Disease Info Card

Misalignment

Information about Misalignment: 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 Misalignment

Most recent studies have shown that Misalignment shares some biological mechanisms with abnormal-degeneration, arthritis, arthropathy, bone-malalignment, congenital-abnormality, degenerative-polyarthritis, dislocations, dysplasia, femoral-fractures, flexed-fetal-attitude, fracture, knee-injuries, knee-pain, neoplasms, osteoarthritis-knee, pain, strabismus, subluxation-of-joint, tibial-fractures, ventricular-septal-defects.

Among the many pathways, these few ones have gauged particular interests from scientists studying Misalignment, and have been seen in publications frequently: Aging, Anaphase, Cell Cycle, Chromosome Segregation, Circadian Rhythm, Dna Replication, Localization, Meiosis, Metaphase, Mitosis, Ossification, Pathogenesis, Reflex, Regeneration, Segmentation, Spindle Assembly, Spindle Checkpoint, Translation, Transport, Transposition

Quite a number of genes have been found to play important roles in Misalignment, such as ACLY, ARC, C2, CAT, CRAT, GLYAT, GPSM2, GRIP1, HNRNPC, NOL3, PLK1, PMP22, SLC17A5, SS18L1, TNFSF14. 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.

Misalignment Related Genes

click to see detail information for each gene

ACLY ARC C2
CAT CRAT GLYAT
GPSM2 GRIP1 HNRNPC
NOL3 PLK1 PMP22
SLC17A5 SS18L1 TNFSF14