Research of Sebastian Syndrome has been linked to Fechtner Syndrome (disorder), Nephritis, Hereditary Nephritis, Blood Platelet Disorders, Complete Hearing Loss. The study of Sebastian Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Sebastian Syndrome include Pathogenesis, Localization, Platelet Aggregation, Granulocyte Differentiation. These pathways complement our catalog of research reagents for the study of Sebastian Syndrome including antibodies and ELISA kits against NONMUSCLE MYOSIN HEAVY CHAIN, MYOSIN IIA, NONMUSCLE MYOSIN HEAVY CHAIN-A, NMMHC-A, ITP.
Sebastian 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 Sebastian Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 806 products for the study of Sebastian Syndrome that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.