Research of Prader-willi Syndrome has been linked to Obesity, Angelman Syndrome, Uniparental Disomy, Muscle Hypotonia, Port-wine Stain. The study of Prader-willi Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Prader-willi Syndrome include Methylation, Dna Methylation, Secretion, Pathogenesis, Meiosis. These pathways complement our catalog of research reagents for the study of Prader-willi Syndrome including antibodies and ELISA kits against GROWTH HORMONE, GHRELIN, GABRB3, GH1, IGF1.
Prader-willi Syndrome Bioinformatics Tool
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Prader-willi Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 1237 products for the study of Prader-willi Syndrome that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Flow Cytometry, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Prader-willi Syndrome is also known as prader-willi syndrome, obesity, muscular hypotonia, mental retardation, short stature, hypogonadotropic hypogonadism, and small hands and feet, prader-willi syndrome (disorder), prader - willi syndrome, prader willi syndrome.