Creutzfeldt-jakob Disease, Familial

Overview of Creutzfeldt-jakob Disease, Familial

Most recent studies have shown that Creutzfeldt-jakob Disease, Familial shares some biological mechanisms with alzheimers-disease, ataxia, creutzfeldt-jakob-disease, dementia, encephalopathies, fatal-familial-insomnia, gerstmann-straussler-scheinker-disease, gliosis, kuru, myoclonus, nervousness, neurodegenerative-disorders, prion-diseases, scrapie, sleep-initiation-and-maintenance-disorders, sleeplessness, spongy-degeneration, sporadic-cjd.

Among the many pathways, these few ones have gauged particular interests from scientists studying Creutzfeldt-jakob Disease, Familial, and have been seen in publications frequently: Aging, Cell Growth, Cellular Localization, Glycosylation, Inflammatory Response, Localization, Pathogenesis, Protein Folding, Rna Interference, Segmentation, Transport

Quite a number of genes have been found to play important roles in Creutzfeldt-jakob Disease, Familial, such as ABCB6, APOE, APP, C4BPA, CARD14, CSF2, GNPDA1, GPI, GSS, LAMC2, MAPT, MRPL13, PRDX2, PRND, PRNP, PSEN1, YWHAQ. 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.

Creutzfeldt-jakob Disease, Familial Related Genes

click to see detail information for each gene

Pathways Related to Creutzfeldt-jakob Disease, Familial

This information is being compiled and will come in a future update

Related Diseases