CTNNBIP1
من أرابيكا، الموسوعة العربية الحرة
المزيد من اللغات
المزيد من الإجراءات
An Error has occured retrieving Wikidata item for infobox CTNNBIP1 (Catenin beta interacting protein 1) هوَ بروتين يُشَفر بواسطة جين CTNNBIP1 في الإنسان.[1][2]
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
- ^ Tago K، Nakamura T، Nishita M، Hyodo J، Nagai S، Murata Y، Adachi S، Ohwada S، Morishita Y، Shibuya H، Akiyama T (يوليو 2000). "Inhibition of Wnt signaling by ICAT, a novel beta-catenin-interacting protein". Genes Dev. ج. 14 ع. 14: 1741–9. PMC:316784. PMID:10898789.
- ^ "Entrez Gene: catenin". مؤرشف من الأصل في 2010-12-05.
قراءة متعمقة
- Yochum GS، Cleland R، Goodman RH (2008). "A genome-wide screen for beta-catenin binding sites identifies a downstream enhancer element that controls c-Myc gene expression". Mol. Cell. Biol. ج. 28 ع. 24: 7368–79. DOI:10.1128/MCB.00744-08. PMC:2593444. PMID:18852287.
- Sharma M، Henderson BR (2007). "IQ-domain GTPase-activating protein 1 regulates beta-catenin at membrane ruffles and its role in macropinocytosis of N-cadherin and adenomatous polyposis coli". J. Biol. Chem. ج. 282 ع. 11: 8545–56. DOI:10.1074/jbc.M610272200. PMID:17255093.
- Takeda K، Kinoshita I، Shimizu Y، وآخرون (2008). "Clinicopathological significance of expression of p-c-Jun, TCF4 and beta-Catenin in colorectal tumors". BMC Cancer. ج. 8: 328. DOI:10.1186/1471-2407-8-328. PMC:2585585. PMID:18992165.
- Wang W، Zhang X، Deng K، وآخرون (2009). "ICAT as a potential enhancer of monocytic differentiation: implications from the comparative proteome analysis of the HL60 cell line stimulated by all-trans retinoic acid and NSC67657". Cell Biochem. Funct. ج. 27 ع. 6: 329–37. DOI:10.1002/cbf.1576. PMID:19569129.
- Wang WJ، Tang W، Qiu ZY (2009). "Comparative proteomics analysis on differentiation of human promyelocytic leukemia HL-60 cells into granulocyte and monocyte lineages". Ai Zheng. ج. 28 ع. 2: 117–21. PMID:19550115.
- Reichel O، Mayr D، Durst F، Berghaus A (2008). "E-cadherin but not beta-catenin expression is decreased in laryngeal biopsies from patients with laryngopharyngeal reflux". Eur Arch Otorhinolaryngol. ج. 265 ع. 8: 937–42. DOI:10.1007/s00405-007-0568-6. PMID:18183411.
- Bazas VM، Lukyanova NY، Demash DV، وآخرون (2008). "Relation between cell-to-cell adhesion and angiogenesis and clinico-morphological prognostic factors in patients with gastric cancer". Exp. Oncol. ج. 30 ع. 3: 235–9. PMID:18806748.
- Kohler EM، Chandra SH، Behrens J، Schneikert J (2009). "Beta-catenin degradation mediated by the CID domain of APC provides a model for the selection of APC mutations in colorectal, desmoid and duodenal tumours". Hum. Mol. Genet. ج. 18 ع. 2: 213–26. DOI:10.1093/hmg/ddn338. PMID:18854359.
- Seo E، Jho EH (2007). "Axin-independent phosphorylation of APC controls beta-catenin signaling via cytoplasmic retention of beta-catenin". Biochem. Biophys. Res. Commun. ج. 357 ع. 1: 81–6. DOI:10.1016/j.bbrc.2007.03.117. PMID:17418091.
- Ladeiro Y، Couchy G، Balabaud C، وآخرون (2008). "MicroRNA profiling in hepatocellular tumors is associated with clinical features and oncogene/tumor suppressor gene mutations". Hepatology. ج. 47 ع. 6: 1955–63. DOI:10.1002/hep.22256. PMID:18433021.
- Zhang H، Xue Y (2008). "Wnt pathway is involved in advanced gastric carcinoma". Hepatogastroenterology. ج. 55 ع. 84: 1126–30. PMID:18705344.
- Wang HX، Tekpetey FR، Kidder GM (2009). "Identification of WNT/beta-CATENIN signaling pathway components in human cumulus cells". Mol. Hum. Reprod. ج. 15 ع. 1: 11–7. DOI:10.1093/molehr/gan070. PMID:19038973.
- Matono H، Oda Y، Nakamori M، وآخرون (2008). "Correlation between beta-catenin widespread nuclear expression and matrix metalloproteinase-7 overexpression in sporadic desmoid tumors". Hum. Pathol. ج. 39 ع. 12: 1802–8. DOI:10.1016/j.humpath.2008.05.005. PMID:18715618.
- Wang L، O'Leary H، Fortney J، Gibson LF (2007). "Ph+/VE-cadherin+ identifies a stem cell like population of acute lymphoblastic leukemia sustained by bone marrow niche cells". Blood. ج. 110 ع. 9: 3334–44. DOI:10.1182/blood-2007-01-068122. PMC:2200915. PMID:17638851.
- von Koch CS، Gulati M، Aldape K، Berger MS (2002). "Familial medulloblastoma: case report of one family and review of the literature". Neurosurgery. ج. 51 ع. 1: 227–33, discussion 233. DOI:10.1097/00006123-200207000-00035. PMID:12182422.
- Wang L، Li H، Zhang Y، وآخرون (2009). "HINT1 inhibits beta-catenin/TCF4, USF2 and NFkappaB activity in human hepatoma cells". Int. J. Cancer. ج. 124 ع. 7: 1526–34. DOI:10.1002/ijc.24072. PMC:2667231. PMID:19089909.
- Chen Y، Bodles AM (2007). "Amyloid precursor protein modulates beta-catenin degradation". Journal of Neuroinflammation. ج. 4: 29. DOI:10.1186/1742-2094-4-29. PMC:2231348. PMID:18070361.
- Kastritis E، Murray S، Kyriakou F، وآخرون (2009). "Somatic mutations of adenomatous polyposis coli gene and nuclear b-catenin accumulation have prognostic significance in invasive urothelial carcinomas: evidence for Wnt pathway implication". Int. J. Cancer. ج. 124 ع. 1: 103–8. DOI:10.1002/ijc.23917. PMID:18844223.
- Turbiner J، Moreno-Bueno G، Dahiya S، وآخرون (2008). "Clinicopathological and molecular analysis of endometrial carcinoma associated with tamoxifen". Mod. Pathol. ج. 21 ع. 8: 925–36. DOI:10.1038/modpathol.2008.49. PMID:18500270.
- 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.