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Oncogene, ISSN 0950-9232, 11/2016, Volume 35, Issue 47, pp. 6077 - 6086
Journal Article
EMBO Molecular Medicine, ISSN 1757-4676, 06/2015, Volume 7, Issue 6, pp. 848 - 858
Journal Article
PLoS Genetics, ISSN 1553-7390, 10/2014, Volume 10, Issue 10
  The Notch3 signaling pathway is thought to play a critical role in cancer development, as evidenced by the Notch3 amplification and rearrangement observed in... 
Proteins | Datasets | Cell cycle | Ligands | Smooth muscle | Genomes | Mutation | Gene expression | Experiments | Ovarian cancer
Journal Article
Development (Cambridge), ISSN 0950-1991, 01/2014, Volume 141, Issue 2, pp. 307 - 317
Journal Article
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2013, Volume 8, Issue 9, pp. e75035 - e75035
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 8/2009, Volume 18, Issue 15, pp. 2761 - 2767
Journal Article
BRAIN, ISSN 0006-8950, 06/2013, Volume 136, pp. 1830 - 1845
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, or CADASIL, one of the most common inherited small vessel diseases... 
SUBCORTICAL INFARCTS | LIGAND-BINDING | cerebrovasculature | extracellular matrix proteins | NEUROSCIENCES | CLINICAL NEUROLOGY | SORSBYS FUNDUS DYSTROPHY | CADASIL | MUTANT NOTCH3 | SIGNALING PATHWAY | protein aggregation | SMALL-VESSEL DISEASE | Notch3 | TISSUE INHIBITOR | AUTOSOMAL-DOMINANT ARTERIOPATHY | SMOOTH-MUSCLE-CELLS | METALLOPROTEINASES-3 TIMP3
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 06/2018, Volume 89, Issue 6, pp. A25 - A26
IntroductionCerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary small vessel disease caused by... 
Convulsions & seizures | Nuclear magnetic resonance--NMR | Mutation | Epilepsy | Age | Cognitive ability
Journal Article
Journal of Neurology, ISSN 0340-5354, 6/2018, Volume 265, Issue 6, pp. 1338 - 1342
Journal Article