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TRIP10
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An Error has occured retrieving Wikidata item for infobox TRIP10 (Thyroid hormone receptor interactor 10) هوَ بروتين يُشَفر بواسطة جين TRIP10 في الإنسان.[1][2][3][4]
الوظيفة
![[أيقونة]](/%D9%85%D9%84%D9%81:Crystal_xedit.svg){kind=small} | هذا القسم فارغ أو غير مكتمل. ساهم في توسيعه. (يوليو 2018) |
الأهمية السريرية
| هذا القسم فارغ أو غير مكتمل. ساهم في توسيعه. (يوليو 2018) |
المراجع
- ^ Tsuji E، Tsuji Y (أبريل 2001). "Molecular cloning and chromosomal localization of human salt-tolerant protein". Genetica. ج. 108 ع. 3: 259–62. DOI:10.1023/A:1004132919896. PMID:11294612.
- ^ Lee JW، Choi HS، Gyuris J، Brent R، Moore DD (يوليو 1995). "Two classes of proteins dependent on either the presence or absence of thyroid hormone for interaction with the thyroid hormone receptor". Mol Endocrinol. ج. 9 ع. 2: 243–54. DOI:10.1210/me.9.2.243. PMID:7776974.
- ^ Aspenstrom P (أغسطس 1997). "A Cdc42 target protein with homology to the non-kinase domain of FER has a potential role in regulating the actin cytoskeleton". Curr Biol. ج. 7 ع. 7: 479–87. DOI:10.1016/S0960-9822(06)00219-3. PMID:9210375.
- ^ "Entrez Gene: TRIP10 thyroid hormone receptor interactor 10". مؤرشف من الأصل في 2010-12-05.
قراءة متعمقة
- Maruyama K، Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. ج. 138 ع. 1–2: 171–4. DOI:10.1016/0378-1119(94)90802-8. PMID:8125298.
- Suzuki Y، Yoshitomo-Nakagawa K، Maruyama K، وآخرون (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. ج. 200 ع. 1–2: 149–56. DOI:10.1016/S0378-1119(97)00411-3. PMID:9373149.
- Tian L، Nelson DL، Stewart DM (2000). "Cdc42-interacting protein 4 mediates binding of the Wiskott-Aldrich syndrome protein to microtubules". J. Biol. Chem. ج. 275 ع. 11: 7854–61. DOI:10.1074/jbc.275.11.7854. PMID:10713100.
- Linder S، Hüfner K، Wintergerst U، Aepfelbacher M (2001). "Microtubule-dependent formation of podosomal adhesion structures in primary human macrophages". J. Cell Sci. 113 Pt 23: 4165–76. PMID:11069762.
- Richnau N، Aspenström P (2001). "Rich, a rho GTPase-activating protein domain-containing protein involved in signaling by Cdc42 and Rac1". J. Biol. Chem. ج. 276 ع. 37: 35060–70. DOI:10.1074/jbc.M103540200. PMID:11431473.
- Yuan R، Fan S، Achary M، وآخرون (2001). "Altered gene expression pattern in cultured human breast cancer cells treated with hepatocyte growth factor/scatter factor in the setting of DNA damage". Cancer Res. ج. 61 ع. 21: 8022–31. PMID:11691828.
- Wang L، Rudert WA، Grishin A، وآخرون (2002). "Identification and genetic analysis of human and mouse activated Cdc42 interacting protein-4 isoforms". Biochem. Biophys. Res. Commun. ج. 293 ع. 5: 1426–30. DOI:10.1016/S0006-291X(02)00398-4. PMID:12054674.
- Chang L، Adams RD، Saltiel AR (2002). "The TC10-interacting protein CIP4/2 is required for insulin-stimulated Glut4 translocation in 3T3L1 adipocytes". Proc. Natl. Acad. Sci. U.S.A. ج. 99 ع. 20: 12835–40. Bibcode:2002PNAS...9912835C. DOI:10.1073/pnas.202495599. PMC:130546. PMID:12242347.
- Dombrosky-Ferlan P، Grishin A، Botelho RJ، وآخرون (2003). "Felic (CIP4b), a novel binding partner with the Src kinase Lyn and Cdc42, localizes to the phagocytic cup". Blood. ج. 101 ع. 7: 2804–9. DOI:10.1182/blood-2002-03-0851. PMID:12456510.
- Strausberg RL، Feingold EA، Grouse LH، وآخرون (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. ج. 99 ع. 26: 16899–903. Bibcode:2002PNAS...9916899M. DOI:10.1073/pnas.242603899. PMC:139241. PMID:12477932.
- Holbert S، Dedeoglu A، Humbert S، وآخرون (2003). "Cdc42-interacting protein 4 binds to huntingtin: neuropathologic and biological evidence for a role in Huntington's disease". Proc. Natl. Acad. Sci. U.S.A. ج. 100 ع. 5: 2712–7. Bibcode:2003PNAS..100.2712H. DOI:10.1073/pnas.0437967100. PMC:151406. PMID:12604778.
- Katoh M، Katoh M (2004). "FNBP2 gene on human chromosome 1q32.1 encodes ARHGAP family protein with FCH, FBH, RhoGAP and SH3 domains". Int. J. Mol. Med. ج. 11 ع. 6: 791–7. DOI:10.3892/ijmm.11.6.791. PMID:12736724.
- Morin F، Vannier B، Houdart F، وآخرون (2003). "A proline-rich domain in the gamma subunit of phosphodiesterase 6 mediates interaction with SH3-containing proteins". Mol. Vis. ج. 9: 449–59. PMID:14502124.
- Larocca MC، Shanks RA، Tian L، وآخرون (2004). "AKAP350 interaction with cdc42 interacting protein 4 at the Golgi apparatus". Mol. Biol. Cell. ج. 15 ع. 6: 2771–81. DOI:10.1091/mbc.E03-10-0757. PMC:420101. PMID:15047863.
- Chung YH، Cho NH، Garcia MI، وآخرون (2004). "Activation of Stat3 transcription factor by Herpesvirus saimiri STP-A oncoprotein". J. Virol. ج. 78 ع. 12: 6489–97. DOI:10.1128/JVI.78.12.6489-6497.2004. PMC:416526. PMID:15163742.
- Gerhard DS، Wagner L، Feingold EA، وآخرون (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. ج. 14 ع. 10B: 2121–7. DOI:10.1101/gr.2596504. PMC:528928. PMID:15489334.
- Yin X، Warner DR، Roberts EA، وآخرون (2005). "Identification of novel CBP interacting proteins in embryonic orofacial tissue". Biochem. Biophys. Res. Commun. ج. 329 ع. 3: 1010–7. DOI:10.1016/j.bbrc.2005.02.075. PMID:15752756.
