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Marie-Claude Gingras

Showing results (41-50 of 70) with videos related to

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Science Translational Medicine|June 17, 2011
Whole-genome sequencing for optimized patient managementMatthew N Bainbridge, Wojciech Wiszniewski, David R Murdock, et al.
NPJ Microgravity|May 14, 2025
The GENESTAR manual for biospecimen collection biobanking and omics data generation from commercial space missionsAparna Krishnavajhala, Marie-Claude Gingras, Emmanuel Urquieta, et al.
Medrxiv : the Preprint Server for Health Sciences|January 8, 2026
Expanding the Clinical and Molecular Spectrum of <i>TUBB2B</i> Through Distinct Variants Identified Across Multiple FamiliesShaghayegh T Beheshti, Angad Jolly, Ahmed K Saad, et al.
Molecular Cell|October 17, 2015
Mitochondrial Phosphoenolpyruvate Carboxykinase Regulates Metabolic Adaptation and Enables Glucose-Independent Tumor GrowthEmma E Vincent, Alexey Sergushichev, Takla Griss, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2026
Multi-Omics Characterization of Human Molecular Responses to Spaceflight Across Two Independent MissionsAbirami Santhanam, Zeineen Momin, Xiang Qin, et al.
The Journal of Clinical Investigation|April 26, 2014
The tumor suppressor folliculin regulates AMPK-dependent metabolic transformationMing Yan, Marie-Claude Gingras, Elaine A Dunlop, et al.
Human Mutation|September 2, 2022
Long read sequencing and expression studies of AHDC1 deletions in Xia-Gibbs syndrome reveal a novel genetic regulatory mechanismVaruna Chander, Medhat Mahmoud, Jianhong Hu, et al.
Genetics in Medicine Open|January 16, 2026
An evaluation of genetic predisposition to congenital anomalies and pediatric cancer supports <i>KAT6B</i> as a novel neuroblastoma susceptibility geneHyunjung Gu, Yao Yu, Saumya Dushyant Sisoudiya, et al.
Nature Communications|January 26, 2016
Functional annotation of rare gene aberration drivers of pancreatic cancerYiu Huen Tsang, Turgut Dogruluk, Philip M Tedeschi, et al.
HGG Advances|March 5, 2021
Germline mutation in <i>POLR2A</i>: a heterogeneous, multi-systemic developmental disorder characterized by transcriptional dysregulationAdam W Hansen, Payal Arora, Michael M Khayat, et al.
Pageof 7

Showing results (41-50 of 70) with videos related to

Sort By:
Pageof 7
Science Translational Medicine|June 17, 2011
Whole-genome sequencing for optimized patient managementMatthew N Bainbridge, Wojciech Wiszniewski, David R Murdock, et al.
NPJ Microgravity|May 14, 2025
The GENESTAR manual for biospecimen collection biobanking and omics data generation from commercial space missionsAparna Krishnavajhala, Marie-Claude Gingras, Emmanuel Urquieta, et al.
Medrxiv : the Preprint Server for Health Sciences|January 8, 2026
Expanding the Clinical and Molecular Spectrum of <i>TUBB2B</i> Through Distinct Variants Identified Across Multiple FamiliesShaghayegh T Beheshti, Angad Jolly, Ahmed K Saad, et al.
Molecular Cell|October 17, 2015
Mitochondrial Phosphoenolpyruvate Carboxykinase Regulates Metabolic Adaptation and Enables Glucose-Independent Tumor GrowthEmma E Vincent, Alexey Sergushichev, Takla Griss, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2026
Multi-Omics Characterization of Human Molecular Responses to Spaceflight Across Two Independent MissionsAbirami Santhanam, Zeineen Momin, Xiang Qin, et al.
The Journal of Clinical Investigation|April 26, 2014
The tumor suppressor folliculin regulates AMPK-dependent metabolic transformationMing Yan, Marie-Claude Gingras, Elaine A Dunlop, et al.
Human Mutation|September 2, 2022
Long read sequencing and expression studies of AHDC1 deletions in Xia-Gibbs syndrome reveal a novel genetic regulatory mechanismVaruna Chander, Medhat Mahmoud, Jianhong Hu, et al.
Genetics in Medicine Open|January 16, 2026
An evaluation of genetic predisposition to congenital anomalies and pediatric cancer supports <i>KAT6B</i> as a novel neuroblastoma susceptibility geneHyunjung Gu, Yao Yu, Saumya Dushyant Sisoudiya, et al.
Nature Communications|January 26, 2016
Functional annotation of rare gene aberration drivers of pancreatic cancerYiu Huen Tsang, Turgut Dogruluk, Philip M Tedeschi, et al.
HGG Advances|March 5, 2021
Germline mutation in <i>POLR2A</i>: a heterogeneous, multi-systemic developmental disorder characterized by transcriptional dysregulationAdam W Hansen, Payal Arora, Michael M Khayat, et al.
Pageof 7