CADASIL-associated Notch3 mutations have differential effects both on ligand binding and ligand-induced Notch3 receptor signaling through RBP-Jk
Author:
Publisher
Elsevier BV
Subject
Cell Biology
Reference43 articles.
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1. Protein aggregates containing wild-type and mutant NOTCH3 are major drivers of arterial pathology in CADASIL;Journal of Clinical Investigation;2024-02-22
2. Progress to Clarify How NOTCH3 Mutations Lead to CADASIL, a Hereditary Cerebral Small Vessel Disease;Biomolecules;2024-01-18
3. CADASIL: A NOTCH3-associated cerebral small vessel disease;Journal of Advanced Research;2024-01
4. Case report: CADASIL with cysteine-sparing P572L mutation on exon 11 presenting as focal onset epilepsy;2023-11-25
5. Update on the Epidemiology, Pathogenesis, and Biomarkers of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy;Journal of Clinical Neurology;2023
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