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Disease Info Card
Branchiootic Syndrome 1
Information about Branchiootic Syndrome 1: 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 Branchiootic Syndrome 1
Most recent studies have shown that Branchiootic Syndrome 1 shares some biological mechanisms with branchio-oto-renal-syndrome, bronchiolitis, bronchiolitis-obliterans, chromosomal-duplication, congenital-abnormality, developmental-delay-(disorder), dwarfism, goldenhar-syndrome-with-ipsilateral-radial-defect, malnutrition, multiple-congenital-anomalies, physiological-stress, plant-diseases, stresses-oxidative, trisomy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Branchiootic Syndrome 1, and have been seen in publications frequently: Cell Death, Cellular Localization, Defense Response, Disease Resistance, Hypersensitivity, Localization, Membrane Fusion, Pathogenesis, Protein Transport, Rna Interference, Secretion, Secretory Pathway, Snare Complex Assembly, Sporulation, Transport, Vesicle Docking, Vesicle Fusion, Vesicle Targeting, Vesicle Transport, Virulence
Quite a number of genes have been found to play important roles in Branchiootic Syndrome 1, such as AGFG1, ARF1, BET1, EYA1, GOSR1, GOSR2, IL6, NAPG, RAB1A, SCFD1, SEC22A, SEC61A1, SIX1, SNAP25, STX5, VTI1B, YKT6. 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.