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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.
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.
Annals of Neurology
|
April 21, 2007
Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease
Dominique Loiseau, Arnaud Chevrollier, Christophe Verny, et al.
Annals of Neurology
|
May 23, 2008
Hereditary optic neuropathies share a common mitochondrial coupling defect
Arnaud Chevrollier, Virginie Guillet, Dominique Loiseau, et al.
Annals of Neurology
|
March 25, 2008
Reversible optic neuropathy with OPA1 exon 5b mutation
Karen Cornille, Dan Milea, Patrizia Amati-Bonneau, et al.
Genome Research
|
October 27, 2010
OPA1 links human mitochondrial genome maintenance to mtDNA replication and distribution
Ghizlane Elachouri, Sara Vidoni, Claudia Zanna, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 16) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 16 results.
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.
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.
Annals of Neurology
|
April 21, 2007
Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease
Dominique Loiseau, Arnaud Chevrollier, Christophe Verny, et al.
Annals of Neurology
|
May 23, 2008
Hereditary optic neuropathies share a common mitochondrial coupling defect
Arnaud Chevrollier, Virginie Guillet, Dominique Loiseau, et al.
Annals of Neurology
|
March 25, 2008
Reversible optic neuropathy with OPA1 exon 5b mutation
Karen Cornille, Dan Milea, Patrizia Amati-Bonneau, et al.
Genome Research
|
October 27, 2010
OPA1 links human mitochondrial genome maintenance to mtDNA replication and distribution
Ghizlane Elachouri, Sara Vidoni, Claudia Zanna, et al.
Page
of 2