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Disease Info Card
Neuromuscular Junction Diseases
Information about Neuromuscular Junction Diseases: 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 Neuromuscular Junction Diseases
Most recent studies have shown that Neuromuscular Junction Diseases shares some biological mechanisms with atrophy, autoimmune-diseases, autoimmune-reaction, guillain-barre-syndrome, lambert-eaton-myasthenic-syndrome, muscle-weakness, muscular-atrophy, myasthenia-gravis, myasthenias, myasthenic-syndromes-congenital, myopathy, neoplasms, nervous-system-disorder, nervousness, neuromuscular-diseases, peripheral-neuropathy, spinal-muscular-atrophy, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Neuromuscular Junction Diseases, and have been seen in publications frequently: Aging, Enucleation, Exocytosis, Glycosylation, Immune Response, Localization, Muscle Atrophy, Muscle Contraction, Myelination, Neuromuscular Junction Development, Pathogenesis, Reflex, Regeneration, Regulation Of Gene Expression, Reverse Transcription, Secretion, Swimming, Synaptic Transmission, Transport, Virulence
Quite a number of genes have been found to play important roles in Neuromuscular Junction Diseases, such as ACHE, AGRN, BCHE, CACNA1A, CHAT, CST7, DBNL, EIF3K, MLYCD, NMT1, NOS1, RAPSN, SCN8A, SMN1, SNRPN, STMN1. 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.