FCN3

An Error has occured retrieving Wikidata item for infobox FCN3‏ (Ficolin 3) هوَ بروتين يُشَفر بواسطة جين FCN3 في الإنسان.^[1]^[2]^[3]

الوظيفة

الأهمية السريرية

المراجع

^ Akaiwa M، Yae Y، Sugimoto R، Suzuki SO، Iwaki T، Izuhara K، Hamasaki N (يونيو 1999). "Hakata antigen, a new member of the ficolin/opsonin p35 family, is a novel human lectin secreted into bronchus/alveolus and bile". J Histochem Cytochem. ج. 47 ع. 6: 777–86. DOI:10.1177/002215549904700607. PMID:10330454.
^ "Entrez Gene: FCN3 ficolin (collagen/fibrinogen domain containing) 3 (Hakata antigen)". مؤرشف من الأصل في 2010-03-07.
^ Sugimoto R، Yae Y، Akaiwa M، Kitajima S، Shibata Y، Sato H، Hirata J، Okochi K، Izuhara K، Hamasaki N (سبتمبر 1998). "Cloning and characterization of the Hakata antigen, a member of the ficolin/opsonin p35 lectin family". J Biol Chem. ج. 273 ع. 33: 20721–7. DOI:10.1074/jbc.273.33.20721. PMID:9694814.

قراءة متعمقة

Yae Y، Inaba S، Sato H (1991). "Isolation and characterization of a thermolabile beta-2 macroglycoprotein ('thermolabile substance' or 'Hakata antigen') detected by precipitating (auto) antibody in sera of patients with systemic lupus erythematosus". Biochim. Biophys. Acta. ج. 1078 ع. 3: 369–76. DOI:10.1016/0167-4838(91)90158-v. PMID:1859827.
Inaba S، Okochi K، Yae Y (1991). "Serological studies of an SLE-associated antigen-antibody system discovered as a precipitation reaction in agarose gel: the HAKATA antigen-antibody system". Fukuoka Igaku Zasshi. ج. 81 ع. 9: 284–91. PMID:2276712.
Matsushita M، Kuraya M، Hamasaki N (2002). "Activation of the lectin complement pathway by H-ficolin (Hakata antigen)". J. Immunol. ج. 168 ع. 7: 3502–6. DOI:10.4049/jimmunol.168.7.3502. PMID:11907111.
Tsujimura M، Miyazaki T، Kojima E (2003). "Serum concentration of Hakata antigen, a member of the ficolins, is linked with inhibition of Aerococcus viridans growth". Clin. Chim. Acta. ج. 325 ع. 1–2: 139–46. DOI:10.1016/S0009-8981(02)00274-7. PMID:12367778.
Strausberg RL، Feingold EA، Grouse LH (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.
Zeng L، Dai J، Ying K (2003). "Identification of a novel human angiopoietin-like gene expressed mainly in heart". J. Hum. Genet. ج. 48 ع. 3: 159–62. DOI:10.1007/s100380300025. PMID:12624729.
Clark HF، Gurney AL، Abaya E (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 (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.
Anderson NL، Polanski M، Pieper R (2004). "The human plasma proteome: a nonredundant list developed by combination of four separate sources". Mol. Cell. Proteomics. ج. 3 ع. 4: 311–26. DOI:10.1074/mcp.M300127-MCP200. PMID:14718574.
Zhang Z، Henzel WJ (2005). "Signal peptide prediction based on analysis of experimentally verified cleavage sites". Protein Sci. ج. 13 ع. 10: 2819–24. DOI:10.1110/ps.04682504. PMC:2286551. PMID:15340161.
Gerhard DS، Wagner L، Feingold EA (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.
Otsuki T، Ota T، Nishikawa T (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.
Liu T، Qian WJ، Gritsenko MA (2006). "Human plasma N-glycoproteome analysis by immunoaffinity subtraction, hydrazide chemistry, and mass spectrometry". J. Proteome Res. ج. 4 ع. 6: 2070–80. DOI:10.1021/pr0502065. PMC:1850943. PMID:16335952.
Muzny DM، Scherer SE، Kaul R (2006). "The DNA sequence, annotation and analysis of human chromosome 3". Nature. ج. 440 ع. 7088: 1194–8. DOI:10.1038/nature04728. PMID:16641997.
Garlatti V، Belloy N، Martin L (2007). "Structural insights into the innate immune recognition specificities of L- and H-ficolins". EMBO J. ج. 26 ع. 2: 623–33. DOI:10.1038/sj.emboj.7601500. PMC:1783469. PMID:17215869.
Honoré C، Hummelshoj T، Hansen BE (2007). "The innate immune component ficolin 3 (Hakata antigen) mediates the clearance of late apoptotic cells". Arthritis Rheum. ج. 56 ع. 5: 1598–607. DOI:10.1002/art.22564. PMID:17469142.

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

[1] Akaiwa M، Yae Y، Sugimoto R، Suzuki SO، Iwaki T، Izuhara K، Hamasaki N (يونيو 1999). "Hakata antigen, a new member of the ficolin/opsonin p35 family, is a novel human lectin secreted into bronchus/alveolus and bile". J Histochem Cytochem. ج. 47 ع. 6: 777–86. DOI:10.1177/002215549904700607. PMID:10330454.

[2] "Entrez Gene: FCN3 ficolin (collagen/fibrinogen domain containing) 3 (Hakata antigen)". مؤرشف من الأصل في 2010-03-07.

[3] Sugimoto R، Yae Y، Akaiwa M، Kitajima S، Shibata Y، Sato H، Hirata J، Okochi K، Izuhara K، Hamasaki N (سبتمبر 1998). "Cloning and characterization of the Hakata antigen, a member of the ficolin/opsonin p35 lectin family". J Biol Chem. ج. 273 ع. 33: 20721–7. DOI:10.1074/jbc.273.33.20721. PMID:9694814.

[1]

[2]

[3]