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5mC and 5hmC genes in the aetiology of dilated cardiomyopathy
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创建时间：
2019-02-10
相关数据集
Circulating Proteome Profiling Identifies the Hub Proteins and Biological Processes in Ischemic and Non-ischemic Dilated Cardiomyopathy
Circulating Proteome Profiling Identifies the Hub Proteins and Biological Processes in Ischemic and Non-ischemic Dilated Cardiomyopathy
integrated proteome resources40
Targeting MRTF/SRF in CAP2-dependent dilated cardiomyopathy delays disease onset
About one third of dilated cardiomyopathy (DCM) cases are caused by mutations in sarcomere or cytoskeletal proteins. Yet treating the cytoskeleton directly is not possible because drugs that bind to
NIAID Data Ecosystem20
TBX5 R264K acts as a modifier to develop dilated cardiomyopathy in mice independently of T-box pathway
BackgroundTBX5 is a transcription factor that has an important role in development of heart. TBX5 variants in the region encoding the T-box domain have been shown to cause cardiac defects, such as atr
Figshare2020-04-01 更新10
Data_Sheet_1_Cardiomyocyte Proliferative Capacity Is Restricted in Mice With Lmna Mutation.pdf
LMNA is one of the leading causative genes of genetically inherited dilated cardiomyopathy (DCM). Unlike most DCM-causative genes, which encode sarcomeric or sarcomere-related proteins, LMNA encodes n
NIAID Data Ecosystem20
Table1_Construction of Immune-Related ceRNA Network in Dilated Cardiomyopathy: Based on Sex Differences.DOCX
Background: Immune targeted therapy has become an attractive therapeutic approach for patients with dilated cardiomyopathy (DCM) recently. Genetic predisposition and gender play a critical role in imm
NIAID Data Ecosystem10
