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Jamel Chelly

Showing results (51-60 of 226) with videos related to

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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|June 5, 2003
IL1 receptor accessory protein like, a protein involved in X-linked mental retardation, interacts with Neuronal Calcium Sensor-1 and regulates exocytosisNadia Bahi, Gaelle Friocourt, Alain Carrié, 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.
Movement Disorders : Official Journal of the Movement Disorder Society|May 19, 2022
De Novo Mutation in TMEM151A and Paroxysmal Kinesigenic DyskinesiaThomas Wirth, Aurélie Méneret, Nathalie Drouot, et al.
Orphanet Journal of Rare Diseases|July 11, 2012
Assessment of the structural and functional impact of in-frame mutations of the DMD gene, using the tools included in the eDystrophin online databaseAurélie Nicolas, Céline Lucchetti-Miganeh, Rabah Ben Yaou, 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.
Human Mutation|February 1, 2011
A missense mutation within the fork-head domain of the forkhead box G1 Gene (FOXG1) affects its nuclear localizationTangui Le Guen, Yann Fichou, Juliette Nectoux, et al.
Nature Neuroscience|August 30, 2011
A circadian clock in hippocampus is regulated by interaction between oligophrenin-1 and Rev-erbαPamela Valnegri, Malik Khelfaoui, Olivier Dorseuil, et al.
The European Journal of Neuroscience|March 8, 2006
Human disorders of cortical development: from past to presentFiona Francis, Gundela Meyer, Catherine Fallet-Bianco, et al.
Trends in Genetics : TIG|June 13, 2003
Nonsyndromic X-linked mental retardation: where are the missing mutations?Hans-Hilger Ropers, Maria Hoeltzenbein, Vera Kalscheuer, et al.
Pageof 23

Showing results (51-60 of 226) with videos related to

Sort By:
Pageof 23
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|June 5, 2003
IL1 receptor accessory protein like, a protein involved in X-linked mental retardation, interacts with Neuronal Calcium Sensor-1 and regulates exocytosisNadia Bahi, Gaelle Friocourt, Alain Carrié, 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.
Movement Disorders : Official Journal of the Movement Disorder Society|May 19, 2022
De Novo Mutation in TMEM151A and Paroxysmal Kinesigenic DyskinesiaThomas Wirth, Aurélie Méneret, Nathalie Drouot, et al.
Orphanet Journal of Rare Diseases|July 11, 2012
Assessment of the structural and functional impact of in-frame mutations of the DMD gene, using the tools included in the eDystrophin online databaseAurélie Nicolas, Céline Lucchetti-Miganeh, Rabah Ben Yaou, 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.
Human Mutation|February 1, 2011
A missense mutation within the fork-head domain of the forkhead box G1 Gene (FOXG1) affects its nuclear localizationTangui Le Guen, Yann Fichou, Juliette Nectoux, et al.
Nature Neuroscience|August 30, 2011
A circadian clock in hippocampus is regulated by interaction between oligophrenin-1 and Rev-erbαPamela Valnegri, Malik Khelfaoui, Olivier Dorseuil, et al.
The European Journal of Neuroscience|March 8, 2006
Human disorders of cortical development: from past to presentFiona Francis, Gundela Meyer, Catherine Fallet-Bianco, et al.
Trends in Genetics : TIG|June 13, 2003
Nonsyndromic X-linked mental retardation: where are the missing mutations?Hans-Hilger Ropers, Maria Hoeltzenbein, Vera Kalscheuer, et al.
Pageof 23