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Disease Info Card
Developmental Delay (disorder)
Information about Developmental Delay (disorder): 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 Developmental Delay (disorder)
Most recent studies have shown that Developmental Delay (disorder) shares some biological mechanisms with autistic-disorder, cerebral-palsy, congenital-abnormality, congenital-heart-defects, cytogenetic-abnormality, developmental-disabilities, dwarfism, epilepsy, growth-disorders, growth-retardation, hypoplasia, microcephaly, muscle-hypotonia, nervousness, trisomy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Developmental Delay (disorder), and have been seen in publications frequently: Brain Development, Cell Death, Cell Proliferation, Cognition, Embryo Development, Excretion, Fertilization, Glucose Transport, Glycosylation, Insulin Secretion, Localization, Metaphase, Methylation, Myelination, Ossification, Pathogenesis, Pigmentation, Reflex, Secretion, Transport
Quite a number of genes have been found to play important roles in Developmental Delay (disorder), such as ABCC8, AKR1C2, ATP2A2, CSF2, ENDOU, EXOSC6, FGFR3, FMR1, INS, INVS, KCNJ11, LAMC2, LMLN, MB, MECP2, NSD1, S100A10, SLC2A1. 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.