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- Table of Contents
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pathway Info Card
Dna Deamination
Information about Dna Deamination: 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 Dna Deamination
Most recent studies have shown that Dna Deamination shares some biological mechanisms with cell-activation, cytidine-deamination, dna-cytosine-deamination, dna-recombination, dna-repair, dna-replication, electron-transport, gene-conversion, immune-response, isotype-switching, localization, meiosis, mismatch-repair, oncogenesis, pathogenesis, reverse-transcription, t-cell-activation, transport, transposition, v(d)j-recombination.
Among the many pathways, these few ones have gauged particular interests from scientists studying Dna Deamination, and have been seen in publications frequently: cell-activation, cytidine-deamination, dna-cytosine-deamination, dna-recombination, dna-repair, dna-replication, electron-transport, gene-conversion, immune-response, isotype-switching, localization, meiosis, mismatch-repair, oncogenesis, pathogenesis, reverse-transcription, t-cell-activation, transport, transposition, v(d)j-recombination
Quite a number of genes have been found to play important roles in Dna Deamination, such as A4GALT, APEX1, APOBEC1, APOBEC2, APOBEC3B, APOBEC3G, Aicda, Apobec3, B3GALNT1, CDA, CDKN1A, IL4, MSH2, MSH6, SCARA3, SMUG1, UNG. 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.