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RBM20 gene

Known as: RBM20, RNA binding motif protein 20, RNA-BINDING MOTIF PROTEIN 20 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
5 A Mutation in the Glutamate-rich Region of RBM 20 Causes Dilated Cardiomyopathy through Missplicing of Titin and Impaired Frank-Starling Mechanism
Review
2017
Review
2017
RBM20, a potential target for treatment of cardiomyopathy via titin isoform switching
Cardiomyopathy, also known as heart muscle disease, is an unfavorable condition leading to alterations in myocardial contraction… 
2017
2017
Response by Methawasin and Granzier to Letter Regarding Article, "Experimentally Increasing the Compliance of Titin Through RNA Binding Motif-20 (RBM20) Inhibition Improves Diastolic Function in a…
We thank Lewis and Miller for discussing important questions regarding the possible benefits of Rbm20 inhibition in patients with… 
2017
2017
Abstracts zum 123. Kongress der Deutschen Gesellschaft für Innere Medizin e.V
YIA 1 A comprehensive Analysis of RBM20 and Titin variants in Left Ventricular Non-compaction Cardiomyopathy Dr. Farbod Sedaghat… 
2016
2016
Reducing RBM20 activity improves diastolic dysfunction and cardiac atrophy
Impaired diastolic filling is a main contributor to heart failure with preserved ejection fraction (HFpEF), a syndrome with… 
2015
2015
Whole exome sequencing in a large pedigree with DCM identifies a novel mutation in RBM20
Abstract Background: Familial dilated cardiomyopathy (DCM) is genetically heterogeneous and is associated with mutations in at… 
2015
2015
Searching for DNA motifs that affect splicing of exons regulated by RBM20
2015
2015
A study to find sequence motifs that affect splicing of exons regulated by RBM20
2013
2013
INVESTIGATIONS INTO THE EFFECTS OF ALTERED TITIN ISOFORM EXPRESSION IN STRIATED MUSCLE
The giant protein titin is found primarily in striated muscle, where it is responsible for a number of roles. In order to… 
2012
2012
Abstract 11966: Exome Sequencing of Remotely Related Individuals Plus Bioinformatic Analysis Identifies Rbm20 as a Cause Of DCM in a Large Pedigree as Well as Hdac7 a Potential Genetic Modifier
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