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Arnaud Monteil

Showing results (41-50 of 47) with videos related to

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Frontiers in Pharmacology|October 20, 2025
Electrophysiological classification of <i>CACNA1G</i> gene variants associated with neurodevelopmental and neurological disordersAmaël Davakan, Leos Cmarko, Barbara Ribeiro Oliveira-Mendes, et al.
Human Mutation|April 3, 2007
Mutational analysis of CACNA1G in idiopathic generalized epilepsy. Mutation in brief #962. OnlineBaljinder Singh, Arnaud Monteil, Isabelle Bidaud, et al.
The Journal of Biological Chemistry|December 2, 2011
A Ca(v)3.2/syntaxin-1A signaling complex controls T-type channel activity and low-threshold exocytosisNorbert Weiss, Shahid Hameed, José M Fernández-Fernández, et al.
Scientific Reports|March 1, 2019
Cav3.2 T-type calcium channels shape electrical firing in mouse Lamina II neuronsMiriam Candelas, Ana Reynders, Margarita Arango-Lievano, et al.
Neurology|March 6, 2025
Genotype-Phenotype Landscape of <i>NALCN</i> and <i>UNC80</i>-Related DisordersPaloma Parra-Díaz, Arnaud Monteil, Daniel Calame, et al.
The EMBO Journal|June 6, 2023
NALCN-mediated sodium influx confers metastatic prostate cancer cell invasivenessAntoine Folcher, Dmitri Gordienko, Oksana Iamshanova, et al.
American Journal of Human Genetics|February 17, 2015
De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delayJessica X Chong, Margaret J McMillin, Kathryn M Shively, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Frontiers in Pharmacology|October 20, 2025
Electrophysiological classification of <i>CACNA1G</i> gene variants associated with neurodevelopmental and neurological disordersAmaël Davakan, Leos Cmarko, Barbara Ribeiro Oliveira-Mendes, et al.
Human Mutation|April 3, 2007
Mutational analysis of CACNA1G in idiopathic generalized epilepsy. Mutation in brief #962. OnlineBaljinder Singh, Arnaud Monteil, Isabelle Bidaud, et al.
The Journal of Biological Chemistry|December 2, 2011
A Ca(v)3.2/syntaxin-1A signaling complex controls T-type channel activity and low-threshold exocytosisNorbert Weiss, Shahid Hameed, José M Fernández-Fernández, et al.
Scientific Reports|March 1, 2019
Cav3.2 T-type calcium channels shape electrical firing in mouse Lamina II neuronsMiriam Candelas, Ana Reynders, Margarita Arango-Lievano, et al.
Neurology|March 6, 2025
Genotype-Phenotype Landscape of <i>NALCN</i> and <i>UNC80</i>-Related DisordersPaloma Parra-Díaz, Arnaud Monteil, Daniel Calame, et al.
The EMBO Journal|June 6, 2023
NALCN-mediated sodium influx confers metastatic prostate cancer cell invasivenessAntoine Folcher, Dmitri Gordienko, Oksana Iamshanova, et al.
American Journal of Human Genetics|February 17, 2015
De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delayJessica X Chong, Margaret J McMillin, Kathryn M Shively, et al.
Pageof 5