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Annals of Neurology
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January 6, 2004
De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency
Robert McFarland, Denise M Kirby, Kerry J Fowler, et al.
Human Molecular Genetics
|
July 11, 2015
COA6 is a mitochondrial complex IV assembly factor critical for biogenesis of mtDNA-encoded COX2
David A Stroud, Megan J Maher, Caroline Lindau, et al.
Aging Cell
|
May 15, 2023
The African killifish: A short-lived vertebrate model to study the biology of sarcopenia and longevity
Avnika A Ruparelia, Adrian Salavaty, Christopher K Barlow, et al.
Current Biology : CB
|
December 8, 2009
Mitochondrial cardiolipin involved in outer-membrane protein biogenesis: implications for Barth syndrome
Natalia Gebert, Amit S Joshi, Stephan Kutik, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 5, 2012
Tissue-specific splicing of an Ndufs6 gene-trap insertion generates a mitochondrial complex I deficiency-specific cardiomyopathy
Bi-Xia Ke, Salvatore Pepe, David R Grubb, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 25, 2022
Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module
Thomas D Jackson, Jordan J Crameri, Linden Muellner-Wong, et al.
Elife
|
November 5, 2019
Function of hTim8a in complex IV assembly in neuronal cells provides insight into pathomechanism underlying Mohr-Tranebjærg syndrome
Yilin Kang, Alexander J Anderson, Thomas Daniel Jackson, et al.
Elife
|
March 19, 2020
Correction: Function of hTim8a in complex IV assembly in neuronal cells provides insight into pathomechanism underlying Mohr-Tranebjærg syndrome
Yilin Kang, Alexander J Anderson, Thomas Daniel Jackson, et al.
Human Mutation
|
August 28, 2022
Biallelic pathogenic variants in COX11 are associated with an infantile-onset mitochondrial encephalopathy
Rocio Rius, Neal K Bennett, Kaustuv Bhattacharya, et al.
EMBO Reports
|
June 5, 2023
Human Tim8a, Tim8b and Tim13 are auxiliary assembly factors of mature Complex IV
Alexander J Anderson, Jordan J Crameri, Ching-Seng Ang, et al.
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of 14
Search research articles
Search
Showing results (101-110 of 136) with videos related to
Sort By:
Page
of 14
Annals of Neurology
|
January 6, 2004
De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency
Robert McFarland, Denise M Kirby, Kerry J Fowler, et al.
Human Molecular Genetics
|
July 11, 2015
COA6 is a mitochondrial complex IV assembly factor critical for biogenesis of mtDNA-encoded COX2
David A Stroud, Megan J Maher, Caroline Lindau, et al.
Aging Cell
|
May 15, 2023
The African killifish: A short-lived vertebrate model to study the biology of sarcopenia and longevity
Avnika A Ruparelia, Adrian Salavaty, Christopher K Barlow, et al.
Current Biology : CB
|
December 8, 2009
Mitochondrial cardiolipin involved in outer-membrane protein biogenesis: implications for Barth syndrome
Natalia Gebert, Amit S Joshi, Stephan Kutik, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 5, 2012
Tissue-specific splicing of an Ndufs6 gene-trap insertion generates a mitochondrial complex I deficiency-specific cardiomyopathy
Bi-Xia Ke, Salvatore Pepe, David R Grubb, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 25, 2022
Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module
Thomas D Jackson, Jordan J Crameri, Linden Muellner-Wong, et al.
Elife
|
November 5, 2019
Function of hTim8a in complex IV assembly in neuronal cells provides insight into pathomechanism underlying Mohr-Tranebjærg syndrome
Yilin Kang, Alexander J Anderson, Thomas Daniel Jackson, et al.
Elife
|
March 19, 2020
Correction: Function of hTim8a in complex IV assembly in neuronal cells provides insight into pathomechanism underlying Mohr-Tranebjærg syndrome
Yilin Kang, Alexander J Anderson, Thomas Daniel Jackson, et al.
Human Mutation
|
August 28, 2022
Biallelic pathogenic variants in COX11 are associated with an infantile-onset mitochondrial encephalopathy
Rocio Rius, Neal K Bennett, Kaustuv Bhattacharya, et al.
EMBO Reports
|
June 5, 2023
Human Tim8a, Tim8b and Tim13 are auxiliary assembly factors of mature Complex IV
Alexander J Anderson, Jordan J Crameri, Ching-Seng Ang, et al.
Page
of 14