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Congenital Ureterocele: Disease Bioinformatics
Research of Congenital Ureterocele has been linked to Ureterocele, Blepharoptosis, Urethral Diseases, Gastroesophageal Reflux Disease, Hydronephrosis. The study of Congenital Ureterocele has been mentioned in research publications which can be found using our bioinformatics tool below. Congenital Ureterocele has been researched in relation to the Peristalsis Pathway. This pathway complements our catalog of research reagents for the study of Congenital Ureterocele including antibodies and ELISA kits against TSC22D3, PIAS2, NCKIPSD.
Congenital Ureterocele 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 Congenital Ureterocele below!
For more information on how to use Laverne, please read the How to Guide
Top Research Reagents
We have 68 products for the study of Congenital Ureterocele that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Species Human, Rat
Applications WB, ELISA
Species Human, Mouse
Applications WB, IHC, IHC-P
Applications WB, ELISA, ICC/IF
Congenital Ureterocele has been researched against:
Congenital Ureterocele has been linked to:
Congenital Ureterocele has been studied in relation to diseases such as:
Alternate NamesCongenital Ureterocele is also known as Simple Ureterocele.