EFEMP2

An Error has occured retrieving Wikidata item for infobox EFEMP2‏ (EGF containing fibulin extracellular matrix protein 2) هوَ بروتين يُشَفر بواسطة جين EFEMP2 في الإنسان.^[1]^[1]^[2]^[3]

الوظيفة

الأهمية السريرية

المراجع

^ ^أ ^ب "Entrez Gene: EFEMP2 EGF-containing fibulin-like extracellular matrix protein 2". مؤرشف من الأصل في 2010-03-07.
^ Giltay R، Timpl R، Kostka G (فبراير 2000). "Sequence, recombinant expression and tissue localization of two novel extracellular matrix proteins, fibulin-3 and fibulin-4". Matrix Biol. ج. 18 ع. 5: 469–80. DOI:10.1016/S0945-053X(99)00038-4. PMID:10601734.
^ Katsanis N، Venable S، Smith JR، Lupski JR (سبتمبر 2000). "Isolation of a paralog of the Doyne honeycomb retinal dystrophy gene from the multiple retinopathy critical region on 11q13". Hum Genet. ج. 106 ع. 1: 66–72. DOI:10.1007/s004390051011. PMID:10982184.

قراءة متعمقة

Gallagher WM، Argentini M، Sierra V، وآخرون (1999). "MBP1: a novel mutant p53-specific protein partner with oncogenic properties". Oncogene. ج. 18 ع. 24: 3608–16. DOI:10.1038/sj.onc.1202937. PMID:10380882.
Gallagher WM، Greene LM، Ryan MP، وآخرون (2001). "Human fibulin-4: analysis of its biosynthetic processing and mRNA expression in normal and tumour tissues". FEBS Lett. ج. 489 ع. 1: 59–66. DOI:10.1016/S0014-5793(00)02389-9. PMID:11231014.
Wistow G، Bernstein SL، Wyatt MK، وآخرون (2002). "Expressed sequence tag analysis of human retina for the NEIBank Project: retbindin, an abundant, novel retinal cDNA and alternative splicing of other retina-preferred gene transcripts". Mol. Vis. ج. 8: 196–204. PMID:12107411.
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. Bibcode:2002PNAS...9916899M. DOI:10.1073/pnas.242603899. PMC:139241. PMID:12477932.
Clark HF، Gurney AL، Abaya E، وآخرون (2003). "The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment". Genome Res. ج. 13 ع. 10: 2265–70. DOI:10.1101/gr.1293003. PMC:403697. PMID:12975309.
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.
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.
Rual JF، Venkatesan K، Hao T، وآخرون (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. ج. 437 ع. 7062: 1173–8. Bibcode:2005Natur.437.1173R. DOI:10.1038/nature04209. PMID:16189514.
Otsuki T، Ota T، Nishikawa T، وآخرون (2007). "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries". DNA Res. ج. 12 ع. 2: 117–26. DOI:10.1093/dnares/12.2.117. PMID:16303743.
Xiang Y، Sekine T، Nakamura H، وآخرون (2006). "Fibulin-4 is a target of autoimmunity predominantly in patients with osteoarthritis". J. Immunol. ج. 176 ع. 5: 3196–204. DOI:10.4049/jimmunol.176.5.3196. PMID:16493080.
Taylor TD، Noguchi H، Totoki Y، وآخرون (2006). "Human chromosome 11 DNA sequence and analysis including novel gene identification". Nature. ج. 440 ع. 7083: 497–500. Bibcode:2006Natur.440..497T. DOI:10.1038/nature04632. PMID:16554811.
Hucthagowder V، Sausgruber N، Kim KH، وآخرون (2006). "Fibulin-4: a novel gene for an autosomal recessive cutis laxa syndrome". Am. J. Hum. Genet. ج. 78 ع. 6: 1075–80. DOI:10.1086/504304. PMC:1474103. PMID:16685658.
El-Hallous E، Sasaki T، Hubmacher D، وآخرون (2007). "Fibrillin-1 interactions with fibulins depend on the first hybrid domain and provide an adaptor function to tropoelastin". J. Biol. Chem. ج. 282 ع. 12: 8935–46. DOI:10.1074/jbc.M608204200. PMID:17255108.

هذه بذرة مقالة عن بروتين بحاجة للتوسيع. فضلًا شارك في تحريرها.

[entrez-1] أ ^ب "Entrez Gene: EFEMP2 EGF-containing fibulin-like extracellular matrix protein 2". مؤرشف من الأصل في 2010-03-07.

[pmid10601734-2] Giltay R، Timpl R، Kostka G (فبراير 2000). "Sequence, recombinant expression and tissue localization of two novel extracellular matrix proteins, fibulin-3 and fibulin-4". Matrix Biol. ج. 18 ع. 5: 469–80. DOI:10.1016/S0945-053X(99)00038-4. PMID:10601734.

[pmid10982184-3] Katsanis N، Venable S، Smith JR، Lupski JR (سبتمبر 2000). "Isolation of a paralog of the Doyne honeycomb retinal dystrophy gene from the multiple retinopathy critical region on 11q13". Hum Genet. ج. 106 ع. 1: 66–72. DOI:10.1007/s004390051011. PMID:10982184.

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