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Human Mutation
|
November 10, 2020
Multiomic analysis elucidates Complex I deficiency caused by a deep intronic variant in NDUFB10
Guy Helman, Alison G Compton, Daniella H Hock, 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.
Science Advances
|
August 15, 2025
Complex II assembly drives metabolic adaptation to OXPHOS dysfunction
Roopasingam Kugapreethan, Sheik Nadeem Elahee Doomun, Joanna Sacharz, et al.
Mitochondrion
|
October 16, 2024
An integrated multi-omics approach allowed ultra-rapid diagnosis of a deep intronic pathogenic variant in PDHX and precision treatment in a neonate critically ill with lactic acidosis
Rodrigo T Starosta, Austin A Larson, Naomi J L Meeks, 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.
Nature Communications
|
December 4, 2021
High-intensity training induces non-stoichiometric changes in the mitochondrial proteome of human skeletal muscle without reorganisation of respiratory chain content
Cesare Granata, Nikeisha J Caruana, Javier Botella, et al.
Molecular Metabolism
|
December 28, 2020
Metabolic remodeling of dystrophic skeletal muscle reveals biological roles for dystrophin and utrophin in adaptation and plasticity
Justin P Hardee, Karen J B Martins, Paula M Miotto, et al.
The Journal of Experimental Medicine
|
July 9, 2020
Mutations in the exocyst component EXOC2 cause severe defects in human brain development
Nicole J Van Bergen, Syed Mukhtar Ahmed, Felicity Collins, et al.
Cell
|
August 6, 2013
Coupling of mitochondrial import and export translocases by receptor-mediated supercomplex formation
Jian Qiu, Lena-Sophie Wenz, Ralf M Zerbes, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 109) with videos related to
Sort By:
Page
of 11
Human Mutation
|
November 10, 2020
Multiomic analysis elucidates Complex I deficiency caused by a deep intronic variant in NDUFB10
Guy Helman, Alison G Compton, Daniella H Hock, 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.
Science Advances
|
August 15, 2025
Complex II assembly drives metabolic adaptation to OXPHOS dysfunction
Roopasingam Kugapreethan, Sheik Nadeem Elahee Doomun, Joanna Sacharz, et al.
Mitochondrion
|
October 16, 2024
An integrated multi-omics approach allowed ultra-rapid diagnosis of a deep intronic pathogenic variant in PDHX and precision treatment in a neonate critically ill with lactic acidosis
Rodrigo T Starosta, Austin A Larson, Naomi J L Meeks, 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.
Nature Communications
|
December 4, 2021
High-intensity training induces non-stoichiometric changes in the mitochondrial proteome of human skeletal muscle without reorganisation of respiratory chain content
Cesare Granata, Nikeisha J Caruana, Javier Botella, et al.
Molecular Metabolism
|
December 28, 2020
Metabolic remodeling of dystrophic skeletal muscle reveals biological roles for dystrophin and utrophin in adaptation and plasticity
Justin P Hardee, Karen J B Martins, Paula M Miotto, et al.
The Journal of Experimental Medicine
|
July 9, 2020
Mutations in the exocyst component EXOC2 cause severe defects in human brain development
Nicole J Van Bergen, Syed Mukhtar Ahmed, Felicity Collins, et al.
Cell
|
August 6, 2013
Coupling of mitochondrial import and export translocases by receptor-mediated supercomplex formation
Jian Qiu, Lena-Sophie Wenz, Ralf M Zerbes, et al.
Page
of 11