This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Disease Info Card
Coronary Microvascular Disease
Information about Coronary Microvascular Disease: 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 Coronary Microvascular Disease
Most recent studies have shown that Coronary Microvascular Disease shares some biological mechanisms with congenital-muscular-dystrophy-(disorder), craniomandibular-disorders, depressive-disorder, dysplasia, dystrophy, facial-pain, headache, mental-disorders, muscle-contracture, muscle-hypotonia, muscle-weakness, muscular-dystrophy, myopathy, nervousness, pain, temporomandibular-joint-disorders, temporomandibular-joint-dysfunction-syndrome, walker-warburg-congenital-muscular-dystrophy, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Coronary Microvascular Disease, and have been seen in publications frequently: Angiogenesis, Bone Mineralization, Cell Adhesion, Cell Death, Cell Differentiation, Cell Growth, Cell Proliferation, Conjugation, Excretion, Glomerular Filtration, Glycosylation, Localization, Mastication, Myelination, Pathogenesis, Reflex, Regeneration, Secretion, Translation, Transport
Quite a number of genes have been found to play important roles in Coronary Microvascular Disease, such as ACAN, AKR1B1, ANKH, BCR, CHKA, CHKB, DAG1, DMD, FKRP, FKTN, JAK2, LAMA2, POMGNT1, POMT1, POMT2, SLC25A5, TNF. 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.