MSX2Gene Duplication in a Patient with Eye Development Defects-Reference-Cited by-同舟云学术

MSX2Gene Duplication in a Patient with Eye Development Defects

Published:2014-03-25 Issue:4 Volume:36 Page:353-358
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Plaisancié Julie,Collet Corinne,Pelletier Valerie,Perdomo Yaumara,Studer Fouzia,Fradin Mélanie,Schaefer Elise,Speeg-Schatz Claude,Bloch-Zupan Agnès,Flori Elisabeth,Dollfus Hélène

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

http://www.tandfonline.com/doi/pdf/10.3109/13816810.2014.886270

Reference37 articles.

1. Premature suture closure and ectopic cranial bone in mice expressing Msx2 transgenes in the developing skull.

2. Perinatal Lethality and Multiple Craniofacial Malformations in MSX2 Transgenic Mice

3. Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation

4. Msx homeobox gene family and craniofacial development

5. Transcriptional Regulatory Cascades in Runx2-Dependent Bone Development

Cited by 6 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. Amelogenesis imperfecta: Next-generation sequencing sheds light on Witkop’s classification;Frontiers in Physiology;2023-05-09

2. Genetics of syndromic ocular coloboma: CHARGE and COACH syndromes;Experimental Eye Research;2020-04

3. Inherited Eye Diseases with Retinal Manifestations through the Eyes of Homeobox Genes;International Journal of Molecular Sciences;2020-02-26

4. Experimental periodontitis in Msx2 mutant mice induces alveolar bone necrosis;Journal of Periodontology;2019-10-15

5. Genes and pathways in optic fissure closure;Seminars in Cell & Developmental Biology;2019-07