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Disease Info Card
Ciliary Motility Disorders
Information about Ciliary Motility Disorders: 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 Ciliary Motility Disorders
Most recent studies have shown that Ciliary Motility Disorders shares some biological mechanisms with asthma, bronchiectasis, bronchitis, chronic-sinusitis, coughing, cystic-fibrosis, dyskinetic-syndrome, ear-inflammation, fibrosis, infective-disorder, infertility, kartagener-syndrome, lung-diseases, male-infertility, respiration-disorders, respiratory-tract-diseases, respiratory-tract-infections, rhinorrhea, sinusitis, situs-inversus.
Among the many pathways, these few ones have gauged particular interests from scientists studying Ciliary Motility Disorders, and have been seen in publications frequently: Aging, Cell Cycle, Cell Differentiation, Cell Motility, Chemotaxis, Fertilization, Hypersensitivity, Inflammatory Response, Intraflagellar Transport, Localization, Mucus Secretion, Neutrophil Chemotaxis, Pathogenesis, Phagocytosis, Regeneration, Secretion, Sperm Motility, Spermatogenesis, Transport, Transposition
Quite a number of genes have been found to play important roles in Ciliary Motility Disorders, such as AK7, ALB, CFTR, COL18A1, DNAH11, DNAH5, DNAH9, DNAI1, DNASE1, FEV, IL13, MCC, MKS1, NME8, OXSM, PCBD1, RPGR, RPGRIP1L, SHH, TMEM67. 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.