TUSC3
TUSC3 (Tumor suppressor candidate 3) هوَ بروتين يُشَفر بواسطة جين TUSC3 في الإنسان.[1][2][3]
الوظيفة
الأهمية السريرية
المراجع
- ^ MacGrogan D، Levy A، Bova GS، Isaacs WB، Bookstein R (سبتمبر 1996). "Structure and methylation-associated silencing of a gene within a homozygously deleted region of human chromosome band 8p22". Genomics. ج. 35 ع. 1: 55–65. DOI:10.1006/geno.1996.0322. PMID:8661104.
- ^ "Entrez Gene: TUSC3 tumor suppressor candidate 3". مؤرشف من الأصل في 2010-12-05.
- ^ Ishii H، Baffa R، Numata SI، Murakumo Y، Rattan S، Inoue H، Mori M، Fidanza V، Alder H، Croce CM (مايو 1999). "The FEZ1 gene at chromosome 8p22 encodes a leucine-zipper protein, and its expression is altered in multiple human tumors". Proc Natl Acad Sci U S A. ج. 96 ع. 7: 3928–33. DOI:10.1073/pnas.96.7.3928. PMC:22397. PMID:10097140.
قراءة متعمقة
- Pak BJ، Park H، Chang ER، وآخرون (1998). "Differential display analysis of oxygen-mediated changes in gene expression in first trimester human trophoblast cells". Placenta. ج. 19 ع. 7: 483–8. DOI:10.1016/S0143-4004(98)91041-4. PMID:9778121.
- 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. DOI:10.1073/pnas.242603899. PMC:139241. PMID:12477932.
- Kelleher DJ، Karaoglu D، Mandon EC، Gilmore R (2003). "Oligosaccharyltransferase isoforms that contain different catalytic STT3 subunits have distinct enzymatic properties". Mol. Cell. ج. 12 ع. 1: 101–11. DOI:10.1016/S1097-2765(03)00243-0. PMID:12887896.
- Anderson NL، Polanski M، Pieper R، وآخرون (2004). "The human plasma proteome: a nonredundant list developed by combination of four separate sources". Mol. Cell. Proteomics. ج. 3 ع. 4: 311–26. DOI:10.1074/mcp.M300127-MCP200. PMID:14718574.
{استشهاد بدورية محكمة}
: صيانة الاستشهاد: دوي مجاني غير معلم (link) - Colland F، Jacq X، Trouplin V، وآخرون (2004). "Functional proteomics mapping of a human signaling pathway". Genome Res. ج. 14 ع. 7: 1324–32. DOI:10.1101/gr.2334104. PMC:442148. PMID:15231748.
- 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.
- Shibatani T، David LL، McCormack AL، وآخرون (2005). "Proteomic analysis of mammalian oligosaccharyltransferase reveals multiple subcomplexes that contain Sec61, TRAP, and two potential new subunits". Biochemistry. ج. 44 ع. 16: 5982–92. DOI:10.1021/bi047328f. PMID:15835887.
- Rual JF، Venkatesan K، Hao T، وآخرون (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. ج. 437 ع. 7062: 1173–8. DOI:10.1038/nature04209. PMID:16189514.
- Pils D، Horak P، Gleiss A، وآخرون (2006). "Five genes from chromosomal band 8p22 are significantly down-regulated in ovarian carcinoma: N33 and EFA6R have a potential impact on overall survival". Cancer. ج. 104 ع. 11: 2417–29. DOI:10.1002/cncr.21538. PMID:16270321.
- Guervós MA، Marcos CA، Hermsen M، وآخرون (2007). "Deletions of N33, STK11 and TP53 are involved in the development of lymph node metastasis in larynx and pharynx carcinomas". Cell. Oncol. ج. 29 ع. 4: 327–34. PMID:17641416.