Macular Corneal Dystrophy Type I: Disease Bioinformatics
Research of Macular Corneal Dystrophy Type I has been linked to Glomerulonephritis, Minimal Change, Angiolymphoid Hyperplasia, Multicentric Angiofollicular Lymphoid Hyperplasia, Nephrotic Syndrome, Focal Glomerulosclerosis. The study of Macular Corneal Dystrophy Type I has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Macular Corneal Dystrophy Type I include Pathogenesis, Fatty Acid Oxidation, Localization, Secretion, Excretion. These pathways complement our catalog of research reagents for the study of Macular Corneal Dystrophy Type I including antibodies and ELISA kits against MLYCD, IL6, TNF, ACTN4, EPR.
Macular Corneal Dystrophy Type I 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 Macular Corneal Dystrophy Type I below!
For more information on how to use Laverne, please read the How to Guide.
We have 2290 products for the study of Macular Corneal Dystrophy Type I that can be applied to Western Blot, Chromatin Immunoprecipitation, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Chromatin Immunoprecipitation (ChIP), Immunohistochemistry from our catalog of antibodies and ELISA kits.
Macular Corneal Dystrophy Type I is also known as Mcd, Mcdc1.
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