Human cardiomyopathy mutations induce myocyte hyperplasia and activate hypertrophic pathways during cardiogenesis in zebrafish (Q30500300)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21245263%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

title

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

1 reference

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20 January 2020

0 references

1 reference

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20 January 2020

Jason R Becker

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20 January 2020

Rahul C Deo

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20 January 2020

Andreas A Werdich

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20 January 2020

Shannon Coy

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20 January 2020

Calum A MacRae

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20 January 2020

publication date

18 January 2011

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Disease Models & Mechanisms

20 January 2020

published in

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20 January 2020

volume

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20 January 2020

issue

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20 January 2020

page(s)

400-410

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describes a project that uses

20 January 2020

ImageJ

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3097461/fullTextXML

inferred from PubMed Central ID database lookup

limma

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22 June 2022

https://europepmc.org/article/PMC/3097461

inferred from PubMed Central ID database lookup

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Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia

20 June 2018

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Somatic events modify hypertrophic cardiomyopathy pathology and link hypertrophy to arrhythmia

20 June 2018

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Modulation of cytosolic and intra-sarcoplasmic reticulum calcium waves by calsequestrin in rat cardiac myocytes

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Direct actions of urotensin II on the heart: implications for cardiac fibrosis and hypertrophy

20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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Cardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathy

20 June 2018

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A truncated cardiac troponin T molecule in transgenic mice suggests multiple cellular mechanisms for familial hypertrophic cardiomyopathy

20 June 2018

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20 June 2018

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

20 June 2018

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26 November 2018

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Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathy

26 November 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/21245263

12 December 2020

inferred from PubMed ID database lookup

Hemodynamic alteration by fetal surgery accelerates myocyte proliferation in fetal guinea pig hearts

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21245263

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1242/DMM.006148

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21245263%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21245263%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

PubMed publication ID

21245263

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21245263%20AND%20SRC:MED&resulttype=core&format=json