The LINC complex and human disease (Q37958956)

25 August 2017

The LINC complex and human disease (English)

1 reference

25 August 2017

Peter Meinke

1

1 reference

25 August 2017

Thuy Duong Nguyen

series ordinal

2

1 reference

25 August 2017

Manfred S Wehnert

series ordinal

3

1 reference

25 August 2017

language of work or name

1 reference

1 December 2011

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Biochemical Society Transactions

25 August 2017

1 reference

25 August 2017

39

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25 August 2017

1693-1697

1 reference

25 August 2017

6

1 reference

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

25 August 2017

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

Dynamics and molecular interactions of linker of nucleoskeleton and cytoskeleton (LINC) complex proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

Linear arrays of nuclear envelope proteins harness retrograde actin flow for nuclear movement.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

21 January 2018

Emery-Dreifuss syndrome

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

Myofiber degeneration in autosomal dominant Emery-Dreifuss muscular dystrophy (AD-EDMD) (LGMD1B).

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

Frequent low penetrance mutations in the Lamin A/C gene, causing Emery Dreifuss muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

"Laminopathies": a wide spectrum of human diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

Clinical and genetic heterogeneity in laminopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

Nesprin-1 and -2 are involved in the pathogenesis of Emery Dreifuss muscular dystrophy and are critical for nuclear envelope integrity

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

Disease severity in dominant Emery Dreifuss is increased by mutations in both emerin and desmin proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

Direct interaction between emerin and lamin A

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

An X-linked myopathy with postural muscle atrophy and generalized hypertrophy, termed XMPMA, is caused by mutations in FHL1

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

TMEM43 mutations in Emery-Dreifuss muscular dystrophy-related myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

Mammalian SUN protein interaction networks at the inner nuclear membrane and their role in laminopathy disease processes

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

Severe clinical expression in X-linked Emery–Dreifuss muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBST20110658

21 January 2018

Identifiers

DOI

10.1042/BST20110658

1 reference

release_fd2yfkitbvfmdkcdf3ise3ceqm

25 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/fd2yfkitbvfmdkcdf3ise3ceqm

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference