(Q24304005)

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Distinct functional domains in nesprin-1alpha and nesprin-2beta bind directly to emerin and both interactions are disrupted in X-linked Emery-Dreifuss muscular dystrophy

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29 December 2019

Distinct functional domains in nesprin-1alpha and nesprin-2beta bind directly to emerin and both interactions are disrupted in X-linked Emery-Dreifuss muscular dystrophy (English)

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29 December 2019

Emery-Dreifuss muscular dystrophy

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based on heuristic

inferred from title

3

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29 December 2019

Catherine Shanahan

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29 December 2019

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Matthew A Wheeler

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29 December 2019

John D Davies

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29 December 2019

Lindsay J Emerson

4

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29 December 2019

James Hunt

5

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29 December 2019

Juliet A Ellis

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29 December 2019

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publication date

30 March 2007

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29 December 2019

Experimental Cell Research

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29 December 2019

313

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29 December 2019

2845-2857

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29 December 2019

13

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29 December 2019

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

MAN1, an inner nuclear membrane protein that shares the LEM domain with lamina-associated polypeptide 2 and emerin

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Barrier-to-autointegration factor (BAF) bridges DNA in a discrete, higher-order nucleoprotein complex

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Multiple and surprising new functions for emerin, a nuclear membrane protein

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Lmo7 is an emerin-binding protein that regulates the transcription of emerin and many other muscle-relevant genes

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Emery-Dreifuss muscular dystrophy - a 40 year retrospective

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

The nuclear envelope, muscular dystrophy and gene expression

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Abnormal nuclear shape and impaired mechanotransduction in emerin-deficient cells

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Decreased mechanical stiffness in LMNA-/- cells is caused by defective nucleo-cytoskeletal integrity: implications for the development of laminopathies.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Nesprin-2 is a multi-isomeric protein that binds lamin and emerin at the nuclear envelope and forms a subcellular network in skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Nesprin-3, a novel outer nuclear membrane protein, associates with the cytoskeletal linker protein plectin

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Nesprins: intracellular scaffolds that maintain cell architecture and coordinate cell function?

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Nesprin-1alpha self-associates and binds directly to emerin and lamin A in vitro

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Lamin A/C-dependent localization of Nesprin-2, a giant scaffolder at the nuclear envelope

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

SUN1 interacts with nuclear lamin A and cytoplasmic nesprins to provide a physical connection between the nuclear lamina and the cytoskeleton

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

The inner nuclear membrane protein Sun1 mediates the anchorage of Nesprin-2 to the nuclear envelope

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Nesprin-1alpha contributes to the targeting of mAKAP to the cardiac myocyte nuclear envelope

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Coupling of the nucleus and cytoplasm: role of the LINC complex

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

The inner nuclear membrane protein emerin regulates beta-catenin activity by restricting its accumulation in the nucleus

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

The Emery-Dreifuss Muscular Dystrophy Mutation Database

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Direct interaction between emerin and lamin A

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Transcriptional repressor germ cell-less (GCL) and barrier to autointegration factor (BAF) compete for binding to emerin in vitro

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Emerin binding to Btf, a death-promoting transcriptional repressor, is disrupted by a missense mutation that causes Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Emerin caps the pointed end of actin filaments: evidence for an actin cortical network at the nuclear inner membrane

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Emerin interacts in vitro with the splicing-associated factor, YT521-B

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Comparative analysis of coiled-coil prediction methods.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblasts

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Structural analysis of emerin, an inner nuclear membrane protein mutated in X-linked Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Dynamic interaction between BAF and emerin revealed by FRAP, FLIP, and FRET analyses in living HeLa cells.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Robust phosphoproteomic profiling of tyrosine phosphorylation sites from human T cells using immobilized metal affinity chromatography and tandem mass spectrometry

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Dissociation of emerin from barrier-to-autointegration factor is regulated through mitotic phosphorylation of emerin in a xenopus egg cell-free system

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

Identification of tyrosine-phosphorylation sites in the nuclear membrane protein emerin.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

The Emery-Dreifuss muscular dystrophy associated-protein emerin is phosphorylated on serine 49 by protein kinase A.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2007.03.025

7 January 2021

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10.1016/J.YEXCR.2007.03.025

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Europe PubMed Central

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29 December 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17462627%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

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