pathway Info Card

Amyloid Fibril Formation

Information about Amyloid Fibril Formation: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.

Overview of Amyloid Fibril Formation

Most recent studies have shown that Amyloid Fibril Formation shares some biological mechanisms with aging, cell-adhesion, cell-death, cytokine-production, endocytosis, glycosylation, hyperphosphorylation, immune-response, insulin-secretion, lipid-oxidation, pathogenesis, phagocytosis, protein-folding, protein-stabilization, protein-unfolding, proteolysis, secretion, translation, transport, tropism.

Among the many pathways, these few ones have gauged particular interests from scientists studying Amyloid Fibril Formation, and have been seen in publications frequently: aging, cell-adhesion, cell-death, cytokine-production, endocytosis, glycosylation, hyperphosphorylation, immune-response, insulin-secretion, lipid-oxidation, pathogenesis, phagocytosis, protein-folding, protein-stabilization, protein-unfolding, proteolysis, secretion, translation, transport, tropism

Quite a number of genes have been found to play important roles in Amyloid Fibril Formation, such as ABCB6, ACHE, APOA1, APOC2, APP, C4BPA, CARD14, CEL, FAP, GLMN, IAPP, INS, LYZ, PRDX2, PRNP, SFTPC, SNCA, TNFSF14, TTR. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this pathway. Plesae stay updated.