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Monnot

Showing results (291-300 of 338) with videos related to

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Biomaterials|December 12, 2018
Development of a human skeletal micro muscle platform with pacing capabilitiesRichard J Mills, Benjamin L Parker, Pauline Monnot, et al.
Cell Reports|May 27, 2014
Data from artificial models of mitochondrial DNA disorders are not always applicable to humansJulie Steffann, Nadine Gigarel, David C Samuels, et al.
Experimental Neurology|December 24, 2024
Early alterations of functional connectivity, regional brain volumes and astrocyte markers in the beta-sitosterol beta-d-glucoside (BSSG) rat model of parkinsonismC Monnot, M Kalomoiri, E MacNicol, et al.
Regulatory Toxicology and Pharmacology : RTP|February 16, 2021
A comprehensive weight of evidence assessment of published acetaminophen genotoxicity data: Implications for its carcinogenic hazard potentialDavid Kirkland, Michael Kovochich, Sharlee L More, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 11, 2020
A retrospective study on the efficacy of prenatal diagnosis for pregnancies at risk of mitochondrial DNA disordersJulie Steffann, Sophie Monnot, Maryse Magen, et al.
Journal of Medical Genetics|May 13, 2006
Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke-like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal developmentC Bouchet, J Steffann, J Corcos, et al.
Human Molecular Genetics|February 8, 2013
Mutation dependance of the mitochondrial DNA copy number in the first stages of human embryogenesisSophie Monnot, David C Samuels, Laetitia Hesters, et al.
European Journal of Gastroenterology & Hepatology|March 15, 2001
Treatment of mild chronic hepatitis C with interferon alpha-2b: results of a multi-centre randomized study in 80 patientsP E Queneau, F Osaer, J P Bronowicki, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 13, 2025
Quantifying cell traction forces at the single-fiber scale in 3D: An approach based on deformable photopolymerized fiber arraysPierre Ucla, Joanne Lê-Chesnais, Henri Ver Hulst, et al.
American Journal of Human Genetics|April 9, 2011
Poor correlations in the levels of pathogenic mitochondrial DNA mutations in polar bodies versus oocytes and blastomeres in humansNadine Gigarel, Laetitia Hesters, David C Samuels, et al.
Pageof 34

Showing results (291-300 of 338) with videos related to

Sort By:
Pageof 34
Biomaterials|December 12, 2018
Development of a human skeletal micro muscle platform with pacing capabilitiesRichard J Mills, Benjamin L Parker, Pauline Monnot, et al.
Cell Reports|May 27, 2014
Data from artificial models of mitochondrial DNA disorders are not always applicable to humansJulie Steffann, Nadine Gigarel, David C Samuels, et al.
Experimental Neurology|December 24, 2024
Early alterations of functional connectivity, regional brain volumes and astrocyte markers in the beta-sitosterol beta-d-glucoside (BSSG) rat model of parkinsonismC Monnot, M Kalomoiri, E MacNicol, et al.
Regulatory Toxicology and Pharmacology : RTP|February 16, 2021
A comprehensive weight of evidence assessment of published acetaminophen genotoxicity data: Implications for its carcinogenic hazard potentialDavid Kirkland, Michael Kovochich, Sharlee L More, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 11, 2020
A retrospective study on the efficacy of prenatal diagnosis for pregnancies at risk of mitochondrial DNA disordersJulie Steffann, Sophie Monnot, Maryse Magen, et al.
Journal of Medical Genetics|May 13, 2006
Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke-like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal developmentC Bouchet, J Steffann, J Corcos, et al.
Human Molecular Genetics|February 8, 2013
Mutation dependance of the mitochondrial DNA copy number in the first stages of human embryogenesisSophie Monnot, David C Samuels, Laetitia Hesters, et al.
European Journal of Gastroenterology & Hepatology|March 15, 2001
Treatment of mild chronic hepatitis C with interferon alpha-2b: results of a multi-centre randomized study in 80 patientsP E Queneau, F Osaer, J P Bronowicki, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 13, 2025
Quantifying cell traction forces at the single-fiber scale in 3D: An approach based on deformable photopolymerized fiber arraysPierre Ucla, Joanne Lê-Chesnais, Henri Ver Hulst, et al.
American Journal of Human Genetics|April 9, 2011
Poor correlations in the levels of pathogenic mitochondrial DNA mutations in polar bodies versus oocytes and blastomeres in humansNadine Gigarel, Laetitia Hesters, David C Samuels, et al.
Pageof 34