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Disease Info Card
Werner Syndrome
Information about Werner Syndrome: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Werner Syndrome
Most recent studies have shown that Werner Syndrome shares some biological mechanisms with arteriosclerosis, ataxia-telangiectasia, atherosclerosis, atrophy, bloom-syndrome, cataract, cockayne-syndrome, cytogenetic-abnormality, diabetes-mellitus, dwarfism, genomic-instability, hereditary-diseases, insulin-resistance, malignant-neoplasms, neoplasms, osteoporosis, premature-aging-syndrome, progeria, rothmund-thomson-syndrome, ulcer.
Among the many pathways, these few ones have gauged particular interests from scientists studying Werner Syndrome, and have been seen in publications frequently: Aging, Cell Cycle, Cell Death, Cell Growth, Cell Proliferation, Cellular Senescence, Chromosome Breakage, Dna Recombination, Dna Repair, Dna Replication, Hypersensitivity, Localization, Methylation, Mismatch Repair, Pathogenesis, Replicative Senescence, S Phase, Secretion, Senescence, Telomere Maintenance
Quite a number of genes have been found to play important roles in Werner Syndrome, such as BLM, CDKN1A, ELN, FEN1, GP1BB, INS, LMNA, MECP2, PARP1, PCNA, RECQL, RECQL4, TERF2, TP53, WRN, XRCC5. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.