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Elife
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July 27, 2017
Maturation of selected human mitochondrial tRNAs requires deadenylation
Sarah F Pearce, Joanna Rorbach, Lindsey Van Haute, et al.
Nucleic Acids Research
|
October 31, 2019
METTL15 introduces N4-methylcytidine into human mitochondrial 12S rRNA and is required for mitoribosome biogenesis
Lindsey Van Haute, Alan G Hendrick, Aaron R D'Souza, et al.
The Journal of Biological Chemistry
|
January 14, 2017
The Pseudouridine Synthase RPUSD4 Is an Essential Component of Mitochondrial RNA Granules
Sofia Zaganelli, Pedro Rebelo-Guiomar, Kinsey Maundrell, et al.
EMBO Molecular Medicine
|
April 9, 2025
Clinically translatable mitochondrial gene therapy in muscle using tandem mtZFN architecture
Pavel A Nash, Keira M Turner, Christopher A Powell, et al.
Molecular Cell
|
November 14, 2021
Balancing of mitochondrial translation through METTL8-mediated m<sup>3</sup>C modification of mitochondrial tRNAs
Eva Schöller, James Marks, Virginie Marchand, et al.
JIMD Reports
|
May 8, 2023
Severe neonatal onset neuroregression with paroxysmal dystonia and apnoea: Expanding the phenotypic and genotypic spectrum of <i>CARS2</i>-related mitochondrial disease
Jessie Poquérusse, Melinda Nolan, David R Thorburn, et al.
Elife
|
December 23, 2021
Disruption of the TCA cycle reveals an ATF4-dependent integration of redox and amino acid metabolism
Dylan Gerard Ryan, Ming Yang, Hiran A Prag, et al.
Orphanet Journal of Rare Diseases
|
July 3, 2016
TRNT1 deficiency: clinical, biochemical and molecular genetic features
Yehani Wedatilake, Rojeen Niazi, Elisa Fassone, et al.
Nucleic Acids Research
|
July 6, 2019
NSUN2 introduces 5-methylcytosines in mammalian mitochondrial tRNAs
Lindsey Van Haute, Song-Yi Lee, Beverly J McCann, et al.
Molecular Genetics and Metabolism
|
November 12, 2017
New insights into the phenotype of FARS2 deficiency
Elise Vantroys, Austin Larson, Marisa Friederich, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 33) with videos related to
Sort By:
Page
of 4
Elife
|
July 27, 2017
Maturation of selected human mitochondrial tRNAs requires deadenylation
Sarah F Pearce, Joanna Rorbach, Lindsey Van Haute, et al.
Nucleic Acids Research
|
October 31, 2019
METTL15 introduces N4-methylcytidine into human mitochondrial 12S rRNA and is required for mitoribosome biogenesis
Lindsey Van Haute, Alan G Hendrick, Aaron R D'Souza, et al.
The Journal of Biological Chemistry
|
January 14, 2017
The Pseudouridine Synthase RPUSD4 Is an Essential Component of Mitochondrial RNA Granules
Sofia Zaganelli, Pedro Rebelo-Guiomar, Kinsey Maundrell, et al.
EMBO Molecular Medicine
|
April 9, 2025
Clinically translatable mitochondrial gene therapy in muscle using tandem mtZFN architecture
Pavel A Nash, Keira M Turner, Christopher A Powell, et al.
Molecular Cell
|
November 14, 2021
Balancing of mitochondrial translation through METTL8-mediated m<sup>3</sup>C modification of mitochondrial tRNAs
Eva Schöller, James Marks, Virginie Marchand, et al.
JIMD Reports
|
May 8, 2023
Severe neonatal onset neuroregression with paroxysmal dystonia and apnoea: Expanding the phenotypic and genotypic spectrum of <i>CARS2</i>-related mitochondrial disease
Jessie Poquérusse, Melinda Nolan, David R Thorburn, et al.
Elife
|
December 23, 2021
Disruption of the TCA cycle reveals an ATF4-dependent integration of redox and amino acid metabolism
Dylan Gerard Ryan, Ming Yang, Hiran A Prag, et al.
Orphanet Journal of Rare Diseases
|
July 3, 2016
TRNT1 deficiency: clinical, biochemical and molecular genetic features
Yehani Wedatilake, Rojeen Niazi, Elisa Fassone, et al.
Nucleic Acids Research
|
July 6, 2019
NSUN2 introduces 5-methylcytosines in mammalian mitochondrial tRNAs
Lindsey Van Haute, Song-Yi Lee, Beverly J McCann, et al.
Molecular Genetics and Metabolism
|
November 12, 2017
New insights into the phenotype of FARS2 deficiency
Elise Vantroys, Austin Larson, Marisa Friederich, et al.
Page
of 4