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Disease Info Card
Alstrom Syndrome
Information about Alstrom 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 Alstrom Syndrome
Most recent studies have shown that Alstrom Syndrome shares some biological mechanisms with acanthosis-nigricans, bardet-biedl-syndrome, blind-vision, cardiomyopathies, complete-hearing-loss, diabetes-mellitus, diabetes-mellitus-non-insulin-dependent, dwarfism, hereditary-diseases, hyperinsulinism, hypertensive-disease, insulin-resistance, kidney-diseases, neuroblastoma, obesity, retinal-degeneration, retinitis-pigmentosa, sensorineural-hearing-loss-(disorder).
Among the many pathways, these few ones have gauged particular interests from scientists studying Alstrom Syndrome, and have been seen in publications frequently: Anaphase, Bicarbonate Transport, Cell Activation, Cell Adhesion, Cell Cycle, Cell Death, Cell Migration, Cilium Assembly, Cytokinesis, Intracellular Transport, Keratinocyte Differentiation, Localization, Pathogenesis, Programmed Cell Death, Secretion, Sexual Reproduction, Stem Cell Proliferation, T Cell Activation, Transport, Wound Healing
Quite a number of genes have been found to play important roles in Alstrom Syndrome, such as ALMS1, BBS2, CASP8, CBLB, CFLAR, CXCR4, FADD, IL2, INS, MADD, MKKS, MYCN, NFKB1, NLRP3, RALBP1, RPGRIP1L, SLC4A4, SLC4A5, TNF. 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.