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Maria Falkenberg

Showing results (51-60 of 104) with videos related to

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Human Molecular Genetics|March 1, 2013
Subnormal levels of POLγA cause inefficient initiation of light-strand DNA synthesis and lead to mitochondrial DNA deletions and progressive external ophthalmoplegia [corrected]Sara Roos, Bertil Macao, Javier Miralles Fusté, et al.
Current Genetics|September 30, 2005
A family of putative transcription termination factors shared amongst metazoans and plantsTomas Linder, Chan Bae Park, Jordi Asin-Cayuela, et al.
Nucleic Acids Research|August 14, 2018
A two-nuclease pathway involving RNase H1 is required for primer removal at human mitochondrial OriLAli Al-Behadili, Jay P Uhler, Anna-Karin Berglund, et al.
EMBO Reports|October 24, 2012
In vivo mutagenesis reveals that OriL is essential for mitochondrial DNA replicationSjoerd Wanrooij, Javier Miralles Fusté, James B Stewart, et al.
Journal of Perinatal Medicine|October 28, 2021
Second trimester fetal thymus size in association to preterm birthChristian Porschen, Ralf Schmitz, Rene Schmidt, et al.
Plos One|April 29, 2017
Selective mitochondrial DNA degradation following double-strand breaksAmandine Moretton, Frédéric Morel, Bertil Macao, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 21, 2009
Unraveling the structure of DNA during overstretching by using multicolor, single-molecule fluorescence imagingJoost van Mameren, Peter Gross, Geraldine Farge, et al.
Nucleic Acids Research|June 23, 2010
Maintenance of respiratory chain function in mouse hearts with severely impaired mtDNA transcriptionChristoph Freyer, Chan Bae Park, Mats I Ekstrand, et al.
Neurology. Genetics|February 12, 2020
Deep sequencing of mitochondrial DNA and characterization of a novel <i>POLG</i> mutation in a patient with arPEOCarola Hedberg-Oldfors, Bertil Macao, Swaraj Basu, et al.
Neuromuscular Disorders : NMD|February 13, 2021
Functional analysis of a novel POLγA mutation associated with a severe perinatal mitochondrial encephalomyopathyNiklas Darin, Triinu Siibak, Bradley Peter, et al.
Pageof 11

Showing results (51-60 of 104) with videos related to

Sort By:
Pageof 11
Human Molecular Genetics|March 1, 2013
Subnormal levels of POLγA cause inefficient initiation of light-strand DNA synthesis and lead to mitochondrial DNA deletions and progressive external ophthalmoplegia [corrected]Sara Roos, Bertil Macao, Javier Miralles Fusté, et al.
Current Genetics|September 30, 2005
A family of putative transcription termination factors shared amongst metazoans and plantsTomas Linder, Chan Bae Park, Jordi Asin-Cayuela, et al.
Nucleic Acids Research|August 14, 2018
A two-nuclease pathway involving RNase H1 is required for primer removal at human mitochondrial OriLAli Al-Behadili, Jay P Uhler, Anna-Karin Berglund, et al.
EMBO Reports|October 24, 2012
In vivo mutagenesis reveals that OriL is essential for mitochondrial DNA replicationSjoerd Wanrooij, Javier Miralles Fusté, James B Stewart, et al.
Journal of Perinatal Medicine|October 28, 2021
Second trimester fetal thymus size in association to preterm birthChristian Porschen, Ralf Schmitz, Rene Schmidt, et al.
Plos One|April 29, 2017
Selective mitochondrial DNA degradation following double-strand breaksAmandine Moretton, Frédéric Morel, Bertil Macao, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 21, 2009
Unraveling the structure of DNA during overstretching by using multicolor, single-molecule fluorescence imagingJoost van Mameren, Peter Gross, Geraldine Farge, et al.
Nucleic Acids Research|June 23, 2010
Maintenance of respiratory chain function in mouse hearts with severely impaired mtDNA transcriptionChristoph Freyer, Chan Bae Park, Mats I Ekstrand, et al.
Neurology. Genetics|February 12, 2020
Deep sequencing of mitochondrial DNA and characterization of a novel <i>POLG</i> mutation in a patient with arPEOCarola Hedberg-Oldfors, Bertil Macao, Swaraj Basu, et al.
Neuromuscular Disorders : NMD|February 13, 2021
Functional analysis of a novel POLγA mutation associated with a severe perinatal mitochondrial encephalomyopathyNiklas Darin, Triinu Siibak, Bradley Peter, et al.
Pageof 11