Anne Joutel - Publications

Université Paris 5 
Notch3 signaling, Small vessel disease of the brain, Smooth muscle cell, Transcriptome, Myogenic response,

32 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Ghezali L, Capone C, Baron-Menguy C, Ratelade J, Christensen S, Pedersen LØ, Domenga-Denier V, Pedersen JT, Joutel A. Notch3 immunotherapy improves cerebrovascular responses in CADASIL mice. Annals of Neurology. PMID 30014602 DOI: 10.1002/ana.25284  0.68
2018 Huneau C, Houot M, Joutel A, Béranger B, Giroux C, Benali H, Chabriat H. Altered dynamics of neurovascular coupling in CADASIL. Annals of Clinical and Translational Neurology. 5: 788-802. PMID 30009197 DOI: 10.1002/acn3.574  0.32
2018 Zellner A, Scharrer E, Arzberger T, Oka C, Domenga-Denier V, Joutel A, Lichtenthaler SF, Müller SA, Dichgans M, Haffner C. CADASIL brain vessels show a HTRA1 loss-of-function profile. Acta Neuropathologica. PMID 29725820 DOI: 10.1007/s00401-018-1853-8  0.44
2017 Ratelade J, Mezouar N, Domenga-Denier V, Rochey A, Plaisier E, Joutel A. Severity of arterial defects in the retina correlates with the burden of intracerebral haemorrhage in COL4A1-related stroke. The Journal of Pathology. PMID 29266233 DOI: 10.1002/path.5023  0.44
2017 Joutel A, Chabriat H. Pathogenesis of white matter changes in cerebral small vessel diseases: beyond vessel-intrinsic mechanisms. Clinical Science (London, England : 1979). 131: 635-651. PMID 28351960 DOI: 10.1042/CS20160380  0.32
2016 Baron-Menguy C, Domenga-Denier V, Ghezali L, Faraci FM, Joutel A. Increased Notch3 Activity Mediates Pathological Changes in Structure of Cerebral Arteries. Hypertension (Dallas, Tex. : 1979). PMID 27821617 DOI: 10.1161/HYPERTENSIONAHA.116.08015  0.68
2016 Capone C, Dabertrand F, Baron-Menguy C, Chalaris A, Ghezali L, Domenga-Denier V, Schmidt S, Huneau C, Rose-John S, Nelson MT, Joutel A. Mechanistic insights into a TIMP3-sensitive pathway constitutively engaged in the regulation of cerebral hemodynamics. Elife. 5. PMID 27476853 DOI: 10.7554/eLife.17536  0.68
2015 Capone C, Cognat E, Ghezali L, Baron-Menguy C, Aubin D, Mesnard L, Stöhr H, Domenga-Denier V, Nelson MT, Joutel A. Reducing Timp3 or vitronectin ameliorates disease manifestations in CADASIL mice. Annals of Neurology. PMID 26648042 DOI: 10.1002/ana.24573  0.68
2015 Dabertrand F, Krøigaard C, Bonev AD, Cognat E, Dalsgaard T, Domenga-Denier V, Hill-Eubanks DC, Brayden JE, Joutel A, Nelson MT. Potassium channelopathy-like defect underlies early-stage cerebrovascular dysfunction in a genetic model of small vessel disease. Proceedings of the National Academy of Sciences of the United States of America. 112: E796-805. PMID 25646445 DOI: 10.1073/pnas.1420765112  0.44
2014 Tikka S, Baumann M, Siitonen M, Pasanen P, Pöyhönen M, Myllykangas L, Viitanen M, Fukutake T, Cognat E, Joutel A, Kalimo H. CADASIL and CARASIL. Brain Pathology (Zurich, Switzerland). 24: 525-44. PMID 25323668 DOI: 10.1111/bpa.12181  0.44
2014 Cognat E, Cleophax S, Domenga-Denier V, Joutel A. Early white matter changes in CADASIL: evidence of segmental intramyelinic oedema in a pre-clinical mouse model. Acta Neuropathologica Communications. 2: 49. PMID 24886907 DOI: 10.1186/2051-5960-2-49  0.44
2014 Cognat E, Hervé D, Joutel A. Response to letter regarding article, "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: e129. PMID 24867925 DOI: 10.1161/STROKEAHA.114.005616  0.44
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  0.68
2013 Dichgans M, Joutel A, Chabriat H. Letter by Dichgans et al regarding article, "Peripheral artery disease as a manifestation of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) and practical implications". Circulation. 128: e363. PMID 24146128 DOI: 10.1161/CIRCULATIONAHA.113.003657  0.32
2013 Monet-Leprêtre M, Haddad I, Baron-Menguy C, Fouillot-Panchal M, Riani M, Domenga-Denier V, Dussaule C, Cognat E, Vinh J, Joutel A. Abnormal recruitment of extracellular matrix proteins by excess Notch3 ECD: a new pathomechanism in CADASIL. Brain : a Journal of Neurology. 136: 1830-45. PMID 23649698 DOI: 10.1093/brain/awt092  0.68
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  0.68
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  0.68
