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Anne Joutel

Showing results (31-40 of 74) with videos related to

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Genesis (New York, N.Y. : 2000)|May 19, 2006
Nas transgenic mouse line allows visualization of Notch pathway activity in vivoCéline Souilhol, Sarah Cormier, Marie Monet, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|November 3, 2012
Transcriptome analysis for Notch3 target genes identifies Grip2 as a novel regulator of myogenic response in the cerebrovasculatureCharles Fouillade, Céline Baron-Menguy, Valérie Domenga-Denier, et al.
Acta Neuropathologica Communications|November 23, 2019
Blood brain barrier leakage is not a consistent feature of white matter lesions in CADASILRikesh M Rajani, Julien Ratelade, Valérie Domenga-Denier, et al.
Stroke|December 1, 2004
Impaired vascular mechanotransduction in a transgenic mouse model of CADASIL arteriopathyCaroline Dubroca, Pierre Lacombe, Valérie Domenga, et al.
Genesis (New York, N.Y. : 2000)|November 5, 2003
Characterization of Notch3-deficient mice: normal embryonic development and absence of genetic interactions with a Notch1 mutationLuke T Krebs, Yingzi Xue, Christine R Norton, et al.
Stroke|January 16, 2014
Archetypal Arg169Cys mutation in NOTCH3 does not drive the pathogenesis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy via a loss-of-function mechanismEmmanuel Cognat, Céline Baron-Menguy, Valérie Domenga-Denier, et al.
Archives of Neurology|May 11, 2011
Stroke-related translational researchLouis R Caplan, Juan Arenillas, Steven C Cramer, et al.
Annals of Neurology|January 13, 2006
A novel hereditary small vessel disease of the brainSteve Verreault, Anne Joutel, Florence Riant, et al.
European Journal of Human Genetics : EJHG|October 31, 2002
Spectrum and expression analysis of KRIT1 mutations in 121 consecutive and unrelated patients with Cerebral Cavernous MalformationsFlorence Cavé-Riant, Christian Denier, Pierre Labauge, et al.
Human Mutation|February 15, 2008
Activating NOTCH3 mutation in a patient with small-vessel-disease of the brainCharles Fouillade, Hugues Chabriat, Florence Riant, et al.
Pageof 8

Showing results (31-40 of 74) with videos related to

Sort By:
Pageof 8
Genesis (New York, N.Y. : 2000)|May 19, 2006
Nas transgenic mouse line allows visualization of Notch pathway activity in vivoCéline Souilhol, Sarah Cormier, Marie Monet, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|November 3, 2012
Transcriptome analysis for Notch3 target genes identifies Grip2 as a novel regulator of myogenic response in the cerebrovasculatureCharles Fouillade, Céline Baron-Menguy, Valérie Domenga-Denier, et al.
Acta Neuropathologica Communications|November 23, 2019
Blood brain barrier leakage is not a consistent feature of white matter lesions in CADASILRikesh M Rajani, Julien Ratelade, Valérie Domenga-Denier, et al.
Stroke|December 1, 2004
Impaired vascular mechanotransduction in a transgenic mouse model of CADASIL arteriopathyCaroline Dubroca, Pierre Lacombe, Valérie Domenga, et al.
Genesis (New York, N.Y. : 2000)|November 5, 2003
Characterization of Notch3-deficient mice: normal embryonic development and absence of genetic interactions with a Notch1 mutationLuke T Krebs, Yingzi Xue, Christine R Norton, et al.
Stroke|January 16, 2014
Archetypal Arg169Cys mutation in NOTCH3 does not drive the pathogenesis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy via a loss-of-function mechanismEmmanuel Cognat, Céline Baron-Menguy, Valérie Domenga-Denier, et al.
Archives of Neurology|May 11, 2011
Stroke-related translational researchLouis R Caplan, Juan Arenillas, Steven C Cramer, et al.
Annals of Neurology|January 13, 2006
A novel hereditary small vessel disease of the brainSteve Verreault, Anne Joutel, Florence Riant, et al.
European Journal of Human Genetics : EJHG|October 31, 2002
Spectrum and expression analysis of KRIT1 mutations in 121 consecutive and unrelated patients with Cerebral Cavernous MalformationsFlorence Cavé-Riant, Christian Denier, Pierre Labauge, et al.
Human Mutation|February 15, 2008
Activating NOTCH3 mutation in a patient with small-vessel-disease of the brainCharles Fouillade, Hugues Chabriat, Florence Riant, et al.
Pageof 8