823 KB

english, 2001

11

Mitochondrial involvement in temporal lobe epilepsy

Alexei P. Kudin, Gábor Zsurka, Christian E. Elger, Wolfram S. Kunz

Journal:

Experimental Neurology

Year:

2009

Language:

english

File:

PDF, 359 KB

english, 2009

12

Inheritance of Mitochondrial DNA Recombinants in Double-Heteroplasmic Families: Potential Implications for Phylogenetic Analysis

Gábor Zsurka, Kevin G. Hampel, Tatiana Kudina, Cornelia Kornblum, Yevgenia Kraytsberg, Christian E. Elger, Konstantin Khrapko, Wolfram S. Kunz

Journal:

The American Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 1.43 MB

english, 2007

13

No mitochondrial haplotype was found to increase risk for alzheimer’s disease

Gábor Zsurka, János Kálmán, Anna Juhász, Albert Császár, István Raskó, Zoltán Janka, Pál Venetianer

Journal:

Biological Psychiatry

Year:

1998

Language:

english

File:

PDF, 23 KB

english, 1998

14

Mitochondrial involvement in neurodegenerative diseases

Zsurka, Gábor, Kunz, Wolfram S.

Journal:

Year:

2013

Language:

english

File:

PDF, 436 KB

english, 2013

15

Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease

Kornblum, Cornelia, Nicholls, Thomas J, Haack, Tobias B, Schöler, Susanne, Peeva, Viktoriya, Danhauser, Katharina, Hallmann, Kerstin, Zsurka, Gábor, Rorbach, Joanna, Iuso, Arcangela, Wieland, Thomas,

Journal:

Nature Genetics

Year:

2013

Language:

english

File:

PDF, 710 KB

english, 2013

16

Mutation in the mitochondrial tRNAIle gene causes progressive myoclonus epilepsy

Zsurka, Gábor, Becker, Felicitas, Heinen, Markus, Gdynia, Hans-Jürgen, Lerche, Holger, Kunz, Wolfram S., Weber, Yvonne G.

Journal:

Year:

2013

Language:

english

File:

PDF, 1.22 MB

english, 2013

17

Oxyphil Cell Metaplasia in the Parathyroids Is Characterized by Somatic Mitochondrial DNA Mutations in NADH Dehydrogenase Genes and Cytochrome c Oxidase Activity–Impairing Genes

Müller-Höcker, Josef, Schäfer, Sabine, Krebs, Stefan, Blum, Helmut, Zsurka, Gábor, Kunz, Wolfram S., Prokisch, Holger, Seibel, Peter, Jung, Andreas

Journal:

The American Journal of Pathology

Year:

2014

Language:

english

File:

PDF, 4.37 MB

english, 2014

18

Mitochondrial DNA damage and the aging process–facts and imaginations*

Wiesner, Rudolf J., Zsurka, Gábor, Kunz, Wolfram S., Wiesner, Rudolf J., Zsurka, Gábor, Kunz, Wolfram S.

Journal:

Free Radical Research

Year:

2006

Language:

english

File:

PDF, 266 KB

english, 2006

19

Mosaic Deficiency in Mitochondrial Oxidative Metabolism Promotes Cardiac Arrhythmia during Aging

Baris, Olivier R., Ederer, Stefan, Neuhaus, Johannes F.G., von Kleist-Retzow, Jürgen-Christoph, Wunderlich, Claudia M., Pal, Martin, Wunderlich, F. Thomas, Peeva, Viktoriya, Zsurka, Gabor, Kunz, Wolfr

Journal:

Cell Metabolism

Year:

2015

Language:

english

File:

PDF, 2.70 MB

english, 2015

20

Concerted action of two novel tRNA mtDNA point mutations in chronic progressive external ophthalmoplegia

Kornblum, Cornelia, Zsurka, Gábor, Wiesner, Rudolf J., Schröder, Rolf, Kunz, Wolfram S.

