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Biochimica Et Biophysica Acta
|
December 4, 2004
Respiratory chain defects: what do we know for sure about their consequences in vivo?
Jean-Jacques Brière, Dominique Chrétien, Paule Bénit, et al.
Journal of Clinical Medicine
|
June 9, 2017
An Effective, Versatile, and Inexpensive Device for Oxygen Uptake Measurement
Paule Bénit, Dominique Chrétien, Mathieu Porceddu, et al.
Molecular Genetics and Metabolism
|
October 3, 2002
Coenzyme Q(10) and idebenone in the therapy of respiratory chain diseases: rationale and comparative benefits
Vanna Geromel, Niklas Darin, Dominique Chrétien, et al.
Annals of Neurology
|
August 28, 2007
Twinkle helicase (PEO1) gene mutation causes mitochondrial DNA depletion
Emmanuelle Sarzi, Steffi Goffart, Valérie Serre, et al.
American Journal of Medical Genetics. Part A
|
November 18, 2008
Developmental delay, dysmorphic features, neonatal spontaneous fractures, wrinkled skin, and hepatic failure: a new metabolic syndrome?
André Mégarbané, Leila Samaras, Rima Chédid, et al.
Clinical Science (London, England : 1979)
|
February 6, 2016
Mitochondrial cytochrome c oxidase deficiency
Malgorzata Rak, Paule Bénit, Dominique Chrétien, et al.
Plos One
|
June 23, 2011
Nuclear outsourcing of RNA interference components to human mitochondria
Simonetta Bandiera, Silvia Rüberg, Muriel Girard, et al.
The Journal of Pediatrics
|
April 25, 2007
Mitochondrial DNA depletion is a prevalent cause of multiple respiratory chain deficiency in childhood
Emmanuelle Sarzi, Alice Bourdon, Dominique Chrétien, et al.
Plos Biology
|
January 26, 2018
Mitochondria are physiologically maintained at close to 50 °C
Dominique Chrétien, Paule Bénit, Hyung-Ho Ha, et al.
International Journal of Molecular Sciences
|
March 20, 2020
Defects in Galactose Metabolism and Glycoconjugate Biosynthesis in a UDP-Glucose Pyrophosphorylase-Deficient Cell Line Are Reversed by Adding Galactose to the Growth Medium
Christelle Durrant, Jana I Fuehring, Alexandra Willemetz, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 21) with videos related to
Sort By:
Page
of 3
Biochimica Et Biophysica Acta
|
December 4, 2004
Respiratory chain defects: what do we know for sure about their consequences in vivo?
Jean-Jacques Brière, Dominique Chrétien, Paule Bénit, et al.
Journal of Clinical Medicine
|
June 9, 2017
An Effective, Versatile, and Inexpensive Device for Oxygen Uptake Measurement
Paule Bénit, Dominique Chrétien, Mathieu Porceddu, et al.
Molecular Genetics and Metabolism
|
October 3, 2002
Coenzyme Q(10) and idebenone in the therapy of respiratory chain diseases: rationale and comparative benefits
Vanna Geromel, Niklas Darin, Dominique Chrétien, et al.
Annals of Neurology
|
August 28, 2007
Twinkle helicase (PEO1) gene mutation causes mitochondrial DNA depletion
Emmanuelle Sarzi, Steffi Goffart, Valérie Serre, et al.
American Journal of Medical Genetics. Part A
|
November 18, 2008
Developmental delay, dysmorphic features, neonatal spontaneous fractures, wrinkled skin, and hepatic failure: a new metabolic syndrome?
André Mégarbané, Leila Samaras, Rima Chédid, et al.
Clinical Science (London, England : 1979)
|
February 6, 2016
Mitochondrial cytochrome c oxidase deficiency
Malgorzata Rak, Paule Bénit, Dominique Chrétien, et al.
Plos One
|
June 23, 2011
Nuclear outsourcing of RNA interference components to human mitochondria
Simonetta Bandiera, Silvia Rüberg, Muriel Girard, et al.
The Journal of Pediatrics
|
April 25, 2007
Mitochondrial DNA depletion is a prevalent cause of multiple respiratory chain deficiency in childhood
Emmanuelle Sarzi, Alice Bourdon, Dominique Chrétien, et al.
Plos Biology
|
January 26, 2018
Mitochondria are physiologically maintained at close to 50 °C
Dominique Chrétien, Paule Bénit, Hyung-Ho Ha, et al.
International Journal of Molecular Sciences
|
March 20, 2020
Defects in Galactose Metabolism and Glycoconjugate Biosynthesis in a UDP-Glucose Pyrophosphorylase-Deficient Cell Line Are Reversed by Adding Galactose to the Growth Medium
Christelle Durrant, Jana I Fuehring, Alexandra Willemetz, et al.
Page
of 3