Research of Raine Syndrome has been linked to Osteosclerosis, Bone Diseases, Developmental, Dysplasia, Microcephaly, Exophthalmos. The study of Raine Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Raine Syndrome include Protein Phosphorylation, Secretory Pathway, Osteoblast Differentiation, Bone Development, Blood Circulation. These pathways complement our catalog of research reagents for the study of Raine Syndrome including antibodies and ELISA kits against OSTEOSCLEROTIC, DMP4, CHONDRODYSPLASIA, E14, GOLGI-LOCALIZED PROTEIN.
Raine 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 Raine Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 169 products for the study of Raine Syndrome that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Raine Syndrome is also known as raine syndrome, combination of microcephaly, exophthalmos, hypoplastic nose and midface, gum hyperplasia, cleft palate, apparently low-set ears, and osteosclerosis, osteosclerotic dysplasia, neonatal severe, lethal osteosclerotic bone dysplasia, osteosclerosis.