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Disease Info Card
Progressive Aphasia
Information about Progressive Aphasia: 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 Progressive Aphasia
Most recent studies have shown that Progressive Aphasia shares some biological mechanisms with abnormal-degeneration, alzheimers-disease, anomia, aphasia, aphasia-broca, apraxias, atrophy, cognition-disorders, corticobasal-degeneration, dementia, frontotemporal-dementia, frontotemporal-lobar-degeneration, language-disorders, malnutrition, neurodegenerative-disorders, pick-disease-of-the-brain, primary-progressive-aphasia-(disorder), primary-progressive-nonfluent-aphasia, progressive-supranuclear-palsy, semantic-dementia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Progressive Aphasia, and have been seen in publications frequently: Aging, Brain Development, Cognition, Eating Behavior, Inflammatory Response, Innervation, Localization, Long-term Memory, Pathogenesis, Reflex, Segmentation, Short-term Memory, Social Behavior, Translation, Transport, Transposition
Quite a number of genes have been found to play important roles in Progressive Aphasia, such as APOE, BPIFA2, COPS2, CSF2, GRN, LAMC2, LPA, MAPT, MSMB, PRNP, PSEN1, PSPH, PSPN, RANGAP1, REG1A, SLC17A5, STXBP3, TARDBP. 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.