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Disease Info Card
Mobility Poor
Information about Mobility Poor: 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 Mobility Poor
Most recent studies have shown that Mobility Poor shares some biological mechanisms with cerebrovascular-accident, cognition-disorders, confusion, dementia, depressive-disorder, diabetes-mellitus, femoral-neck-fractures, fracture, heart-diseases, hip-fractures, hypertensive-disease, impaired-cognition, malignant-neoplasms, mobility-limitation, neoplasms, pain, pressure-ulcer, ulcer, urinary-incontinence.
Among the many pathways, these few ones have gauged particular interests from scientists studying Mobility Poor, and have been seen in publications frequently: Aging, Angiogenesis, Brain Development, Cell Growth, Cell Migration, Cellular Senescence, Chemotaxis, Coagulation, Cognition, Endothelial Cell Migration, Glomerular Filtration, Immune Response, Lateral Root Formation, Menopause, Micturition, Pathogenesis, Reflex, Senescence, Transport, Wound Healing
Quite a number of genes have been found to play important roles in Mobility Poor, such as ALB, AMBP, BEST1, CCDC6, CREG1, DMD, GRIP1, HGF, HPSE, IGF1, ILK, INS, LDHA, LDHC, MTOR, SF3B1, SGCA, SHBG, VEGFA, YWHAE. 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.