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Disease Info Card
Primary Familial Dilated Cardiomyopathy
Information about Primary Familial Dilated Cardiomyopathy: 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 Primary Familial Dilated Cardiomyopathy
Most recent studies have shown that Primary Familial Dilated Cardiomyopathy shares some biological mechanisms with cardiac-arrhythmia, cardiac-death, cardiomyopathies, cardiomyopathy-dilated, cardiomyopathy-familial-idiopathic, cardiomyopathy-hypertrophic-familial, dilatation-ventricular, dystrophy, familial-disease, heart-diseases, heart-failure, hypertrophic-cardiomyopathy, hypertrophy, left-ventricular-hypertrophy, myocarditis, myopathy, pathological-dilatation, sudden-cardiac-death, sudden-death, ventricular-dysfunction-left.
Among the many pathways, these few ones have gauged particular interests from scientists studying Primary Familial Dilated Cardiomyopathy, and have been seen in publications frequently: Cardiac Conduction, Cardiac Muscle Contraction, Cell Cycle, Cell Death, Glycosylation, Heart Development, Induction Of Apoptosis, Localization, Meiosis, Meiosis I, Mrna Transcription, Muscle Contraction, Oogenesis, Pachytene, Pathogenesis, Prophase, Regulation Of Striated Muscle Contraction, Rna Splicing, Spermatogenesis, Striated Muscle Contraction
Quite a number of genes have been found to play important roles in Primary Familial Dilated Cardiomyopathy, such as ACTC1, DES, DMD, FST, GBGT1, LDB3, LMNA, MYH14, MYH7, PLN, SCN5A, SGCA, SGCD, TAZ, TNNC1, TNNI3, TNNT2, TPM1, TTN. 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.