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Disease Info Card
Anterior Segment Mesenchymal Dysgenesis
Information about Anterior Segment Mesenchymal Dysgenesis: 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 Anterior Segment Mesenchymal Dysgenesis
Most recent studies have shown that Anterior Segment Mesenchymal Dysgenesis shares some biological mechanisms with aniridia, aphakia, cataract, congenital-abnormality, congenital-anomaly-of-brain, corneal-diseases, eye-abnormalities, hyperplasia, irido-corneal-dysgenesis, irido-corneo-trabecular-dysgenesis-(disorder), keloid, lens-diseases, lens-subluxation, microphthalmos, nervousness, neurocutaneous-syndromes, orbital-separation-excessive, tissue-adhesions.
Among the many pathways, these few ones have gauged particular interests from scientists studying Anterior Segment Mesenchymal Dysgenesis, and have been seen in publications frequently: Brain Development, Cell Cycle, Cell Differentiation
Quite a number of genes have been found to play important roles in Anterior Segment Mesenchymal Dysgenesis, such as CDKN1B, CDKN1C, CHP1, DCTN3, DYNC1H1, FLNA, FOXE3, GYPE, PAX6, PITX1, PITX2, PITX3, PROX1, STS. 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.
Pathways Related to Anterior Segment Mesenchymal Dysgenesis
This information is being compiled and will come in a future update
| Brain Development | Cell Cycle | Cell Differentiation |