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2 documents found
1: Title: EFR3s are palmitoylated plasma membrane proteins that control responsiveness to G-protein-coupled receptors.
Authors: Bojjireddy, Naveen, et.al. .
Journal: Journal of cell science (J Cell Sci), Vol. 128 (1): 118-28, 2015 .
Snippet: siRNA-mediated depletion of EFR3A and EFR3B impaired the sustained phase of cytosolic Ca(2+) response to high concentration of AngII in HEK293 cells that express wild type but not truncated AGTR1 (AT1a receptor), missing the phosphorylation sites.
Affiliation: Section on Molecular Signal Transduction, Program for Developmental Neuroscience, Eunice Kennedy Shriver NICHD, National Institutes of Health, Bethesda, MD 20892, USA. Swammerdam Institute for Life Sciences, University of Amsterdam, 1012 WX Amsterdam, The Netherlands. Section on Molecular Signal Transduction, Program for Developmental Neuroscience, Eunice Kennedy Shriver NICHD, National Institutes of Health, Bethesda, MD 20892, USA ballat@mail.nih.gov. .
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2: Title: A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci.
Authors: Bradfield, Jonathan P, et.al. .
Journal: PLoS genetics (Plos Genet), Vol. 7 (9): e1002293, 2011 .
Snippet: The second most significantly associated SNP (rs478222, P = 3.50×10⁻⁹ resides in an intronic region of the EFR3B (protein EFR3 homolog B) gene on 2p23; however, the region of linkage disequilibrium is approximately 800 kb and harbors additional multiple genes, including NCOA1, C2orf79, CENPO, ADCY3, DNAJC27, POMC, and DNMT3A.
Affiliation: The Center for Applied Genomics, The Children's Hospital Philadelphia, Philadelphia, Pennsylvania, United States of America. .
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