Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

David Pacheu-Grau

Showing results (31-40 of 39) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 39 results.
Environmental Toxicology|January 28, 2026
Effects of Tributyltin Chloride on Human Neuronal Differentiation and Mice Brain DevelopmentEster López-Gallardo, Patricia Meade, Irene Jiménez-Salvador, et al.
Redox Biology|June 11, 2017
Pharmacologic concentrations of linezolid modify oxidative phosphorylation function and adipocyte secretomeLaura Llobet, M Pilar Bayona-Bafaluy, David Pacheu-Grau, et al.
Human Molecular Genetics|November 20, 2018
Mutations of the mitochondrial carrier translocase channel subunit TIM22 cause early-onset mitochondrial myopathyDavid Pacheu-Grau, Sylvie Callegari, Sonia Emperador, et al.
Elife|December 4, 2019
Impaired lysosomal acidification triggers iron deficiency and inflammation in vivoKing Faisal Yambire, Christine Rostosky, Takashi Watanabe, et al.
Clinical Genetics|July 9, 2022
Toxic and nutritional factors trigger Leber hereditary optic neuropathy due to a mitochondrial tRNA mutationAna Vela-Sebastián, Ester López-Gallardo, Sonia Emperador, et al.
The EMBO Journal|June 23, 2020
MICOS assembly controls mitochondrial inner membrane remodeling and crista junction redistribution to mediate cristae formationTill Stephan, Christian Brüser, Markus Deckers, et al.
The EMBO Journal|July 16, 2019
Redox signals at the ER-mitochondria interface control melanoma progressionXin Zhang, Christine S Gibhardt, Thorsten Will, et al.
Circulation Research|January 25, 2021
Caveolin3 Stabilizes McT1-Mediated Lactate/Proton Transport in CardiomyocytesJonas Peper, Daniel Kownatzki-Danger, Gunnar Weninger, et al.
Orphanet Journal of Rare Diseases|April 6, 2024
Identification and characterization of a new pathologic mutation in a large Leber hereditary optic neuropathy pedigreeSonia Emperador, Mouna Habbane, Ester López-Gallardo, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Environmental Toxicology|January 28, 2026
Effects of Tributyltin Chloride on Human Neuronal Differentiation and Mice Brain DevelopmentEster López-Gallardo, Patricia Meade, Irene Jiménez-Salvador, et al.
Redox Biology|June 11, 2017
Pharmacologic concentrations of linezolid modify oxidative phosphorylation function and adipocyte secretomeLaura Llobet, M Pilar Bayona-Bafaluy, David Pacheu-Grau, et al.
Human Molecular Genetics|November 20, 2018
Mutations of the mitochondrial carrier translocase channel subunit TIM22 cause early-onset mitochondrial myopathyDavid Pacheu-Grau, Sylvie Callegari, Sonia Emperador, et al.
Elife|December 4, 2019
Impaired lysosomal acidification triggers iron deficiency and inflammation in vivoKing Faisal Yambire, Christine Rostosky, Takashi Watanabe, et al.
Clinical Genetics|July 9, 2022
Toxic and nutritional factors trigger Leber hereditary optic neuropathy due to a mitochondrial tRNA mutationAna Vela-Sebastián, Ester López-Gallardo, Sonia Emperador, et al.
The EMBO Journal|June 23, 2020
MICOS assembly controls mitochondrial inner membrane remodeling and crista junction redistribution to mediate cristae formationTill Stephan, Christian Brüser, Markus Deckers, et al.
The EMBO Journal|July 16, 2019
Redox signals at the ER-mitochondria interface control melanoma progressionXin Zhang, Christine S Gibhardt, Thorsten Will, et al.
Circulation Research|January 25, 2021
Caveolin3 Stabilizes McT1-Mediated Lactate/Proton Transport in CardiomyocytesJonas Peper, Daniel Kownatzki-Danger, Gunnar Weninger, et al.
Orphanet Journal of Rare Diseases|April 6, 2024
Identification and characterization of a new pathologic mutation in a large Leber hereditary optic neuropathy pedigreeSonia Emperador, Mouna Habbane, Ester López-Gallardo, et al.
Pageof 4