Modeling inherited cardiac disorders (Q27024060)

title

Modeling inherited cardiac disorders (English)

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author name string

Karim Sallam

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6530482&resulttype=core&format=json

14 May 2020

Kazuki Kodo

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6530482&resulttype=core&format=json

14 May 2020

Joseph C Wu

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6530482&resulttype=core&format=json

14 May 2020

language of work or name

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2014

1 reference

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6530482&resulttype=core&format=json

14 May 2020

volume

78

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6530482&resulttype=core&format=json

14 May 2020

issue

4

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6530482&resulttype=core&format=json

14 May 2020

page(s)

784-794

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6530482&resulttype=core&format=json

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

14 May 2020

cites work

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Repolarization reserve: a moving target

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Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations

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Drug evaluation in cardiomyocytes derived from human induced pluripotent stem cells carrying a long QT syndrome type 2 mutation

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Generation of isogenic pluripotent stem cells differing exclusively at two early onset Parkinson point mutations

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HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

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Use of human stem cell derived cardiomyocytes to examine sunitinib mediated cardiotoxicity and electrophysiological alterations

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Human Pompe disease-induced pluripotent stem cells for pathogenesis modeling, drug testing and disease marker identification

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Cardiomyocytes generated from CPVTD307H patients are arrhythmogenic in response to β-adrenergic stimulation

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Model for long QT syndrome type 2 using human iPS cells demonstrates arrhythmogenic characteristics in cell culture

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Dantrolene rescues arrhythmogenic RYR2 defect in a patient-specific stem cell model of catecholaminergic polymorphic ventricular tachycardia

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In vitro modeling of ryanodine receptor 2 dysfunction using human induced pluripotent stem cells

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Patient-specific induced pluripotent stem cells as a model for familial dilated cardiomyopathy.

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Disease characterization using LQTS-specific induced pluripotent stem cells

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Modeling of catecholaminergic polymorphic ventricular tachycardia with patient-specific human-induced pluripotent stem cells

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Generation of patient-specific induced pluripotent stem cell-derived cardiomyocytes as a cellular model of arrhythmogenic right ventricular cardiomyopathy.

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Mechanisms of zolpidem-induced long QT syndrome: acute inhibition of recombinant hERG K(+) channels and action potential prolongation in human cardiomyocytes derived from induced pluripotent stem cells

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Repolarization reserve determines drug responses in human pluripotent stem cell derived cardiomyocytes

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Hypertrophic cardiomyopathy: diagnosis, risk stratification and treatment

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Distinct metabolic flow enables large-scale purification of mouse and human pluripotent stem cell-derived cardiomyocytes

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Induced pluripotent stem cells used to reveal drug actions in a long QT syndrome family with complex genetics

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Abnormal calcium handling properties underlie familial hypertrophic cardiomyopathy pathology in patient-specific induced pluripotent stem cells

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Patient-specific induced-pluripotent stem cells-derived cardiomyocytes recapitulate the pathogenic phenotypes of dilated cardiomyopathy due to a novel DES mutation identified by whole exome sequencing.

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12 December 2020

Ultrastructural maturation of human-induced pluripotent stem cell-derived cardiomyocytes in a long-term culture

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Drug screening using a library of human induced pluripotent stem cell-derived cardiomyocytes reveals disease-specific patterns of cardiotoxicity

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The effect of cyclic stretch on maturation and 3D tissue formation of human embryonic stem cell-derived cardiomyocytes

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Identifiers

DOI

10.1253/CIRCJ.CJ-14-0182

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6530482&resulttype=core&format=json

14 May 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6530482&resulttype=core&format=json

14 May 2020

PubMed publication ID

2 references