Zebrafish mab21l2 mutants possess severe defects in optic cup morphogenesis, lens and cornea development-Reference-Cited by-同舟云学术

Zebrafish mab21l2 mutants possess severe defects in optic cup morphogenesis, lens and cornea development

Published:2019-05-21 Issue:7 Volume:248 Page:514-529
ISSN:1058-8388
Container-title:Developmental Dynamics
language:en
Short-container-title:Developmental Dynamics

Author:

Gath Natalie¹²^ORCID,Gross Jeffrey M.¹²^ORCID

Affiliation:

1. Department of Molecular BiosciencesInstitute for Cellular and Molecular Biology, The University of Texas at Austin Austin Texas

2. Departments of Ophthalmology and Developmental Biology, Louis J. Fox Center for Vision RestorationThe University of Pittsburgh School of Medicine Pittsburgh Pennsylvania

Funder

Eye and Ear Foundation of Pittsburgh

National Eye Institute

Research to Prevent Blindness

Publisher

Wiley

Subject

Developmental Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/dvdy.44

Reference67 articles.

1. Two Murine and Human Homologs of Mab-21, a Cell Fate Determination Gene Involved in Caenorhabditis Elegans Neural Development

2. Requirement for Mab21l2 during development of murine retina and ventral body wall

3. Monoallelic and Biallelic Mutations in MAB21L2 Cause a Spectrum of Major Eye Malformations

4. Mutations in MAB21L2 Result in Ocular Coloboma, Microcornea and Cataracts

5. Temporal Requirement ofMab21l2During Eye Development in Chick Reveals Stage-Dependent Functions for Retinogenesis

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