May 05, 2009 article CADASIL mutations enhance spontaneous multimerization of NOTCH3 Human Molecular Genetics DOI: 10.1093/hmg/ddp211 OpenAlex Authors 0 Author list not loaded yet. Cited by 5 stored of 89 Search Sort Most cited Newest Oldest Patent citations Title Any typearticle review book-chapter conference-paper preprint dissertation book dataset other Any fieldAgricultural and Biological Sciences Arts and Humanities Biochemistry, Genetics and Molecular Biology Business, Management and Accounting Chemical Engineering Chemistry Computer Science Decision Sciences Dentistry Earth and Planetary Sciences Economics, Econometrics and Finance Energy Engineering Environmental Science Health Professions Immunology and Microbiology Materials Science Mathematics Medicine Neuroscience Nursing Pharmacology, Toxicology and Pharmaceutics Physics and Astronomy Psychology Social Sciences Veterinary Open access NOTCH3 CADASIL Variant Receptor Aggregation Requires NOTCH3 Wild‐Type Receptors: Identification of Highly Selective Inhibitors That Block the Process 2026 The FASEB Journal article Medicine Cerebrovascular and genetic disorders Open access 1 citations Active immunotherapy reduces NOTCH3 deposition in brain capillaries in a CADASIL mouse model 2022 EMBO Molecular Medicine article Medicine Cerebrovascular and genetic disorders Open access 29 citations NOTCH3 active immunotherapy reduces NOTCH3 deposition in brain capillaries in a CADASIL mouse model 2022 bioRxiv (Cold Spring Harbor Laboratory) preprint Medicine Cerebrovascular and genetic disorders Open access 0 citations Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Family Members With a Pathogenic NOTCH3 Variant Can Have a Normal Brain Magnetic Resonance Imaging and Skin Biopsy Beyond Age 50 Years 2022 Stroke article Medicine Cerebrovascular and genetic disorders Open access 23 citations NO TCH3 variant position is associated with NOTCH3 aggregation load in CADASIL vasculature 2021 Neuropathology and Applied Neurobiology article Medicine Cerebrovascular and genetic disorders Open access 43 citations 5 results References 0