Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Marie Monet-Leprêtre"'
Autor:
Charles Fouillade, Anne Joutel, Mieke Dewerchin, Céline Baron-Menguy, Marie Monet-Leprêtre, Sabine Cleophax, Emmanuel Cognat, Valérie Domenga-Denier
Publikováno v:
Stroke. 45:842-849
Background and Purpose— Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy, the most common heritable small vessel disease of the brain, is caused by dominant mutations in the NOTCH3 receptor that stereotypic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27251c96aecfc442189880c8ddd3d4c9
https://doi.org/10.1161/strokeaha.113.003339
https://doi.org/10.1161/strokeaha.113.003339
Publikováno v:
Cardiovascular Research. 95:138-146
The Notch signalling pathway is a highly conserved cell-cell signalling mechanism that plays a central role in the development and maturation of most vertebrate organs. In vertebrates, Notch receptors, several ligands, and components of the downstrea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b648d3e269a8f5d0bed28c85990e4857
https://doi.org/10.1093/cvr/cvs019
https://doi.org/10.1093/cvr/cvs019
Autor:
Claire Dussaule, Meriem Riani, Maï Fouillot-Panchal, Emmanuel Cognat, Joëlle Vinh, Anne Joutel, Iman Haddad, Valérie Domenga-Denier, Marie Monet-Leprêtre, Céline Baron-Menguy
Publikováno v:
Brain-A Journal of Neurology
Brain-A Journal of Neurology, Oxford University Press (OUP), 2013, 136 (Pt 6), pp.1830-45. ⟨10.1093/brain/awt092⟩
Brain-A Journal of Neurology, Oxford University Press (OUP), 2013, 136 (Pt 6), pp.1830-45. ⟨10.1093/brain/awt092⟩
International audience; Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, or CADASIL, one of the most common inherited small vessel diseases of the brain, is characterized by a progressive loss of vascular sm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ca4c72cd8e9355ef5b312ad983039d8
https://pubmed.ncbi.nlm.nih.gov/23649698
https://pubmed.ncbi.nlm.nih.gov/23649698
Autor:
Annette Hammes, Pierre Lacombe, Marie Monet-Leprêtre, Anne Joutel, Valérie Domenga, Andreas Schedl, Claudia Gosele, Sabine Schmidt, Barbara Lemaire-Carrette, Norbert Hubner, Céline Baron-Menguy
Cerebral ischemic small vessel disease (SVD) is the leading cause of vascular dementia and a major contributor to stroke in humans. Dominant mutations in NOTCH3 cause cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencepha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85d6408d09653850a6dbad8317672606
https://europepmc.org/articles/PMC2810078/
https://europepmc.org/articles/PMC2810078/
Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain
Autor:
Valérie Domenga, Barbara Lemaire, Ophélia Godin, Marie Monet-Leprêtre, Hugues Chabriat, Anne Joutel, Michel Cohen-Tannoudji, Elisabeth Tournier-Lasserve, Boris Bardot, Martin Dichgans
Publikováno v:
Brain-A Journal of Neurology
Brain-A Journal of Neurology, 2009, 132 (6), pp.1601-1612. ⟨10.1093/brain/awp049⟩
Brain-A Journal of Neurology, Oxford University Press (OUP), 2009, 132 (6), pp.1601-1612. ⟨10.1093/brain/awp049⟩
Brain-A Journal of Neurology, 2009, 132 (6), pp.1601-1612. ⟨10.1093/brain/awp049⟩
Brain-A Journal of Neurology, Oxford University Press (OUP), 2009, 132 (6), pp.1601-1612. ⟨10.1093/brain/awp049⟩
International audience; Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an autosomal dominant small-vessel disease of the brain caused by mutations in the NOTCH3 receptor. The highly stereotyped
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dacaef39e41c7561d7752f2965cea348
https://hal-pasteur.archives-ouvertes.fr/pasteur-02075498
https://hal-pasteur.archives-ouvertes.fr/pasteur-02075498