(Q24315475)

English

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

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scholarly article

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

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Emery-Dreifuss muscular dystrophy

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James M Holaska

object named as

James M Holaska

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Yasushi Hiraoka

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Yasushi Hiraoka

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author name string

Tokuko Haraguchi

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Miho Yamane

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Takako Koujin

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Noriyo Hashiguchi

5

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Chie Mori

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Katherine L Wilson

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publication date

March 2004

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271

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1035-45

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5

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Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse

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https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

21 January 2018

Btf, a novel death-promoting transcriptional repressor that interacts with Bcl-2-related proteins

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

21 January 2018

Molecular cloning and genomic organization of mouse homologue of Drosophila germ cell-less and its expression in germ lineage cells.

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https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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Direct interaction between emerin and lamin A

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https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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germ cell-less is required only during the establishment of the germ cell lineage of Drosophila and has activities which are dependent and independent of its localization to the nuclear envelope.

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https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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Emerin, deficiency of which causes Emery-Dreifuss muscular dystrophy, is localized at the inner nuclear membrane

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https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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

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https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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

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https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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Fluorescence microscopy in three dimensions.

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https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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LMNA mutations in atypical Werner's syndrome

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https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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Emery-Dreifuss muscular dystrophy - a 40 year retrospective

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https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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108th ENMC International Workshop, 3rd Workshop of the MYO-CLUSTER project: EUROMEN, 7th International Emery-Dreifuss Muscular Dystrophy (EDMD) Workshop, 13-15 September 2002, Naarden, The Netherlands

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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The nuclear envelope, muscular dystrophy and gene expression

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https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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Transcriptional repression, apoptosis, human disease and the functional evolution of the nuclear lamina

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https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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Identity between TRAP and SMCC complexes indicates novel pathways for the function of nuclear receptors and diverse mammalian activators

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https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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Life at the edge: the nuclear envelope and human disease

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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The nuclear muscular dystrophies.

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https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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MAN1 and emerin have overlapping function(s) essential for chromosome segregation and cell division in Caenorhabditis elegans

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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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/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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Barrier to autointegration factor interacts with the cone-rod homeobox and represses its transactivation function

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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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/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

based on heuristic

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Barrier-to-autointegration factor: major roles in chromatin decondensation and nuclear assembly

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

based on heuristic

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A cell-killing monoclonal antibody (anti-Fas) to a cell surface antigen co-downregulated with the receptor of tumor necrosis factor

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

based on heuristic

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Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

based on heuristic

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Prediction of the coding sequences of unidentified human genes. V. The coding sequences of 40 new genes (KIAA0161-KIAA0200) deduced by analysis of cDNA clones from human cell line KG-1

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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LAP2 binds to BAF.DNA complexes: requirement for the LEM domain and modulation by variable regions

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

based on heuristic

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Heart to heart: from nuclear proteins to Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

based on heuristic

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Nuclear envelope proteins and associated diseases

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Lamin a truncation in Hutchinson-Gilford progeria.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

based on heuristic

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Emery-Dreifuss syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1432-1033.2004.04007.X

7 January 2021

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Identifiers

10.1111/J.1432-1033.2004.04007.X

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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ResearchGate publication ID

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