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Disease Info Card
Bardet-biedl Syndrome
Information about Bardet-biedl 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 Bardet-biedl Syndrome
Most recent studies have shown that Bardet-biedl Syndrome shares some biological mechanisms with blind-vision, diabetes-mellitus, dystrophy, hereditary-diseases, hypertensive-disease, hypogonadism, kidney-diseases, kidney-failure, kidney-failure-chronic, laurence-moon-syndrome, learning-disabilities, obesity, polycystic-kidney-diseases, polydactyly, retinal-degeneration, retinal-diseases, retinal-dystrophies, retinitis-pigmentosa.
Among the many pathways, these few ones have gauged particular interests from scientists studying Bardet-biedl Syndrome, and have been seen in publications frequently: Cell Cycle, Cell Death, Cell Division, Cell Migration, Cell Proliferation, Energy Homeostasis, Excretion, Gastrulation, Intracellular Transport, Intraflagellar Transport, Limb Development, Localization, Melanosome Transport, Pathogenesis, Pigmentation, Protein Transport, Rna Interference, Secretion, Tissue Homeostasis, Transport
Quite a number of genes have been found to play important roles in Bardet-biedl Syndrome, such as ARL4D, ARL6, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, CEP290, ERG, INS, LEP, MKKS, MKS1, PCM1, RAB8A, TRIM32, TTC8. 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.