RHOQ
RHOQ (Ras homolog family member Q) هوَ بروتين يُشَفر بواسطة جين RHOQ في الإنسان.[1][2][3][2]
المراجع
- "Characterization of four novel ras-like genes expressed in a human teratocarcinoma cell line"، Mol Cell Biol، 10 (4): 1793–8، مايو 1990، PMC 362288، PMID 2108320.
- "Entrez Gene: RHOQ ras homolog gene family, member Q"، مؤرشف من الأصل في 05 ديسمبر 2010.
- "Novel MITF targets identified using a two-step DNA microarray strategy"، Pigment Cell Melanoma Res.، 21 (6): 665–76، 2008، doi:10.1111/j.1755-148X.2008.00505.x، PMID 19067971.
قراءة متعمقة
- "Cellular functions of TC10, a Rho family GTPase: regulation of morphology, signal transduction and cell growth"، Oncogene، 18 (26): 3831–45، 1999، doi:10.1038/sj.onc.1202758، PMID 10445846.
- "The Borgs, a new family of Cdc42 and TC10 GTPase-interacting proteins"، Mol. Cell. Biol.، 19 (10): 6585–97، 2000، PMC 84628، PMID 10490598.
- "The cell-polarity protein Par6 links Par3 and atypical protein kinase C to Cdc42"، Nat. Cell Biol.، 2 (8): 531–9، 2000، doi:10.1038/35019573، PMID 10934474.
- "Characterization of TCL, a new GTPase of the rho family related to TC10 andCcdc42"، J. Biol. Chem.، 275 (46): 36457–64، 2000، doi:10.1074/jbc.M003487200، PMID 10967094.
- "Differential localization of Rho GTPases in live cells: regulation by hypervariable regions and RhoGDI binding"، J. Cell Biol.، 152 (1): 111–26، 2001، doi:10.1083/jcb.152.1.111، PMC 2193662، PMID 11149925.
- "PIST: a novel PDZ/coiled-coil domain binding partner for the rho-family GTPase TC10"، Biochem. Biophys. Res. Commun.، 280 (2): 541–7، 2001، doi:10.1006/bbrc.2000.4160، PMID 11162552.
- "Cloning and functional characterization of related TC10 isoforms, a subfamily of Rho proteins involved in insulin-stimulated glucose transport"، J. Biol. Chem.، 277 (15): 13067–73، 2002، doi:10.1074/jbc.M109471200، PMID 11821390.
- "Small GTP-binding protein TC10 differentially regulates two distinct populations of filamentous actin in 3T3L1 adipocytes"، Mol. Biol. Cell، 13 (7): 2334–46، 2003، doi:10.1091/mbc.01-10-0490، PMC 117317، PMID 12134073.
- "The TC10-interacting protein CIP4/2 is required for insulin-stimulated Glut4 translocation in 3T3L1 adipocytes"، Proc. Natl. Acad. Sci. U.S.A.، 99 (20): 12835–40، 2002، doi:10.1073/pnas.202495599، PMC 130546، PMID 12242347.
- "Small GTPase Tc10 and its homologue RhoT induce N-WASP-mediated long process formation and neurite outgrowth"، J. Cell Sci.، 116 (Pt 1): 155–68، 2003، doi:10.1242/jcs.00208، PMID 12456725.
- "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 DNA sequence and analysis of human chromosome 14"، Nature، 421 (6923): 601–7، 2003، doi:10.1038/nature01348، PMID 12508121.
- "The exocytotic trafficking of TC10 occurs through both classical and nonclassical secretory transport pathways in 3T3L1 adipocytes"، Mol. Cell. Biol.، 23 (3): 961–74، 2003، doi:10.1128/MCB.23.3.961-974.2003، PMC 140699، PMID 12529401.
- "The exocyst complex is required for targeting of Glut4 to the plasma membrane by insulin"، Nature، 422 (6932): 629–33، 2003، doi:10.1038/nature01533، PMID 12687004.
- "Lipid Raft targeting of the TC10 amino terminal domain is responsible for disruption of adipocyte cortical actin"، Mol. Biol. Cell، 14 (9): 3578–91، 2004، doi:10.1091/mbc.E03-01-0012، PMC 196551، PMID 12972548.
- "Complete sequencing and characterization of 21,243 full-length human cDNAs"، Nat. Genet.، 36 (1): 40–5، 2004، doi:10.1038/ng1285، PMID 14702039.
- "Expression of the human myotonic dystrophy kinase-related Cdc42-binding kinase gamma is regulated by promoter DNA methylation and Sp1 binding"، J. Biol. Chem.، 279 (33): 34156–64، 2004، doi:10.1074/jbc.M405252200، PMID 15194684.
- "Isolation and characterisation of DOCK8, a member of the DOCK180-related regulators of cell morphology"، FEBS Lett.، 572 (1–3): 159–66، 2004، doi:10.1016/j.febslet.2004.06.095، PMID 15304341.
- "Activation of endogenous Cdc42 visualized in living cells"، Science، 305 (5690): 1615–9، 2004، doi:10.1126/science.1100367، PMID 15361624.
بوابة الكيمياء الحيوية
بوابة علم الأحياء الخلوي والجزيئي
بوابة طب
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