This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
Information about Pronephros Formation: 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.
Most recent studies have shown that Pronephros Formation shares some biological mechanisms with convergent-extension, eye-development, gastrulation, kidney-development, pronephros-development, pronephros-morphogenesis, ribosome-assembly, translation.
Among the many pathways, these few ones have gauged particular interests from scientists studying Pronephros Formation, and have been seen in publications frequently: convergent-extension, eye-development, gastrulation, kidney-development, pronephros-development, pronephros-morphogenesis, ribosome-assembly, translation
Quite a number of genes have been found to play important roles in Pronephros Formation, such as DBT, E4F1, EIF6, Gstk1, HNF1A, HNF1B, HNRNPC, Invs, LHX1, MAPK8, NOG, Osr2, PAX8, SFRP2, SNAI2, SS18L1, ZFP36L1. 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 pathway. Plesae stay updated.
congenital abnormality | congenital absence | crest syndrome |
cystic kidney diseases | diabetes mellitus | diabetes mellitus non insulin dependent |
dysplasia | edema | hypoplasia |
kidney diseases | nephronophthisis |