Hypo- and Hypermorphic FOXC1 Mutations in Dominant Glaucoma: Transactivation and Phenotypic Variability

Newborn primary congenital glaucoma: Histopathologic features of the anterior chamber filtration angle

(2012) Lynn P. Perry et al.   JOURNAL OF AAPOS

Null CYP1B1 Genotypes in Primary Congenital and Nondominant Juvenile Glaucoma

(2012) María-Pilar López-Garrido et al.   OPHTHALMOLOGY

Variants in ASB10 are associated with open-angle glaucoma

(2011) F. Pasutto et al.   HUMAN MOLECULAR GENETICS

Reversible Ponceau staining as a loading control alternative to actin in Western blots

(2010) Isabel Romero-Calvo et al.   ANALYTICAL BIOCHEMISTRY

Null Mutations in LTBP2 Cause Primary Congenital Glaucoma

(2009) Manir Ali et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A novel mutation in the FOXC1 gene in a family with Axenfeld-Rieger syndrome and Peters’ anomaly

(2009) N Weisschuh et al.   CLINICAL GENETICS

Forkhead transcription factors regulate expression of the chemokine receptor CXCR4 in endothelial cells and CXCL12-induced cell migration

(2008) Hisaki Hayashi et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS