Research of Cockayne Syndrome has been linked to Xeroderma Pigmentosum, Xeroderma, Dwarfism, Malignant Neoplasms, Trichothiodystrophy Syndromes. The study of Cockayne Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Cockayne Syndrome include Dna Repair, Aging, Hypersensitivity, Cell Cycle, Dna Replication. These pathways complement our catalog of research reagents for the study of Cockayne Syndrome including antibodies and ELISA kits against ERCC8, CS, CSH1, CSH2, ERCC1.
Cockayne 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 Cockayne Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 633 products for the study of Cockayne Syndrome that can be applied to Western Blot, Chromatin Immunoprecipitation, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Chromatin Immunoprecipitation (ChIP) from our catalog of antibodies and ELISA kits.
Cockayne Syndrome is also known as cockayne syndrome, dwarfism-retinal atrophy-deafness syndrome, cockayne's syndrome, trigonocephaly, cs, dwarfism with retinal atrohpy and deafness, trigonocephaly c syndrome, trigonocephaly syndrome, neill-dingwall syndrome, c syndrome, progeria.