scholarly article | Q13442814 |
P50 | author | Daniela Panáková | Q80563531 |
P2093 | author name string | Andreas A Werdich | |
Calum A MacRae | |||
Rahul C Deo | |||
Shannon Coy | |||
Jason R Becker | |||
P2860 | cites work | Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere | Q24316399 |
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Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia | Q28235110 | ||
A truncated cardiac troponin T molecule in transgenic mice suggests multiple cellular mechanisms for familial hypertrophic cardiomyopathy | Q28508653 | ||
Growth hormone-releasing hormone promotes survival of cardiac myocytes in vitro and protects against ischaemia-reperfusion injury in rat heart | Q28576178 | ||
A mouse model of familial hypertrophic cardiomyopathy | Q28588233 | ||
Cardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathy | Q28588821 | ||
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Myofilament Ca2+ sensitization causes susceptibility to cardiac arrhythmia in mice. | Q30484558 | ||
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Polony multiplex analysis of gene expression (PMAGE) in mouse hypertrophic cardiomyopathy | Q33287095 | ||
The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy. | Q33350170 | ||
Next generation software for functional trend analysis | Q33567100 | ||
Somatic events modify hypertrophic cardiomyopathy pathology and link hypertrophy to arrhythmia | Q34195775 | ||
Impaired Ca2+ store functions in skeletal and cardiac muscle cells from sarcalumenin-deficient mice. | Q34371988 | ||
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Genetic basis of hypertrophic cardiomyopathy: from bench to the clinics | Q36960609 | ||
Resolution of established cardiac hypertrophy and fibrosis and prevention of systolic dysfunction in a transgenic rabbit model of human cardiomyopathy through thiol-sensitive mechanisms | Q37413082 | ||
fdrtool: a versatile R package for estimating local and tail area-based false discovery rates | Q38426781 | ||
Characterizing gene sets with FuncAssociate | Q38522379 | ||
Cardiac myocyte nuclear size and ploidy status decrease after mechanical support | Q39571676 | ||
Diurnal profiling of neuroendocrine genes in murine heart, and shift in proopiomelanocortin gene expression with pressure-overload cardiac hypertrophy | Q39972664 | ||
Parathyroid hormone accelerates decompensation following left ventricular hypertrophy | Q41891365 | ||
Direct actions of urotensin II on the heart: implications for cardiac fibrosis and hypertrophy | Q42169441 | ||
Modulation of cytosolic and intra-sarcoplasmic reticulum calcium waves by calsequestrin in rat cardiac myocytes | Q42469181 | ||
Prevalence, clinical profile, and significance of left ventricular remodeling in the end-stage phase of hypertrophic cardiomyopathy | Q43954826 | ||
Familial hypertrophic cardiomyopathy-linked mutant troponin T causes stress-induced ventricular tachycardia and Ca2+-dependent action potential remodeling. | Q44324598 | ||
Effect of increased pressure loading on heart growth in neonatal rats. | Q44391074 | ||
heart of glass regulates the concentric growth of the heart in zebrafish. | Q44696937 | ||
Cardiac troponin T is essential in sarcomere assembly and cardiac contractility | Q46049216 | ||
Calpastatin domain L is involved in the regulation of L-type Ca2+ channels in guinea pig cardiac myocytes | Q46470281 | ||
RNA induction and inheritance of epigenetic cardiac hypertrophy in the mouse | Q48748791 | ||
Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathy | Q73316865 | ||
Hemodynamic alteration by fetal surgery accelerates myocyte proliferation in fetal guinea pig hearts | Q73676353 | ||
P4510 | describes a project that uses | ImageJ | Q1659584 |
limma | Q112236343 | ||
P433 | issue | 3 | |
P921 | main subject | Danio rerio | Q169444 |
cardiomyopathy | Q847583 | ||
P304 | page(s) | 400-410 | |
P577 | publication date | 2011-01-18 | |
P1433 | published in | Disease Models & Mechanisms | Q1524006 |
P1476 | title | Human cardiomyopathy mutations induce myocyte hyperplasia and activate hypertrophic pathways during cardiogenesis in zebrafish | |
P478 | volume | 4 |
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Q89637300 | Autophagy Activation in Zebrafish Heart Regeneration |
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Q38944373 | Cardiac and somatic parameters in zebrafish: tools for the evaluation of cardiovascular function |
Q38998289 | Cardiomyocyte proliferation in zebrafish and mammals: lessons for human disease |
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Q38806486 | LITTLE FISH, BIG DATA: ZEBRAFISH AS A MODEL FOR CARDIOVASCULAR AND METABOLIC DISEASE. |
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Q36873848 | The zebrafish as a novel animal model to study the molecular mechanisms of mechano-electrical feedback in the heart |
Q37659191 | The zebrafish model system in cardiovascular research: A tiny fish with mighty prospects |
Q27024639 | Understanding cardiac sarcomere assembly with zebrafish genetics |
Q38165614 | Zebrafish approaches enhance the translational research tackle box. |
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