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Disease Info Card
Joint Laxity
Information about Joint Laxity: 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 Joint Laxity
Most recent studies have shown that Joint Laxity shares some biological mechanisms with arthralgia, arthropathy, blepharoptosis, connective-tissue-diseases, degenerative-polyarthritis, dislocations, dwarfism, dysplasia, ehlers-danlos-syndrome, flexed-fetal-attitude, hypermobility-syndrome, knee-injuries, ligament-injury, muscle-hypotonia, pain, scoliosis-unspecified, subluxation-of-joint.
Among the many pathways, these few ones have gauged particular interests from scientists studying Joint Laxity, and have been seen in publications frequently: Aging, Bone Resorption, Coagulation, Dentinogenesis, Excretion, Lactation, Localization, Muscle Atrophy, Muscle Contraction, Ossification, Ovulation, Pathogenesis, Platelet Aggregation, Proprioception, Protein Folding, Reflex, Secretion, Swimming, Translation, Wound Healing
Quite a number of genes have been found to play important roles in Joint Laxity, such as ACLY, COL1A1, COL1A2, COL3A1, COL5A1, COL5A2, COMP, FBN1, FH, HOPX, PES1, PLOD1, SLC2A10, ST13, STIP1, TNXB, TTN, VPS13B. 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.