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Showing results (1271-1280 of 1,344) with videos related to

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Neuromuscular Disorders : NMD|October 31, 2020
The importance of an integrated genotype-phenotype strategy to unravel the molecular bases of titinopathiesAurélien Perrin, Raul Juntas Morales, François Rivier, et al.
Medrxiv : the Preprint Server for Health Sciences|December 25, 2025
Host Genetic Architecture between Epstein-Barr Virus Activity and Multiple Sclerosis Reveals Shared PathwaysYoshiaki Yasumizu, Namkwon Kim, Cyprien A Rivier, et al.
Medrxiv : the Preprint Server for Health Sciences|October 4, 2023
Polygenic Risk of Epilepsy and Post-Stroke EpilepsyCyprien A Rivier, Santiago Clocchiatti-Tuozzo, Shubham Misra, et al.
Pediatric Pulmonology|September 29, 2021
Interstitial lung disease in children with Rubinstein-Taybi syndromeLauren Bradford, Mindy K Ross, Jagila Minso, et al.
Journal of Medical Genetics|June 5, 2010
Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndromeChristel Depienne, Oriane Trouillard, Isabelle Gourfinkel-An, et al.
Stroke|November 6, 2024
Polygenic Risk of Epilepsy and Poststroke EpilepsySantiago Clocchiatti-Tuozzo, Cyprien A Rivier, Shubham Misra, et al.
European Journal of Human Genetics : EJHG|May 16, 2013
Expanding the phenotype of IQSEC2 mutations: truncating mutations in severe intellectual disabilityFrederic Tran Mau-Them, Marjolaine Willems, Beate Albrecht, et al.
Journal of the American Heart Association|August 29, 2025
Characterizing Stroke Clots Using Single-Cell SequencingDaniela Renedo, Tanyeri Barak, Jonathan DeLong, et al.
The British Journal of Dermatology|July 6, 2018
Nonclinical and human pharmacology of the potent and selective topical retinoic acid receptor-γ agonist trifaroteneJ Aubert, D Piwnica, B Bertino, et al.
Nature Structural & Molecular Biology|September 13, 2016
A minimized human insulin-receptor-binding motif revealed in a Conus geographus venom insulinJohn G Menting, Joanna Gajewiak, Christopher A MacRaild, et al.
Pageof 135

Showing results (1271-1280 of 1,344) with videos related to

Sort By:
Pageof 135
Neuromuscular Disorders : NMD|October 31, 2020
The importance of an integrated genotype-phenotype strategy to unravel the molecular bases of titinopathiesAurélien Perrin, Raul Juntas Morales, François Rivier, et al.
Medrxiv : the Preprint Server for Health Sciences|December 25, 2025
Host Genetic Architecture between Epstein-Barr Virus Activity and Multiple Sclerosis Reveals Shared PathwaysYoshiaki Yasumizu, Namkwon Kim, Cyprien A Rivier, et al.
Medrxiv : the Preprint Server for Health Sciences|October 4, 2023
Polygenic Risk of Epilepsy and Post-Stroke EpilepsyCyprien A Rivier, Santiago Clocchiatti-Tuozzo, Shubham Misra, et al.
Pediatric Pulmonology|September 29, 2021
Interstitial lung disease in children with Rubinstein-Taybi syndromeLauren Bradford, Mindy K Ross, Jagila Minso, et al.
Journal of Medical Genetics|June 5, 2010
Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndromeChristel Depienne, Oriane Trouillard, Isabelle Gourfinkel-An, et al.
Stroke|November 6, 2024
Polygenic Risk of Epilepsy and Poststroke EpilepsySantiago Clocchiatti-Tuozzo, Cyprien A Rivier, Shubham Misra, et al.
European Journal of Human Genetics : EJHG|May 16, 2013
Expanding the phenotype of IQSEC2 mutations: truncating mutations in severe intellectual disabilityFrederic Tran Mau-Them, Marjolaine Willems, Beate Albrecht, et al.
Journal of the American Heart Association|August 29, 2025
Characterizing Stroke Clots Using Single-Cell SequencingDaniela Renedo, Tanyeri Barak, Jonathan DeLong, et al.
The British Journal of Dermatology|July 6, 2018
Nonclinical and human pharmacology of the potent and selective topical retinoic acid receptor-γ agonist trifaroteneJ Aubert, D Piwnica, B Bertino, et al.
Nature Structural & Molecular Biology|September 13, 2016
A minimized human insulin-receptor-binding motif revealed in a Conus geographus venom insulinJohn G Menting, Joanna Gajewiak, Christopher A MacRaild, et al.
Pageof 135