Emerin interacts in vitro with the splicing-associated factor, YT521-B (Q28205048)

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3 November 2019

title

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

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3 November 2019

2

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3 November 2019

author name string

Fiona L Wilkinson

1

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3 November 2019

Zhayi Zhang

3

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3 November 2019

Aarti Sharma

4

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3 November 2019

Sushila Manilal

5

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3 November 2019

Ian Holt

6

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3 November 2019

Stefan Stamm

7

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3 November 2019

Katherine L Wilson

8

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3 November 2019

Glenn E Morris

9

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3 November 2019

language of work or name

English

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publication date

1 June 2003

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3 November 2019

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3 November 2019

volume

270

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3 November 2019

page(s)

2459-2466

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3 November 2019

issue

11

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

3 November 2019

cites work

1 reference

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1046/J.1432-1033.2003.03617.X

Nuclear envelope proteins and associated diseases

21 April 2017

1 reference

https://api.crossref.org/works/10.1046/J.1432-1033.2003.03617.X

Direct interaction between emerin and lamin A

21 April 2017

1 reference

https://api.crossref.org/works/10.1046/J.1432-1033.2003.03617.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1046/J.1432-1033.2003.03617.X

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

21 April 2017

1 reference

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1046/J.1432-1033.2003.03617.X

Cloning of a gene, YT521, for a novel RNA splicing-related protein induced by hypoxia/reoxygenation

21 April 2017

1 reference

https://api.crossref.org/works/10.1046/J.1432-1033.2003.03617.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1046/J.1432-1033.2003.03617.X

Vav family proteins couple to diverse cell surface receptors

21 April 2017

1 reference

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Distribution of emerin and lamins in the heart and implications for Emery-Dreifuss muscular dystrophy

21 April 2017

1 reference

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A novel interaction between lamin A and SREBP1: implications for partial lipodystrophy and other laminopathies

21 April 2017

1 reference

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Lamin A/C binding protein LAP2alpha is required for nuclear anchorage of retinoblastoma protein

21 April 2017

1 reference

https://api.crossref.org/works/10.1046/J.1432-1033.2003.03617.X

Interaction between emerin and nuclear lamins

21 April 2017

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1033.2003.03617.X

Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeats.

21 January 2018

1 reference

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

21 January 2018

1 reference

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The interaction and colocalization of Sam68 with the splicing-associated factor YT521-B in nuclear dots is regulated by the Src family kinase p59(fyn)

21 January 2018

1 reference

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Identification of an NTF2-related factor that binds Ran-GTP and regulates nuclear protein export.

21 January 2018

1 reference

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The in vivo minigene approach to analyze tissue-specific splicing

21 January 2018

1 reference

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Coupling of signal transduction to alternative pre-mRNA splicing by a composite splice regulator

21 January 2018

1 reference

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Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing

21 January 2018

1 reference

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Expanded CUG repeats trigger aberrant splicing of ClC-1 chloride channel pre-mRNA and hyperexcitability of skeletal muscle in myotonic dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1033.2003.03617.X

Disruption of splicing regulated by a CUG-binding protein in myotonic dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1033.2003.03617.X

Defects in pre-mRNA processing as causes of and predisposition to diseases

21 January 2018

1 reference

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X-linked emery-dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sample

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1033.2003.03617.X

The R482Q lamin A/C mutation that causes lipodystrophy does not prevent nuclear targeting of lamin A in adipocytes or its interaction with emerin

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1033.2003.03617.X

The role of the nuclear envelope in Emery-Dreifuss muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1033.2003.03617.X

How does a g993t mutation in the emerin gene cause Emery-Dreifuss muscular dystrophy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1432-1033.2003.03617.X

Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy

21 January 2018

1 reference

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