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Flora Nolent

Showing results (11-20 of 16) with videos related to

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Nature Microbiology|November 7, 2022
Tecovirimat is effective against human monkeypox virus in vitro at nanomolar concentrationsGaëlle Frenois-Veyrat, Franck Gallardo, Olivier Gorgé, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|May 27, 2022
Investigation of a COVID-19 outbreak on the Charles de Gaulle aircraft carrier, March to April 2020: a retrospective cohort studyFranck de Laval, Hervé Chaudet, Olivier Gorgé, et al.
American Journal of Human Genetics|May 26, 2015
Mutations of GPR126 are responsible for severe arthrogryposis multiplex congenitaGianina Ravenscroft, Flora Nolent, Sulekha Rajagopalan, et al.
Human Molecular Genetics|December 10, 2013
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defectsAnnie Laquérriere, Jérome Maluenda, Adrien Camus, et al.
The Journal of Clinical Investigation|September 25, 2014
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathyMichaela Yuen, Sarah A Sandaradura, James J Dowling, et al.
Journal of Medical Genetics|April 6, 2021
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenitaAnnie Laquerriere, Dana Jaber, Emanuela Abiusi, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Nature Microbiology|November 7, 2022
Tecovirimat is effective against human monkeypox virus in vitro at nanomolar concentrationsGaëlle Frenois-Veyrat, Franck Gallardo, Olivier Gorgé, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|May 27, 2022
Investigation of a COVID-19 outbreak on the Charles de Gaulle aircraft carrier, March to April 2020: a retrospective cohort studyFranck de Laval, Hervé Chaudet, Olivier Gorgé, et al.
American Journal of Human Genetics|May 26, 2015
Mutations of GPR126 are responsible for severe arthrogryposis multiplex congenitaGianina Ravenscroft, Flora Nolent, Sulekha Rajagopalan, et al.
Human Molecular Genetics|December 10, 2013
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defectsAnnie Laquérriere, Jérome Maluenda, Adrien Camus, et al.
The Journal of Clinical Investigation|September 25, 2014
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathyMichaela Yuen, Sarah A Sandaradura, James J Dowling, et al.
Journal of Medical Genetics|April 6, 2021
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenitaAnnie Laquerriere, Dana Jaber, Emanuela Abiusi, et al.
Pageof 2