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Alice Karam

Showing results (1-10 of 7) with videos related to

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Advances in Experimental Medicine and Biology|February 11, 2018
Molecular Mechanisms and Therapeutic Strategies in Spinocerebellar Ataxia Type 7Alice Karam, Yvon Trottier
BMC Bioinformatics|September 16, 2019
A multiscale mathematical model of cell dynamics during neurogenesis in the mouse cerebral cortexMarie Postel, Alice Karam, Guillaume Pézeron, et al.
Human Molecular Genetics|November 17, 2018
Loss of zebrafish Ataxin-7, a SAGA subunit responsible for SCA7 retinopathy, causes ocular coloboma and malformation of photoreceptorsSamantha Carrillo-Rosas, Chantal Weber, Lorraine Fievet, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 30, 2019
The Ciliopathy Gene <i>Ftm/Rpgrip1l</i> Controls Mouse Forebrain Patterning via Region-Specific Modulation of Hedgehog/Gli SignalingAbraham Andreu-Cervera, Isabelle Anselme, Alice Karam, et al.
Neurobiology of Disease|May 20, 2015
A novel function of Huntingtin in the cilium and retinal ciliopathy in Huntington's disease miceAlice Karam, Lars Tebbe, Chantal Weber, et al.
Neurobiology of Disease|July 6, 2010
Polyglutamine toxicity induces rod photoreceptor division, morphological transformation or death in spinocerebellar ataxia 7 mouse retinaMarina G Yefimova, Nadia Messaddeq, Alice Karam, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 23, 2021
SCA7 Mouse Cerebellar Pathology Reveals Preferential Downregulation of Key Purkinje Cell-Identity Genes and Shared Disease Signature with SCA1 and SCA2Anna Niewiadomska-Cimicka, Frédéric Doussau, Jean-Baptiste Perot, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Advances in Experimental Medicine and Biology|February 11, 2018
Molecular Mechanisms and Therapeutic Strategies in Spinocerebellar Ataxia Type 7Alice Karam, Yvon Trottier
BMC Bioinformatics|September 16, 2019
A multiscale mathematical model of cell dynamics during neurogenesis in the mouse cerebral cortexMarie Postel, Alice Karam, Guillaume Pézeron, et al.
Human Molecular Genetics|November 17, 2018
Loss of zebrafish Ataxin-7, a SAGA subunit responsible for SCA7 retinopathy, causes ocular coloboma and malformation of photoreceptorsSamantha Carrillo-Rosas, Chantal Weber, Lorraine Fievet, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 30, 2019
The Ciliopathy Gene <i>Ftm/Rpgrip1l</i> Controls Mouse Forebrain Patterning via Region-Specific Modulation of Hedgehog/Gli SignalingAbraham Andreu-Cervera, Isabelle Anselme, Alice Karam, et al.
Neurobiology of Disease|May 20, 2015
A novel function of Huntingtin in the cilium and retinal ciliopathy in Huntington's disease miceAlice Karam, Lars Tebbe, Chantal Weber, et al.
Neurobiology of Disease|July 6, 2010
Polyglutamine toxicity induces rod photoreceptor division, morphological transformation or death in spinocerebellar ataxia 7 mouse retinaMarina G Yefimova, Nadia Messaddeq, Alice Karam, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 23, 2021
SCA7 Mouse Cerebellar Pathology Reveals Preferential Downregulation of Key Purkinje Cell-Identity Genes and Shared Disease Signature with SCA1 and SCA2Anna Niewiadomska-Cimicka, Frédéric Doussau, Jean-Baptiste Perot, et al.
Pageof 1