Journal:

Bioscience Reports

Year:

2008

Language:

english

File:

PDF, 442 KB

english, 2008

21

Mitochondrial dysfunction and seizures: the neuronal energy crisis

Zsurka, Gábor, Kunz, Wolfram S

Journal:

The Lancet Neurology

Year:

2015

Language:

english

File:

PDF, 696 KB

english, 2015

22

Neuropathological signs of inflammation correlate with mitochondrial DNA deletions in mesial temporal lobe epilepsy

Volmering, Elisa, Niehusmann, Pitt, Peeva, Viktoriya, Grote, Alexander, Zsurka, Gábor, Altmüller, Janine, Nürnberg, Peter, Becker, Albert J., Schoch, Susanne, Elger, Christian E., Kunz, Wolfram S.

Journal:

Acta Neuropathologica

Year:

2016

Language:

english

File:

PDF, 2.09 MB

english, 2016

23

Clonally Expanded Mitochondrial DNA Mutations in Epileptic Individuals With Mutated DNA Polymerase γ

Zsurka, Gábor, Baron, Miriam, Stewart, Joanna D., Kornblum, Cornelia, Bös, Monika, Sassen, Robert, Taylor, Robert W., Elger, Christian E., Chinnery, Patrick F., Kunz, Wolfram S.

Journal:

Journal of Neuropathology and Experimental Neurology

Year:

2008

Language:

english

File:

PDF, 706 KB

english, 2008

24

Loss of subunit COX8A reduces stability of human cytochrome c oxidase (COX) complex

Kunz, Wolfram S., Kudin, Alexei P., Zsurka, Gábor, Kornblum, Cornelia, Reimann, Jens, Rüb, Cornelia, Voos, Wolfgang

Journal:

Biochimica et Biophysica Acta (BBA) - Bioenergetics

Year:

2016

Language:

english

File:

PDF, 49 KB

english, 2016

25

Homozygous mutation in TXNRD1 is associated with genetic generalized epilepsy

Kudin, Alexei P., Baron, Gregor, Zsurka, Gábor, Hampel, Kevin G., Elger, Christian E., Grote, Alexander, Weber, Yvonne, Lerche, Holger, Thiele, Holger, Nürnberg, Peter, Schulz, Herbert, Ruppert, Ann-K

Journal:

Free Radical Biology and Medicine

Year:

2017

Language:

english

File:

PDF, 914 KB

english, 2017

26

Is There Still Any Role for Oxidative Stress in Mitochondrial DNA-Dependent Aging?

Zsurka, Gábor, Peeva, Viktoriya, Kotlyar, Alexander, Kunz, Wolfram

Journal:

Year:

2018

Language:

english

File:

PDF, 1.49 MB

english, 2018

27

Retinoencephalopathy with occipital lobe epilepsy in an OPA-1 mutation carrier

Nass, Robert Daniel, Hansen, Niels, Quesada, Carlos, Rüber, Theodor, Kornblum, Cornelia, Zsurka, Gábor, Hermann, Philipp, Becker, Albert, Gärtner, Florian, Hattingen, Elke, Block, Wolfgang, Steidl, Ei

Journal:

Year:

2019

Language:

english

File:

PDF, 839 KB

english, 2019

28

Distinct segregation of the pathogenic m.5667G>A mitochondrial tRNAAsn mutation in extraocular and skeletal muscle in chronic progressive external ophthalmoplegia

Schlapakow, Elena, Peeva, Viktoriya, Zsurka, Gábor, Jeub, Monika, Wabbels, Bettina, Kornblum, Cornelia, Kunz, Wolfram S.

Journal:

Neuromuscular Disorders

Year:

2019

Language:

english

File:

PDF, 1.20 MB

english, 2019

29

Replication fork rescue in mammalian mitochondria

Torregrosa-Muñumer, Rubén, Hangas, Anu, Goffart, Steffi, Blei, Daniel, Zsurka, Gábor, Griffith, Jack, Kunz, Wolfram S., Pohjoismäki, Jaakko L. O.

Journal:

Scientific Reports

Year:

2019

Language:

english

File:

PDF, 7.21 MB

english, 2019

30

MitoWheel, visualizing the human mitochondrial genome

Zsurka, Gábor, Csordás, Attila

Journal:

Bioentrepreneur

Year:

2009

Language:

english

File:

PDF, 319 KB

english, 2009

31

MitoWheel, visualizing the human mitochondrial genome

Zsurka, Gábor, Csordás, Attila

Journal:

Bioentrepreneur

Year:

2009

File:

PDF, 319 KB

2009

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