Correction of a CADASIL point mutation using adenine base editors in hiPSCs and blood vessel organoids
Author:
Publisher
Elsevier BV
Subject
Genetics,Molecular Biology
Reference45 articles.
1. Search-and-replace genome editing without double-strand breaks or donor DNA;Anzalone;Nature,2019
2. Basic biology of adeno-associated virus (AAV) vectors used in gene therapy;Balakrishnan;Curr. Gene Ther.,2014
3. Clinical features and mutation spectrum in Chinese patients with CADASIL: a multicenter retrospective study;Chen;CNS Neurosci. Ther.,2017
4. Development of highly efficient dual-AAV split adenosine base editor for in vivo gene therapy;Chen;Small Methods,2020
5. Immunolocalization of platelet-derived growth factor receptor- (PDGFR-) and pericytes in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL);Craggs;Neuropath. Appl. Neuro.,2015
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