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Nucleic Acids Research
|
August 1, 2024
LRPPRC and SLIRP synergize to maintain sufficient and orderly mammalian mitochondrial translation
Diana Rubalcava-Gracia, Kristina Bubb, Fredrik Levander, et al.
Journal of Neurology
|
July 14, 2020
Behr syndrome and hypertrophic cardiomyopathy in a family with a novel UCHL1 deletion
Grace McMacken, Hanns Lochmüller, Boglarka Bansagi, et al.
Nature
|
October 5, 2022
Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes
Wei Wei, Katherine R Schon, Greg Elgar, et al.
Cerebellum & Ataxias
|
December 8, 2015
Mitochondrial pathology in progressive cerebellar ataxia
David Bargiela, Priya Shanmugarajah, Christine Lo, et al.
Annals of Clinical and Translational Neurology
|
April 2, 2024
7T MRI detects widespread brain iron deposition in neuroferritinopathy
Alexander G Murley, Catarina Rua, Heather Biggs, et al.
Molecular Genetics and Metabolism
|
May 22, 2012
In vitro supplementation with deoxynucleoside monophosphates rescues mitochondrial DNA depletion
Stefanie Bulst, Elke Holinski-Feder, Brendan Payne, et al.
Circulation
|
December 2, 2025
Mitochondrial Genetics in Cardiovascular Health and Disease: A Scientific Statement From the American Heart Association
Jessica L Fetterman, Patrick F Chinnery, Rebecca McClellan, et al.
Plos Genetics
|
January 6, 2023
A role for BCL2L13 and autophagy in germline purifying selection of mtDNA
Laura S Kremer, Lyuba V Bozhilova, Diana Rubalcava-Gracia, et al.
Annals of Clinical and Translational Neurology
|
August 2, 2024
Mitochondrial DNA disorders in neuromuscular diseases in diverse populations
Fei Gao, Katherine R Schon, Jana Vandrovcova, et al.
Neuromuscular Disorders : NMD
|
April 27, 2020
Chronic pain is common in mitochondrial disease
Jelle van den Ameele, Joshua Fuge, Robert D S Pitceathly, et al.
Page
of 37
Search research articles
Search
Showing results (151-160 of 370) with videos related to
Sort By:
Page
of 37
Nucleic Acids Research
|
August 1, 2024
LRPPRC and SLIRP synergize to maintain sufficient and orderly mammalian mitochondrial translation
Diana Rubalcava-Gracia, Kristina Bubb, Fredrik Levander, et al.
Journal of Neurology
|
July 14, 2020
Behr syndrome and hypertrophic cardiomyopathy in a family with a novel UCHL1 deletion
Grace McMacken, Hanns Lochmüller, Boglarka Bansagi, et al.
Nature
|
October 5, 2022
Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes
Wei Wei, Katherine R Schon, Greg Elgar, et al.
Cerebellum & Ataxias
|
December 8, 2015
Mitochondrial pathology in progressive cerebellar ataxia
David Bargiela, Priya Shanmugarajah, Christine Lo, et al.
Annals of Clinical and Translational Neurology
|
April 2, 2024
7T MRI detects widespread brain iron deposition in neuroferritinopathy
Alexander G Murley, Catarina Rua, Heather Biggs, et al.
Molecular Genetics and Metabolism
|
May 22, 2012
In vitro supplementation with deoxynucleoside monophosphates rescues mitochondrial DNA depletion
Stefanie Bulst, Elke Holinski-Feder, Brendan Payne, et al.
Circulation
|
December 2, 2025
Mitochondrial Genetics in Cardiovascular Health and Disease: A Scientific Statement From the American Heart Association
Jessica L Fetterman, Patrick F Chinnery, Rebecca McClellan, et al.
Plos Genetics
|
January 6, 2023
A role for BCL2L13 and autophagy in germline purifying selection of mtDNA
Laura S Kremer, Lyuba V Bozhilova, Diana Rubalcava-Gracia, et al.
Annals of Clinical and Translational Neurology
|
August 2, 2024
Mitochondrial DNA disorders in neuromuscular diseases in diverse populations
Fei Gao, Katherine R Schon, Jana Vandrovcova, et al.
Neuromuscular Disorders : NMD
|
April 27, 2020
Chronic pain is common in mitochondrial disease
Jelle van den Ameele, Joshua Fuge, Robert D S Pitceathly, et al.
Page
of 37