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Molecular Metabolism
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June 20, 2014
Studying mitochondrial CB1 receptors: Yes we can
Etienne Hebert-Chatelain, Leire Reguero, Nagore Puente, et al.
European Journal of Human Genetics : EJHG
|
October 21, 2016
Complete loss of function of the ubiquitin ligase HERC2 causes a severe neurodevelopmental phenotype
Fanny Morice-Picard, Giovanni Benard, Hamid R Rezvani, et al.
Molecular Metabolism
|
June 20, 2014
Cannabinoid control of brain bioenergetics: Exploring the subcellular localization of the CB1 receptor
Etienne Hebert-Chatelain, Leire Reguero, Nagore Puente, et al.
Biochimica Et Biophysica Acta
|
December 21, 2010
XPC silencing in normal human keratinocytes triggers metabolic alterations through NOX-1 activation-mediated reactive oxygen species
Hamid Reza Rezvani, Rodrigue Rossignol, Nsrein Ali, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
November 9, 2016
High glucose repatterns human podocyte energy metabolism during differentiation and diabetic nephropathy
Toshiyuki Imasawa, Emilie Obre, Nadège Bellance, et al.
The Journal of Experimental Medicine
|
December 7, 2007
Bronchial smooth muscle remodeling involves calcium-dependent enhanced mitochondrial biogenesis in asthma
Thomas Trian, Giovanni Benard, Hugues Begueret, et al.
Antioxidants & Redox Signaling
|
February 29, 2012
Adaptative capacity of mitochondrial biogenesis and of mitochondrial dynamics in response to pathogenic respiratory chain dysfunction
Giovanni Benard, Thomas Trian, Nadège Bellance, et al.
Hepatology (Baltimore, Md.)
|
September 11, 2012
Disruption of the histidine triad nucleotide-binding hint2 gene in mice affects glycemic control and mitochondrial function
Juliette Martin, Olivier Maurhofer, Nadège Bellance, et al.
Biochimica Et Biophysica Acta
|
March 21, 2012
Metabolic consequences of NDUFS4 gene deletion in immortalized mouse embryonic fibroblasts
Federica Valsecchi, Claire Monge, Marleen Forkink, et al.
Human Mutation
|
October 17, 2017
CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56
Christelle M Durand, Laura Dhers, Christelle Tesson, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 22) with videos related to
Sort By:
Page
of 3
Molecular Metabolism
|
June 20, 2014
Studying mitochondrial CB1 receptors: Yes we can
Etienne Hebert-Chatelain, Leire Reguero, Nagore Puente, et al.
European Journal of Human Genetics : EJHG
|
October 21, 2016
Complete loss of function of the ubiquitin ligase HERC2 causes a severe neurodevelopmental phenotype
Fanny Morice-Picard, Giovanni Benard, Hamid R Rezvani, et al.
Molecular Metabolism
|
June 20, 2014
Cannabinoid control of brain bioenergetics: Exploring the subcellular localization of the CB1 receptor
Etienne Hebert-Chatelain, Leire Reguero, Nagore Puente, et al.
Biochimica Et Biophysica Acta
|
December 21, 2010
XPC silencing in normal human keratinocytes triggers metabolic alterations through NOX-1 activation-mediated reactive oxygen species
Hamid Reza Rezvani, Rodrigue Rossignol, Nsrein Ali, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
November 9, 2016
High glucose repatterns human podocyte energy metabolism during differentiation and diabetic nephropathy
Toshiyuki Imasawa, Emilie Obre, Nadège Bellance, et al.
The Journal of Experimental Medicine
|
December 7, 2007
Bronchial smooth muscle remodeling involves calcium-dependent enhanced mitochondrial biogenesis in asthma
Thomas Trian, Giovanni Benard, Hugues Begueret, et al.
Antioxidants & Redox Signaling
|
February 29, 2012
Adaptative capacity of mitochondrial biogenesis and of mitochondrial dynamics in response to pathogenic respiratory chain dysfunction
Giovanni Benard, Thomas Trian, Nadège Bellance, et al.
Hepatology (Baltimore, Md.)
|
September 11, 2012
Disruption of the histidine triad nucleotide-binding hint2 gene in mice affects glycemic control and mitochondrial function
Juliette Martin, Olivier Maurhofer, Nadège Bellance, et al.
Biochimica Et Biophysica Acta
|
March 21, 2012
Metabolic consequences of NDUFS4 gene deletion in immortalized mouse embryonic fibroblasts
Federica Valsecchi, Claire Monge, Marleen Forkink, et al.
Human Mutation
|
October 17, 2017
CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56
Christelle M Durand, Laura Dhers, Christelle Tesson, et al.
Page
of 3