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Maria Falkenberg

Professor

Maria Falkenberg
Professor
maria.falkenberg@medkem.gu.se
+46 31 786 3444
0732-309119

Room number: 5374
Postal Address: Box 440, 40530 Göteborg
Visiting Address: Medicinaregatan 9A , 41390 Göteborg


Department of Medical Biochemistry and Cell biology at Institute of Biomedicine (More Information)
Box 440
405 30 Göteborg
Fax: +46 31416108
Visiting Address: Medicinaregatan 9 A-B , 413 90 Göteborg

Latest publications

SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder
V. Del Dotto, F. Ullah, I. Di Meo, P. Magini, M. Gusic et al.
Journal of Clinical Investigation, Journal article 2020
Journal article

Dinucleotide Degradation by REXO2 Maintains Promoter Specificity in Mammalian Mitochondria
Thomas J. Nicholls, H. Spahr, S. Jiang, S. J. Siira, C. Koolmeister et al.
Molecular Cell, Journal article 2019
Journal article

Organization of DNA in mammalian mitochondria
G. É R. Farge, Maria Falkenberg
International Journal of Molecular Sciences, Journal article 2019
Journal article

Structural basis for adPEO-causing mutations in the mitochondrial TWINKLE helicase.
Bradley Peter, Geraldine Farge, Carlos Pardo-Hernandez, Stefan Tångefjord, Maria Falkenberg
Human molecular genetics, Journal article 2019
Journal article

Mice lacking the mitochondrial exonuclease MGME1 accumulate mtDNA deletions without developing progeria
S. Matic, M. Jiang, Thomas J. Nicholls, Jay Uhler, C. Dirksen-Schwanenland et al.
Nature Communications, Journal article 2018
Journal article

Defective mitochondrial protease LonP1 can cause classical mitochondrial disease
Bradley Peter, C. L. Waddington, M. Olahova, E. W. Sommerville, S. Hopton et al.
Human Molecular Genetics, Journal article 2018
Journal article

Showing 21 - 30 of 71

2015

Cross-strand binding of TFAM to a single mtDNA molecule forms the mitochondrial nucleoid
C. Kukat, K. M. Davies, C. A. Wurm, H. Spahr, N. A. Bonekamp et al.
Proceedings of the National Academy of Sciences of the United States of America, Journal article 2015
Journal article

2014

A human mitochondrial poly(A) polymerase mutation reveals the complexities of post-transcriptional mitochondrial gene expression
W. C. Wilson, H. T. Hornig-Do, F. Bruni, J. H. Chang, A. A. Jourdain et al.
Human Molecular Genetics, Journal article 2014
Journal article

In Vitro-Reconstituted Nucleoids Can Block Mitochondrial DNA Replication and Transcription
G. Farge, Majda Mehmedovic, M. Baclayon, Smjl van den Wildenberg, W. H. Roos et al.
Cell Reports, Journal article 2014
Journal article

The UbL protein UBTD1 stably interacts with the UBE2D family of E2 ubiquitin conjugating enzymes
Jay Uhler, H. Spahr, G. Farge, S. Clavel, N. G. Larsson et al.
Biochemical and Biophysical Research Communications, Journal article 2014
Journal article

2013

MTERF1 Binds mtDNA to Prevent Transcriptional Interference at the Light-Strand Promoter but Is Dispensable for rRNA Gene Transcription Regulation
M. Terzioglu, B. Ruzzenente, J. Harmel, A. Mourier, Elisabeth Jemt et al.
Cell Metabolism, Journal article 2013
Journal article

Showing 21 - 30 of 71

Page Manager: Evelyn Vilkman|Last update: 8/28/2017
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Utskriftsdatum: 2020-02-22