EPB41L3
EPB41L3 (Erythrocyte membrane protein band 4.1 like 3) هوَ بروتين يُشَفر بواسطة جين EPB41L3 في الإنسان.[1][2][3]
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
- ^ Tran YK، Bögler O، Gorse KM، Wieland I، Green MR، Newsham IF (يناير 1999). "A novel member of the NF2/ERM/4.1 superfamily with growth suppressing properties in lung cancer". Cancer Research. ج. 59 ع. 1: 35–43. PMID:9892180.
- ^ "Entrez Gene: EPB41L3 erythrocyte membrane protein band 4.1-like 3". مؤرشف من الأصل في 2010-12-05.
- ^ Peters LL، Weier HU، Walensky LD، Snyder SH، Parra M، Mohandas N، Conboy JG (ديسمبر 1998). "Four paralogous protein 4.1 genes map to distinct chromosomes in mouse and human". Genomics. ج. 54 ع. 2: 348–50. DOI:10.1006/geno.1998.5537. PMID:9828140.
قراءة متعمقة
- Calinisan V، Gravem D، Chen RP، Brittin S، Mohandas N، Lecomte MC، Gascard P (2006). "New insights into potential functions for the protein 4.1 superfamily of proteins in kidney epithelium". Frontiers in Bioscience. ج. 11: 1646–66. DOI:10.2741/1911. PMID:16368544.
- Adams MD، Kerlavage AR، Fleischmann RD، Fuldner RA، Bult CJ، Lee NH، Kirkness EF، Weinstock KG، Gocayne JD، White O (سبتمبر 1995). "Initial assessment of human gene diversity and expression patterns based upon 83 million nucleotides of cDNA sequence" (PDF). Nature. ج. 377 ع. 6547 Suppl: 3–174. PMID:7566098. مؤرشف من الأصل (PDF) في 2016-03-04.
- Adams MD، Soares MB، Kerlavage AR، Fields C، Venter JC (أغسطس 1993). "Rapid cDNA sequencing (expressed sequence tags) from a directionally cloned human infant brain cDNA library". Nature Genetics. ج. 4 ع. 4: 373–80. DOI:10.1038/ng0893-373. PMID:8401585.
- Nagase T، Ishikawa K، Suyama M، Kikuno R، Hirosawa M، Miyajima N، Tanaka A، Kotani H، Nomura N، Ohara O (فبراير 1999). "Prediction of the coding sequences of unidentified human genes. XIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro". DNA Research. ج. 6 ع. 1: 63–70. DOI:10.1093/dnares/6.1.63. PMID:10231032.
- Gutmann DH، Donahoe J، Perry A، Lemke N، Gorse K، Kittiniyom K، Rempel SA، Gutierrez JA، Newsham IF (يونيو 2000). "Loss of DAL-1, a protein 4.1-related tumor suppressor, is an important early event in the pathogenesis of meningiomas". Human Molecular Genetics. ج. 9 ع. 10: 1495–500. DOI:10.1093/hmg/9.10.1495. PMID:10888600.
- Yu T، Robb VA، Singh V، Gutmann DH، Newsham IF (أغسطس 2002). "The 4.1/ezrin/radixin/moesin domain of the DAL-1/Protein 4.1B tumour suppressor interacts with 14-3-3 proteins". The Biochemical Journal. ج. 365 ع. Pt 3: 783–9. DOI:10.1042/BJ20020060. PMC:1222735. PMID:11996670.
- Charboneau AL، Singh V، Yu T، Newsham IF (يوليو 2002). "Suppression of growth and increased cellular attachment after expression of DAL-1 in MCF-7 breast cancer cells". International Journal of Cancer. ج. 100 ع. 2: 181–8. DOI:10.1002/ijc.10470. PMID:12115567.
- Yageta M، Kuramochi M، Masuda M، Fukami T، Fukuhara H، Maruyama T، Shibuya M، Murakami Y (سبتمبر 2002). "Direct association of TSLC1 and DAL-1, two distinct tumor suppressor proteins in lung cancer". Cancer Research. ج. 62 ع. 18: 5129–33. PMID:12234973.
- Nakayama M، Kikuno R، Ohara O (نوفمبر 2002). "Protein-protein interactions between large proteins: two-hybrid screening using a functionally classified library composed of long cDNAs". Genome Research. ج. 12 ع. 11: 1773–84. DOI:10.1101/gr.406902. PMC:187542. PMID:12421765.
- Heinrich B، Hartmann C، Stemmer-Rachamimov AO، Louis DN، MacCollin M (فبراير 2003). "Multiple meningiomas: Investigating the molecular basis of sporadic and familial forms". International Journal of Cancer. ج. 103 ع. 4: 483–8. DOI:10.1002/ijc.10840. PMID:12478663.
- Denisenko-Nehrbass N، Oguievetskaia K، Goutebroze L، Galvez T، Yamakawa H، Ohara O، Carnaud M، Girault JA (يناير 2003). "Protein 4.1B associates with both Caspr/paranodin and Caspr2 at paranodes and juxtaparanodes of myelinated fibres". The European Journal of Neuroscience. ج. 17 ع. 2: 411–6. DOI:10.1046/j.1460-9568.2003.02441.x. PMID:12542678.
- Robb VA، Li W، Gutmann DH (أبريل 2004). "Disruption of 14-3-3 binding does not impair Protein 4.1B growth suppression". Oncogene. ج. 23 ع. 20: 3589–96. DOI:10.1038/sj.onc.1207445. PMID:15116094.
- Kittiniyom K، Mastronardi M، Roemer M، Wells WA، Greenberg ER، Titus-Ernstoff L، Newsham IF (يوليو 2004). "Allele-specific loss of heterozygosity at the DAL-1/4.1B (EPB41L3) tumor-suppressor gene locus in the absence of mutation". Genes, Chromosomes & Cancer. ج. 40 ع. 3: 190–203. DOI:10.1002/gcc.20034. PMID:15138999.
- Jin J، Smith FD، Stark C، Wells CD، Fawcett JP، Kulkarni S، Metalnikov P، O'Donnell P، Taylor P، Taylor L، Zougman A، Woodgett JR، Langeberg LK، Scott JD، Pawson T (أغسطس 2004). "Proteomic, functional, and domain-based analysis of in vivo 14-3-3 binding proteins involved in cytoskeletal regulation and cellular organization". Current Biology. ج. 14 ع. 16: 1436–50. DOI:10.1016/j.cub.2004.07.051. PMID:15324660.
- Singh V، Miranda TB، Jiang W، Frankel A، Roemer ME، Robb VA، Gutmann DH، Herschman HR، Clarke S، Newsham IF (أكتوبر 2004). "DAL-1/4.1B tumor suppressor interacts with protein arginine N-methyltransferase 3 (PRMT3) and inhibits its ability to methylate substrates in vitro and in vivo". Oncogene. ج. 23 ع. 47: 7761–71. DOI:10.1038/sj.onc.1208057. PMID:15334060.
- Ballif BA، Villén J، Beausoleil SA، Schwartz D، Gygi SP (نوفمبر 2004). "Phosphoproteomic analysis of the developing mouse brain". Molecular & Cellular Proteomics. ج. 3 ع. 11: 1093–101. DOI:10.1074/mcp.M400085-MCP200. PMID:15345747.
{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
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