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V Procaccio

Showing results (21-30 of 33) with videos related to

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Neurology|April 27, 2011
Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMTJ Cassereau, C Casasnovas, N Gueguen, et al.
Eye (London, England)|November 19, 2016
Multiethnic involvement in autosomal-dominant optic atrophy in SingaporeJ L Loo, S Singhal, A V Rukmini, et al.
The Journal of Clinical Investigation|July 7, 1999
Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblastsV Procaccio, B Mousson, R Beugnot, et al.
Diabetes & Metabolism|October 29, 2008
Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitisC Verny, P Amati-Bonneau, F Letournel, et al.
Journal of Assisted Reproduction and Genetics|October 27, 2018
The mitochondrial DNA content of cumulus cells may help predict embryo implantationA Taugourdeau, V Desquiret-Dumas, J F Hamel, et al.
Mitochondrion|August 19, 2014
Mitochondrial macro-haplogroup JT may play a protective role in ovarian ageingP May-Panloup, V Desquiret, C Morinière, et al.
Human Reproduction (Oxford, England)|September 24, 2017
Deep sequencing shows that oocytes are not prone to accumulate mtDNA heteroplasmic mutations during ovarian ageingL Boucret, C Bris, V Seegers, et al.
Human Reproduction (Oxford, England)|October 18, 2017
Targeted metabolomics reveals reduced levels of polyunsaturated choline plasmalogens and a smaller dimethylarginine/arginine ratio in the follicular fluid of patients with a diminished ovarian reserveJ M Chao de la Barca, T Boueilh, G Simard, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 5, 2013
Key role of estrogens and endothelial estrogen receptor α in blood flow-mediated remodeling of resistance arteriesK Tarhouni, A L Guihot, M L Freidja, et al.
Molecular Genetics and Metabolism Reports|April 17, 2025
The recurrent p.Glu3Lys variant in <i>EHHADH</i> is responsible for Fanconi syndrome with early liver dysfunction and mitochondrial abnormalitiesP Rollier, A Cospain, M Barth, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Neurology|April 27, 2011
Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMTJ Cassereau, C Casasnovas, N Gueguen, et al.
Eye (London, England)|November 19, 2016
Multiethnic involvement in autosomal-dominant optic atrophy in SingaporeJ L Loo, S Singhal, A V Rukmini, et al.
The Journal of Clinical Investigation|July 7, 1999
Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblastsV Procaccio, B Mousson, R Beugnot, et al.
Diabetes & Metabolism|October 29, 2008
Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitisC Verny, P Amati-Bonneau, F Letournel, et al.
Journal of Assisted Reproduction and Genetics|October 27, 2018
The mitochondrial DNA content of cumulus cells may help predict embryo implantationA Taugourdeau, V Desquiret-Dumas, J F Hamel, et al.
Mitochondrion|August 19, 2014
Mitochondrial macro-haplogroup JT may play a protective role in ovarian ageingP May-Panloup, V Desquiret, C Morinière, et al.
Human Reproduction (Oxford, England)|September 24, 2017
Deep sequencing shows that oocytes are not prone to accumulate mtDNA heteroplasmic mutations during ovarian ageingL Boucret, C Bris, V Seegers, et al.
Human Reproduction (Oxford, England)|October 18, 2017
Targeted metabolomics reveals reduced levels of polyunsaturated choline plasmalogens and a smaller dimethylarginine/arginine ratio in the follicular fluid of patients with a diminished ovarian reserveJ M Chao de la Barca, T Boueilh, G Simard, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 5, 2013
Key role of estrogens and endothelial estrogen receptor α in blood flow-mediated remodeling of resistance arteriesK Tarhouni, A L Guihot, M L Freidja, et al.
Molecular Genetics and Metabolism Reports|April 17, 2025
The recurrent p.Glu3Lys variant in <i>EHHADH</i> is responsible for Fanconi syndrome with early liver dysfunction and mitochondrial abnormalitiesP Rollier, A Cospain, M Barth, et al.
Pageof 4