Combinatorial effects of double cardiomyopathy mutant alleles in rodent myocytes: a predictive cellular model of myofilament dysregulation in disease - Wikidata - wikimedia - TriplyDB

Combinatorial effects of double cardiomyopathy mutant alleles in rodent myocytes: a predictive cellular model of myofilament dysregulation in disease

Combinatorial effects of double cardiomyopathy mutant alleles in rodent myocytes: a predictive cellular model of myofilament dysregulation in disease

http://www.wikidata.org/entity/Q28472836

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Cell biology of sarcomeric protein engineering: disease modeling and therapeutic potential Ca(2+)-regulatory function of the inhibitory peptide region of cardiac troponin I is aided by the C-terminus of cardiac troponin T: Effects of familial hypertrophic cardiomyopathy mutations cTnI R145G and cTnT R278C, alone and in combination, on fil Extracellular signal-regulated kinases 1 and 2 regulate the balance between eccentric and concentric cardiac growth A Tension-Based Model Distinguishes Hypertrophic versus Dilated Cardiomyopathy.Experimental models of inherited cardiomyopathy and its therapeutics.

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Combinatorial effects of double cardiomyopathy mutant alleles in rodent myocytes: a predictive cellular model of myofilament dysregulation in disease

http://www.wikidata.org/entity/Q28472836

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2010 nî lūn-bûn

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2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի փետրվարին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Combinatorial effects of doubl ...... ament dysregulation in disease

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Combinatorial effects of doubl ...... ament dysregulation in disease

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Combinatorial effects of doubl ...... ament dysregulation in disease

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Combinatorial effects of doubl ...... ament dysregulation in disease

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Jennifer Davis

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Joseph M Metzger

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Dilated cardiomyopathy mutant tropomyosin mice develop cardiac dysfunction with significantly decreased fractional shortening and myofilament calcium sensitivity

Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy

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

Hypertrophic cardiomyopathy in cardiac myosin binding protein-C knockout mice

Prevalence and severity of "benign" mutations in the beta-myosin heavy chain, cardiac troponin T, and alpha-tropomyosin genes in hypertrophic cardiomyopathy

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

A novel mutant cardiac troponin C disrupts molecular motions critical for calcium binding affinity and cardiomyocyte contractility

Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy

Turnover of cardiac troponin subunits. Kinetic evidence for a precursor pool of troponin-I

Contemporary definitions and classification of the cardiomyopathies: an American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and F

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