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Disease Info Card
Bloch Sulzberger Syndrome
Information about Bloch Sulzberger Syndrome: 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 Bloch Sulzberger Syndrome
Most recent studies have shown that Bloch Sulzberger Syndrome shares some biological mechanisms with dermatologic-disorders, dysplasia, ectodermal-dysplasia, embryonic-mosaic, exanthema, eye-abnormalities, hyperpigmentation, hypopigmentation-disorder, incontinentia-pigmenti-achromians, melanocytic-nevus, nervousness, neurocutaneous-syndromes, pigmentation-disorders, retinal-detachment, retinal-diseases, skin-diseases-genetic, skin-neoplasms, tooth-abnormalities.
Among the many pathways, these few ones have gauged particular interests from scientists studying Bloch Sulzberger Syndrome, and have been seen in publications frequently: Cell Adhesion, Cell Maturation, Chemotaxis, Exocytosis, Fertilization, Gene Conversion, Gene Silencing, Hair Follicle Morphogenesis, Immune Response, Localization, Methylation, Myelination, Neutrophil Chemotaxis, Pathogenesis, Phagocytosis, Pigmentation, Response To Tumor Necrosis Factor, Skin Development, Tooth Eruption, Translation
Quite a number of genes have been found to play important roles in Bloch Sulzberger Syndrome, such as AR, CCL11, CHUK, ENDOU, EXOSC6, F8, G6PD, IKBKB, IKBKE, IKBKG, NFKB1, POMC, S100A10, TNF, UBL4A. 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.