OGN
اُستئوگلیسین (انگلیسی: Osteoglycin) که با نام «میمیکَن» هم شناخته میشود، نام پروتئینی است که در انسان توسط ژن «OGN» کُد میشود.[4]
این پروتئین در کنار TGF-β موجب استخوانسازی نابجا در بافتهای دیگر میشود.
میزان بیان ژنی این پروتئین، با بروز کاردیومگالی و بهویژه هیپرتروفی بطن چپ در ارتباط است.[5][6]
منابع
- GRCm38: Ensembl release 89: ENSMUSG00000021390 - Ensembl, May 2017
- "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- "Entrez Gene: OGN osteoglycin".
- "Big hearts 'have genetic problem'". Health. BBC News. 2008-06-06. Retrieved 2008-06-07.
- Petretto E, Sarwar R, Grieve I, Lu H, Kumaran MK, Muckett PJ, Mangion J, Schroen B, Benson M, Punjabi PP, Prasad SK, Pennell DJ, Kiesewetter C, Tasheva ES, Corpuz LM, Webb MD, Conrad GW, Kurtz TW, Kren V, Fischer J, Hubner N, Pinto YM, Pravenec M, Aitman TJ, Cook SA (May 2008). "Integrated genomic approaches implicate osteoglycin (Ogn) in the regulation of left ventricular mass". Nat. Genet. 40 (5): 546–52. doi:10.1038/ng.134. PMC 2742198. PMID 18443592.
- مشارکتکنندگان ویکیپدیا. «OGN (gene)». در دانشنامهٔ ویکیپدیای انگلیسی، بازبینیشده در ۲۲ دسامبر ۲۰۱۷.
بیشتر بخوانید
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