Genetic disruption of zebrafish mab21l1 reveals a conserved role in eye development and affected pathways-Reference-Cited by-同舟云学术

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Genetic disruption of zebrafish mab21l1 reveals a conserved role in eye development and affected pathways

Published:2021-03-12 Issue:8 Volume:250 Page:1056-1073
ISSN:1058-8388
Container-title:Developmental Dynamics
language:en
Short-container-title:Developmental Dynamics

Author:

Seese Sarah E.¹²,Deml Brett¹²³,Muheisen Sanaa¹,Sorokina Elena¹,Semina Elena V.¹²⁴⁵^ORCID

Affiliation:

1. Department of Pediatrics The Medical College of Wisconsin Milwaukee Wisconsin USA

2. Cell Biology, Neurobiology and Anatomy The Medical College of Wisconsin Milwaukee Wisconsin USA

3. PreventionGenetics Marshfield Wisconsin USA

4. Department of Ophthalmology and Visual Sciences Medical College of Wisconsin, Children's of Wisconsin Milwaukee Wisconsin USA

5. Children's Research Institute Medical College of Wisconsin, Children's of Wisconsin Milwaukee Wisconsin USA

Funder

National Eye Institute

Publisher

Wiley

Subject

Developmental Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/dvdy.312

Reference91 articles.

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

2. A Novel Oculo-Skeletal syndrome with intellectual disability caused by a particular MAB21L2 mutation

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

4. Autosomal recessive truncatingMAB21L1mutation associated with a syndromic scrotal agenesis

5. MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome)

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Congenital anterior segment ocular disorders: Genotype-phenotype correlations and emerging novel mechanisms;Progress in Retinal and Eye Research;2024-09

2. Monoallelic missense variants in MAB21L1 cause a novel autosomal dominant microphthalmia;Ophthalmic Genetics;2024-07-17

3. External genitalia phenotypes of a Mab21l1‐null mouse model for cerebellar, ocular, craniofacial, and genital (COFG) syndrome;The Anatomical Record;2023-09-26

4. Single cell transcriptome analyses of the developing zebrafish eye— perspectives and applications;Frontiers in Cell and Developmental Biology;2023-06-29

5. Missense Mutations in MAB21L1: Causation of Novel Autosomal Dominant Ocular BAMD Syndrome;Investigative Opthalmology & Visual Science;2023-03-09

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