(Q38461361)

English

Transgenic overexpression of human DMPK accumulates into hypertrophic cardiomyopathy, myotonic myopathy and hypotension traits of myotonic dystrophy

scientific article published on 18 August 2004

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scholarly article

1 reference

Europe PubMed Central

3 September 2017

Transgenic overexpression of human DMPK accumulates into hypertrophic cardiomyopathy, myotonic myopathy and hypotension traits of myotonic dystrophy (English)

1 reference

Europe PubMed Central

3 September 2017

1 reference

based on heuristic

inferred from title

hypertrophic cardiomyopathy

1 reference

based on heuristic

inferred from title

author name string

D Fearghas O'Cochlain

1

1 reference

Europe PubMed Central

3 September 2017

Carmen Perez-Terzic

2

1 reference

Europe PubMed Central

3 September 2017

Santiago Reyes

3

1 reference

Europe PubMed Central

3 September 2017

Garvan C Kane

4

1 reference

Europe PubMed Central

3 September 2017

Atta Behfar

5

1 reference

Europe PubMed Central

3 September 2017

Denice M Hodgson

6

1 reference

Europe PubMed Central

3 September 2017

Jeffrey A Strommen

7

1 reference

Europe PubMed Central

3 September 2017

Xiao-Ke Liu

8

1 reference

Europe PubMed Central

3 September 2017

Walther van den Broek

9

1 reference

Europe PubMed Central

3 September 2017

Derick G Wansink

10

1 reference

Europe PubMed Central

3 September 2017

Bé Wieringa

11

1 reference

Europe PubMed Central

3 September 2017

Andre Terzic

12

1 reference

Europe PubMed Central

3 September 2017

publication date

18 August 2004

1 reference

Europe PubMed Central

3 September 2017

Human Molecular Genetics

1 reference

Europe PubMed Central

3 September 2017

13

1 reference

Europe PubMed Central

3 September 2017

2505-2518

1 reference

Europe PubMed Central

3 September 2017

20

1 reference

Europe PubMed Central

3 September 2017

The protein kinase complement of the human genome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Rocks: multifunctional kinases in cell behaviour

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Alternative splicing controls myotonic dystrophy protein kinase structure, enzymatic activity, and subcellular localization

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Transgenic mouse models for myotonic dystrophy type 1 (DM1)

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Characterization of the myotonic dystrophy region predicts multiple protein isoform-encoding mRNAs

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Skeletal muscle sodium channel gating in mice deficient in myotonic dystrophy protein kinase

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Abnormal contractile activity and calcium cycling in cardiac myocytes isolated from DMPK knockout mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Abnormal Na channel gating in murine cardiac myocytes deficient in myotonic dystrophy protein kinase

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Inactivation of muscle chloride channel by transposon insertion in myotonic mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Modulation of skeletal muscle sodium channels by human myotonin protein kinase

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Myotonic dystrophy protein kinase is involved in the modulation of the Ca2+ homeostasis in skeletal muscle cells

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

The expression of ion channel mRNAs in skeletal muscles from patients with myotonic muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Expanded CUG repeats trigger aberrant splicing of ClC-1 chloride channel pre-mRNA and hyperexcitability of skeletal muscle in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Myotonic dystrophy protein kinase phosphorylates the myosin phosphatase targeting subunit and inhibits myosin phosphatase activity

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

An unstable triplet repeat in a gene related to myotonic muscular dystrophy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Cloning of the essential myotonic dystrophy region and mapping of the putative defect

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Overexpression of 3'-untranslated region of the myotonic dystrophy kinase cDNA inhibits myoblast differentiation in vitro

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Inhibition of myogenesis in transgenic mice expressing the human DMPK 3'-UTR.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Myogenic defects in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

RNA leaching of transcription factors disrupts transcription in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Myotonic dystrophy: RNA pathogenesis comes into focus

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Definition of regulatory sequence elements in the promoter region and the first intron of the myotonic dystrophy protein kinase gene

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Characterization of a monoclonal antibody panel shows that the myotonic dystrophy protein kinase, DMPK, is expressed almost exclusively in muscle and heart

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

ATP-sensitive K+ channel knockout compromises the metabolic benefit of exercise training, resulting in cardiac deficits

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Stress pathways and heart failure

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Cardiac hypertrophy: the good, the bad, and the ugly

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Converging pathways and principles in heart development and disease: CV@CSH.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Myotonic dystrophy reviewed: back to the future?

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Absence of the skeletal muscle sarcolemma chloride channel ClC-1 in myotonic mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

A muscleblind knockout model for myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

A role for myotonic dystrophy protein kinase in synaptic plasticity

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

The aging process

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Molecular Biology of Aging

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Cellular remodeling in heart failure disrupts K(ATP) channel-dependent stress tolerance

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Kir6.2 is required for adaptation to stress

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Pathology of the cardiac conduction system in myotonic dystrophy: a study of 12 cases

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

THE HEART IN MYOTONIA ATROPHICA.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Mutagenic stress modulates the dynamics of CTG repeat instability associated with myotonic dystrophy type 1.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Expanded CUG repeat RNAs form hairpins that activate the double-stranded RNA-dependent protein kinase PKR

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Overexpression of Human Myotonic Dystrophy Protein Kinase in Schizosaccharomyces pombe Induces an Abnormal Polarized and Swollen Cell Morphology

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Structural adaptation of the nuclear pore complex in stem cell-derived cardiomyocytes.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Directed inhibition of nuclear import in cellular hypertrophy.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Stable benefit of embryonic stem cell therapy in myocardial infarction.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Genetic disruption of Kir6.2, the pore-forming subunit of ATP-sensitive K+ channel, predisposes to catecholamine-induced ventricular dysrhythmia

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDH266

21 January 2018

Identifiers

10.1093/HMG/DDH266

1 reference

Europe PubMed Central

3 September 2017

1 reference

Europe PubMed Central

3 September 2017

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