Cell signaling abnormalities in cardiomyopathy caused by lamin A/C gene mutations.

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Role of Lamin A/C Gene Mutations in the Signaling Defects Leading to Cardiomyopathies

P2860

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P2860

Cell signaling abnormalities in cardiomyopathy caused by lamin A/C gene mutations.

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http://www.wikidata.org/entity/Q47340107

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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Cell signaling abnormalities in cardiomyopathy caused by lamin A/C gene mutations.

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Cell signaling abnormalities in cardiomyopathy caused by lamin A/C gene mutations.

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Item

label

Cell signaling abnormalities in cardiomyopathy caused by lamin A/C gene mutations.

@en

Cell signaling abnormalities in cardiomyopathy caused by lamin A/C gene mutations.

@nl

prefLabel

Cell signaling abnormalities in cardiomyopathy caused by lamin A/C gene mutations.

@en

Cell signaling abnormalities in cardiomyopathy caused by lamin A/C gene mutations.

@nl

P1476

Cell signaling abnormalities in cardiomyopathy caused by lamin A/C gene mutations.

@en

P2093

Howard J Worman

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P2860

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

Homologies in both primary and secondary structure between nuclear envelope and intermediate filament proteins

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

Activation of MAPK pathways links LMNA mutations to cardiomyopathy in Emery-Dreifuss muscular dystrophy.

Lamin-binding Proteins

Pharmacological inhibition of c-Jun N-terminal kinase signaling prevents cardiomyopathy caused by mutation in LMNA gene

Activation of MAPK in hearts of EMD null mice: similarities between mouse models of X-linked and autosomal dominant Emery Dreifuss muscular dystrophy.

Mitogen-activated protein kinase inhibitors improve heart function and prevent fibrosis in cardiomyopathy caused by mutation in lamin A/C gene.

Late gadolinium enhanced cardiovascular magnetic resonance of lamin A/C gene mutation related dilated cardiomyopathy.

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37-42

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scholarly article

review article

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10.1042/BST20170236

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2017-12-01T00:00:00Z

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29196611

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6521696

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Cell signaling abnormalities in cardiomyopathy caused by lamin A/C gene mutations.

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P2860

P2860

Cell signaling abnormalities in cardiomyopathy caused by lamin A/C gene mutations.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932