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pathway Info Card
Somatic Hypermutation Of Immunoglobulin Genes
Information about Somatic Hypermutation Of Immunoglobulin Genes: 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 Somatic Hypermutation Of Immunoglobulin Genes
Most recent studies have shown that Somatic Hypermutation Of Immunoglobulin Genes shares some biological mechanisms with aging, b-cell-affinity-maturation, cell-development, cell-differentiation, cytidine-deamination, dna-repair, dna-replication, gene-conversion, immune-response, localization, mismatch-repair, mutualism, plasma-cell-differentiation, secretion, translesion-synthesis, v(d)j-recombination.
Among the many pathways, these few ones have gauged particular interests from scientists studying Somatic Hypermutation Of Immunoglobulin Genes, and have been seen in publications frequently: aging, b-cell-affinity-maturation, cell-development, cell-differentiation, cytidine-deamination, dna-repair, dna-replication, gene-conversion, immune-response, localization, mismatch-repair, mutualism, plasma-cell-differentiation, secretion, translesion-synthesis, v(d)j-recombination
Quite a number of genes have been found to play important roles in Somatic Hypermutation Of Immunoglobulin Genes, such as APOBEC3B, Aicda, BCL6, BLM, CDA, DNTT, FUS, HES1, MAD2L2, MSH2, MYC, PCNA, POLH, POLI, POLM, POLQ, PRDM1, Polk, REV1, REV3L. 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.