Reduced expression of A-type lamins and emerin activates extracellular signal-regulated kinase in cultured cells. (Q37106817)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19022376%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

title

Reduced expression of A-type lamins and emerin activates extracellular signal-regulated kinase in cultured cells (English)

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17 January 2020

1

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17 January 2020

author name string

Wei Wu

series ordinal

2

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17 January 2020

Howard J Worman

series ordinal

3

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17 January 2020

language of work or name

English

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publication date

5 November 2008

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17 January 2020

number of pages

7

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Biochimica et Biophysica Acta

inferred from page(s)

published in

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17 January 2020

volume

1792

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17 January 2020

page(s)

75-81

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17 January 2020

issue

1

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Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins.

17 January 2020

cites work

1 reference

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Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan.

14 September 2017

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P2Y nucleotide receptor signaling through MAPK/ERK is regulated by extracellular matrix: involvement of beta3 integrins

14 September 2017

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

14 September 2017

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The role of ERK signaling in protein hydrogel remodeling by vascular smooth muscle cells

14 September 2017

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"Laminopathies": a wide spectrum of human diseases

14 September 2017

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

14 September 2017

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Proteasome-mediated degradation of integral inner nuclear membrane protein emerin in fibroblasts lacking A-type lamins

14 September 2017

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The nuclear envelope and human disease

14 September 2017

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Real-time PCR based on SYBR-Green I fluorescence: an alternative to the TaqMan assay for a relative quantification of gene rearrangements, gene amplifications and micro gene deletions

14 September 2017

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Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.

14 September 2017

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Involvement of extracellular signal-regulated kinases 1/2 in cardiac hypertrophy and cell death

14 September 2017

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The inner nuclear membrane

14 September 2017

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Emery-Dreifuss muscular dystrophy - a 40 year retrospective

14 September 2017

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

14 September 2017

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Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy.

14 September 2017

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Direct interaction between emerin and lamin A

14 September 2017

1 reference

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

14 September 2017

1 reference

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Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646592

Changes at P183 of emerin weaken its protein-protein interactions resulting in X-linked Emery-Dreifuss muscular dystrophy

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646592

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

14 September 2017

1 reference

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The Emery-Dreifuss muscular dystrophy protein, emerin, is a nuclear membrane protein

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646592

Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophy

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646592

Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C

14 September 2017

1 reference

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Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2646592

PD 098059 is a specific inhibitor of the activation of mitogen-activated protein kinase kinase in vitro and in vivo

14 September 2017

1 reference

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Phenotypic clustering of lamin A/C mutations in neuromuscular patients.

14 September 2017

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The Emery-Dreifuss muscular dystrophy phenotype arises from aberrant targeting and binding of emerin at the inner nuclear membrane.

29 September 2017

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Distinct regions specify the nuclear membrane targeting of emerin, the responsible protein for Emery-Dreifuss muscular dystrophy

29 September 2017

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Activation of JNK/SAPK and ERK by mechanical strain in vascular smooth muscle cells depends on extracellular matrix composition

29 September 2017

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Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene

3 September 2018

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12 December 2020

Properties of lamin A mutants found in Emery-Dreifuss muscular dystrophy, cardiomyopathy and Dunnigan-type partial lipodystrophy

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12 December 2020

Nuclear envelope defects associated with LMNA mutations cause dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy

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12 December 2020

Genotype-phenotype analysis in X-linked Emery-Dreifuss muscular dystrophy and identification of a missense mutation associated with a milder phenotype

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12 December 2020

Emery-Dreifuss muscular dystrophy

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12 December 2020

Lamin A/C Gene Mutation Associated With Dilated Cardiomyopathy With Variable Skeletal Muscle Involvement

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12 December 2020

10.1016/J.BBADIS.2008.10.012

Identifiers

DOI

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17 January 2020

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17 January 2020

1 reference

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