This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Disease Info Card
Russell-silver Syndrome
Information about Russell-silver 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 Russell-silver Syndrome
Most recent studies have shown that Russell-silver Syndrome shares some biological mechanisms with beckwith-wiedemann-syndrome, clinodactyly, craniofacial-abnormalities, craniofacial-dysostosis, cytogenetic-abnormality, diabetes-mellitus, dwarfism, embryonic-mosaic, fetal-growth-retardation, growth-disorders, growth-retardation, macrocephaly, prader-willi-syndrome, precocious-puberty, shwachman-syndrome, trisomy, uniparental-disomy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Russell-silver Syndrome, and have been seen in publications frequently: Aging, Angiogenesis, Bone Maturation, Cell Death, Cell Proliferation, Demethylation, Dna Hypomethylation, Dna Methylation, Fertilization, Glycosylation, Growth Hormone Secretion, Hormone Secretion, Localization, Meiosis, Meiosis I, Methylation, Pathogenesis, Pigmentation, Secretion, Transport
Quite a number of genes have been found to play important roles in Russell-silver Syndrome, such as BSCL2, CDKN1C, EGFR, GGH, GH1, GRB10, IGF1, IGF1R, IGF2, IGFBP1, IGFBP3, MEST, SMS, TGM1, UROD, WDR20. 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.