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David Pla-Martín

Showing results (1-10 of 14) with videos related to

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Autophagy|January 24, 2023
Endosomal-dependent mitophagy coordinates mitochondrial nucleoid and mtDNA eliminationAyesha Sen, Julia Boix, David Pla-Martín
Frontiers in Molecular Biosciences|July 23, 2021
Selective Neuron Vulnerability in Common and Rare Diseases-Mitochondria in the FocusThomas Paß, Rudolf J Wiesner, David Pla-Martín
Methods in Molecular Biology (Clifton, N.J.)|February 22, 2023
Localization of Mitochondrial Nucleoids by Transmission Electron Microscopy Using the Transgenic Expression of the Mitochondrial Helicase Twinkle and APEX2David Pla-Martín, Felix Babatz, Astrid C Schauss
Advances in Experimental Medicine and Biology|March 13, 2010
The role of mitochondrial network dynamics in the pathogenesis of Charcot-Marie-Tooth diseaseFrancesc Palau, Anna Estela, David Pla-Martín, et al.
The Journal of Biological Chemistry|September 6, 2011
Charcot-Marie-Tooth-related gene GDAP1 complements cell cycle delay at G2/M phase in Saccharomyces cerevisiae fis1 gene-defective cellsAnna Estela, David Pla-Martín, Maribel Sánchez-Piris, et al.
Frontiers in Cellular Neuroscience|May 27, 2014
Mitochondrial dysfunction induced by frataxin deficiency is associated with cellular senescence and abnormal calcium metabolismArantxa Bolinches-Amorós, Belén Mollá, David Pla-Martín, et al.
The EMBO Journal|March 10, 2020
CLUH granules coordinate translation of mitochondrial proteins with mTORC1 signaling and mitophagyDavid Pla-Martín, Désirée Schatton, Janica L Wiederstein, et al.
Human Molecular Genetics|August 30, 2014
Junctophilin-1 is a modifier gene of GDAP1-related Charcot-Marie-Tooth diseaseDavid Pla-Martín, Eduardo Calpena, Vincenzo Lupo, et al.
Scientific Reports|February 22, 2017
CMT-linked loss-of-function mutations in GDAP1 impair store-operated Ca<sup>2+</sup> entry-stimulated respirationPaloma González-Sánchez, David Pla-Martín, Paula Martínez-Valero, et al.
Journal of Cachexia, Sarcopenia and Muscle|June 29, 2022
Combined fibre atrophy and decreased muscle regeneration capacity driven by mitochondrial DNA alterations underlie the development of sarcopeniaSammy Kimoloi, Ayesha Sen, Stefan Guenther, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Autophagy|January 24, 2023
Endosomal-dependent mitophagy coordinates mitochondrial nucleoid and mtDNA eliminationAyesha Sen, Julia Boix, David Pla-Martín
Frontiers in Molecular Biosciences|July 23, 2021
Selective Neuron Vulnerability in Common and Rare Diseases-Mitochondria in the FocusThomas Paß, Rudolf J Wiesner, David Pla-Martín
Methods in Molecular Biology (Clifton, N.J.)|February 22, 2023
Localization of Mitochondrial Nucleoids by Transmission Electron Microscopy Using the Transgenic Expression of the Mitochondrial Helicase Twinkle and APEX2David Pla-Martín, Felix Babatz, Astrid C Schauss
Advances in Experimental Medicine and Biology|March 13, 2010
The role of mitochondrial network dynamics in the pathogenesis of Charcot-Marie-Tooth diseaseFrancesc Palau, Anna Estela, David Pla-Martín, et al.
The Journal of Biological Chemistry|September 6, 2011
Charcot-Marie-Tooth-related gene GDAP1 complements cell cycle delay at G2/M phase in Saccharomyces cerevisiae fis1 gene-defective cellsAnna Estela, David Pla-Martín, Maribel Sánchez-Piris, et al.
Frontiers in Cellular Neuroscience|May 27, 2014
Mitochondrial dysfunction induced by frataxin deficiency is associated with cellular senescence and abnormal calcium metabolismArantxa Bolinches-Amorós, Belén Mollá, David Pla-Martín, et al.
The EMBO Journal|March 10, 2020
CLUH granules coordinate translation of mitochondrial proteins with mTORC1 signaling and mitophagyDavid Pla-Martín, Désirée Schatton, Janica L Wiederstein, et al.
Human Molecular Genetics|August 30, 2014
Junctophilin-1 is a modifier gene of GDAP1-related Charcot-Marie-Tooth diseaseDavid Pla-Martín, Eduardo Calpena, Vincenzo Lupo, et al.
Scientific Reports|February 22, 2017
CMT-linked loss-of-function mutations in GDAP1 impair store-operated Ca<sup>2+</sup> entry-stimulated respirationPaloma González-Sánchez, David Pla-Martín, Paula Martínez-Valero, et al.
Journal of Cachexia, Sarcopenia and Muscle|June 29, 2022
Combined fibre atrophy and decreased muscle regeneration capacity driven by mitochondrial DNA alterations underlie the development of sarcopeniaSammy Kimoloi, Ayesha Sen, Stefan Guenther, et al.
Pageof 2