Charles Fouillade - Publications
Affiliations: | Université Paris 5 |
Area:
Notch3 signaling, Small vessel disease of the brain, Smooth muscle cell, Transcriptome, Myogenic responseYear | Citation | Score | |||
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2014 | Cognat E, Baron-Menguy C, Domenga-Denier V, Cleophax S, Fouillade C, Monet-Leprêtre M, Dewerchin M, Joutel A. 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 mechanism. Stroke. 45: 842-9. PMID 24425116 DOI: 10.1161/Strokeaha.113.003339 | 0.546 | |||
2013 | Fouillade C, Baron-Menguy C, Domenga-Denier V, Thibault C, Takamiya K, Huganir R, Joutel A. Transcriptome analysis for Notch3 target genes identifies Grip2 as a novel regulator of myogenic response in the cerebrovasculature. Arteriosclerosis, Thrombosis, and Vascular Biology. 33: 76-86. PMID 23117660 DOI: 10.1161/Atvbaha.112.251736 | 0.532 | |||
2012 | Fouillade C, Monet-Leprêtre M, Baron-Menguy C, Joutel A. Notch signalling in smooth muscle cells during development and disease. Cardiovascular Research. 95: 138-46. PMID 22266753 DOI: 10.1093/Cvr/Cvs019 | 0.532 | |||
2009 | Fouillade C, Monet Lepretre M, Carrette B, Domenga V, Joutel A. J022 Effecteurs du récepteur Notch3 dans la cellule musculaire lisse des petites artères Archives of Cardiovascular Diseases. 102: S110. DOI: 10.1016/S1875-2136(09)72397-6 | 0.425 | |||
2008 | Fouillade C, Chabriat H, Riant F, Mine M, Arnoud M, Magy L, Bousser MG, Tournier-Lasserve E, Joutel A. Activating NOTCH3 mutation in a patient with small-vessel-disease of the brain. Human Mutation. 29: 452. PMID 18273901 DOI: 10.1002/Humu.9527 | 0.55 | |||
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