This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Disease Info Card
Cri Du Chat
Information about Cri Du Chat: 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 Cri Du Chat
Most recent studies have shown that Cri Du Chat shares some biological mechanisms with autistic-disorder, chromosomal-translocation, congenital-abnormality, cornelia-de-lange-syndrome, cri-du-chat-syndrome, cytogenetic-abnormality, developmental-disabilities, down-syndrome, embryonic-mosaic, hereditary-diseases, loss-of-chromosome-5, microcephaly, micrognathism, monosomy, multiple-congenital-anomalies, muscle-hypotonia, orbital-separation-excessive, partial-trisomy, trisomy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Cri Du Chat, and have been seen in publications frequently: Cell Adhesion, Cell Division, Cell Proliferation, Cognition, Dna Replication, Endocytosis, Fertilization, Hypersensitivity, Interphase, Localization, Male Sex Determination, Metaphase, Mitosis, Rumination, Sex Determination, Telomere Maintenance, Tooth Eruption
Quite a number of genes have been found to play important roles in Cri Du Chat, such as CAT, CDK2AP2, CDKN2A, CDKN2B, CHAT, CRAT, EXOSC1, GLYAT, INVS, LAMTOR2, LMLN, MRPL28, NXT1, RPP14, S100A9, SH2D3C, SUB1. 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.