WNT2B

An Error has occured retrieving Wikidata item for infobox WNT2B‏ (Wnt family member 2B) هوَ بروتين يُشَفر بواسطة جين WNT2B في الإنسان.^[1]^[2]^[3]^[4]

الوظيفة

الأهمية السريرية

المراجع

^ Katoh M، Hirai M، Sugimura T، Terada M (أكتوبر 1996). "Cloning, expression and chromosomal localization of Wnt-13, a novel member of the Wnt gene family". Oncogene. ج. 13 ع. 4: 873–6. PMID:8761309.
^ "Entrez Gene: WNT2B wingless-type MMTV integration site family, member 2B". مؤرشف من الأصل في 2010-12-05.
^ Katoh M، Kirikoshi H، Saitoh T، Sagara N، Koike J (سبتمبر 2000). "Alternative splicing of the WNT-2B/WNT-13 gene". Biochem Biophys Res Commun. ج. 275 ع. 1: 209–16. DOI:10.1006/bbrc.2000.3252. PMID:10944466.
^ Kubo F، Takeichi M، Nakagawa S (2003). "Wnt2b controls retinal cell differentiation at the ciliary marginal zone". Development. ج. 130 ع. 3: 587–98. PMID:12490564.

قراءة متعمقة

Katoh M (2006). "WNT2B: comparative integromics and clinical applications (Review)". Int. J. Mol. Med. ج. 16 ع. 6: 1103–8. DOI:10.3892/ijmm.16.6.1103. PMID:16273293.
Smolich BD، McMahon JA، McMahon AP، Papkoff J (1994). "Wnt family proteins are secreted and associated with the cell surface". Mol. Biol. Cell. ج. 4 ع. 12: 1267–75. DOI:10.1091/mbc.4.12.1267. PMC:275763. PMID:8167409.
Bergstein I، Eisenberg LM، Bhalerao J، وآخرون (1998). "Isolation of two novel WNT genes, WNT14 and WNT15, one of which (WNT15) is closely linked to WNT3 on human chromosome 17q21". Genomics. ج. 46 ع. 3: 450–8. DOI:10.1006/geno.1997.5041. PMID:9441749.
Katoh M (2002). "Differential regulation of WNT2 and WNT2B expression in human cancer". Int. J. Mol. Med. ج. 8 ع. 6: 657–60. DOI:10.3892/ijmm.8.6.657. PMID:11712082.
Yarden RI، Brody LC (2002). "Identification of proteins that interact with BRCA1 by Far-Western library screening". J. Cell. Biochem. ج. 83 ع. 4: 521–31. DOI:10.1002/jcb.1257. PMID:11746496.
Ricken A، Lochhead P، Kontogiannea M، Farookhi R (2002). "Wnt signaling in the ovary: identification and compartmentalized expression of wnt-2, wnt-2b, and frizzled-4 mRNAs". Endocrinology. ج. 143 ع. 7: 2741–9. DOI:10.1210/en.143.7.2741. PMID:12072409.
Ota T، Suzuki Y، Nishikawa T، وآخرون (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. ج. 36 ع. 1: 40–5. DOI:10.1038/ng1285. PMID:14702039.
Katoh M (2005). "Molecular evolution of Wnt2b orthologs". Int. J. Oncol. ج. 26 ع. 4: 1135–9. DOI:10.3892/ijo.26.4.1135. PMID:15754012.
Struewing IT، Toborek A، Mao CD (2006). "Mitochondrial and nuclear forms of Wnt13 are generated via alternative promoters, alternative RNA splicing, and alternative translation start sites". J. Biol. Chem. ج. 281 ع. 11: 7282–93. DOI:10.1074/jbc.M511182200. PMID:16407296.

هذه بذرة مقالة عن جين على كروموسوم 1 بحاجة للتوسيع. فضلًا شارك في تحريرها.

[1] Katoh M، Hirai M، Sugimura T، Terada M (أكتوبر 1996). "Cloning, expression and chromosomal localization of Wnt-13, a novel member of the Wnt gene family". Oncogene. ج. 13 ع. 4: 873–6. PMID:8761309.

[2] "Entrez Gene: WNT2B wingless-type MMTV integration site family, member 2B". مؤرشف من الأصل في 2010-12-05.

[3] Katoh M، Kirikoshi H، Saitoh T، Sagara N، Koike J (سبتمبر 2000). "Alternative splicing of the WNT-2B/WNT-13 gene". Biochem Biophys Res Commun. ج. 275 ع. 1: 209–16. DOI:10.1006/bbrc.2000.3252. PMID:10944466.

[4] Kubo F، Takeichi M، Nakagawa S (2003). "Wnt2b controls retinal cell differentiation at the ciliary marginal zone". Development. ج. 130 ع. 3: 587–98. PMID:12490564.

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