WNT10B

An Error has occured retrieving Wikidata item for infobox WNT10B‏ (Wnt family member 10B) هوَ بروتين يُشَفر بواسطة جين WNT10B في الإنسان.^[1]^[2]^[3]^[3]^[4]^[5]^[6]

الوظيفة

الأهمية السريرية

المراجع

^ Schubert M، Holland LZ، Holland ND، Jacobs DK (2000). "A phylogenetic tree of the Wnt genes based on all available full-length sequences, including five from the cephalochordate amphioxus". Molecular Biology and Evolution. ج. 17 ع. 12: 1896–903. DOI:10.1093/oxfordjournals.molbev.a026291. PMID:11110906.
^ Paik DT, Rai M, Ryzhov S, Sanders LN, Aisagbonhi O, Funke MJ, Feoktistov I, Hatzopoulos AK. Wnt10b gain-of-function improves cardiac repair by arteriole formation and attenuation of fibrosis. Circ Res. 2015; 117:804-816.
^ ^أ ^ب "Entrez Gene: WNT10B wingless-type MMTV integration site family, member 10B". مؤرشف من الأصل في 2010-03-07.
^ Ugur SA، Tolun A (أغسطس 2008). "Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation". Hum Mol Genet. ج. 17 ع. 17: 2644–53. DOI:10.1093/hmg/ddn164. PMID:18515319.
^ Bui TD، Rankin J، Smith K، Huguet EL، Ruben S، Strachan T، Harris AL، Lindsay S (أبريل 1997). "A novel human Wnt gene, WNT10B, maps to 12q13 and is expressed in human breast carcinomas". Oncogene. ج. 14 ع. 10: 1249–53. DOI:10.1038/sj.onc.1200936. PMID:9121776.
^ Hardiman G، Kastelein RA، Bazan JF (سبتمبر 1997). "Isolation, characterization and chromosomal localization of human WNT10B". Cytogenet Cell Genet. ج. 77 ع. 3–4: 278–82. DOI:10.1159/000134597. PMID:9284937.

قراءة متعمقة

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.
Ross SE، Hemati N، Longo KA، وآخرون (2000). "Inhibition of adipogenesis by Wnt signaling". Science. ج. 289 ع. 5481: 950–3. DOI:10.1126/science.289.5481.950. PMID:10937998.
Kirikoshi H، Sekihara H، Katoh M (2001). "WNT10A and WNT6, clustered in human chromosome 2q35 region with head-to-tail manner, are strongly coexpressed in SW480 cells". Biochem. Biophys. Res. Commun. ج. 283 ع. 4: 798–805. DOI:10.1006/bbrc.2001.4855. PMID:11350055.
Saitoh T، Kirikoshi H، Mine T، Katoh M (2002). "Proto-oncogene WNT10B is up-regulated by tumor necrosis factor alpha in human gastric cancer cell line MKN45". Int. J. Oncol. ج. 19 ع. 6: 1187–92. DOI:10.3892/ijo.19.6.1187. PMID:11713588.
Kasat K، Go V، Pogo BG (2003). "Effects of pyrethroid insecticides and estrogen on WNT10B proto-oncogene expression". Environment international. ج. 28 ع. 5: 429–32. DOI:10.1016/S0160-4120(02)00072-7. PMID:12437293.
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.
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.
Christodoulides C، Scarda A، Granzotto M، وآخرون (2006). "WNT10B mutations in human obesity". Diabetologia. ج. 49 ع. 4: 678–84. DOI:10.1007/s00125-006-0144-4. PMC:4304000. PMID:16477437.
Thrasivoulou C، Millar M، Ahmed A (2013). "Activation of intracellular calcium by multiple Wnt ligands and translocation of ß-catenin into the nucleus: a convergent model of Wnt/Ca2+ and Wnt/ß-catenin pathways". J. Biol. Chem. ج. 288 ع. 50: 35651–35659. DOI:10.1074/jbc.M112.437913. PMC:3861617. PMID:24158438. {{استشهاد بدورية محكمة}}: الوسيط غير المعروف |last-author-amp= تم تجاهله يقترح استخدام |name-list-style= (مساعدة)

هذه بذرة مقالة عن جين على كروموسوم 12 بحاجة للتوسيع. فضلًا شارك في تحريرها.

[1] Schubert M، Holland LZ، Holland ND، Jacobs DK (2000). "A phylogenetic tree of the Wnt genes based on all available full-length sequences, including five from the cephalochordate amphioxus". Molecular Biology and Evolution. ج. 17 ع. 12: 1896–903. DOI:10.1093/oxfordjournals.molbev.a026291. PMID:11110906.

[2] Paik DT, Rai M, Ryzhov S, Sanders LN, Aisagbonhi O, Funke MJ, Feoktistov I, Hatzopoulos AK. Wnt10b gain-of-function improves cardiac repair by arteriole formation and attenuation of fibrosis. Circ Res. 2015; 117:804-816.

[entrez-3] أ ^ب "Entrez Gene: WNT10B wingless-type MMTV integration site family, member 10B". مؤرشف من الأصل في 2010-03-07.

[pmid18515319-4] Ugur SA، Tolun A (أغسطس 2008). "Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation". Hum Mol Genet. ج. 17 ع. 17: 2644–53. DOI:10.1093/hmg/ddn164. PMID:18515319.

[pmid9121776-5] Bui TD، Rankin J، Smith K، Huguet EL، Ruben S، Strachan T، Harris AL، Lindsay S (أبريل 1997). "A novel human Wnt gene, WNT10B, maps to 12q13 and is expressed in human breast carcinomas". Oncogene. ج. 14 ع. 10: 1249–53. DOI:10.1038/sj.onc.1200936. PMID:9121776.

[pmid9284937-6] Hardiman G، Kastelein RA، Bazan JF (سبتمبر 1997). "Isolation, characterization and chromosomal localization of human WNT10B". Cytogenet Cell Genet. ج. 77 ع. 3–4: 278–82. DOI:10.1159/000134597. PMID:9284937.

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