Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy. - Wikidata - awgldk - TriplyDB

Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.

Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.

http://www.wikidata.org/entity/Q34781987

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Ahnak1 is a tuneable modulator of cardiac Ca(v)1.2 calcium channel activity Muscle lim protein isoform negatively regulates striated muscle actin dynamics and differentiation A novel custom resequencing array for dilated cardiomyopathy KaPPA-View4: a metabolic pathway database for representation and analysis of correlation networks of gene co-expression and metabolite co-accumulation and omics data Muscle LIM protein interacts with cofilin 2 and regulates F-actin dynamics in cardiac and skeletal muscle Titin-based tension in the cardiac sarcomere: molecular origin and physiological adaptations Clinical and Mechanistic Insights Into the Genetics of Cardiomyopathy The vertebrate muscle Z-disc: sarcomere anchor for structure and signalling A differential wiring analysis of expression data correctly identifies the gene containing the causal mutation.Transcriptomic and proteomic analysis of global ischemia and cardioprotection in the rabbit heart.Human muscle LIM protein dimerizes along the actin cytoskeleton and cross-links actin filaments Genetics of hypertrophic cardiomyopathy.Drosophila melanogaster muscle LIM protein and alpha-actinin function together to stabilize muscle cytoarchitecture: a potential role for Mlp84B in actin-crosslinking.Myocyte remodeling in response to hypertrophic stimuli requires nucleocytoplasmic shuttling of muscle LIM protein.Neuronal expression of muscle LIM protein in postnatal retinae of rodents.Mechanotransduction in cardiac hypertrophy and failure.Progesterone signalling in broiler skeletal muscle is associated with divergent feed efficiency.CRP2, a new invadopodia actin bundling factor critically promotes breast cancer cell invasion and metastasis MLP and CARP are linked to chronic PKCα signalling in dilated cardiomyopathy.Targeted sequence capture and GS-FLX Titanium sequencing of 23 hypertrophic and dilated cardiomyopathy genes: implementation into diagnostics.The titin-telethonin complex is a directed, superstable molecular bond in the muscle Z-disk.Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction.Are biological sensors modulated by their structural scaffolds? The role of the structural muscle proteins alpha-actinin-2 and alpha-actinin-3 as modulators of biological sensors.The interactome of LIM domain proteins: the contributions of LIM domain proteins to heart failure and heart development.Genetic testing for inherited cardiac disease.Early postmortem gene expression and its relationship to composition and quality traits in pig Longissimus dorsi muscle.Animal Models of Congenital Cardiomyopathies Associated With Mutations in Z-Line Proteins.Muscle hypertrophy as the presenting sign in a patient with a complete FHL1 deletion.Defining the genetic architecture of hypertrophic cardiomyopathy: re-evaluating the role of non-sarcomeric genes.Nuclear accumulation of myocyte muscle LIM protein is regulated by heme oxygenase 1 and correlates with cardiac function in the transition to failure.A One Health Approach to Hypertrophic Cardiomyopathy.Nociceptive DRG neurons express muscle lim protein upon axonal injury Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy.When signalling goes wrong: pathogenic variants in structural and signalling proteins causing cardiomyopathies.Application of Large Scale Aptamer-Based Proteomic Profiling to "Planned" Myocardial Infarctions.Age-dependent changes in contractile function and passive elastic properties of myocardium from mice lacking muscle LIM protein (MLP).Mutant Muscle LIM Protein C58G causes cardiomyopathy through protein depletion

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P2860

Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.

http://www.wikidata.org/entity/Q34781987

description

2008 nî lūn-bûn

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2008 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2008 թվականի մայիսին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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name

Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.

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Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.

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Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.

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type

label

Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.

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Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.

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Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.

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Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.

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Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.

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Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.

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Human Molecular Genetics

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Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.

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P2093

Andreas Perrot

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Angelika Bublak

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Bettina Erdmann

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Cemil Ozcelik

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Christian Geier

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Dieter O Fürst

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Florian Krackhardt

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Herbert Nägele

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Karl J Osterziel

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Katja Gehmlich

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P2860

Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy

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

Muscle LIM protein promotes myogenesis by enhancing the activity of MyoD

Unusual splicing events result in distinct Xin isoforms that associate differentially with filamin c and Mena/VASP

Muscle LIM protein, a novel essential regulator of myogenesis, promotes myogenic differentiation

The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy

Paxillin and ponsin interact in nascent costameres of muscle cells

Decreased interactions of mutant muscle LIM protein (MLP) with N-RAP and alpha-actinin and their implication for hypertrophic cardiomyopathy

Alterations at the intercalated disk associated with the absence of muscle LIM protein

Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

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2753-2765

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10.1093/HMG/DDN160

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18

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17

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Peter Nürnberg

Elisabeth Ehler

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2008-05-27T00:00:00Z

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18505755

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