A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathy. - Wikidata - awgldk - TriplyDB

A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathy.

A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathy.

http://www.wikidata.org/entity/Q30351668

about

Initial sequence and comparative analysis of the cat genome Animal and in silico models for the study of sarcomeric cardiomyopathies Myosin binding protein C: implications for signal-transduction How do MYBPC3 mutations cause hypertrophic cardiomyopathy?Mybpc3 gene therapy for neonatal cardiomyopathy enables long-term disease prevention in mice MYBPC3 in hypertrophic cardiomyopathy: from mutation identification to RNA-based correction In the thick of it: HCM-causing mutations in myosin binding proteins of the thick filament Genetic testing in domestic cats The A31P missense mutation in cardiac myosin binding protein C alters protein structure but does not cause haploinsufficiency.Pharmacodynamic effects of ivabradine, a negative chronotropic agent, in healthy cats.Investigations into the Sarcomeric Protein and Ca2+-Regulation Abnormalities Underlying Hypertrophic Cardiomyopathy in Cats (Felix catus).Comparative echocardiographic and clinical features of hypertrophic cardiomyopathy in 5 breeds of cats: a retrospective analysis of 344 cases (2001-2011).Variation of cats under domestication: genetic assignment of domestic cats to breeds and worldwide random-bred populations.Myosin-binding protein C DNA variants in domestic cats (A31P, A74T, R820W) and their association with hypertrophic cardiomyopathy Hypertrophic cardiomyopathy in young Maine Coon cats caused by the p.A31P cMyBP-C mutation--the clinical significance of having the mutation.Feline genetics: clinical applications and genetic testing.Mucopolysaccharidosis VI in cats - clarification regarding genetic testing A Small Molecule Inhibitor of Sarcomere Contractility Acutely Relieves Left Ventricular Outflow Tract Obstruction in Feline Hypertrophic Cardiomyopathy Assessment of regional left ventricular systolic function by strain imaging echocardiography in phenotypically normal and abnormal Maine coon cats tested for the A31P mutation in the MYBPC3 gene.Left Ventricular Hypertrophy in Rhesus Macaques (Macaca mulatta) at the California National Primate Research Center (1992-2014)A High-Resolution SNP Array-Based Linkage Map Anchors a New Domestic Cat Draft Genome Assembly and Provides Detailed Patterns of Recombination.Cardiac troponin I and T as prognostic markers in cats with hypertrophic cardiomyopathy.A high-resolution cat radiation hybrid and integrated FISH mapping resource for phylogenomic studies across Felidae A 1.5-Mb-resolution radiation hybrid map of the cat genome and comparative analysis with the canine and human genomes Health and Behavioral Survey of over 8000 Finnish Cats.Feline myocardial disease 2: diagnosis, prognosis and clinical management.MYBPC3's alternate ending: consequences and therapeutic implications of a highly prevalent 25 bp deletion mutation DNA mutations of the cat: the good, the bad and the ugly.Veterinary cardiology: a journey through time.The practical use of genome sequencing data in the management of a feline colony pedigree.The genetic basis of hypertrophic cardiomyopathy in cats and humans.The age, breed and sex pattern of diagnosis for veterinary care in insured cats in Japan.Murine Electrophysiological Models of Cardiac Arrhythmogenesis.Haematological and biochemical reference intervals in adult Maine Coon cat blood donors.A One Health Approach to Hypertrophic Cardiomyopathy.An international parentage and identification panel for the domestic cat (Felis catus)Naturally Occurring Biventricular Noncompaction in an Adult Domestic Cat.Structure and interactions of myosin-binding protein C domain C0: cardiac-specific regulation of myosin at its neck?Familial cardiomyopathy in Norwegian Forest cats.Genomic Insights into Cardiomyopathies: A Comparative Cross-Species Review.

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P2860

A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathy.

http://www.wikidata.org/entity/Q30351668

description

2005 nî lūn-bûn

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2005 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2005 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年學術文章

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name

A cardiac myosin binding prote ...... l hypertrophic cardiomyopathy.

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A cardiac myosin binding prote ...... l hypertrophic cardiomyopathy.

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type

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A cardiac myosin binding prote ...... l hypertrophic cardiomyopathy.

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A cardiac myosin binding prote ...... l hypertrophic cardiomyopathy.

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A cardiac myosin binding prote ...... l hypertrophic cardiomyopathy.

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A cardiac myosin binding prote ...... l hypertrophic cardiomyopathy.

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Human Molecular Genetics

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A cardiac myosin binding prote ...... l hypertrophic cardiomyopathy.

@en

P2093

Judith A Kittleson

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Kathryn M Meurs

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Keith Dryburgh

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Kristin A Macdonald

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Marcia J Munro

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Mark D Kittleson

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Neil E Bowles

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Peter J Reiser

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Ryan M David

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Ximena Sanchez

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P2860

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

A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetrance

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

Assignment of the human gene for the sarcomeric M-band protein myomesin (MYOM1) to 18p11.31-p11.32

Structural evidence for the interaction of C-protein (MyBP-C) with actin and sequence identification of a possible actin-binding domain.

Familial hypertrophic cardiomyopathy in maine coon cats: an animal model of human disease.

Myosin binding protein C: structural abnormalities in familial hypertrophic cardiomyopathy.

Expression and functional assessment of a truncated cardiac troponin T that causes hypertrophic cardiomyopathy. Evidence for a dominant negative action.

Anomalous electrophoretic mobility of Drosophila phosphorylated H1 histone: is it related to the compaction of satellite DNA into heterochromatin?

COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fetal rat cardiomyocytes.

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3587-3593

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10.1093/HMG/DDI386

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23

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14

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Jeffrey A Towbin

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2005-10-19T00:00:00Z

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7529274

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16236761

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