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Disease Info Card
Holoprosencephaly
Information about Holoprosencephaly: 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 Holoprosencephaly
Most recent studies have shown that Holoprosencephaly shares some biological mechanisms with alobar-holoprosencephaly, cleft-lip, cleft-palate, congenital-abnormality, congenital-absence, congenital-anomaly-of-brain, cyclocephaly, cytogenetic-abnormality, dysplasia, eye-abnormalities, fetal-diseases, hydrocephalus, hypoplasia, hypotelorism-of-orbit, microcephaly, nervousness, patau-syndrome, semi-lobar-holoprosencephaly, trisomy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Holoprosencephaly, and have been seen in publications frequently: Brain Development, Cell Death, Cell Differentiation, Cell Proliferation, Central Nervous System Development, Eye Development, Forebrain Development, Gastrulation, Head Development, Localization, Myelination, Nervous System Development, Neural Tube Closure, Pathogenesis, Secretion, Segmentation, System Development, Transport, Transposition, Tube Closure
Quite a number of genes have been found to play important roles in Holoprosencephaly, such as AVP, BMP4, CDON, DHCR7, FGF8, FUT1, GLI1, GLI2, GLI3, HFE, IL10, NODAL, PTCH1, SHH, SIX3, SS18L1, TGIF1, ZIC1, ZIC2. 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.