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David A Keays

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

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Plos Genetics|February 6, 2013
Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypesDawn E Watkins-Chow, Joanna Cooke, Ruth Pidsley, et al.
Human Molecular Genetics|August 22, 2015
Mutations in PIGY: expanding the phenotype of inherited glycosylphosphatidylinositol deficienciesBiljana Ilkovski, Alistair T Pagnamenta, Gina L O'Grady, et al.
Current Biology : CB|March 11, 2008
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficitsMatthias Groszer, David A Keays, Robert M J Deacon, et al.
Human Mutation|June 23, 2007
Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A)Karine Poirier, David A Keays, Fiona Francis, et al.
Nature Neuroscience|June 8, 2018
Publisher Correction: Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humansThomas Gstrein, Andrew Edwards, Anna Přistoupilová, et al.
Nature Neuroscience|January 10, 2018
Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humansThomas Gstrein, Andrew Edwards, Anna Přistoupilová, et al.
Brain : a Journal of Neurology|September 24, 2013
Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 geneValerio Conti, Aurelie Carabalona, Emilie Pallesi-Pocachard, 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.
Plos Genetics|February 6, 2013
Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypesDawn E Watkins-Chow, Joanna Cooke, Ruth Pidsley, et al.
Human Molecular Genetics|August 22, 2015
Mutations in PIGY: expanding the phenotype of inherited glycosylphosphatidylinositol deficienciesBiljana Ilkovski, Alistair T Pagnamenta, Gina L O'Grady, et al.
Current Biology : CB|March 11, 2008
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficitsMatthias Groszer, David A Keays, Robert M J Deacon, et al.
Human Mutation|June 23, 2007
Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A)Karine Poirier, David A Keays, Fiona Francis, et al.
Nature Neuroscience|June 8, 2018
Publisher Correction: Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humansThomas Gstrein, Andrew Edwards, Anna Přistoupilová, et al.
Nature Neuroscience|January 10, 2018
Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humansThomas Gstrein, Andrew Edwards, Anna Přistoupilová, et al.
Brain : a Journal of Neurology|September 24, 2013
Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 geneValerio Conti, Aurelie Carabalona, Emilie Pallesi-Pocachard, et al.
Pageof 5