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Disease Info Card
Blepharophimosis
Information about Blepharophimosis: 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 Blepharophimosis
Most recent studies have shown that Blepharophimosis shares some biological mechanisms with blepharophimosis-syndrome, blepharoptosis, cleft-palate, congenital-abnormality, congenital-epicanthus, cytogenetic-abnormality, developmental-delay-(disorder), developmental-disabilities, dwarfism, eye-abnormalities, eyelid-diseases, growth-retardation, hypoplasia, microcephaly, micrognathism, muscle-contracture, ovarian-failure-premature, premature-menopause.
Among the many pathways, these few ones have gauged particular interests from scientists studying Blepharophimosis, and have been seen in publications frequently: Aging, Bone Maturation, Cell Cycle, Cell Death, Cell Proliferation, Female Sex Determination, Interphase, Limb Development, Localization, Menopause, Muscle Hypertrophy, Myelination, Pathogenesis, Pigmentation, Proteolysis, Reflex, Regulation Of Gene Expression, Sex Determination, System Development, Transdifferentiation
Quite a number of genes have been found to play important roles in Blepharophimosis, such as ATR, CDKN2B, DIAPH2, DLK1, FMR1, FOXL2, KAT6B, LHCGR, MRPL28, NXT1, RBP1, SIRT1, SOX14, SRY, SUB1, TWIST1. 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.