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Disease Info Card
Skin Abnormalities
Information about Skin Abnormalities: 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 Skin Abnormalities
Most recent studies have shown that Skin Abnormalities shares some biological mechanisms with aplasia-cutis-congenita, aplasia-nos, atrophy, cardio-facio-cutaneous-syndrome, congenital-abnormality, congenital-heart-defects, costello-syndrome-(disorder), craniofacial-abnormalities, dermatologic-disorders, dwarfism, dysplasia, ectodermal-dysplasia, eye-abnormalities, growth-disorders, hypoplasia, malignant-neoplasms, melanocytic-nevus, neoplasms, skin-neoplasms.
Among the many pathways, these few ones have gauged particular interests from scientists studying Skin Abnormalities, and have been seen in publications frequently: Aging, Cell Adhesion, Cell Death, Cell Proliferation, Dna Repair, Excretion, Hair Cycle, Hair Follicle Development, Hair Follicle Morphogenesis, Keratinization, Keratinocyte Differentiation, Localization, Methylation, Pathogenesis, Pigmentation, Secretion, Skin Development, Transport, Transposition, Wound Healing
Quite a number of genes have been found to play important roles in Skin Abnormalities, such as BRAF, ELN, FBN1, FLG, FOXL2, HRAS, IKBKG, IL10, IRF6, KRAS, KRT14, LMNA, MAP2K1, MAP2K2, PTPN11, SHH, ZMPSTE24. 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.