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Fabien Fauchereau

Showing results (11-20 of 24) with videos related to

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Cerebral Cortex (New York, N.Y. : 1991)|May 15, 2014
Genetic and Environmental Influences on the Visual Word Form and Fusiform Face AreasPhilippe Pinel, Christophe Lalanne, Thomas Bourgeron, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 21, 2012
Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regionsPhilippe Pinel, Fabien Fauchereau, Antonio Moreno, et al.
Molecular and Cellular Neurosciences|December 21, 2004
Doublecortin interacts with the ubiquitin protease DFFRX, which associates with microtubules in neuronal processesGaëlle Friocourt, Caroline Kappeler, Yoann Saillour, et al.
Scientific Reports|May 20, 2017
Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disordersCécile Pagan, Hany Goubran-Botros, Richard Delorme, et al.
BMC Medical Genetics|January 27, 2009
An investigation of ribosomal protein L10 gene in autism spectrum disordersXiaohong Gong, Richard Delorme, Fabien Fauchereau, et al.
Plos One|March 12, 2011
Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populationsMarina Konyukh, Richard Delorme, Pauline Chaste, et al.
Human Molecular Genetics|April 25, 2002
ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardationThierry Bienvenu, Karine Poirier, Gaelle Friocourt, et al.
Nature Genetics|December 19, 2006
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disordersChristelle M Durand, Catalina Betancur, Tobias M Boeckers, et al.
Journal of Pineal Research|May 28, 2011
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disordersPauline Chaste, Nathalie Clement, Hany Goubran Botros, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2008
Analysis of X chromosome inactivation in autism spectrum disordersXiaohong Gong, Elena Bacchelli, Francesca Blasi, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Cerebral Cortex (New York, N.Y. : 1991)|May 15, 2014
Genetic and Environmental Influences on the Visual Word Form and Fusiform Face AreasPhilippe Pinel, Christophe Lalanne, Thomas Bourgeron, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 21, 2012
Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regionsPhilippe Pinel, Fabien Fauchereau, Antonio Moreno, et al.
Molecular and Cellular Neurosciences|December 21, 2004
Doublecortin interacts with the ubiquitin protease DFFRX, which associates with microtubules in neuronal processesGaëlle Friocourt, Caroline Kappeler, Yoann Saillour, et al.
Scientific Reports|May 20, 2017
Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disordersCécile Pagan, Hany Goubran-Botros, Richard Delorme, et al.
BMC Medical Genetics|January 27, 2009
An investigation of ribosomal protein L10 gene in autism spectrum disordersXiaohong Gong, Richard Delorme, Fabien Fauchereau, et al.
Plos One|March 12, 2011
Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populationsMarina Konyukh, Richard Delorme, Pauline Chaste, et al.
Human Molecular Genetics|April 25, 2002
ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardationThierry Bienvenu, Karine Poirier, Gaelle Friocourt, et al.
Nature Genetics|December 19, 2006
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disordersChristelle M Durand, Catalina Betancur, Tobias M Boeckers, et al.
Journal of Pineal Research|May 28, 2011
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disordersPauline Chaste, Nathalie Clement, Hany Goubran Botros, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2008
Analysis of X chromosome inactivation in autism spectrum disordersXiaohong Gong, Elena Bacchelli, Francesca Blasi, et al.
Pageof 3