Lista de obras - Abdelaziz Beqqali - Dominio Público Uruguay

A mutation in the glutamate-rich region of RNA-binding motif protein 20 causes dilated cardiomyopathy through missplicing of titin and impaired Frank-Starling mechanism.

artículo científico publicado en 2016

A targeted metabolomics assay for cardiac metabolism and demonstration using a mouse model of dilated cardiomyopathy

artículo científico publicado en 2016

Alternative splicing in cardiomyopathy

artículo científico publicado en 2018

CAZIP, a novel protein expressed in the developing heart and nervous system

artículo científico publicado en 2009

CHAP is a newly identified Z-disc protein essential for heart and skeletal muscle function

scientific journal article

Cardiac circRNAs arise mainly from constitutive exons rather than alternatively spliced exons.

artículo científico publicado en 2018

Cytoskeletal heart-enriched actin-associated protein (CHAP) is expressed in striated and smooth muscle cells in chick and mouse during embryonic and adult stages

artículo científico publicado en 2011

Genome-wide transcriptional profiling of human embryonic stem cells differentiating to cardiomyocytes

artículo científico publicado en 2006

Heterozygous loss of Rbm24 in the adult mouse heart increases sarcomere slack length but does not affect function

scientific article published on 06 May 2020

Human stem cells as a model for cardiac differentiation and disease.

artículo científico publicado en 2009

Insights into alternative splicing of sarcomeric genes in the heart.

artículo científico publicado en 2015

Long Non-Coding RNA Malat-1 Is Dispensable during Pressure Overload-Induced Cardiac Remodeling and Failure in Mice

artículo científico publicado en 2016

RBM20 Mutations Induce an Arrhythmogenic Dilated Cardiomyopathy Related to Disturbed Calcium Handling.

artículo científico publicado en 2018

RBM20 Regulates Circular RNA Production From the Titin Gene.

artículo científico publicado en 2016

Sarcosin (Krp1) in skeletal muscle differentiation: gene expression profiling and knockdown experiments

scientific journal article

TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT

artículo científico publicado en 2016

The LMNA mutation p.Arg321Ter associated with dilated cardiomyopathy leads to reduced expression and a skewed ratio of lamin A and lamin C proteins

artículo científico publicado en 2013

The MEF2 transcriptional target DMPK induces loss of sarcomere structure and cardiomyopathy

artículo científico publicado en 2018

The RNA-binding protein Rbm38 is dispensable during pressure overload-induced cardiac remodeling in mice

artículo científico publicado en 2017

The clinical outcome of LMNA missense mutations can be associated with the amount of mutated protein in the nuclear envelope

artículo científico publicado en 2018

Z-disc protein CHAPb induces cardiomyopathy and contractile dysfunction in the postnatal heart

artículo científico publicado en 2017

Lista de obras de Abdelaziz Beqqali

A mutation in the glutamate-rich region of RNA-binding motif protein 20 causes dilated cardiomyopathy through missplicing of titin and impaired Frank-Starling mechanism.

A targeted metabolomics assay for cardiac metabolism and demonstration using a mouse model of dilated cardiomyopathy

Alternative splicing in cardiomyopathy

CAZIP, a novel protein expressed in the developing heart and nervous system

CHAP is a newly identified Z-disc protein essential for heart and skeletal muscle function

Cardiac circRNAs arise mainly from constitutive exons rather than alternatively spliced exons.

Cytoskeletal heart-enriched actin-associated protein (CHAP) is expressed in striated and smooth muscle cells in chick and mouse during embryonic and adult stages

Genome-wide transcriptional profiling of human embryonic stem cells differentiating to cardiomyocytes

Heterozygous loss of Rbm24 in the adult mouse heart increases sarcomere slack length but does not affect function

Human stem cells as a model for cardiac differentiation and disease.

Insights into alternative splicing of sarcomeric genes in the heart.

Long Non-Coding RNA Malat-1 Is Dispensable during Pressure Overload-Induced Cardiac Remodeling and Failure in Mice

RBM20 Mutations Induce an Arrhythmogenic Dilated Cardiomyopathy Related to Disturbed Calcium Handling.

RBM20 Regulates Circular RNA Production From the Titin Gene.

Sarcosin (Krp1) in skeletal muscle differentiation: gene expression profiling and knockdown experiments

TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT

The LMNA mutation p.Arg321Ter associated with dilated cardiomyopathy leads to reduced expression and a skewed ratio of lamin A and lamin C proteins

The MEF2 transcriptional target DMPK induces loss of sarcomere structure and cardiomyopathy

The RNA-binding protein Rbm38 is dispensable during pressure overload-induced cardiac remodeling in mice

The clinical outcome of LMNA missense mutations can be associated with the amount of mutated protein in the nuclear envelope

Z-disc protein CHAPb induces cardiomyopathy and contractile dysfunction in the postnatal heart