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Disease Info Card
Patau Syndrome
Information about Patau Syndrome: 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 Patau Syndrome
Most recent studies have shown that Patau Syndrome shares some biological mechanisms with aneuploidy, chromosomal-translocation, cleft-lip, cleft-palate, complete-trisomy-18-syndrome, congenital-abnormality, congenital-heart-defects, cytogenetic-abnormality, down-syndrome, embryonic-mosaic, fetal-diseases, holoprosencephaly, leukemia, monosomy, partial-trisomy, polydactyly, triploidy, trisomy, turner-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Patau Syndrome, and have been seen in publications frequently: Cell Growth, Chromosome Segregation, Fertilization, Forebrain Development, Immune Response, Interphase, Limb Development, Meiosis, Meiosis I, Meiosis Ii, Mesoderm Formation, Metaphase, Mitosis, Ossification, Pathogenesis, Pigmentation, Proteolysis, Skin Development, Transport, Transposition
Quite a number of genes have been found to play important roles in Patau Syndrome, such as AFP, BBS9, BCR, CTLA4, DNTT, ESD, FANCB, FLT3, HLA-DQA1, IL31RA, LGALS13, LMOD1, NOD2, NT5E, NTM, NTS, PAPPA, PGF, TRIM26. 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.