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Disease Info Card
Xeroderma Pigmentosum, Group B
Information about Xeroderma Pigmentosum, Group B: 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 Xeroderma Pigmentosum, Group B
Most recent studies have shown that Xeroderma Pigmentosum, Group B shares some biological mechanisms with basal-cell-carcinoma, cockayne-syndrome, dna-repair-disorder, genomic-instability, hereditary-diseases, leukemia, malignant-neoplasm-of-skin, malignant-neoplasms, melanoma, neoplasms, papilloma, photosensitivity-disorders, skin-neoplasms, trichothiodystrophy-syndromes, xeroderma, xeroderma-pigmentosum, xeroderma-pigmentosum-complementation-group-a, xeroderma-pigmentosum-group-d, xeroderma-pigmentosum-group-f, xeroderma-pigmentosum-group-g.
Among the many pathways, these few ones have gauged particular interests from scientists studying Xeroderma Pigmentosum, Group B, and have been seen in publications frequently: Cell Cycle, Cell Death, Cellular Homeostasis, Dna Excision, Dna Repair, Dna Replication, Drug Resistance, Hypersensitivity, Induction Of Apoptosis, Localization, Mrna Transcription, Pathogenesis, Programmed Cell Death, Response To Uv, S Phase, Senescence, Sensitization, Somatic Hypermutation Of Immunoglobulin Genes, Translation
Quite a number of genes have been found to play important roles in Xeroderma Pigmentosum, Group B, such as BCR, BTN2A2, CS, DCTN4, ERCC1, ERCC2, ERCC3, ERCC5, GTF2H1, GTF2H2, GTF2H3, GTF2H4, GTF2H5, NR1H2, PCNA, TP53, XPA, XPC. 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 disease. Plesae stay updated.