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Disease Info Card
Frontotemporal Lobar Degeneration
Information about Frontotemporal Lobar Degeneration: 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 Frontotemporal Lobar Degeneration
Most recent studies have shown that Frontotemporal Lobar Degeneration shares some biological mechanisms with alzheimers-disease, amyotrophic-lateral-sclerosis, aphasia, atrophy, cognition-disorders, dementia, frontotemporal-dementia, impaired-cognition, lewy-body-disease, motor-neuron-disease, nerve-degeneration, neurodegenerative-disorders, primary-lateral-sclerosis, progressive-aphasia, progressive-supranuclear-palsy, sclerosis, semantic-dementia, supranuclear-palsy, tauopathies, tdp-43-proteinopathies.
Among the many pathways, these few ones have gauged particular interests from scientists studying Frontotemporal Lobar Degeneration, and have been seen in publications frequently: Aging, Autophagy, Cell Cycle, Cell Death, Cognition, Hyperphosphorylation, Localization, Long-term Memory, Neurogenesis, Nuclear Import, Nuclear Transport, Pathogenesis, Regulation Of Gene Expression, Rna Processing, Rna Splicing, Secretion, Segmentation, Social Behavior, Translation, Transport
Quite a number of genes have been found to play important roles in Frontotemporal Lobar Degeneration, such as APOE, C9ORF72, CHMP2B, CSF2, DCTN4, FUS, GRN, IGFALS, KHDRBS1, LAMC2, MAPT, NUP62, RANGAP1, RBM8A, SLC17A5, SNCA, SOD1, SQSTM1, TARDBP, VCP. 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.