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- Table of Contents
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Disease Info Card
Communication Impairment
Information about Communication Impairment: 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 Communication Impairment
Most recent studies have shown that Communication Impairment shares some biological mechanisms with alzheimers-disease, aphasia, autism-spectrum-disorders, autistic-disorder, brain-injuries, cerebrovascular-accident, cognition-disorders, complete-hearing-loss, dementia, depressive-disorder, developmental-disabilities, hearing-problem, impairment-(finding), language-development-disorders, language-disorders, malnutrition, mental-disorders, schizophrenia, speech-disorders.
Among the many pathways, these few ones have gauged particular interests from scientists studying Communication Impairment, and have been seen in publications frequently: Aging, Brain Development, Cognition, Developmental Process, Eating Behavior, Hypersensitivity, Immune Response, Localization, Locomotion, Pathogenesis, Platelet Activation, Reflex, Regeneration, Short-term Memory, Social Behavior, Synaptic Transmission, Translation, Transposition, Visual Perception, Vocal Learning
Quite a number of genes have been found to play important roles in Communication Impairment, such as ACHE, AKR1C4, APOE, BCHE, CHAT, CP, CSF2, DNMT3B, EBP, FOXP2, GLB1, IGFALS, LAMC2, RHD, RUNX1T1, SH3D19, SLC17A5, SLC6A3, SOD1. 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.