EMP3

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Epithelial membrane protein 3
Identifiers
Symbols EMP3 ; YMP
External IDs Template:OMIM5 Template:MGI HomoloGene1090
RNA expression pattern
More reference expression data
Orthologs
Template:GNF Ortholog box
Species Human Mouse
Entrez n/a n/a
Ensembl n/a n/a
UniProt n/a n/a
RefSeq (mRNA) n/a n/a
RefSeq (protein) n/a n/a
Location (UCSC) n/a n/a
PubMed search n/a n/a

Epithelial membrane protein 3, also known as EMP3, is a human gene.[1]


References

  1. "Entrez Gene: EMP3 epithelial membrane protein 3".

Further reading

  • Lobsiger CS, Magyar JP, Taylor V; et al. (1997). "Identification and characterization of a cDNA and the structural gene encoding the mouse epithelial membrane protein-1". Genomics. 36 (3): 379–87. PMID 8884260.
  • Taylor V, Suter U (1996). "Epithelial membrane protein-2 and epithelial membrane protein-3: two novel members of the peripheral myelin protein 22 gene family". Gene. 175 (1–2): 115–20. PMID 8917086.
  • Ben-Porath I, Benvenisty N (1997). "Characterization of a tumor-associated gene, a member of a novel family of genes encoding membrane glycoproteins". Gene. 183 (1–2): 69–75. PMID 8996089.
  • Bolin LM, McNeil T, Lucian LA; et al. (1997). "HNMP-1: a novel hematopoietic and neural membrane protein differentially regulated in neural development and injury". J. Neurosci. 17 (14): 5493–502. PMID 9204931.
  • Liehr T, Kuhlenbäumer G, Wulf P; et al. (1999). "Regional localization of the human epithelial membrane protein genes 1, 2, and 3 (EMP1, EMP2, EMP3) to 12p12.3, 16p13.2, and 19q13.3". Genomics. 58 (1): 106–8. doi:10.1006/geno.1999.5803. PMID 10331954.
  • Yus-Najera E, Santana-Castro I, Villarroel A (2002). "The identification and characterization of a noncontinuous calmodulin-binding site in noninactivating voltage-dependent KCNQ potassium channels". J. Biol. Chem. 277 (32): 28545–53. doi:10.1074/jbc.M204130200. PMID 12032157.
  • Wilson HL, Wilson SA, Surprenant A, North RA (2002). "Epithelial membrane proteins induce membrane blebbing and interact with the P2X7 receptor C terminus". J. Biol. Chem. 277 (37): 34017–23. doi:10.1074/jbc.M205120200. PMID 12107182.
  • Strausberg RL, Feingold EA, Grouse LH; et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932.
  • Schwake M, Jentsch TJ, Friedrich T (2003). "A carboxy-terminal domain determines the subunit specificity of KCNQ K+ channel assembly". EMBO Rep. 4 (1): 76–81. doi:10.1038/sj.embor.embor715. PMID 12524525.
  • Yus-Nájera E, Muñoz A, Salvador N; et al. (2003). "Localization of KCNQ5 in the normal and epileptic human temporal neocortex and hippocampal formation". Neuroscience. 120 (2): 353–64. PMID 12890507.
  • Gerhard DS, Wagner L, Feingold EA; et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMID 15489334.
  • Nielsen K, Heegaard S, Vorum H; et al. (2005). "Altered expression of CLC, DSG3, EMP3, S100A2, and SLPI in corneal epithelium from keratoconus patients". Cornea. 24 (6): 661–8. PMID 16015083.
  • Li KK, Pang JC, Chung NY; et al. (2007). "EMP3 overexpression is associated with oligodendroglial tumors retaining chromosome arms 1p and 19q". Int. J. Cancer. 120 (4): 947–50. doi:10.1002/ijc.22415. PMID 17187361.
  • Kunitz A, Wolter M, van den Boom J; et al. (2007). "DNA hypermethylation and aberrant expression of the EMP3 gene at 19q13.3 in Human Gliomas". Brain Pathol. 17 (4): 363–70. doi:10.1111/j.1750-3639.2007.00083.x. PMID 17610521.

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