(Q28589708)

31 January 2017

title

Cardiomyopathy in α-kinase 3 (ALPK3)-deficient mice (English)

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31 January 2017

main subject

Alpha-protein kinase 3

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GOA release 2020-03-11

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I. Van Sligtenhorst

1

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31 January 2017

Z.-M. Ding

2

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31 January 2017

Z.-Z. Shi

3

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31 January 2017

R. W. Read

4

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31 January 2017

G. Hansen

5

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31 January 2017

P. Vogel

6

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31 January 2017

publication date

1 January 2012

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31 January 2017

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31 January 2017

volume

49

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31 January 2017

issue

1

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31 January 2017

page(s)

131–141

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The transitional junction: a new functional subcellular domain at the intercalated disc

31 January 2017

cites work

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Alterations at the intercalated disk associated with the absence of muscle LIM protein

21 April 2017

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A novel myocyte-specific gene Midori promotes the differentiation of P19CL6 cells into cardiomyocytes

21 April 2017

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Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

21 April 2017

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Control of mouse cardiac morphogenesis and myogenesis by transcription factor MEF2C

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Shared genetic causes of cardiac hypertrophy in children and adults

21 April 2017

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Dilated cardiomyopathy: a disease of the intercalated disc?

21 April 2017

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Developmental defects in mouse embryos lacking N-cadherin

21 April 2017

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Wnk1 kinase deficiency lowers blood pressure in mice: A gene-trap screen to identify potential targets for therapeutic intervention

21 April 2017

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21 April 2017

Gene trap mutagenesis

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MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure

21 January 2018

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Genetic mechanisms controlling cardiovascular development

21 January 2018

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The developmental genetics of congenital heart disease.

21 January 2018

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Sarcomeric protein mutations in dilated cardiomyopathy

21 January 2018

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Genomic circuits and the integrative biology of cardiac diseases

21 January 2018

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The alpha-kinases TRPM6 and TRPM7, but not eEF-2 kinase, phosphorylate the assembly domain of myosin IIA, IIB and IIC.

21 January 2018

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Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene

21 January 2018

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Alpha-kinases: analysis of the family and comparison with conventional protein kinases

21 January 2018

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Large-scale gene trapping in C57BL/6N mouse embryonic stem cells.

21 January 2018

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Cardiac manifestations in the mouse model of mucopolysaccharidosis I.

21 January 2018

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Molecular etiology and pathogenesis of hereditary cardiomyopathy

21 January 2018

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The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma

21 January 2018

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Desmin mutation responsible for idiopathic dilated cardiomyopathy

21 January 2018

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Cardiovascular lesions and skeletal myopathy in mice lacking desmin.

21 January 2018

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Mechanisms and models in heart failure: A combinatorial approach

21 January 2018

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21 January 2018

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Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults

21 January 2018

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The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated Cardiomyopathy

21 January 2018

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Genetic causes of human heart failure

21 January 2018

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Metavinculin mutations alter actin interaction in dilated cardiomyopathy.

21 January 2018

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Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies.

21 January 2018

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Null mutation in the desmin gene gives rise to a cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811402841

Incidence, causes, and outcomes of dilated cardiomyopathy in children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811402841

Identification of a metavinculin missense mutation, R975W, associated with both hypertrophic and dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811402841

Cytoskeletal control of myogenesis: a desmin null mutation blocks the myogenic pathway during embryonic stem cell differentiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811402841

Disruption and sequence identification of 2,000 genes in mouse embryonic stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985811402841

21 January 2018

Identifiers

DOI

10.1177/0300985811402841

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31 January 2017

1 reference