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David Pacheu-Grau

Showing results (21-30 of 39) with videos related to

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Mutation Research. Reviews in Mutation Research|December 19, 2020
Genetic aspects of the oxidative phosphorylation dysfunction in dilated cardiomyopathyM Pilar Bayona-Bafaluy, Eldris Iglesias, Ester López-Gallardo, et al.
Orphanet Journal of Rare Diseases|February 5, 2021
Sulthiame impairs mitochondrial function in vitro and may trigger onset of visual loss in Leber hereditary optic neuropathyMarie-Christine Reinert, David Pacheu-Grau, Claudia B Catarino, et al.
Biochimica Et Biophysica Acta|May 8, 2012
Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathyAurora Gómez-Durán, David Pacheu-Grau, Iñigo Martínez-Romero, et al.
Human Molecular Genetics|August 11, 2011
'Progress' renders detrimental an ancient mitochondrial DNA genetic variantDavid Pacheu-Grau, Aurora Gómez-Durán, Ester López-Gallardo, et al.
Cell Metabolism|May 12, 2015
Cooperation between COA6 and SCO2 in COX2 maturation during cytochrome c oxidase assembly links two mitochondrial cardiomyopathiesDavid Pacheu-Grau, Bettina Bareth, Jan Dudek, et al.
Frontiers in Genetics|February 3, 2015
An MRPS12 mutation modifies aminoglycoside sensitivity caused by 12S rRNA mutationsSonia Emperador, David Pacheu-Grau, M Pilar Bayona-Bafaluy, et al.
Cell Reports|February 11, 2025
A microscopy-based screen identifies cellular kinases modulating mitochondrial translationRoya Yousefi, Luis Daniel Cruz-Zaragoza, Anusha Valpadashi, et al.
Cell|December 25, 2012
MITRAC links mitochondrial protein translocation to respiratory-chain assembly and translational regulationDavid U Mick, Sven Dennerlein, Heike Wiese, et al.
FEBS Letters|October 9, 2016
TIM29 is a subunit of the human carrier translocase required for protein transportSylvie Callegari, Frank Richter, Katarzyna Chojnacka, et al.
Journal of Molecular Biology|February 17, 2020
COA6 Facilitates Cytochrome c Oxidase Biogenesis as Thiol-reductase for Copper Metallochaperones in MitochondriaDavid Pacheu-Grau, Michał Wasilewski, Silke Oeljeklaus, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Mutation Research. Reviews in Mutation Research|December 19, 2020
Genetic aspects of the oxidative phosphorylation dysfunction in dilated cardiomyopathyM Pilar Bayona-Bafaluy, Eldris Iglesias, Ester López-Gallardo, et al.
Orphanet Journal of Rare Diseases|February 5, 2021
Sulthiame impairs mitochondrial function in vitro and may trigger onset of visual loss in Leber hereditary optic neuropathyMarie-Christine Reinert, David Pacheu-Grau, Claudia B Catarino, et al.
Biochimica Et Biophysica Acta|May 8, 2012
Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathyAurora Gómez-Durán, David Pacheu-Grau, Iñigo Martínez-Romero, et al.
Human Molecular Genetics|August 11, 2011
'Progress' renders detrimental an ancient mitochondrial DNA genetic variantDavid Pacheu-Grau, Aurora Gómez-Durán, Ester López-Gallardo, et al.
Cell Metabolism|May 12, 2015
Cooperation between COA6 and SCO2 in COX2 maturation during cytochrome c oxidase assembly links two mitochondrial cardiomyopathiesDavid Pacheu-Grau, Bettina Bareth, Jan Dudek, et al.
Frontiers in Genetics|February 3, 2015
An MRPS12 mutation modifies aminoglycoside sensitivity caused by 12S rRNA mutationsSonia Emperador, David Pacheu-Grau, M Pilar Bayona-Bafaluy, et al.
Cell Reports|February 11, 2025
A microscopy-based screen identifies cellular kinases modulating mitochondrial translationRoya Yousefi, Luis Daniel Cruz-Zaragoza, Anusha Valpadashi, et al.
Cell|December 25, 2012
MITRAC links mitochondrial protein translocation to respiratory-chain assembly and translational regulationDavid U Mick, Sven Dennerlein, Heike Wiese, et al.
FEBS Letters|October 9, 2016
TIM29 is a subunit of the human carrier translocase required for protein transportSylvie Callegari, Frank Richter, Katarzyna Chojnacka, et al.
Journal of Molecular Biology|February 17, 2020
COA6 Facilitates Cytochrome c Oxidase Biogenesis as Thiol-reductase for Copper Metallochaperones in MitochondriaDavid Pacheu-Grau, Michał Wasilewski, Silke Oeljeklaus, et al.
Pageof 4