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2024年12月25日 · FGB (Fibrinogen Beta Chain) is a Protein Coding gene. Diseases associated with FGB include Dysfibrinogenemia, Congenital and Afibrinogenemia, Congenital. Among its …

该基因编码的蛋白质是纤维蛋白原的β成分，纤维蛋白原是一种由三对不同的多肽链组成的血源性糖蛋白。 血管损伤后，纤维蛋白原被凝血酶裂解形成纤维蛋白，它是血块中最丰富的成分。 …

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Fibrinogen beta chain, also known as FGB, is a gene found in humans and most other vertebrates with a similar system of blood coagulation. The protein encoded by this gene is the beta …

In this review we discuss regulation of the fibrinogen genes from proximal promoters and enhancers, the influence of acute-phase stimulation, post-transcriptional regulation by miRNAs …

2025年1月5日 · The protein encoded by this gene is the beta component of fibrinogen, a blood-borne glycoprotein comprised of three pairs of nonidentical polypeptide chains. Following …

Gene ID: 2244, updated on 8-Feb-2025. The protein encoded by this gene is the beta component of fibrinogen, a blood-borne glycoprotein comprised of three pairs of nonidentical polypeptide …

Congenital fibrinogen deficiencies are rare bleeding disorders, characterized by extensive genetic heterogeneity in all the three genes: FGA, FGB, and FGG (enconding the Aα, Bβ, and γ chain, …

2025年2月8日 · The protein encoded by this gene is the beta component of fibrinogen, a blood-borne glycoprotein comprised of three pairs of nonidentical polypeptide chains. Following …