Evaluating neural crest cell migration in a Col4a1 mutant mouse model of ocular anterior segment dysgenesis-Reference-Cited by-同舟云学术

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Evaluating neural crest cell migration in a Col4a1 mutant mouse model of ocular anterior segment dysgenesis

Published:2024-09 Issue: Volume:179 Page:203926
ISSN:2667-2901
Container-title:Cells & Development
language:en
Short-container-title:Cells & Development

Author:

Cozzitorto Corinna,Peltz Zoe,Flores Lourdes M.,Della Santina Luca,Mao Mao,Gould Douglas B.

Funder

National Eye Institute

Knights Templar Eye Foundation

University of California, San Francisco

National Institutes of Health

Research to Prevent Blindness

Publisher

Elsevier BV

Reference69 articles.

1. Roles of ephrinB ligands and EphB receptors in cardiovascular development: demarcation of arterial/venous domains, vascular morphogenesis, and sprouting angiogenesis;Adams;Genes Dev.,1999

2. Col4a1 mutations cause progressive retinal neovascular defects and retinopathy;Alavi;Sci. Rep.,2016

3. Epilepsy and related challenges in children with COL4A1 and COL4A2 mutations: a Gould syndrome patient registry;Boyce;Epilepsy Behav.,2021

4. Elevated TGFβ signaling contributes to cerebral small vessel disease in mouse models of Gould syndrome;Branyan;Matrix Biol.,2022

5. Somite as a morphological reference for staging and axial levels of developing structures in mouse embryos, Neuroembryology;Chan;Aging,2004

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