Disease and disorder research has been conducted in relation to the Fin Development Pathway and Crest Syndrome, Holt-oram Syndrome, Congenital Heart Defects, Overlying Behavior, Cryptophthalmos Syndrome. The study of the Fin Development Pathway has been mentioned in research publications which can be found using our bioinformatics tool below. The Fin Development Pathway has been researched in relation to Pectoral Fin Development, Regeneration, Limb Development, Somitogenesis, Fin Morphogenesis. The Fin Development Pathway complements our catalog of research reagents including antibodies and ELISA kits against SHH, TBX5, BMP2, BMP4, FGF4.
Fin Development 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 Fin Development below!
For more information on how to use Laverne, please read the How to Guide.
We have 839 products for the study of the Fin Development Pathway that can be applied to Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.