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资源简介：
identified mutation in a pedigree of familial dilated cardiomyopathy
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创建时间：
2017-11-21
相关数据集
Clinical characteristics of the patients with dilated cardiomyopathy whose tissues were examined by RNA-Seq and western blot analyses.
Clinical characteristics of the patients with dilated cardiomyopathy whose tissues were examined by RNA-Seq and western blot analyses.
NIAID Data Ecosystem50
The parameter values used in the child atria and ventricle models; the parameter values used in the simulation of DCM are shown in the brackets.
The parameter values used in the child atria and ventricle models; the parameter values used in the simulation of DCM are shown in the brackets.
NIAID Data Ecosystem30
Transcription profiling of wild type and delK210 cTnT knock-in mouse heart to study dilated cardiomyopathy
Transcription profiling of wild type and delK210 cTnT knock-in mouse heart to study dilated cardiomyopathy
ChEBI2008-09-04 更新10
Cardiomyocyte-Specific Expression of Lamin A Improves Cardiac Function in Lmna −/− Mice
Lmna−/− mice display multiple tissue defects and die by 6–8 weeks of age reportedly from dilated cardiomyopathy with associated conduction defects. We sought to determine whether restoration of lamin
NIAID Data Ecosystem50
Table_6_Differential Expression Profiles and Functional Analysis of Long Non-coding RNAs in Children With Dilated Cardiomyopathy.XLSX
Aim: To evaluate the expression profile of long non-coding RNAs (lncRNAs) in different left ventricular function of dilated cardiomyopathy (DCM) in children and explore their possible functions. Metho
NIAID Data Ecosystem20
