Research of Kearns-sayre Syndrome has been linked to Ophthalmoplegia, External Ophthalmoplegia, Chronic Progressive External Ophthalmoplegia, Myopathy, Mitochondrial Myopathies. The study of Kearns-sayre Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Kearns-sayre Syndrome include Cardiac Conduction, Pathogenesis, Oxidative Phosphorylation, Transport, Translation. These pathways complement our catalog of research reagents for the study of Kearns-sayre Syndrome including antibodies and ELISA kits against NAD(P)H DEHYDROGENASE (QUINONE), GROWTH HORMONE, COX8A, CPOX, CS.
Kearns-sayre 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 Kearns-sayre Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 1134 products for the study of Kearns-sayre Syndrome that can be applied to Western Blot, Chromatin Immunoprecipitation, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Kearns-sayre Syndrome is also known as kearns-sayre syndrome, kss, ophthalmoplegia, pigmentary degeneration of retina, and cardiomyopathy, ophthalmoplegia, progressive external, with ragged red fibers, chronic progressive external ophthalmoplegia with myopathy, kearns-sayre syndrome (disorder), ophthalmoplegia plus syndrome, oculocraniosomatic syndrome, cpeo with ragged red fibers, mitochondrial cytopathy, cpeo with myopathy.