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Plos Genetics
|
December 17, 2013
Somatic mtDNA mutation spectra in the aging human putamen
Siôn L Williams, Deborah C Mash, Stephan Züchner, et al.
Carcinogenesis
|
October 14, 2005
Oxidative phosphorylation dysfunction modulates expression of extracellular matrix--remodeling genes and invasion
Corina van Waveren, Yubo Sun, Herman S Cheung, et al.
Methods in Enzymology
|
November 23, 2014
The use of mitochondria-targeted endonucleases to manipulate mtDNA
Sandra R Bacman, Sion L Williams, Milena Pinto, et al.
Nature Communications
|
June 29, 2018
The mitochondrial DNA polymerase gamma degrades linear DNA fragments precluding the formation of deletions
Nadee Nissanka, Sandra R Bacman, Melanie J Plastini, et al.
The Journal of Biological Chemistry
|
October 9, 2022
Precise and simultaneous quantification of mitochondrial DNA heteroplasmy and copy number by digital PCR
Wendy K Shoop, Cassandra L Gorsuch, Sandra R Bacman, et al.
Molecular Neurobiology
|
September 8, 2018
Ablation of Cytochrome c in Adult Forebrain Neurons Impairs Oxidative Phosphorylation Without Detectable Apoptosis
Milena Pinto, Uma D Vempati, Francisca Diaz, et al.
Human Molecular Genetics
|
August 17, 2005
Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency
Francisca Diaz, Christine K Thomas, Sofia Garcia, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 8, 2011
The striatum is highly susceptible to mitochondrial oxidative phosphorylation dysfunctions
Alicia M Pickrell, Hirokazu Fukui, Xiao Wang, et al.
Human Molecular Genetics
|
March 20, 2009
PGC-1alpha/beta induced expression partially compensates for respiratory chain defects in cells from patients with mitochondrial disorders
Sarika Srivastava, Francisca Diaz, Luisa Iommarini, et al.
Nature Medicine
|
August 6, 2013
Specific elimination of mutant mitochondrial genomes in patient-derived cells by mitoTALENs
Sandra R Bacman, Siôn L Williams, Milena Pinto, et al.
Page
of 16
Search research articles
Search
Showing results (71-80 of 152) with videos related to
Sort By:
Page
of 16
Plos Genetics
|
December 17, 2013
Somatic mtDNA mutation spectra in the aging human putamen
Siôn L Williams, Deborah C Mash, Stephan Züchner, et al.
Carcinogenesis
|
October 14, 2005
Oxidative phosphorylation dysfunction modulates expression of extracellular matrix--remodeling genes and invasion
Corina van Waveren, Yubo Sun, Herman S Cheung, et al.
Methods in Enzymology
|
November 23, 2014
The use of mitochondria-targeted endonucleases to manipulate mtDNA
Sandra R Bacman, Sion L Williams, Milena Pinto, et al.
Nature Communications
|
June 29, 2018
The mitochondrial DNA polymerase gamma degrades linear DNA fragments precluding the formation of deletions
Nadee Nissanka, Sandra R Bacman, Melanie J Plastini, et al.
The Journal of Biological Chemistry
|
October 9, 2022
Precise and simultaneous quantification of mitochondrial DNA heteroplasmy and copy number by digital PCR
Wendy K Shoop, Cassandra L Gorsuch, Sandra R Bacman, et al.
Molecular Neurobiology
|
September 8, 2018
Ablation of Cytochrome c in Adult Forebrain Neurons Impairs Oxidative Phosphorylation Without Detectable Apoptosis
Milena Pinto, Uma D Vempati, Francisca Diaz, et al.
Human Molecular Genetics
|
August 17, 2005
Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency
Francisca Diaz, Christine K Thomas, Sofia Garcia, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 8, 2011
The striatum is highly susceptible to mitochondrial oxidative phosphorylation dysfunctions
Alicia M Pickrell, Hirokazu Fukui, Xiao Wang, et al.
Human Molecular Genetics
|
March 20, 2009
PGC-1alpha/beta induced expression partially compensates for respiratory chain defects in cells from patients with mitochondrial disorders
Sarika Srivastava, Francisca Diaz, Luisa Iommarini, et al.
Nature Medicine
|
August 6, 2013
Specific elimination of mutant mitochondrial genomes in patient-derived cells by mitoTALENs
Sandra R Bacman, Siôn L Williams, Milena Pinto, et al.
Page
of 16