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Disease Info Card
Rett Syndrome
Information about Rett 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 Rett Syndrome
Most recent studies have shown that Rett Syndrome shares some biological mechanisms with angelman-syndrome, ataxia, atrophy, autism-spectrum-disorders, autistic-disorder, brain-diseases, dementia, developmental-disabilities, encephalopathies, epilepsy, fragile-x-syndrome, microcephaly, movement-disorders, nervous-system-disorder, nervousness, scoliosis-unspecified, stereotyped-behavior.
Among the many pathways, these few ones have gauged particular interests from scientists studying Rett Syndrome, and have been seen in publications frequently: Aging, Brain Development, Chromatin Remodeling, Cognition, Dna Methylation, Gene Silencing, Histone Modification, Innervation, Localization, Locomotion, Methylation, Neurogenesis, Pathogenesis, Reflex, Regulation Of Gene Expression, Secretion, Social Behavior, Synaptic Transmission, Translation, Transport
Quite a number of genes have been found to play important roles in Rett Syndrome, such as AR, BDNF, CDKL5, CSF2, CXXC1, DLX5, DPEP1, FMR1, FOXG1, LAMC2, MBD1, MBD2, MECP2, NGF, POMC, TAC1, UBE3A. 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.