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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Aug 2016.

Ral GEF with PH domain and SH3 binding motif 2

Top mentioned proteins: Notch2, POLYMERASE, Desmoglein 2, EPDR, Insulin
Papers on RALGPS2
Peripheral blood signature of vasodilator-responsive pulmonary arterial hypertension.
West et al., Nashville, United States. In Circulation, Feb 2015
Thirteen of 25 genes tested in whole blood were significantly different: EPDR1, DSG2, SCD5, P2RY5, MGAT5, RHOQ, UCHL1, ZNF652, RALGPS2, TPD52, MKNL1, RAPGEF2, and PIAS1.
Contribution of common genetic variation to the risk of type 2 diabetes in the Mexican Mestizo population.
TusiƩ-Luna et al., Mexico. In Diabetes, 2012
Twenty-four single nucleotide polymorphisms (SNPs) in or near genes (KCNJ11, PPARG, TCF7L2, SLC30A8, HHEX, CDKN2A/2B, CDKAL1, IGF2BP2, ARHGEF11, JAZF1, CDC123/CAMK1D, FTO, TSPAN8/LGR5, KCNQ1, THADA, ADAMTS9, NOTCH2, NXPH1, RORA, UBQLNL, and RALGPS2) were genotyped in Mexican Mestizos.
Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies.
Hanis et al., Chicago, United States. In Diabetes, 2007
A query of our top approximately 1% of SNPs (P < 0.01) revealed SNPs in or near four genes that showed evidence for association (P < 0.05) in multiple other GWAS interrogated: rs979752 and rs10500641 near UBQLNL and OR52H1 on chromosome 11, rs2773080 and rs3922812 in or near RALGPS2 on chromosome 1, and rs1509957 near EGR2 on chromosome 10.
A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch population.
van Duijn et al., Rotterdam, Netherlands. In Am J Hum Genet, 2007
With use of cognitive function as an endophenotype of AD, our study indicates the that the RGSL2, RALGPS2, and C1orf49 genes are the potential disease-causing genes at 1q25.
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