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Yoann Saillour

Showing results (1-10 of 41) with videos related to

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Developmental Neuroscience|December 14, 2007
Alternative transcripts of Dclk1 and Dclk2 and their expression in doublecortin knockout miceFrançoise Phan Dinh Tuy, Yoann Saillour, Caroline Kappeler, et al.
Development (Cambridge, England)|June 25, 2021
Single-cell transcriptomics of the early developing mouse cerebral cortex disentangle the spatial and temporal components of neuronal fate acquisitionMatthieu X Moreau, Yoann Saillour, Andrzej W Cwetsch, et al.
European Journal of Medical Genetics|February 15, 2011
A novel frame shift mutation in the PQBP1 gene identified in a Tunisian family with X-linked mental retardationImen Rejeb, Lamia Ben Jemaa, Leila Abaied, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 21, 2009
Epileptic encephalopathy in a girl with an interstitial deletion of Xp22 comprising promoter and exon 1 of the CDKL5 geneNadia Bahi-Buisson, Benoit Girard, Agnes Gautier, et al.
Glia|February 20, 2020
The intellectual disability protein Oligophrenin-1 controls astrocyte morphology and migrationLaure-Elise Pillet, Noémie Cresto, Yoann Saillour, et al.
European Journal of Medical Genetics|July 7, 2012
Focal polymicrogyria are associated with submicroscopic chromosomal rearrangements detected by CGH microarray analysisChloe Quelin, Yoann Saillour, Karine Poirier, et al.
Brain : a Journal of Neurology|August 2, 2008
Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1ACatherine Fallet-Bianco, Laurence Loeuillet, Karine Poirier, et al.
Human Molecular Genetics|November 2, 2013
Beta tubulin isoforms are not interchangeable for rescuing impaired radial migration due to Tubb3 knockdownYoann Saillour, Loïc Broix, Elodie Bruel-Jungerman, et al.
European Journal of Human Genetics : EJHG|June 5, 2008
A novel splice mutation in PAK3 gene underlying mental retardation with neuropsychiatric featuresImen Rejeb, Yoann Saillour, Laetitia Castelnau, et al.
Human Molecular Genetics|March 31, 2006
Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout miceCaroline Kappeler, Yoann Saillour, Jean-Pierre Baudoin, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
Developmental Neuroscience|December 14, 2007
Alternative transcripts of Dclk1 and Dclk2 and their expression in doublecortin knockout miceFrançoise Phan Dinh Tuy, Yoann Saillour, Caroline Kappeler, et al.
Development (Cambridge, England)|June 25, 2021
Single-cell transcriptomics of the early developing mouse cerebral cortex disentangle the spatial and temporal components of neuronal fate acquisitionMatthieu X Moreau, Yoann Saillour, Andrzej W Cwetsch, et al.
European Journal of Medical Genetics|February 15, 2011
A novel frame shift mutation in the PQBP1 gene identified in a Tunisian family with X-linked mental retardationImen Rejeb, Lamia Ben Jemaa, Leila Abaied, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 21, 2009
Epileptic encephalopathy in a girl with an interstitial deletion of Xp22 comprising promoter and exon 1 of the CDKL5 geneNadia Bahi-Buisson, Benoit Girard, Agnes Gautier, et al.
Glia|February 20, 2020
The intellectual disability protein Oligophrenin-1 controls astrocyte morphology and migrationLaure-Elise Pillet, Noémie Cresto, Yoann Saillour, et al.
European Journal of Medical Genetics|July 7, 2012
Focal polymicrogyria are associated with submicroscopic chromosomal rearrangements detected by CGH microarray analysisChloe Quelin, Yoann Saillour, Karine Poirier, et al.
Brain : a Journal of Neurology|August 2, 2008
Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1ACatherine Fallet-Bianco, Laurence Loeuillet, Karine Poirier, et al.
Human Molecular Genetics|November 2, 2013
Beta tubulin isoforms are not interchangeable for rescuing impaired radial migration due to Tubb3 knockdownYoann Saillour, Loïc Broix, Elodie Bruel-Jungerman, et al.
European Journal of Human Genetics : EJHG|June 5, 2008
A novel splice mutation in PAK3 gene underlying mental retardation with neuropsychiatric featuresImen Rejeb, Yoann Saillour, Laetitia Castelnau, et al.
Human Molecular Genetics|March 31, 2006
Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout miceCaroline Kappeler, Yoann Saillour, Jean-Pierre Baudoin, et al.
Pageof 5