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C Depienne

Showing results (31-40 of 37) with videos related to

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Virology|November 21, 2002
Phylogenetic analysis of 49 newly derived HIV-1 group O strains: high viral diversity but no group M-like subtype structureP Roques, D L Robertson, S Souquière, et al.
Molecular and Cellular Neurosciences|February 27, 2007
Mutations in the SPG3A gene encoding the GTPase atlastin interfere with vesicle trafficking in the ER/Golgi interface and Golgi morphogenesisM Namekawa, M-P Muriel, A Janer, et al.
Neurology|March 15, 2006
Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegiaN Elleuch, C Depienne, A Benomar, et al.
Journal of Medical Genetics|October 22, 2008
Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patientsC Depienne, O Trouillard, C Saint-Martin, et al.
Neurology|January 19, 2011
A novel DCC mutation and genetic heterogeneity in congenital mirror movementsC Depienne, M Cincotta, S Billot, et al.
Translational Psychiatry|October 25, 2012
Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHEC Nava, F Lamari, D Héron, et al.
Clinical Genetics|July 15, 2017
Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patientsE Chérot, B Keren, C Dubourg, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Virology|November 21, 2002
Phylogenetic analysis of 49 newly derived HIV-1 group O strains: high viral diversity but no group M-like subtype structureP Roques, D L Robertson, S Souquière, et al.
Molecular and Cellular Neurosciences|February 27, 2007
Mutations in the SPG3A gene encoding the GTPase atlastin interfere with vesicle trafficking in the ER/Golgi interface and Golgi morphogenesisM Namekawa, M-P Muriel, A Janer, et al.
Neurology|March 15, 2006
Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegiaN Elleuch, C Depienne, A Benomar, et al.
Journal of Medical Genetics|October 22, 2008
Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patientsC Depienne, O Trouillard, C Saint-Martin, et al.
Neurology|January 19, 2011
A novel DCC mutation and genetic heterogeneity in congenital mirror movementsC Depienne, M Cincotta, S Billot, et al.
Translational Psychiatry|October 25, 2012
Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHEC Nava, F Lamari, D Héron, et al.
Clinical Genetics|July 15, 2017
Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patientsE Chérot, B Keren, C Dubourg, et al.
Pageof 4