Research of Crigler-najjar Syndrome has been linked to Hyperbilirubinemia, Gilbert Disease (disorder), Hyperbilirubinemia, Hereditary, Icterus, Unconjugated Hyperbilirubinemia. The study of Crigler-najjar Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Crigler-najjar Syndrome include Excretion, Conjugation, Bilirubin Conjugation, Transport, Immune Response. These pathways complement our catalog of research reagents for the study of Crigler-najjar Syndrome including antibodies and ELISA kits against UDP GLUCURONOSYLTRANSFERASE, SPHEROCYTOSIS, ALB, FECH, G6PD.
Crigler-najjar 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 Crigler-najjar Syndrome below!
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We have 492 products for the study of Crigler-najjar Syndrome that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Crigler-najjar Syndrome is also known as crigler-najjar syndrome, crigler-najjar syndrome, type i, crigler-najjar syndrome (disorder), familial nonhemolytic unconjugated hyperbilirubinemia, bilirubin udp glucuronyl transferase deficiency, crigler-najjar syndrome, type i (disorder), hereditary unconjugated hyperbilirubinemia, crigler najjar syndrome, type 1, hyperbilirubinemia, hereditary, gilbert disease (disorder), crigler najjar syndrome.