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Michelle Simon

Showing results (41-50 of 77) with videos related to

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Journal of Genetics and Genomics = Yi Chuan Xue Bao|April 22, 2020
Asthma-associated polymorphisms in 17q12-21 locus modulate methylation and gene expression of GSDMA in naïve CD4<sup>+</sup> T cellsAnne-Marie Madore, Lucile Pain, Anne-Marie Boucher-Lafleur, et al.
Genome Biology|July 10, 2019
Integrative analysis of vascular endothelial cell genomic features identifies AIDA as a coronary artery disease candidate geneSimon Lalonde, Valérie-Anne Codina-Fauteux, Sébastian Méric de Bellefon, et al.
Human Molecular Genetics|December 27, 2011
Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIbRamakrishna Kurapati, Caoimhe McKenna, Johan Lindqvist, et al.
Cell Genomics|May 25, 2023
Transposable elements are associated with the variable response to influenza infectionXun Chen, Alain Pacis, Katherine A Aracena, et al.
Endocrine Connections|April 30, 2020
Genetic background influences tumour development in heterozygous Men1 knockout miceKate E Lines, Mahsa Javid, Anita A C Reed, et al.
Nature Communications|August 12, 2025
REST/NRSF Preserves muscle stem cell identity by repressing alternate cell fateKorin Sahinyan, Darren M Blackburn, Marie-Michelle Simon, et al.
Human Molecular Genetics|March 7, 2018
A genetic modifier suggests that endurance exercise exacerbates Huntington's diseaseSilvia Corrochano, Gonzalo Blanco, Debbie Williams, et al.
Environmental Health Perspectives|August 9, 2019
Customized MethylC-Capture Sequencing to Evaluate Variation in the Human Sperm DNA Methylome Representative of Altered Folate MetabolismDonovan Chan, Xiaojian Shao, Marie-Charlotte Dumargne, et al.
Developmental Cell|October 16, 2024
LINE1 and PRC2 control nucleolar organization and repression of the 8C state in human ESCsJuan Zhang, Lamisa Ataei, Kirti Mittal, et al.
Genome Biology|December 25, 2015
Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variationStephan Busche, Xiaojian Shao, Maxime Caron, et al.
Pageof 8

Showing results (41-50 of 77) with videos related to

Sort By:
Pageof 8
Journal of Genetics and Genomics = Yi Chuan Xue Bao|April 22, 2020
Asthma-associated polymorphisms in 17q12-21 locus modulate methylation and gene expression of GSDMA in naïve CD4<sup>+</sup> T cellsAnne-Marie Madore, Lucile Pain, Anne-Marie Boucher-Lafleur, et al.
Genome Biology|July 10, 2019
Integrative analysis of vascular endothelial cell genomic features identifies AIDA as a coronary artery disease candidate geneSimon Lalonde, Valérie-Anne Codina-Fauteux, Sébastian Méric de Bellefon, et al.
Human Molecular Genetics|December 27, 2011
Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIbRamakrishna Kurapati, Caoimhe McKenna, Johan Lindqvist, et al.
Cell Genomics|May 25, 2023
Transposable elements are associated with the variable response to influenza infectionXun Chen, Alain Pacis, Katherine A Aracena, et al.
Endocrine Connections|April 30, 2020
Genetic background influences tumour development in heterozygous Men1 knockout miceKate E Lines, Mahsa Javid, Anita A C Reed, et al.
Nature Communications|August 12, 2025
REST/NRSF Preserves muscle stem cell identity by repressing alternate cell fateKorin Sahinyan, Darren M Blackburn, Marie-Michelle Simon, et al.
Human Molecular Genetics|March 7, 2018
A genetic modifier suggests that endurance exercise exacerbates Huntington's diseaseSilvia Corrochano, Gonzalo Blanco, Debbie Williams, et al.
Environmental Health Perspectives|August 9, 2019
Customized MethylC-Capture Sequencing to Evaluate Variation in the Human Sperm DNA Methylome Representative of Altered Folate MetabolismDonovan Chan, Xiaojian Shao, Marie-Charlotte Dumargne, et al.
Developmental Cell|October 16, 2024
LINE1 and PRC2 control nucleolar organization and repression of the 8C state in human ESCsJuan Zhang, Lamisa Ataei, Kirti Mittal, et al.
Genome Biology|December 25, 2015
Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variationStephan Busche, Xiaojian Shao, Maxime Caron, et al.
Pageof 8