Etiology of craniofacial malformations in mouse models of blepharophimosis, ptosis and epicanthus inversus syndrome
出版年份 2014 全文链接
标题
Etiology of craniofacial malformations in mouse models of blepharophimosis, ptosis and epicanthus inversus syndrome
作者
关键词
-
出版物
HUMAN MOLECULAR GENETICS
Volume 24, Issue 6, Pages 1670-1681
出版商
Oxford University Press (OUP)
发表日期
2014-11-22
DOI
10.1093/hmg/ddu579
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- A piggyBac insertion disrupts Foxl2 expression that mimics BPES syndrome in mice
- (2014) Fubiao Shi et al. HUMAN MOLECULAR GENETICS
- The mesenchymal architecture of the cranial mesoderm of mouse embryos is disrupted by the loss of Twist1 function
- (2012) Heidi Bildsoe et al. DEVELOPMENTAL BIOLOGY
- Timetable for Upper Eyelid Development in Staged Human Embryos and Fetuses
- (2011) Tae Ho Byun et al. Anatomical Record-Advances in Integrative Anatomy and Evolutionary Biology
- Insights Into Levator Muscle Dysfunction in a Cohort of Patients With Molecularly Confirmed Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Using High-Resolution Imaging, Anatomic Examination, and Histopathologic Examination
- (2011) Christian E. Decock ARCHIVES OF OPHTHALMOLOGY
- Loss of MAP3K1 enhances proliferation and apoptosis during retinal development
- (2011) M. Mongan et al. DEVELOPMENT
- Notch gain of function in mouse periocular mesenchyme downregulates FoxL2 and impairs eyelid levator muscle formation, leading to congenital blepharophimosis
- (2011) Y. Zhang et al. JOURNAL OF CELL SCIENCE
- Jaw muscularization requires Dlx expression by cranial neural crest cells
- (2010) E. Heude et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Somatic Sex Reprogramming of Adult Ovaries to Testes by FOXL2 Ablation
- (2009) N. Henriette Uhlenhaut et al. CELL
- Congenital Alacrima in a Patient with Blepharophimosis Syndrome
- (2009) Geetha K. Athappilly et al. OPHTHALMIC GENETICS
- Disease-Causing 7.4 kb Cis-Regulatory Deletion Disrupting Conserved Non-Coding Sequences and Their Interaction with the FOXL2 Promotor: Implications for Mutation Screening
- (2009) Barbara D'haene et al. PLoS Genetics
- Dlx genes pattern mammalian jaw primordium by regulating both lower jaw-specific and upper jaw-specific genetic programs
- (2008) J. Jeong et al. DEVELOPMENT
- Development and tissue origins of the mammalian cranial base
- (2008) B. McBratney-Owen et al. DEVELOPMENTAL BIOLOGY
- FOXL2mutations and genomic rearrangements in BPES
- (2008) Diane Beysen et al. HUMAN MUTATION
- Cell lineage in mammalian craniofacial mesenchyme
- (2008) Toshiyuki Yoshida et al. MECHANISMS OF DEVELOPMENT
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now