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Disease Info Card
Resting Tremor
Information about Resting Tremor: 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 Resting Tremor
Most recent studies have shown that Resting Tremor shares some biological mechanisms with atrophy, bradykinesia, dementia, depressive-disorder, dyskinetic-syndrome, dystonia-disorders, essential-tremor, gait-abnormality, hypokinesia, intention-tremor, movement-disorders, muscle-rigidity, neurodegenerative-disorders, parkinson-disease, secondary-parkinson-disease, static-tremor, tremor-unspecified.
Among the many pathways, these few ones have gauged particular interests from scientists studying Resting Tremor, and have been seen in publications frequently: Aging, Blood Circulation, Cell Death, Coagulation, Cognition, Habituation, Innervation, Localization, Locomotion, Muscle Contraction, Neuroprotection, Pathogenesis, Pigmentation, Programmed Cell Death, Proprioception, Protein Phosphorylation, Reflex, Synaptic Transmission, Translation, Transposition
Quite a number of genes have been found to play important roles in Resting Tremor, such as COMT, CSF2, EEF1A2, LRP2, LRRK2, MAPT, MCF2L, MSMB, PARK7, PSPN, REG1A, REST, SIGLEC1, SNCA, STXBP3, TH, VIM. 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.