Etiology of craniofacial malformations in mouse models of blepharophimosis, ptosis and epicanthus inversus syndrome

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