2011 Caplan LR, Arenillas J, Cramer SC, Joutel A, Lo EH, Meschia J, Savitz S, Tournier-Lasserve E. Stroke-related translational research. Archives of Neurology. 68: 1110-23. PMID 21555605 DOI: 10.1001/archneurol.2011.99  0.32
2010 Joutel A, Monet-Leprêtre M, Gosele C, Baron-Menguy C, Hammes A, Schmidt S, Lemaire-Carrette B, Domenga V, Schedl A, Lacombe P, Hubner N. Cerebrovascular dysfunction and microcirculation rarefaction precede white matter lesions in a mouse genetic model of cerebral ischemic small vessel disease. The Journal of Clinical Investigation. 120: 433-45. PMID 20071773 DOI: 10.1172/JCI39733  0.68
2009 Chabriat H, Joutel A, Dichgans M, Tournier-Lasserve E, Bousser MG. Cadasil. The Lancet. Neurology. 8: 643-53. PMID 19539236 DOI: 10.1016/S1474-4422(09)70127-9  0.32
2009 Monet-Leprêtre M, Bardot B, Lemaire B, Domenga V, Godin O, Dichgans M, Tournier-Lasserve E, Cohen-Tannoudji M, Chabriat H, Joutel A. Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain. Brain : a Journal of Neurology. 132: 1601-12. PMID 19293235 DOI: 10.1093/brain/awp049  0.68
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  0.68
2007 Monet M, Domenga V, Lemaire B, Souilhol C, Langa F, Babinet C, Gridley T, Tournier-Lasserve E, Cohen-Tannoudji M, Joutel A. The archetypal R90C CADASIL-NOTCH3 mutation retains NOTCH3 function in vivo. Human Molecular Genetics. 16: 982-92. PMID 17331978 DOI: 10.1093/hmg/ddm042  0.32
2006 Verreault S, Joutel A, Riant F, Neves G, Rui Silva M, Maciazek J, Tournier-Lasserve E, Bousser MG, Chabriat H. A novel hereditary small vessel disease of the brain. Annals of Neurology. 59: 353-7. PMID 16404745 DOI: 10.1002/ana.20775  0.32
2005 Lacombe P, Oligo C, Domenga V, Tournier-Lasserve E, Joutel A. Impaired cerebral vasoreactivity in a transgenic mouse model of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy arteriopathy. Stroke. 36: 1053-8. PMID 15817893 DOI: 10.1161/01.STR.0000163080.82766.eb  0.32
2005 Dubroca C, Lacombe P, Domenga V, Maciazek J, Levy B, Tournier-Lasserve E, Joutel A, Henrion D. Impaired vascular mechanotransduction in a transgenic mouse model of CADASIL arteriopathy. Stroke. 36: 113-7. PMID 15569862 DOI: 10.1161/01.STR.0000149949.92854.45  0.32
2004 Domenga V, Fardoux P, Lacombe P, Monet M, Maciazek J, Krebs LT, Klonjkowski B, Berrou E, Mericskay M, Li Z, Tournier-Lasserve E, Gridley T, Joutel A. Notch3 is required for arterial identity and maturation of vascular smooth muscle cells. Genes & Development. 18: 2730-5. PMID 15545631 DOI: 10.1101/gad.308904  0.32
2004 Vahedi K, Chabriat H, Levy C, Joutel A, Tournier-Lasserve E, Bousser MG. Migraine with aura and brain magnetic resonance imaging abnormalities in patients with CADASIL. Archives of Neurology. 61: 1237-40. PMID 15313840 DOI: 10.1001/archneur.61.8.1237  0.32
2004 Denier C, Labauge P, Brunereau L, Cavé-Riant F, Marchelli F, Arnoult M, Cecillon M, Maciazek J, Joutel A, Tournier-Lasserve E. Clinical features of cerebral cavernous malformations patients with KRIT1 mutations. Annals of Neurology. 55: 213-20. PMID 14755725 DOI: 10.1002/ana.10804  0.32
2004 Joutel A, Monet M, Domenga V, Riant F, Tournier-Lasserve E. Pathogenic mutations associated with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy differently affect Jagged1 binding and Notch3 activity via the RBP/JK signaling Pathway. American Journal of Human Genetics. 74: 338-47. PMID 14714274 DOI: 10.1086/381506  0.32
2003 Ruchoux MM, Domenga V, Brulin P, Maciazek J, Limol S, Tournier-Lasserve E, Joutel A. Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. The American Journal of Pathology. 162: 329-42. PMID 12507916 DOI: 10.1016/S0002-9440(10)63824-2  0.32
2002 Cavé-Riant F, Denier C, Labauge P, Cécillon M, Maciazek J, Joutel A, Laberg-le Couteulx S, Tournier-Lasserve E, Barbieux-Vaquez D, Canaple S, Le Gars D, de Bray JM, Fournier H, Guy G, Penisson-Besnier I, et al. Spectrum and expression analysis of KRIT1 mutations in 121 consecutive and unrelated patients with Cerebral Cavernous Malformations European Journal of Human Genetics. 10: 733-740. PMID 12404106 DOI: 10.1038/sj.ejhg.5200870  0.32
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