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Angela Pyle

Showing results (61-70 of 119) with videos related to

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Neurology. Genetics|December 22, 2017
Opening One's Eyes to Mosaicism in Progressive External OphthalmoplegiaEwen W Sommerville, Rachel L Jones, Steven A Hardy, et al.
Frontiers in Immunology|October 16, 2018
Exposure of Monocytic Cells to Lipopolysaccharide Induces Coordinated Endotoxin Tolerance, Mitochondrial Biogenesis, Mitophagy, and Antioxidant DefensesJohn D Widdrington, Aurora Gomez-Duran, Angela Pyle, et al.
Annals of Neurology|March 24, 2005
Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PDAngela Pyle, Thomas Foltynie, Watcharee Tiangyou, et al.
Biochimica Et Biophysica Acta|December 9, 2010
POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblastsJoanna D Stewart, Susanne Schoeler, Kamil S Sitarz, et al.
Brain : a Journal of Neurology|December 16, 2014
Exome sequencing in undiagnosed inherited and sporadic ataxiasAngela Pyle, Tania Smertenko, David Bargiela, et al.
Clinical Genetics|August 12, 2020
Homozygous TAF1C variants are associated with a novel childhood-onset neurological phenotypeOula Knuutinen, Angela Pyle, Maria Suo-Palosaari, et al.
Trends in Neuroscience and Education|September 12, 2024
Applying the science of learning to teacher professional development and back again: Lessons from 3 country contextsJennifer M Zosh, Angela Pyle, Nikhit D'Sa, et al.
Human Molecular Genetics|March 9, 2018
Defective mitochondrial protease LonP1 can cause classical mitochondrial diseaseBradley Peter, Christie L Waddington, Monika Oláhová, et al.
Human Molecular Genetics|January 24, 2018
A novel mechanism causing imbalance of mitochondrial fusion and fission in human myopathiesMarina Bartsakoulia, Angela Pyle, Diego Troncoso-Chandía, et al.
Human Genomics|February 2, 2019
A genome-wide association study of mitochondrial DNA copy number in two population-based cohortsAnna L Guyatt, Rebecca R Brennan, Kimberley Burrows, et al.
Pageof 12

Showing results (61-70 of 119) with videos related to

Sort By:
Pageof 12
Neurology. Genetics|December 22, 2017
Opening One's Eyes to Mosaicism in Progressive External OphthalmoplegiaEwen W Sommerville, Rachel L Jones, Steven A Hardy, et al.
Frontiers in Immunology|October 16, 2018
Exposure of Monocytic Cells to Lipopolysaccharide Induces Coordinated Endotoxin Tolerance, Mitochondrial Biogenesis, Mitophagy, and Antioxidant DefensesJohn D Widdrington, Aurora Gomez-Duran, Angela Pyle, et al.
Annals of Neurology|March 24, 2005
Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PDAngela Pyle, Thomas Foltynie, Watcharee Tiangyou, et al.
Biochimica Et Biophysica Acta|December 9, 2010
POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblastsJoanna D Stewart, Susanne Schoeler, Kamil S Sitarz, et al.
Brain : a Journal of Neurology|December 16, 2014
Exome sequencing in undiagnosed inherited and sporadic ataxiasAngela Pyle, Tania Smertenko, David Bargiela, et al.
Clinical Genetics|August 12, 2020
Homozygous TAF1C variants are associated with a novel childhood-onset neurological phenotypeOula Knuutinen, Angela Pyle, Maria Suo-Palosaari, et al.
Trends in Neuroscience and Education|September 12, 2024
Applying the science of learning to teacher professional development and back again: Lessons from 3 country contextsJennifer M Zosh, Angela Pyle, Nikhit D'Sa, et al.
Human Molecular Genetics|March 9, 2018
Defective mitochondrial protease LonP1 can cause classical mitochondrial diseaseBradley Peter, Christie L Waddington, Monika Oláhová, et al.
Human Molecular Genetics|January 24, 2018
A novel mechanism causing imbalance of mitochondrial fusion and fission in human myopathiesMarina Bartsakoulia, Angela Pyle, Diego Troncoso-Chandía, et al.
Human Genomics|February 2, 2019
A genome-wide association study of mitochondrial DNA copy number in two population-based cohortsAnna L Guyatt, Rebecca R Brennan, Kimberley Burrows, et al.
Pageof 12