Search research articles
Contact Us
Filters
Showing results (121-130 of 245) with videos related to
Page
of 25
Sort By:
Journal of Clinical Medicine
|
May 7, 2020
Elevated Levels of Monocyte Chemotactic Protein-1 in the Follicular Fluid Reveals Different Populations among Women with Severe Endometriosis
Pierre-Emmanuel Bouet, Juan-Manuel Chao de la Barca, Lisa Boucret, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 7, 2004
Transcriptional profiling reveals coordinated up-regulation of oxidative metabolism genes in thyroid oncocytic tumors
Olivier Baris, Frédérique Savagner, Valéry Nasser, et al.
International Journal of Legal Medicine
|
September 20, 2018
A serum metabolomics signature of hypothermia fatalities involving arginase activity, tryptophan content, and phosphatidylcholine saturation
Guillaume Rousseau, Juan Manuel Chao de la Barca, Clotilde Rougé-Maillart, et al.
The International Journal of Biochemistry & Cell Biology
|
April 15, 2014
Acute intermittent porphyria causes hepatic mitochondrial energetic failure in a mouse model
Chadi Homedan, Jihane Laafi, Caroline Schmitt, et al.
International Journal of Molecular Sciences
|
June 24, 2022
Metabolomic Profiling of Angiotensin-II-Induced Abdominal Aortic Aneurysm in Ldlr<sup>-/-</sup> Mice Points to Alteration of Nitric Oxide, Lipid, and Energy Metabolisms
Juan Manuel Chao de la Barca, Alexis Richard, Pauline Robert, et al.
Human Molecular Genetics
|
June 14, 2015
Mitochondrial energetic defects in muscle and brain of a Hmbs-/- mouse model of acute intermittent porphyria
Chadi Homedan, Caroline Schmitt, Jihane Laafi, et al.
Molecular Neurodegeneration
|
February 26, 2021
Dominant mutations in MIEF1 affect mitochondrial dynamics and cause a singular late onset optic neuropathy
Majida Charif, Yvette C Wong, Soojin Kim, et al.
Molecular Vision
|
March 28, 2009
Acute and late-onset optic atrophy due to a novel OPA1 mutation leading to a mitochondrial coupling defect
Yannick Nochez, Sophie Arsene, Naig Gueguen, et al.
Journal of Proteome Research
|
April 5, 2021
Preliminary Metabolomic Profiling of the Vitreous Humor from Hypothermia Fatalities
Guillaume Rousseau, Juan Manuel Chao de la Barca, Clotilde Rougé-Maillart, et al.
Mitochondrion
|
May 23, 2021
Optic neuropathy linked to ACAD9 pathogenic variants: A potentially riboflavin-responsive disorder?
Naig Gueguen, Julie Piarroux, Emmanuelle Sarzi, et al.
Page
of 25
Search research articles
Search
Showing results (121-130 of 245) with videos related to
Sort By:
Page
of 25
Journal of Clinical Medicine
|
May 7, 2020
Elevated Levels of Monocyte Chemotactic Protein-1 in the Follicular Fluid Reveals Different Populations among Women with Severe Endometriosis
Pierre-Emmanuel Bouet, Juan-Manuel Chao de la Barca, Lisa Boucret, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 7, 2004
Transcriptional profiling reveals coordinated up-regulation of oxidative metabolism genes in thyroid oncocytic tumors
Olivier Baris, Frédérique Savagner, Valéry Nasser, et al.
International Journal of Legal Medicine
|
September 20, 2018
A serum metabolomics signature of hypothermia fatalities involving arginase activity, tryptophan content, and phosphatidylcholine saturation
Guillaume Rousseau, Juan Manuel Chao de la Barca, Clotilde Rougé-Maillart, et al.
The International Journal of Biochemistry & Cell Biology
|
April 15, 2014
Acute intermittent porphyria causes hepatic mitochondrial energetic failure in a mouse model
Chadi Homedan, Jihane Laafi, Caroline Schmitt, et al.
International Journal of Molecular Sciences
|
June 24, 2022
Metabolomic Profiling of Angiotensin-II-Induced Abdominal Aortic Aneurysm in Ldlr<sup>-/-</sup> Mice Points to Alteration of Nitric Oxide, Lipid, and Energy Metabolisms
Juan Manuel Chao de la Barca, Alexis Richard, Pauline Robert, et al.
Human Molecular Genetics
|
June 14, 2015
Mitochondrial energetic defects in muscle and brain of a Hmbs-/- mouse model of acute intermittent porphyria
Chadi Homedan, Caroline Schmitt, Jihane Laafi, et al.
Molecular Neurodegeneration
|
February 26, 2021
Dominant mutations in MIEF1 affect mitochondrial dynamics and cause a singular late onset optic neuropathy
Majida Charif, Yvette C Wong, Soojin Kim, et al.
Molecular Vision
|
March 28, 2009
Acute and late-onset optic atrophy due to a novel OPA1 mutation leading to a mitochondrial coupling defect
Yannick Nochez, Sophie Arsene, Naig Gueguen, et al.
Journal of Proteome Research
|
April 5, 2021
Preliminary Metabolomic Profiling of the Vitreous Humor from Hypothermia Fatalities
Guillaume Rousseau, Juan Manuel Chao de la Barca, Clotilde Rougé-Maillart, et al.
Mitochondrion
|
May 23, 2021
Optic neuropathy linked to ACAD9 pathogenic variants: A potentially riboflavin-responsive disorder?
Naig Gueguen, Julie Piarroux, Emmanuelle Sarzi, et al.
Page
of 25