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Molecular Reproduction and Development
|
May 11, 2026
High-Resolution Imaging Reveals Mitochondrial Protein Imbalance in Sperm of Oligoasthenospermic Men
Pauline Teixeira, Magalie Boguenet, Florence Pascaretti-Grizon, et al.
Journal of Cell Science
|
September 25, 2025
Charcot-Marie-Tooth type 2A variants of mitofusin 2 sensitize cells to apoptotic cell death
Mariana Joaquim, Maria-Bianca Bulimaga, Marie A Mohn, et al.
Current Medicinal Chemistry
|
May 30, 2017
Neurotoxicity of Insecticides
Julien Cassereau, Marc Ferré, Arnaud Chevrollier, et al.
The International Journal of Biochemistry & Cell Biology
|
March 22, 2012
Standardized mitochondrial analysis gives new insights into mitochondrial dynamics and OPA1 function
Arnaud Chevrollier, Julien Cassereau, Marc Ferré, et al.
Neuro-Ophthalmology (Aeolus Press)
|
February 5, 2026
An Apparently Isolated Optic Neuropathy Associated with Biallelic Variants in <i>SLC25A46</i> Gene Encoding the Mitochondrial Ugo1-Like Protein
Pascal Reynier, Patrizia Amati-Bonneau, Valérie Desquiret-Dumas, et al.
Human Mutation
|
September 23, 2014
Improved locus-specific database for OPA1 mutations allows inclusion of advanced clinical data
Marc Ferré, Angélique Caignard, Dan Milea, et al.
Experimental Neurology
|
September 21, 2010
Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutations
Julien Cassereau, Arnaud Chevrollier, Naïg Gueguen, et al.
Neurogenetics
|
July 21, 2009
Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot-Marie-Tooth type 2A disease
Virginie Guillet, Naïg Gueguen, Christophe Verny, et al.
Iscience
|
May 14, 2024
Mitochondrial F0F1-ATP synthase governs the induction of mitochondrial fission
Charlène Lhuissier, Valérie Desquiret-Dumas, Anaïs Girona, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
February 3, 2011
Bioenergetic defect associated with mKATP channel opening in a mouse model carrying a mitofusin 2 mutation
Virginie Guillet, Naïg Gueguen, Romain Cartoni, et al.
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Search research articles
Search
Showing results (21-30 of 79) with videos related to
Sort By:
Page
of 8
Molecular Reproduction and Development
|
May 11, 2026
High-Resolution Imaging Reveals Mitochondrial Protein Imbalance in Sperm of Oligoasthenospermic Men
Pauline Teixeira, Magalie Boguenet, Florence Pascaretti-Grizon, et al.
Journal of Cell Science
|
September 25, 2025
Charcot-Marie-Tooth type 2A variants of mitofusin 2 sensitize cells to apoptotic cell death
Mariana Joaquim, Maria-Bianca Bulimaga, Marie A Mohn, et al.
Current Medicinal Chemistry
|
May 30, 2017
Neurotoxicity of Insecticides
Julien Cassereau, Marc Ferré, Arnaud Chevrollier, et al.
The International Journal of Biochemistry & Cell Biology
|
March 22, 2012
Standardized mitochondrial analysis gives new insights into mitochondrial dynamics and OPA1 function
Arnaud Chevrollier, Julien Cassereau, Marc Ferré, et al.
Neuro-Ophthalmology (Aeolus Press)
|
February 5, 2026
An Apparently Isolated Optic Neuropathy Associated with Biallelic Variants in <i>SLC25A46</i> Gene Encoding the Mitochondrial Ugo1-Like Protein
Pascal Reynier, Patrizia Amati-Bonneau, Valérie Desquiret-Dumas, et al.
Human Mutation
|
September 23, 2014
Improved locus-specific database for OPA1 mutations allows inclusion of advanced clinical data
Marc Ferré, Angélique Caignard, Dan Milea, et al.
Experimental Neurology
|
September 21, 2010
Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutations
Julien Cassereau, Arnaud Chevrollier, Naïg Gueguen, et al.
Neurogenetics
|
July 21, 2009
Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot-Marie-Tooth type 2A disease
Virginie Guillet, Naïg Gueguen, Christophe Verny, et al.
Iscience
|
May 14, 2024
Mitochondrial F0F1-ATP synthase governs the induction of mitochondrial fission
Charlène Lhuissier, Valérie Desquiret-Dumas, Anaïs Girona, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
February 3, 2011
Bioenergetic defect associated with mKATP channel opening in a mouse model carrying a mitofusin 2 mutation
Virginie Guillet, Naïg Gueguen, Romain Cartoni, et al.
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of 8