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TSC22D1
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An Error has occured retrieving Wikidata item for infobox TSC22D1 (TSC22 domain family member 1) هوَ بروتين يُشَفر بواسطة جين TSC22D1 في الإنسان.[1][2][3][4]
الوظيفة
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
- ^ Jay P، Ji JW، Marsollier C، Taviaux S، Berge-Lefranc JL، Berta P (يوليو 1996). "Cloning of the human homologue of the TGF beta-stimulated clone 22 gene". Biochem Biophys Res Commun. ج. 222 ع. 3: 821–6. DOI:10.1006/bbrc.1996.0825. PMID:8651929.
- ^ "Entrez Gene: TSC22D1 TSC22 domain family, member 1". مؤرشف من الأصل في 2010-12-05.
- ^ Kester HA، Blanchetot C، den Hertog J، van der Saag PT، van der Burg B (سبتمبر 1999). "Transforming growth factor-beta-stimulated clone-22 is a member of a family of leucine zipper proteins that can homo- and heterodimerize and has transcriptional repressor activity". J. Biol. Chem. ج. 274 ع. 39: 27439–47. DOI:10.1074/jbc.274.39.27439. PMID:10488076.
- ^ Ohta S، Shimekake Y، Nagata K (مارس 1997). "Molecular cloning and characterization of a transcription factor for the C-type natriuretic peptide gene promoter". Eur J Biochem. ج. 242 ع. 3: 460–6. DOI:10.1111/j.1432-1033.1996.460rr.x. PMID:9022669.
قراءة متعمقة
- Shibanuma M، Kuroki T، Nose K (1992). "Isolation of a gene encoding a putative leucine zipper structure that is induced by transforming growth factor beta 1 and other growth factors". J. Biol. Chem. ج. 267 ع. 15: 10219–24. PMID:1587811.
- Dmitrenko VV، Garifulin OM، Shostak EA، وآخرون (1997). "[The characteristics of different types of mRNA expressed in the human brain]". Tsitol. Genet. ج. 30 ع. 5: 41–7. PMID:9026990.
- Kester HA، Blanchetot C، den Hertog J، وآخرون (1999). "Transforming growth factor-beta-stimulated clone-22 is a member of a family of leucine zipper proteins that can homo- and heterodimerize and has transcriptional repressor activity". J. Biol. Chem. ج. 274 ع. 39: 27439–47. DOI:10.1074/jbc.274.39.27439. PMID:10488076.
- Hino S، Kawamata H، Uchida D، وآخرون (2001). "Nuclear translocation of TSC-22 (TGF-beta-stimulated clone-22) concomitant with apoptosis: TSC-22 as a putative transcriptional regulator". Biochem. Biophys. Res. Commun. ج. 278 ع. 3: 659–64. DOI:10.1006/bbrc.2000.3840. PMID:11095965.
- Hino S، Kawamata H، Omotehara F، وآخرون (2002). "Leucine zipper structure of TSC-22 (TGF-beta stimulated clone-22) markedly inhibits the anchorage-independent growth of salivary gland cancer cells". Oncol. Rep. ج. 9 ع. 2: 371–4. DOI:10.3892/or.9.2.371. PMID:11836610.
- Hino S، Kawamata H، Omotehara F، وآخرون (2002). "Cytoplasmic TSC-22 (transforming growth factor-beta-stimulated clone-22) markedly enhances the radiation sensitivity of salivary gland cancer cells". Biochem. Biophys. Res. Commun. ج. 292 ع. 4: 957–63. DOI:10.1006/bbrc.2002.6776. PMID:11944908.
- Ohara O، Nagase T، Mitsui G، وآخرون (2003). "Characterization of size-fractionated cDNA libraries generated by the in vitro recombination-assisted method". DNA Res. ج. 9 ع. 2: 47–57. DOI:10.1093/dnares/9.2.47. PMID:12056414.
- Gupta RA، Sarraf P، Brockman JA، وآخرون (2003). "Peroxisome proliferator-activated receptor gamma and transforming growth factor-beta pathways inhibit intestinal epithelial cell growth by regulating levels of TSC-22". J. Biol. Chem. ج. 278 ع. 9: 7431–8. DOI:10.1074/jbc.M208076200. PMID:12468551.
- 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.
- Sugawara F، Yamada Y، Watanabe R، وآخرون (2004). "The role of the TSC-22 (-396) A/G variant in the development of diabetic nephropathy". Diabetes Res. Clin. Pract. ج. 60 ع. 3: 191–7. DOI:10.1016/S0168-8227(03)00038-X. PMID:12757981.
- Uchida D، Omotehara F، Nakashiro K، وآخرون (2003). "Posttranscriptional regulation of TSC-22 (TGF-beta-stimulated clone-22) gene by TGF-beta 1". Biochem. Biophys. Res. Commun. ج. 305 ع. 4: 846–54. DOI:10.1016/S0006-291X(03)00854-4. PMID:12767908.
- 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.
- Choi SJ، Moon JH، Ahn YW، وآخرون (2005). "Tsc-22 enhances TGF-beta signaling by associating with Smad4 and induces erythroid cell differentiation". Mol. Cell. Biochem. ج. 271 ع. 1–2: 23–8. DOI:10.1007/s11010-005-3456-7. PMID:15881652.
- Rentsch CA، Cecchini MG، Schwaninger R، وآخرون (2006). "Differential expression of TGFbeta-stimulated clone 22 in normal prostate and prostate cancer". Int. J. Cancer. ج. 118 ع. 4: 899–906. DOI:10.1002/ijc.21449. PMID:16106424.
- Stelzl U، Worm U، Lalowski M، وآخرون (2005). "A human protein-protein interaction network: a resource for annotating the proteome". Cell. ج. 122 ع. 6: 957–68. DOI:10.1016/j.cell.2005.08.029. PMID:16169070.
- Ewing RM، Chu P، Elisma F، وآخرون (2007). "Large-scale mapping of human protein-protein interactions by mass spectrometry". Mol. Syst. Biol. ج. 3 ع. 1: 89. DOI:10.1038/msb4100134. PMC:1847948. PMID:17353931.
- Lu Y، Kitaura J، Oki T، وآخرون (2007). "Identification of TSC-22 as a potential tumor suppressor that is upregulated by Flt3-D835V but not Flt3-ITD". Leukemia. ج. 21 ع. 11: 2246–57. DOI:10.1038/sj.leu.2404883. PMID:17690703.