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Neonatal Hypermethioninemia: Disease Bioinformatics

Research of Neonatal Hypermethioninemia has been linked to Hepatic Methionine Adenosyltransferase Deficiency, Homocystinuria, Lens Subluxation, Pregnancy Complications, Dislocations. The study of Neonatal Hypermethioninemia has been mentioned in research publications which can be found using our bioinformatics tool below. Browse our catalog of research reagents for Neonatal Hypermethioninemia including antibodies and ELISA kits against CBS.

Neonatal Hypermethioninemia 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 Neonatal Hypermethioninemia below! For more information on how to use Laverne, please read the How to Guide.
Vizit™, under license from BioVista Inc.

Top Research Reagents

We have 24 products for the study of Neonatal Hypermethioninemia that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

Western Blot: CBS Antibody (3E1) [H00000875-M01] - CBS monoclonal antibody (M01), clone 3E1. Analysis of CBS expression in MCF-7.Immunohistochemistry-Paraffin: CBS Antibody (3E1) [H00000875-M01] - Analysis of monoclonal antibody to CBS on formalin-fixed paraffin-embedded human hepatocellular carcinoma. Antibody concentration 3 ug/ml.

Mouse Monoclonal
Species Human, Mouse, Rat
Applications WB, ELISA, ICC/IF

     1 Review

42 Publications

Related Genes

Neonatal Hypermethioninemia has been researched against:

Related Pathways

Related PTMs

Alternate Names

Neonatal Hypermethioninemia is also known as Neonatal Hypermethioninaemia.