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Genes and Development, ISSN 0890-9369, 11/2004, Volume 18, Issue 22, pp. 2730 - 2735
Journal Article
Human mutation, ISSN 1059-7794, 2005, Volume 26, Issue 3, pp. 281 - 281
Familial hemiplegic migraine (FHM) is an autosomal dominant form of migraine with aura. The disease is caused by mutations of at least three genes among which... 
Amino Acid Sequence | Sodium-Potassium-Exchanging ATPase - genetics | Exons | Humans | Molecular Sequence Data | Family Health | Male | Mutation, Missense | Polymorphism, Genetic | Sequence Homology, Amino Acid | Animals | Pedigree | Female | Migraine with Aura - genetics | Mutation
Journal Article
Journal Article
Journal Article
by Cavé-Riant, Florence and Denier, Christian and Labauge, Pierre and Cécillon, Michaelle and Maciazek, Jacqueline and Joutel, Anne and Laberg-le Couteulx, Sophie and Tournier-Lasserve, Elisabeth and Barbieux-Vaquez, D and Canaple, S and Le Gars, D and de Bray, J.-M and Fournier, H and Guy, G and Penisson-Besnier, I and Bergouignan, F.-X and Bizette, C and Czorny, A and Godard, J and Jacquet, G and Comoy, J and David, P and Parker, D and Said, G and Castel, J.-P and Guerin, J and Loiseau, H and Houtteville, J.-P and Khoury, S and Viader, F and Attané, F and Tannier, C and Carriere, N and Chazal, J and Clavelou, P and Nivelon, A and Benabid, A.-L and Perret, J and Latinville, D and Christiaens, J.-C and Combelles, G and Lejeune, J.-P and Louis, E and Pasquier, F and Fischer, G and Froment, J.-C and Guyotat, J and Mortelese, A and Sindou, M and Robert, H and Sauvage, P and Savet, J.-F and Gomez Attarian, A and Lena, G and Ricahrd, P and Coubes Cesari, P and Frerebeau Idee, P and Carriere, A and Hepner, H and Lescure, P and Vespignani, H and Weber, M and Martin, S and Resche Mussini, F and Borg, M and Grellier, P and Lonjon Thomas, M and Rougemont Arthuis, D and Clavier, I and Masson, M and Redondo, A and Rey, A and Cophignon, A and Georges, B and Hagueneau, M and Sarrazin, M and Silhouette, B and Chodkiewicz, J.P and Devaux, B and Nataf, F and Roux, F.-X and Agid, Y and Baulac, M and Capelle, L and Clemenceau, S and Dubois, B and Faillot, T and Fohano, D and Philippon, J and Gil, R and Lapierre, F and Neau, J.-P and Rousseaux, P and Carsin, B and Dufour, T and Guegan, Y and Scarabin, J.-M and Freger, P and Brunon, J and Garnier, M and Societe Francaise Neurochirurgie and the Société Française de Neurochirurgie
European Journal of Human Genetics, ISSN 1018-4813, 11/2002, Volume 10, Issue 11, pp. 733 - 740
Journal Article
Stroke, ISSN 0039-2499, 01/2005, Volume 36, Issue 1, pp. 113 - 117
Background and Purpose - CADASIL is an inherited small-vessel disease responsible for lacunar strokes and cognitive impairment. The disease is caused by highly... 
Lacunar infarction | Mice, transgenic | CADASIL | Cognitive disorders | SUBCORTICAL INFARCTS | SIGNALING PATHWAYS | lacunar infarction | MYOGENIC RESPONSE | MICE LACKING | CLINICAL NEUROLOGY | LEUKOENCEPHALOPATHY | SMOOTH-MUSCLE | mice, transgenic | POSITRON-EMISSION-TOMOGRAPHY | CEREBRAL HEMODYNAMICS | PERIPHERAL VASCULAR DISEASE | AUTOSOMAL-DOMINANT ARTERIOPATHY | NOTCH3 MUTATIONS | cognitive disorders | Vasoconstrictor Agents - pharmacology | Vasoconstriction | Stress, Mechanical | CADASIL - physiopathology | Male | Mice, Transgenic | Proto-Oncogene Proteins - genetics | Arteries - drug effects | Pressure | Vasodilation | Mechanotransduction, Cellular | Receptors, Notch | Animals | Phenylephrine - pharmacology | Arteries - physiopathology | Receptor, Notch3 | Mice | CADASIL - etiology | Mutation | In Vitro Techniques | Receptor, Notch4 | Disease Models, Animal | Receptors, Cell Surface - genetics | Phenylephrine/pharmacology | Proto-Oncogene Proteins/genetics | Life Sciences | Rec | Human health and pathology | Arteries/drug effects/physiopathology | CADASIL/etiology/physiopathology | Cardiology and cardiovascular system | Disease Models | Transgenic | Arteries | Receptors | genetics | Cell Surface | Phenylephrine | pharmacology | Proto-Oncogene Proteins | Notch | drug effects | Stress | etiology | physiopathology | Cellular | Vasoconstrictor Agents | Animal | Mechanical | Mechanotransduction
Journal Article
Journal Article
Journal Article
Human Mutation, ISSN 1059-7794, 12/2000, Volume 16, Issue 6, pp. 518 - 526
Notch3 mutations cause CADASIL, an increasingly recognized cause of subcortical ischemic stroke and vascular dementia in human adults. In the absence of any... 
CADASIL | DHPLC | stroke, subcortical ischemic | Notch3 | cysteine | dementia, vascular | G‐C content | Cysteine | Dementia, vascular | Stroke, subcortical ischemic | G-C content
Journal Article
Stroke, ISSN 0039-2499, 01/2005, Volume 36, Issue 1, pp. 113 - 117
BACKGROUND: and Purpose-CADASIL is an inherited small-vessel disease responsible for lacunar strokes and cognitive impairment. The disease is caused by highly... 
Journal Article
Journal Article
Genes & Development, ISSN 0890-9369, 11/2004, Volume 18, Issue 22, pp. 2730 - 2735
Formation of a fully functional artery proceeds through a multistep process. Here we show that Notch3 is required to generate functional arteries in mice by... 
Journal Article