Search research articles
Contact Us
Filters
Showing results (91-100 of 197) with videos related to
Page
of 20
Sort By:
European Journal of Human Genetics : EJHG
|
September 20, 2012
Refractory epilepsy and mitochondrial dysfunction due to GM3 synthase deficiency
Konstantina Fragaki, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Placenta
|
June 27, 2018
Study of mitochondrial function in placental insufficiency
Tiphaine Lefebvre, Ombeline Roche, Valérie Seegers, et al.
BMC Research Notes
|
December 24, 2011
Idebenone increases mitochondrial complex I activity in fibroblasts from LHON patients while producing contradictory effects on respiration
Claire Angebault, Naïg Gueguen, Valérie Desquiret-Dumas, et al.
Orphanet Journal of Rare Diseases
|
February 19, 2018
Cyclosporine A does not prevent second-eye involvement in Leber's hereditary optic neuropathy
Stéphanie Leruez, Christophe Verny, Dominique Bonneau, et al.
The International Journal of Biochemistry & Cell Biology
|
April 25, 2009
OPA1-associated disorders: phenotypes and pathophysiology
Patrizia Amati-Bonneau, Dan Milea, Dominique Bonneau, et al.
Neuroscience Letters
|
July 1, 2009
Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndrome
Hailing Su, Weiwei Fan, Pinar E Coskun, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
November 6, 2016
The addition of ketone bodies alleviates mitochondrial dysfunction by restoring complex I assembly in a MELAS cellular model
Samuel Frey, Guillaume Geffroy, Valerie Desquiret-Dumas, et al.
The Journal of Biological Chemistry
|
November 2, 2013
Resveratrol induces a mitochondrial complex I-dependent increase in NADH oxidation responsible for sirtuin activation in liver cells
Valérie Desquiret-Dumas, Naïg Gueguen, Géraldine Leman, et al.
Annals of Neurology
|
September 27, 2002
Aggregation of actin and cofilin in identical twins with juvenile-onset dystonia
Marla Gearing, Jorge L Juncos, Vincent Procaccio, et al.
Neurogenetics
|
December 18, 2008
Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K)
Julien Cassereau, Arnaud Chevrollier, Naïg Gueguen, et al.
Page
of 20
Search research articles
Search
Showing results (91-100 of 197) with videos related to
Sort By:
Page
of 20
European Journal of Human Genetics : EJHG
|
September 20, 2012
Refractory epilepsy and mitochondrial dysfunction due to GM3 synthase deficiency
Konstantina Fragaki, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Placenta
|
June 27, 2018
Study of mitochondrial function in placental insufficiency
Tiphaine Lefebvre, Ombeline Roche, Valérie Seegers, et al.
BMC Research Notes
|
December 24, 2011
Idebenone increases mitochondrial complex I activity in fibroblasts from LHON patients while producing contradictory effects on respiration
Claire Angebault, Naïg Gueguen, Valérie Desquiret-Dumas, et al.
Orphanet Journal of Rare Diseases
|
February 19, 2018
Cyclosporine A does not prevent second-eye involvement in Leber's hereditary optic neuropathy
Stéphanie Leruez, Christophe Verny, Dominique Bonneau, et al.
The International Journal of Biochemistry & Cell Biology
|
April 25, 2009
OPA1-associated disorders: phenotypes and pathophysiology
Patrizia Amati-Bonneau, Dan Milea, Dominique Bonneau, et al.
Neuroscience Letters
|
July 1, 2009
Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndrome
Hailing Su, Weiwei Fan, Pinar E Coskun, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
November 6, 2016
The addition of ketone bodies alleviates mitochondrial dysfunction by restoring complex I assembly in a MELAS cellular model
Samuel Frey, Guillaume Geffroy, Valerie Desquiret-Dumas, et al.
The Journal of Biological Chemistry
|
November 2, 2013
Resveratrol induces a mitochondrial complex I-dependent increase in NADH oxidation responsible for sirtuin activation in liver cells
Valérie Desquiret-Dumas, Naïg Gueguen, Géraldine Leman, et al.
Annals of Neurology
|
September 27, 2002
Aggregation of actin and cofilin in identical twins with juvenile-onset dystonia
Marla Gearing, Jorge L Juncos, Vincent Procaccio, et al.
Neurogenetics
|
December 18, 2008
Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K)
Julien Cassereau, Arnaud Chevrollier, Naïg Gueguen, et al.
Page
of 20