Human cardiomyopathy mutations induce myocyte hyperplasia and activate hypertrophic pathways during cardiogenesis in zebrafish

scientific article

Human cardiomyopathy mutations induce myocyte hyperplasia and activate hypertrophic pathways during cardiogenesis in zebrafish is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1242/DMM.006148
P932PMC publication ID3097461
P698PubMed publication ID21245263
P5875ResearchGate publication ID49765243

P50authorDaniela PanákováQ80563531
P2093author name stringAndreas A Werdich
Calum A MacRae
Rahul C Deo
Shannon Coy
Jason R Becker
P2860cites workAlpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomereQ24316399
InParanoid 7: new algorithms and tools for eukaryotic orthology analysisQ24643054
The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigmsQ28203734
Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardiaQ28235110
A truncated cardiac troponin T molecule in transgenic mice suggests multiple cellular mechanisms for familial hypertrophic cardiomyopathyQ28508653
Growth hormone-releasing hormone promotes survival of cardiac myocytes in vitro and protects against ischaemia-reperfusion injury in rat heartQ28576178
A mouse model of familial hypertrophic cardiomyopathyQ28588233
Cardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathyQ28588821
The Genetic Basis for CardiomyopathyQ29300961
Myofilament Ca2+ sensitization causes susceptibility to cardiac arrhythmia in mice.Q30484558
Myofibrillogenesis in the developing zebrafish heart: A functional study of tnnt2.Q30494192
Polony multiplex analysis of gene expression (PMAGE) in mouse hypertrophic cardiomyopathyQ33287095
The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy.Q33350170
Next generation software for functional trend analysisQ33567100
Somatic events modify hypertrophic cardiomyopathy pathology and link hypertrophy to arrhythmiaQ34195775
Impaired Ca2+ store functions in skeletal and cardiac muscle cells from sarcalumenin-deficient mice.Q34371988
Phenotypic diversity in hypertrophic cardiomyopathyQ34915396
The Zebrafish Information Network: the zebrafish model organism database provides expanded support for genotypes and phenotypesQ36454027
Cardiac myocyte cell cycle control in development, disease, and regenerationQ36788885
Genetic basis of hypertrophic cardiomyopathy: from bench to the clinicsQ36960609
Resolution of established cardiac hypertrophy and fibrosis and prevention of systolic dysfunction in a transgenic rabbit model of human cardiomyopathy through thiol-sensitive mechanismsQ37413082
fdrtool: a versatile R package for estimating local and tail area-based false discovery ratesQ38426781
Characterizing gene sets with FuncAssociateQ38522379
Cardiac myocyte nuclear size and ploidy status decrease after mechanical supportQ39571676
Diurnal profiling of neuroendocrine genes in murine heart, and shift in proopiomelanocortin gene expression with pressure-overload cardiac hypertrophyQ39972664
Parathyroid hormone accelerates decompensation following left ventricular hypertrophyQ41891365
Direct actions of urotensin II on the heart: implications for cardiac fibrosis and hypertrophyQ42169441
Modulation of cytosolic and intra-sarcoplasmic reticulum calcium waves by calsequestrin in rat cardiac myocytesQ42469181
Prevalence, clinical profile, and significance of left ventricular remodeling in the end-stage phase of hypertrophic cardiomyopathyQ43954826
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 contractilityQ46049216
Calpastatin domain L is involved in the regulation of L-type Ca2+ channels in guinea pig cardiac myocytesQ46470281
RNA induction and inheritance of epigenetic cardiac hypertrophy in the mouseQ48748791
Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathyQ73316865
Hemodynamic alteration by fetal surgery accelerates myocyte proliferation in fetal guinea pig heartsQ73676353
P4510describes a project that usesImageJQ1659584
limmaQ112236343
P433issue3
P921main subjectDanio rerioQ169444
cardiomyopathyQ847583
P304page(s)400-410
P577publication date2011-01-18
P1433published inDisease Models & MechanismsQ1524006
P1476titleHuman cardiomyopathy mutations induce myocyte hyperplasia and activate hypertrophic pathways during cardiogenesis in zebrafish
P478volume4

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cites work (P2860)
Q58752907A Langendorff-like system to quantify cardiac pump function in adult zebrafish
Q41687674A One Health Approach to Hypertrophic Cardiomyopathy
Q34062888A dominantly negative mutation in cardiac troponin I at the interface with troponin T causes early remodeling in ventricular cardiomyocytes
Q89637300Autophagy Activation in Zebrafish Heart Regeneration
Q35834044CDK9 and its repressor LARP7 modulate cardiomyocyte proliferation and response to injury in the zebrafish heart
Q38944373Cardiac and somatic parameters in zebrafish: tools for the evaluation of cardiovascular function
Q38998289Cardiomyocyte proliferation in zebrafish and mammals: lessons for human disease
Q45052413Comparative cardiac pathological changes of Atlantic salmon (Salmo salar L.) affected with heart and skeletal muscle inflammation (HSMI), cardiomyopathy syndrome (CMS) and pancreas disease (PD).
Q51366678Contractility of ventricular myocytes is well preserved despite altered mechanisms of Ca2+ transport and a changing pattern of mRNA in aged type 2 Zucker diabetic fatty rat heart.
Q57973932Deficiency in the nuclear long noncoding RNA causes myogenic defects and heart remodeling in mice
Q41700317Deficient cMyBP-C protein expression during cardiomyocyte differentiation underlies human hypertrophic cardiomyopathy cellular phenotypes in disease specific human ES cell derived cardiomyocytes
Q24635831Hadp1, a newly identified pleckstrin homology domain protein, is required for cardiac contractility in zebrafish
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Q38203157Hypertrophic cardiomyopathy: how do mutations lead to disease?
Q41892305Identification of a new modulator of the intercalated disc in a zebrafish model of arrhythmogenic cardiomyopathy.
Q36135276In vivo natriuretic peptide reporter assay identifies chemical modifiers of hypertrophic cardiomyopathy signalling
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