(Q34214905)

31 July 2017

title

Reversibility of PRKAG2 glycogen-storage cardiomyopathy and electrophysiological manifestations (English)

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31 July 2017

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10

J G Seidman

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31 July 2017

11

Christine E Seidman

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31 July 2017

Ferhaan Ahmad

3

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ORCID Public Data File 2021

Okan Toka

6

object named as

Okan Toka

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31 July 2017

7

Tetsuo Konno

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31 July 2017

1

Cordula M Wolf

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31 July 2017

2

Michael Arad

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31 July 2017

12

Charles I Berul

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31 July 2017

Atsushi Sanbe

4

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31 July 2017

Scott A Bernstein

5

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31 July 2017

Gregory Morley

8

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31 July 2017

Jeffrey Robbins

9

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31 July 2017

language of work or name

English

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publication date

24 December 2007

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31 July 2017

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31 July 2017

volume

117

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31 July 2017

issue

2

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31 July 2017

page(s)

144-154

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describes a project that uses

31 July 2017

ImageQuant

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2957811/fullTextXML

inferred from PubMed Central ID database lookup

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2957811/fullTextXML

inferred from PubMed Central ID database lookup

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Cytoarchitecture and intercalated disks of the working myocardium and the conduction system in the mammalian heart

5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy

5 July 2018

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5 July 2018

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Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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Electrophysiological abnormalities and arrhythmias in alpha MHC mutant familial hypertrophic cardiomyopathy mice

5 July 2018

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High-level production of recombinant human lysosomal acid alpha-glucosidase in Chinese hamster ovary cells which targets to heart muscle and corrects glycogen accumulation in fibroblasts from patients with Pompe disease

5 July 2018

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Transcriptional activation by tetracyclines in mammalian cells

5 July 2018

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Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3

5 July 2018

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5 July 2018

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Pompe's disease presenting as hypertrophic myocardiopathy with Wolff-Parkinson-White syndrome

5 July 2018

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Dilated-hypokinetic evolution of hypertrophic cardiomyopathy: prevalence, incidence, risk factors, and prognostic implications in pediatric and adult patients

5 July 2018

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Sustained correction of glycogen storage disease type II using adeno-associated virus serotype 1 vectors

28 October 2018

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Cell size and communication: role in structural and electrical development and remodeling of the heart

28 October 2018

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Glycogen storage diseases presenting as hypertrophic cardiomyopathy.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957811

Safety and efficacy of recombinant acid alpha-glucosidase (rhGAA) in patients with classical infantile Pompe disease: results of a phase II clinical trial

28 October 2018

1 reference

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Electrophysiologic characterization and postnatal development of ventricular pre-excitation in a mouse model of cardiac hypertrophy and Wolff-Parkinson-White syndrome

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957811

Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957811

Reengineering inducible cardiac-specific transgenesis with an attenuated myosin heavy chain promoter

28 October 2018

1 reference

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Regulation of muscle GLUT-4 transcription by AMP-activated protein kinase

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957811

The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957811

Suppression of atrial myosin gene expression occurs independently in the left and right ventricles of the developing mouse heart.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957811

Molecular mechanisms underlying ionic remodeling in a dog model of atrial fibrillation

28 October 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957811

AMP-activated protein kinase inhibits the glucose-activated expression of fatty acid synthase gene in rat hepatocytes

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957811

Anin vivo analysis of transcriptional elements in the mouse α-myosin heavy chain gene promoter

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957811

Prevalence and electrocardiographic forms of the Wolff-Parkinson-White syndrome

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957811

Wolff-Parkinson-White syndrome and supraventricular tachycardia during infancy: management and follow-up

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957811

Increased alpha2 subunit-associated AMPK activity and PRKAG2 cardiomyopathy

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18158359

12 December 2020

inferred from PubMed ID database lookup

Molecular genetic analysis of PRKAG2 in sporadic Wolff-Parkinson-White syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18158359

12 December 2020

inferred from PubMed ID database lookup

Mutation analysis of AMP-activated protein kinase subunits in inherited cardiomyopathies: implications for kinase function and disease pathogenesis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18158359

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1161/CIRCULATIONAHA.107.726752

1 reference

31 July 2017

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31 July 2017

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