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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

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

Topoisomerase 3α Is Required for Decatenation and Segregation of Human mtDNA
Thomas J. Nicholls, C. A. Nadalutti, E. Motori, E. W. Sommerville, G. S. Gorman et al.
Molecular Cell, Journal article 2018
Journal article

A multi-systemic mitochondrial disorder due to a dominant p.Y955H disease variant in DNA polymerase gamma
Triinu Siibak, P. Clemente, A. Bratic, H. Bruhn, T. E. S. Kauppila et al.
Human Molecular Genetics, Journal article 2017
Journal article

Selective mitochondrial DNA degradation following double-strand breaks
A. Moretton, F. Morel, Bertil Macao, P. Lachaume, L. Ishak et al.
Plos One, Journal article 2017
Journal article

Showing 31 - 40 of 68

2012

Mammalian transcription factor A is a core component of the mitochondrial transcription machinery
Yonghong Shi, Anke Dierckx, Paulina Wanrooij, Sjoerd Wanrooij, N. G. Larsson et al.
Proceedings of the National Academy of Science of the United States of America, Journal article 2012
Journal article

Role of human DNA glycosylase Nei-like 2 (NEIL2) and single strand break repair protein polynucleotide kinase 3'-phosphatase in maintenance of mitochondrial genome.
Santi M Mandal, Muralidhar L Hegde, Arpita Chatterjee, Pavana M Hegde, Bartosz Szczesny et al.
The Journal of biological chemistry, Journal article 2012
Journal article

In vivo mutagenesis reveals that OriL is essential for mitochondrial DNA replication.
Sjoerd Wanrooij, Javier Miralles Fusté, James B Stewart, Paulina H Wanrooij, Tore Samuelsson et al.
EMBO reports, Journal article 2012
Journal article

Protein sliding and DNA denaturation are essential for DNA organization by human mitochondrial transcription factor A
G. Farge, N. Laurens, O. D. Broekmans, Smjl van den Wildenberg, L. C. M. Dekker et al.
Nature Communications, Journal article 2012
Journal article

2011

Adenosine Kinase Deficiency Disrupts the Methionine Cycle and Causes Hypermethioninemia, Encephalopathy, and Abnormal Liver Function
Magnus K. Bjursell, HJ Blom, Jorge Asin-Cayuela, ML Engvall, N Lesko et al.
AMERICAN JOURNAL OF HUMAN GENETICS, Journal article 2011
Journal article

Super-resolution microscopy reveals that mammalian mitochondrial nucleoids have a uniform size and frequently contain a single copy of mtDNA
C Kukat, CA Wurm, H Spahr, Maria Falkenberg, NG Larsson et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, Journal article 2011
Journal article

2010

Human mitochondrial transcription revisited: only TFAM and TFB2M are required for transcription of the mitochondrial genes in vitro.
Dmitry Litonin, Marina Sologub, Yonghong Shi, Maria Savkina, Michael Anikin et al.
The Journal of biological chemistry, Journal article 2010
Journal article

Showing 31 - 40 of 68

Page Manager: Chatrine Butler|Last update: 8/28/2017
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