JAM3
JAM3 (Junctional adhesion molecule 3) هوَ بروتين يُشَفر بواسطة جين JAM3 في الإنسان.[1]
المراجع
- "Entrez Gene: JAM3 junctional adhesion molecule 3"، مؤرشف من الأصل في 05 ديسمبر 2010.
قراءة متعمقة
- Muller WA (2003)، "Leukocyte-endothelial-cell interactions in leukocyte transmigration and the inflammatory response."، Trends Immunol.، 24 (6): 327–34، doi:10.1016/S1471-4906(03)00117-0، PMID 12810109.
- "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides."، Gene، 138 (1–2): 171–4، 1994، doi:10.1016/0378-1119(94)90802-8، PMID 8125298.
- "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library."، Gene، 200 (1–2): 149–56، 1997، doi:10.1016/S0378-1119(97)00411-3، PMID 9373149.
- "Cloning of human junctional adhesion molecule 3 (JAM3) and its identification as the JAM2 counter-receptor."، J. Biol. Chem.، 276 (49): 45826–32، 2002، doi:10.1074/jbc.M105972200، PMID 11590146.
- "Heterogeneity of endothelial junctions is reflected by differential expression and specific subcellular localization of the three JAM family members."، Blood، 98 (13): 3699–707، 2002، doi:10.1182/blood.V98.13.3699، PMID 11739175.
- "Vascular endothelial-junctional adhesion molecule (VE-JAM)/JAM 2 interacts with T, NK, and dendritic cells through JAM 3."، J. Immunol.، 168 (4): 1618–26، 2002، doi:10.4049/jimmunol.168.4.1618، PMID 11823489.
- "Narrowing the critical region within 11q24-qter for hypoplastic left heart and identification of a candidate gene, JAM3, expressed during cardiogenesis."، Genomics، 79 (4): 475–8، 2002، doi:10.1006/geno.2002.6742، PMID 11944976.
- "JAM2 interacts with alpha4beta1. Facilitation by JAM3."، J. Biol. Chem.، 277 (31): 27589–92، 2002، doi:10.1074/jbc.C200331200، PMID 12070135.
- "The junctional adhesion molecule 3 (JAM-3) on human platelets is a counterreceptor for the leukocyte integrin Mac-1."، J. Exp. Med.، 196 (5): 679–91، 2002، doi:10.1084/jem.20020267، PMC 2194005، PMID 12208882.
- "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، 2003، doi:10.1073/pnas.242603899، PMC 139241، PMID 12477932.
- "The junctional adhesion molecule (JAM) family members JAM-2 and JAM-3 associate with the cell polarity protein PAR-3: a possible role for JAMs in endothelial cell polarity."، J. Cell Sci.، 116 (Pt 19): 3879–91، 2004، doi:10.1242/jcs.00704، PMID 12953056.
- "The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment."، Genome Res.، 13 (10): 2265–70، 2003، doi:10.1101/gr.1293003، PMC 403697، PMID 12975309.
- "Complete sequencing and characterization of 21,243 full-length human cDNAs."، Nat. Genet.، 36 (1): 40–5، 2004، doi:10.1038/ng1285، PMID 14702039.
- "JAM-C is a component of desmosomes and a ligand for CD11b/CD18-mediated neutrophil transepithelial migration."، Mol. Biol. Cell، 15 (8): 3926–37، 2005، doi:10.1091/mbc.E04-04-0317، PMC 491847، PMID 15194813.
- "Signal peptide prediction based on analysis of experimentally verified cleavage sites."، Protein Sci.، 13 (10): 2819–24، 2005، doi:10.1110/ps.04682504، PMC 2286551، PMID 15340161.
- "The junctional adhesion molecule-C promotes neutrophil transendothelial migration in vitro and in vivo."، J. Biol. Chem.، 279 (53): 55602–8، 2005، doi:10.1074/jbc.M404676200، PMID 15485832.
- "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."، Genome Res.، 14 (10B): 2121–7، 2004، doi:10.1101/gr.2596504، PMC 528928، PMID 15489334.
- "Junctional adhesion molecule-C regulates the early influx of leukocytes into tissues during inflammation."، J. Immunol.، 174 (10): 6406–15، 2005، doi:10.4049/jimmunol.174.10.6406، PMID 15879142.
- "The homophilic binding of junctional adhesion molecule-C mediates tumor cell-endothelial cell interactions."، J. Biol. Chem.، 280 (43): 36326–33، 2006، doi:10.1074/jbc.M505059200، PMID 16118203.
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