Axenfeld-Rieger syndrome

FOXC1: an emerging marker and therapeutic target for cancer

(2017) B Han et al.   ONCOGENE

Long-term Safety and Efficacy of Latanoprostene Bunod 0.024% in Japanese Subjects with Open-Angle Glaucoma or Ocular Hypertension: The JUPITER Study

(2016) Kazuhide Kawase et al.   ADVANCES IN THERAPY

Comparison of Bioinformatics Prediction, Molecular Modeling, and Functional Analyses ofFOXC1Mutations in Patients with Axenfeld-Rieger Syndrome

(2016) Morteza Seifi et al.   HUMAN MUTATION

Disruptions in a cluster of computationally identified enhancers near FOXC1 and GMDS may influence brain development

(2015) Genevieve D. E. Haliburton et al.   NEUROGENETICS

Whole exome sequencing identifies a heterozygous missense variant in the PRDM5 gene in a family with Axenfeld–Rieger syndrome

(2015) Shazia Micheal et al.   NEUROGENETICS

Novel PITX2c loss-of-function mutations associated with complex congenital heart disease

(2014) DONG WEI et al.   INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE

Prevalence and Spectrum of PITX2c Mutations Associated with Congenital Heart Disease

(2013) Juan Wang et al.   DNA AND CELL BIOLOGY

Cardiac anomalies in Axenfeld-Rieger syndrome due to a novelFOXC1mutation

(2012) Karen W. Gripp et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Overexpression of forkhead box C1 promotes tumor metastasis and indicates poor prognosis in hepatocellular carcinoma

(2012) Limin Xia et al.   HEPATOLOGY

High expression of FOXC1 is associated with poor clinical outcome in non-small cell lung cancer patients

(2012) Long-Xiao Wei et al.   TUMOR BIOLOGY

Axenfeld-Rieger anomaly and Axenfeld-Rieger syndrome: Clinical, molecular-cytogenetic, and DNA array analyses of three patients with chromosomal defects at 6p25

(2011) Hidefumi Tonoki et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Whatʼs new in laser treatment for glaucoma?

(2011) Jay J. Meyer et al.   CURRENT OPINION IN OPHTHALMOLOGY

A complex regulatory network of transcription factors critical for ocular development and disease

(2011) Moulinath Acharya et al.   HUMAN MOLECULAR GENETICS

Forkhead transcription factors: key players in health and disease

(2011) Bérénice A. Benayoun et al.   TRENDS IN GENETICS

FOXC1 Is a Potential Prognostic Biomarker with Functional Significance in Basal-like Breast Cancer

(2010) P. S. Ray et al.   CANCER RESEARCH

Congenital heart defects in two siblings in an Axenfeld–Rieger syndrome family

(2010) Mehmet Necdet Akkus et al.   CLINICAL DYSMORPHOLOGY

Axenfeld–Rieger syndrome and spectrum of PITX2 and FOXC1 mutations

(2009) Zeynep Tümer et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Subtelomeric 6p deletion: Clinical and array-CGH characterization in two patients

(2008) Danielle Martinet et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A