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PLXDC2 gene

Known as: FLJ14623, PLEXIN DOMAIN-CONTAINING PROTEIN 2, tumor endothelial marker 7-related precursor 
National Institutes of Health

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PLXDC1 gene

Papers overview

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2020
2020
Expression Pattern of Plexin Domain Containing 2 in Human Hepatocellular Carcinoma.
Plexin domain containing 2 (PLXDC2) is expressed in endothelial cells of tumor stroma, neural progenitor cells, and pluripotent… 
2018
2018
Improving the quality of a recombinant rabbit monoclonal antibody against PLXDC2 by optimizing transient expression conditions and purification method.
2018
2018
Identification of proteins associated with paclitaxel resistance of epithelial ovarian cancer using iTRAQ-based proteomics
Chemotherapy is an important adjuvant therapy for epithelial ovarian cancer (EOC). The main cause of chemotherapy failure in EOC… 
2017
2017
Genetic Variant Near PLXDC2 Influences the Risk of Primary Open-angle Glaucoma by Increasing Intraocular Pressure in the Japanese Population
Purpose: The purpose of this study is to assess the association between the genetic variants that were previously reported to be… 
2016
2016
Impact of diabetes-related gene polymorphisms on the clinical characteristics of type 2 diabetes Chinese Han population
We investigated the correlation between type 2 diabetes (T2D)-related genes and the clinical characteristics of T2D in the… 
2016
2016
An Integrative Approach Uncovers Biomarkers that Associate with Clinically Relevant Disease Outcomes in Vulvar Carcinoma
Vulvar squamous cell carcinoma (VSCC) is a rare disease that has a high mortality rate (∼40%). However, little is known about its… 
2012
2012
SNP rs1533428 at 2p16.3 as a marker for late-onset primary open-angle glaucoma
Purpose To investigate the associations between gene variants in cholesterol 24S-hydroxylase (CYP46A1), LIM homeobox… 
2011
2011
Plxdc2 Is a Mitogen for Neural Progenitors
The development of different brain regions involves the coordinated control of proliferation and cell fate specification along… 
2010
2010
Genome-Wide SNP Array Analysis in Patients with Features of Sotos Syndrome
Background: Sotos syndrome is characterized by overgrowth, facial dysmorphism and learning impairment. Haploinsufficiency of NSD1… 
2007
2007
Expression of Plxdc2/TEM7R in the developing nervous system of the mouse.
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