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WDR36 gene

Known as: T-CELL ACTIVATION WD REPEAT-CONTAINING PROTEIN, TAWDRP, WD REPEAT-CONTAINING PROTEIN 36 
National Institutes of Health

Related topics

Related topics

1 relation
WD40 Repeats

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
An Application of NGS for WDR36 Gene in Taiwanese Patients with Juvenile-Onset Open-Angle Glaucoma
Primary open-angle glaucoma (POAG) is one of the most important disease in ophthalmology with high prevalence and risk of… 
2016
2016
Two Variants of WDR36 Genes in Primary Open Angle Glaucoma
Background: Glaucoma is the second leading cause of blindness affecting 67 million people worldwide. Primary open angle glaucoma… 
2011
2011
WDR36 acts as a scaffold protein tethering a G-protein-coupled receptor, Gαq and phospholipase Cβ in a signalling complex
We identified the WD-repeat-containing protein, WDR36, as an interacting partner of the β isoform of thromboxane A2 receptor (TP… 
2010
2010
Identification of early transcripts related to male development in chicken embryos.
2010
2010
Variable Clinical Spectrum of the Myocilin Gln368X Mutation in a Dutch Family with Primary Open Angle Glaucoma
Purpose: To describe the clinical phenotype in a family with primary open angle glaucoma harboring a p.Gln368X mutation in MYOC… 
Highly Cited
2009
Highly Cited
2009
Correction of the disease phenotype of myocilin-causing glaucoma by a natural osmolyte.
PURPOSE To characterize a novel Asp384Asn (D384N) mutant myocilin (MYOC) that causes juvenile-onset open-angle glaucoma (JOAG… 
2009
2009
Different WDR36 mutation pattern in Chinese patients with primary open-angle glaucoma
Purpose To determine the distribution of WD repeat domain 36 (WDR36) sequence variants in Chinese patients with primary open… 
2009
2009
Genetic variants of CYP1B1 and WDR36 in the patients with primary congenital glaucoma and primary open angle glaucoma from saint-Petersburg
In 32 unrelated patients with primary congenital glaucoma (PCG), a search for mutations in the myocilin (MYOC), cytochrome P450B1… 
2006
2006
A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5 q
Glaucoma is a leading cause of vision impairment and blindness in both developed and developing countries. Primary open angle… 
2006
2006
Heterozygous CYP 1 B 1 gene mutations in Spanish patients with primary open-angle glaucoma
Glaucoma is a complex and genetically heterogeneous disease characterized by the progressive apoptotic death of retinal ganglion… 
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