Familial exudative vitreoretinopathy and related retinopathies

Antiangiogenic and Antineuroinflammatory Effects of Kallistatin Through Interactions With the Canonical Wnt Pathway

(2013) X. Liu et al.   DIABETES

ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature

(2013) R. W. J. Collin et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Nitrosative Stress Plays an Important Role in Wnt Pathway Activation in Diabetic Retinopathy

(2012) Qiuping Liu et al.   ANTIOXIDANTS & REDOX SIGNALING

Norrin/Frizzled4 Signaling in Retinal Vascular Development and Blood Brain Barrier Plasticity

(2012) Yanshu Wang et al.   CELL

Therapeutic Potential of a Monoclonal Antibody Blocking the Wnt Pathway in Diabetic Retinopathy

(2012) K. Lee et al.   DIABETES

ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous

(2012) Lev Prasov et al.   HUMAN MOLECULAR GENETICS

Clinical Presentation of Familial Exudative Vitreoretinopathy

(2011) Tushar M. Ranchod et al.   OPHTHALMOLOGY

Next-Generation Sequencing of a 40 Mb Linkage Interval Reveals TSPAN12 Mutations in Patients with Familial Exudative Vitreoretinopathy

(2010) Konstantinos Nikopoulos et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy

(2010) James A. Poulter et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Nome's disease: close linkage with genetic markers from the proximal short arm of the X chromosome

(2010) Andreas Gal et al.   CLINICAL GENETICS

Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP

(2010) Konstantinos Nikopoulos et al.   HUMAN MUTATION

Severe retinopathy of prematurity associated withFZD4mutations

(2010) Anna Ells et al.   OPHTHALMIC GENETICS

Three-dimensional structure of human retinal vessels studied by vascular casting

(2009) Toke Bek et al.   ACTA OPHTHALMOLOGICA

CAUSES OF BLINDNESS IN CHILDREN

(2009) GORDON NORRIE   ACTA OPHTHALMOLOGICA

Activation of the Wnt Pathway Plays a Pathogenic Role in Diabetic Retinopathy in Humans and Animal Models

(2009) Ying Chen et al.   AMERICAN JOURNAL OF PATHOLOGY

TSPAN12 Regulates Retinal Vascular Development by Promoting Norrin- but Not Wnt-Induced FZD4/β-Catenin Signaling

(2009) Harald J. Junge et al.   CELL

Norrin, Frizzled-4, and Lrp5 Signaling in Endothelial Cells Controls a Genetic Program for Retinal Vascularization

(2009) Xin Ye et al.   CELL

Müller cell-derived VEGF is a significant contributor to retinal neovascularization

(2009) Yanyan Bai et al.   JOURNAL OF PATHOLOGY

A NovelNDPMutation in an Infant with Unilateral Persistent Fetal Vasculature and Retinal Vasculopathy

(2009) Elisabeth P. Aponte et al.   OPHTHALMIC GENETICS

Phenotypic Overlap of Familial Exudative Vitreoretinopathy (FEVR) with Persistent Fetal Vasculature (PFV) Caused byFZD4Mutations in two Distinct Pedigrees

(2009) Johane M. Robitaille et al.   OPHTHALMIC GENETICS

Familial Exudative Vitreoretinopathy and DiGeorge Syndrome

(2009) David F. Gilmour et al.   OPHTHALMOLOGY

Genetic Contributions to the Development of Retinopathy of Prematurity

(2009) Shakir Mohamed et al.   PEDIATRIC RESEARCH

Prospects for Treatment of Pediatric Vitreoretinal Diseases with Vascular Endothelial Growth Factor Inhibition

(2009) Kristie L. Lin et al.   Seminars in Ophthalmology

Osteoporosis-pseudoglioma syndrome: Description of 9 new cases and beneficial response to bisphosphonates

(2008) Elizabeth A. Streeten et al.   BONE

Lrp5 Controls Bone Formation by Inhibiting Serotonin Synthesis in the Duodenum

(2008) Vijay K. Yadav et al.   CELL

A model for familial exudative vitreoretinopathy caused by LPR5 mutations

(2008) C.-H. Xia et al.   HUMAN MOLECULAR GENETICS

Retinopathy of Prematurity

(2008) Christin L. Sylvester   Seminars in Ophthalmology