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- Table of Contents
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pathway Info Card
Peptidyl-tyrosine Sulfation
Information about Peptidyl-tyrosine Sulfation: 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 Peptidyl-tyrosine Sulfation
Most recent studies have shown that Peptidyl-tyrosine Sulfation shares some biological mechanisms with aging, cell-adhesion, cytolysis, detection-of-mechanical-stimulus, glucose-homeostasis, glycosylation, homophilic-cell-adhesion, iron-sulfur-cluster-assembly, jak-stat-cascade, notch-signaling-pathway, response-to-drug, rrna-processing, sulfation, translational-initiation.
Among the many pathways, these few ones have gauged particular interests from scientists studying Peptidyl-tyrosine Sulfation, and have been seen in publications frequently: aging, cell-adhesion, cytolysis, detection-of-mechanical-stimulus, glucose-homeostasis, glycosylation, homophilic-cell-adhesion, iron-sulfur-cluster-assembly, jak-stat-cascade, notch-signaling-pathway, response-to-drug, rrna-processing, sulfation, translational-initiation
Quite a number of genes have been found to play important roles in Peptidyl-tyrosine Sulfation, such as ALK, CIAO1, Fam126a, NOTCH3, NOTCH4, PTHLH, TSTA3. 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.
Diseases Related to Peptidyl-tyrosine Sulfation
This information is being compiled and will come in a future update
| carcinoma | hepatitis b | liver carcinoma |
| tissue adhesions |