Human chromosome 19p13.1-13.2 contains potential tumor suppressor gene(s) for prostate cancer  Gao AC, Lou W, Ichikawa T, Denmeade SR, Barrett JC, Isaacs JT.

CADASIL caused by mutations in the Notch3 gene with most clustering in exons 3 and 4  Wang T, Sharma SD, Fox N, Rossor M, Brown MJ, Sharma P.

CADASIL. Clinical aspects, neuroradiology, genetics and diagnosis  Mellies JK, Calabrese P, Roth H, Gehlen W.

Differential diagnosis of a vascular leukoencephalopathy within a CADASIL family  Furby A, Vahedi K, Force M, Larrouy S, Ruchoux MM, Joutel A, Tournier-Lasserve E.

Notch3 mutations in CADASIL a mendelian condition causing stroke and vascular dementia  Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, Alamowitch S, Domenga V, Cecillion M, Marechal E, Maciazek J, Vayssiere C, Cruaud C, Cabanis EA, Ruchoux MM, Weissenbach J, Bach JF, Bousser MG, Tournier-Lasserve E.

Expression patterns of Notch1, Notch2, and Notch3 suggest multiple functional roles for the Notch-DSL signaling system during brain development  Irvin DK, Zurcher SD, Nguyen T, Weinmaster G, Kornblum HI.

Analysis of HeyL expression in wild-type and Notch pathway mutant mouse embryos  Leimeister C, Schumacher N, Steidl C, Gessler M.

The phenotypes of pre-malignant thymocytes and of lymphomas indicate a novel and particular role for Notch3 in co-ordinating growth and differentiation of thymocytes  Bellavia D, Campese AF, Alesse E, Vacca A, Felli MP, Balestri A, Stoppacciaro A, Tiveron C, Tatangelo L, Giovarelli M, Gaetano C, Ruco L, Hoffman ES, Hayday AC, Lendahl U, Frati L, Gulino A, Screpanti I.

3D models predict misfolding of Notch3 EGF-like repeat domains in CADASIL  Dichgans M, Ludwig H, Muller-Hocker J, Messerschmidt A, Gasser T.

Interactions between fibroblast growth factors and Notch regulate neuronal differentiation  Faux CH, Turnley AM, Epa R, Cappai R, Bartlett PF.

Notch signalling controls pancreatic cell differentiation  Apelqvist A, Li H, Sommer L, Beatus P, Anderson DJ, Honjo T, Hrabe de Angelis M, Lendahl U, Edlund H.

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke anNotch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementiad dementia  Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, Alamowitch S, Domenga V, Cecillion M, Marechal E, Maciazek J, Vayssiere C, Cruaud C, Cabanis EA, Ruchoux MM, Weissenbach J, Bach JF, Bousser MG, Tournier-Lasserve E.