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RBM20 encodes a protein that likely binds RNA. Zusätzlich bieten wir Ihnen RBM20 Kits (6) und RBM20 Proteine (6) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 41 products:
Mouse (Murine) Polyclonal RBM20 Primary Antibody für ELISA, WB - ABIN4349592
Li, Morales, Gonzalez-Quintana, Norton, Siegfried, Hofmeyer, Hershberger: Identification of novel mutations in RBM20 in patients with dilated cardiomyopathy. in Clinical and translational science 2010
The first light on molecular mechanisms of RBM20-dependent pathological cardiac remodeling leading to DCM.
Mutations in RBM20 cause dilated cardiomyopathy along with dysregulated isoform switch.
Heterozygous loss of RBM20 suffices to profoundly impair myocyte biomechanics by its disturbance of TTN splicing causing dilated cardiomyopathy.
RBM20 is crucial for the formation of a subset of circular RNAs that originate from the I-band of the titin gene.
RBM20 familial dilated cardiomyopathy is a developmental disorder initiated by molecular defects that pattern maladaptive cellular mechanisms of pathological cardiac remodeling.
In failing hearts, reduced expression of RBM20 affected alternative splicing of several direct targets, indicating that differences in RBM20 expression may affect cardiac function.
Study demonstrates that Rbm20 is expressed in early cardiogenesis and functions in the patterning of cardiac gene expression.
The RBM20 c.1907 G>A (p.Arg636His) was confirmed in all 3 affected subjects who underwent exome sequencing.
Nuclear retention domains have been identified in RBM20 which is a nuclear protein regulating alternative splicing of expressed genes.
Mutations in RBM20 identified in approximately 3% of individuals with dilated cardiomyopathy. Mutations in RBM20 did not adversely affect survival or ventricular arrhythmias in subjects with dilated cardiomyopathy.
Deep sequencing of the human and rat cardiac transcriptome revealed an RBM20-dependent regulation of alternative splicing
Dilated cardiomyopathy in patients with RBM20 mutations is associated with advanced disease.
RBM20 as a dilated cardiomyopathy gene and reveal a mutation hotspot in the RS domain. Individuals in each family revealed distinct heterozygous missense mutations in exon 9 of RBM20, encoding ribonucleic acid (RNA) binding motif protein 20.
RBM20 missense mutation is a novel gene underlying one form of dilated cardiomyopathy
Reducing RBM20 activity improves diastolic dysfunction and cardiac atrophy.
Inhibition of the RNA binding motif-20-based titin splicing system upregulates compliant titins, which improves diastolic function and exercise tolerance in the transverse aortic constriction/deoxycorticosterone acetate model
This gene encodes a protein that likely binds RNA. Mutations in this gene have been associated with familial dilated cardiomyopathy.
RNA binding motif protein 20
, RNA-binding motif protein 20
, RNA-binding protein 20
, probable RNA-binding protein 20