Sarcomeric protein isoform transitions in cardiac muscle: a journey to heart failure - Test2 - elhamkhani - TriplyDB

Sarcomeric protein isoform transitions in cardiac muscle: a journey to heart failure

Sarcomeric protein isoform transitions in cardiac muscle: a journey to heart failure

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Fibre typing of intrafusal fibres Heart Failure in Pediatric Patients With Congenital Heart Disease.Aberrant developmental titin splicing and dysregulated sarcomere length in Thymosin β4 knockout mice.Cardiac myosin binding protein C regulates postnatal myocyte cytokinesis.Biomechanics of Cardiac Function Alterations in Multi-Scale Cardiac Architecture in Association With Phosphorylation of Myosin Binding Protein-C.Targeting danger-associated molecular patterns after myocardial infarction.Whole gene sequencing identifies deep-intronic variants with potential functional impact in patients with hypertrophic cardiomyopathy.RBM20, a potential target for treatment of cardiomyopathy via titin isoform switching.Chronic heart failure: Ca(2+), catabolism, and catastrophic cell death.Top-down Proteomics: Technology Advancements and Applications to Heart Diseases.Myocardial plasticity: cardiac development, regeneration and disease.The Zebrafish Heart as a Model of Mammalian Cardiac Function.Pre-mRNA mis-splicing of sarcomeric genes in heart failure.Can Human Pluripotent Stem Cell-Derived Cardiomyocytes Advance Understanding of Muscular Dystrophies?A multidimensional sight on cardiac failure: uncovered from structural to molecular level.Ectopic expression of Cdk8 induces eccentric hypertrophy and heart failure.Region and cell-type resolved quantitative proteomic map of the human heart.HIC2 regulates isoform switching during maturation of the cardiovascular system.Accumulation of 5-oxoproline in myocardial dysfunction and the protective effects of OPLAH.Characterization of TTN Novex Splicing Variants across Species and the Role of RBM20 in Novex-Specific Exon Splicing.Neuro-Cardio Mechanisms in Huntington's Disease and Other Neurodegenerative Disorders.Splicing Factor RBM20 Regulates Transcriptional Network of Titin Associated and Calcium Handling Genes in The Heart.

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P2860

Sarcomeric protein isoform transitions in cardiac muscle: a journey to heart failure

http://www.wikidata.org/entity/Q28252609

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2015 nî lūn-bûn

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2015 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի հունվարին հրատարակված գիտական հոդված

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年學術文章

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Sarcomeric protein isoform transitions in cardiac muscle: a journey to heart failure

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Sarcomeric protein isoform transitions in cardiac muscle: a journey to heart failure

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Sarcomeric protein isoform transitions in cardiac muscle: a journey to heart failure

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Sarcomeric protein isoform transitions in cardiac muscle: a journey to heart failure

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Sarcomeric protein isoform transitions in cardiac muscle: a journey to heart failure

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Sarcomeric protein isoform transitions in cardiac muscle: a journey to heart failure

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Sarcomeric protein isoform transitions in cardiac muscle: a journey to heart failure

@ast

Sarcomeric protein isoform transitions in cardiac muscle: a journey to heart failure

@en

Sarcomeric protein isoform transitions in cardiac muscle: a journey to heart failure

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J.BBADIS.2014.11.003

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Biochimica et Biophysica Acta

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Sarcomeric protein isoform transitions in cardiac muscle: a journey to heart failure

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Jun Ren

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Wei Guo

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Zhiyong Yin

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P2860

Gene regulation, alternative splicing, and posttranslational modification of troponin subunits in cardiac development and adaptation: a focused review

The NH2 terminus of titin spans the Z-disc: its interaction with a novel 19-kD ligand (T-cap) is required for sarcomeric integrity

The complete gene sequence of titin, expression of an unusual approximately 700-kDa titin isoform, and its interaction with obscurin identify a novel Z-line to I-band linking system

Cardiac myosin binding protein C: its role in physiology and disease

RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing

Complete sequence of human fast-type and slow-type muscle myosin-binding-protein C (MyBP-C). Differential expression, conserved domain structure and chromosome assignment

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

Phosphorylation switches specific for the cardiac isoform of myosin binding protein-C: a modulator of cardiac contraction?

The actin gene family: function follows isoform

Titin: major myofibrillar components of striated muscle

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10.1016/J.BBADIS.2014.11.003

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1

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