Syndecan-3
Syndecan-3 (Syndecan 3) هوَ بروتين يُشَفر بواسطة جين Syndecan-3 في الإنسان.[1][2][3]
الوظيفة
المراجع
- "Entrez Gene: SDC3 syndecan 3"، مؤرشف من الأصل في 05 ديسمبر 2010.
- "Molecular cloning and characterization of N-syndecan, a novel transmembrane heparan sulfate proteoglycan"، J Cell Biol، 117 (1): 191–201، مايو 1992، doi:10.1083/jcb.117.1.191، PMC 2289399، PMID 1556152.
- "Cloning and characterization of human syndecan-3"، J Cell Biochem، 82 (2): 246–59، أغسطس 2001، doi:10.1002/jcb.1119، PMID 11527150.
قراءة متعمقة
- "The Tat protein of human immunodeficiency virus type 1, a growth factor for AIDS Kaposi sarcoma and cytokine-activated vascular cells, induces adhesion of the same cell types by using integrin receptors recognizing the RGD amino acid sequence."، Proc. Natl. Acad. Sci. U.S.A.، 90 (17): 7941–5، 1993، doi:10.1073/pnas.90.17.7941، PMC 47263، PMID 7690138.
- "Isolation of a neuronal cell surface receptor of heparin binding growth-associated molecule (HB-GAM). Identification as N-syndecan (syndecan-3)."، J. Biol. Chem.، 269 (17): 12999–3004، 1994، PMID 8175719.
- "N-syndecan (syndecan 3) from neonatal rat brain binds basic fibroblast growth factor."، J. Biol. Chem.، 268 (22): 16810–4، 1993، PMID 8344959.
- "HIV-tat protein is a heparin-binding angiogenic growth factor."، Oncogene، 12 (2): 289–97، 1996، PMID 8570206.
- "Schwann cells secrete a novel collagen-like adhesive protein that binds N-syndecan."، J. Biol. Chem.، 271 (23): 13844–53، 1996، doi:10.1074/jbc.271.23.13844، PMID 8662884.
- "Expression of syndecan-1 and -3 during embryogenesis of the central nervous system in relation to binding with midkine."، J. Biochem.، 121 (2): 197–205، 1997، PMID 9089390.
- "Interaction of HIV-1 Tat protein with heparin. Role of the backbone structure, sulfation, and size."، J. Biol. Chem.، 272 (17): 11313–20، 1997، doi:10.1074/jbc.272.17.11313، PMID 9111037.
- "HIV-1 Tat protein exits from cells via a leaderless secretory pathway and binds to extracellular matrix-associated heparan sulfate proteoglycans through its basic region."، AIDS، 11 (12): 1421–31، 1997، doi:10.1097/00002030-199712000-00006، PMID 9342064.
- "Phosphorylation of recombinant N-syndecan (syndecan 3) core protein."، Biochem. Biophys. Res. Commun.، 240 (2): 502–6، 1997، doi:10.1006/bbrc.1997.7684، PMID 9388509.
- "Characterization of cDNA clones in size-fractionated cDNA libraries from human brain."، DNA Res.، 4 (5): 345–9، 1998، doi:10.1093/dnares/4.5.345، PMID 9455484.
- "Cortactin-Src kinase signaling pathway is involved in N-syndecan-dependent neurite outgrowth."، J. Biol. Chem.، 273 (17): 10702–8، 1998، doi:10.1074/jbc.273.17.10702، PMID 9553134.
- "Regulated expression and subcellular localization of syndecan heparan sulfate proteoglycans and the syndecan-binding protein CASK/LIN-2 during rat brain development."، J. Neurosci.، 19 (17): 7415–25، 1999، PMID 10460248.
- "Multiple interactions of HIV-I Tat protein with size-defined heparin oligosaccharides."، J. Biol. Chem.، 274 (40): 28198–205، 1999، doi:10.1074/jbc.274.40.28198، PMID 10497173.
- "Internalization of HIV-1 tat requires cell surface heparan sulfate proteoglycans."، J. Biol. Chem.، 276 (5): 3254–61، 2001، doi:10.1074/jbc.M006701200، PMID 11024024.
- "The neural cell recognition molecule neurofascin interacts with syntenin-1 but not with syntenin-2, both of which reveal self-associating activity."، J. Biol. Chem.، 276 (14): 10646–54، 2001، doi:10.1074/jbc.M010647200، PMID 11152476.
- "Heparin binding by the HIV-1 tat protein transduction domain."، Protein Sci.، 10 (10): 2138–9، 2001، doi:10.1110/ps.23401، PMC 2374215، PMID 11567105.
- "Schwann cell adhesion to a novel heparan sulfate binding site in the N-terminal domain of alpha 4 type V collagen is mediated by syndecan-3."، J. Biol. Chem.، 277 (9): 7619–25، 2002، doi:10.1074/jbc.M111311200، PMID 11751872.
- "Augmented synthesis and differential localization of heparan sulfate proteoglycans in Duchenne muscular dystrophy."، J. Cell. Biochem.، 85 (4): 703–13، 2002، doi:10.1002/jcb.10184، PMID 11968010.
بوابة الكيمياء الحيوية
بوابة علم الأحياء الخلوي والجزيئي
بوابة طب
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