(Q52162402)

25 April 2018

title

Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy (English)

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25 April 2018

main subject

dilated cardiomyopathy

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20

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25 April 2018

Josef Gotzmann

Josef Gotzmann

18

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Gianfranco Sinagra

Gianfranco Sinagra

9

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Roland Foisner

19

Roland Foisner

1 reference

25 April 2018

Pamela R Fain

6

Pamela R Fain

1 reference

25 April 2018

Sylvia Vlcek

4

Sylvia Vlcek

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25 April 2018

Andreas Gajewski

3

Andreas Gajewski

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25 April 2018

author name string

Matthew R G Taylor

1

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25 April 2018

Dobromir Slavov

2

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25 April 2018

Lisa Ku

5

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25 April 2018

Elisa Carniel

7

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25 April 2018

Andrea Di Lenarda

8

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25 April 2018

Mark M Boucek

10

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25 April 2018

Jean Cavanaugh

11

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25 April 2018

Sharon L Graw

12

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25 April 2018

Patsy Ruegg

13

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25 April 2018

Jennie Feiger

14

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25 April 2018

Xiao Zhu

15

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25 April 2018

Debra A Ferguson

16

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25 April 2018

Michael R Bristow

17

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25 April 2018

Familial Cardiomyopathy Registry Research Group

21

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25 April 2018

publication date

1 December 2005

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25 April 2018

published in

Human Mutation

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25 April 2018

volume

26

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25 April 2018

issue

6

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25 April 2018

page(s)

566-574

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25 April 2018

Interaction between emerin and nuclear lamins

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

The characterization and localization of the mouse thymopoietin/lamina-associated polypeptide 2 gene and its alternatively spliced products

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

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/10.1002%2FHUMU.20250

7 January 2021

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/10.1002%2FHUMU.20250

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Life at the edge: the nuclear envelope and human disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Direct interaction between emerin and lamin A

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Detergent-salt resistance of LAP2alpha in interphase nuclei and phosphorylation-dependent association with chromosomes early in nuclear assembly implies functions in nuclear structure dynamics.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Review: lamina-associated polypeptide 2 isoforms and related proteins in cell cycle-dependent nuclear structure dynamics

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Expression of lamin A mutated in the carboxyl-terminal tail generates an aberrant nuclear phenotype similar to that observed in cells from patients with Dunnigan-type partial lipodystrophy and Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Integral membrane proteins of the nuclear envelope interact with lamins and chromosomes, and binding is modulated by mitotic phosphorylation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

A phosphorylation cluster in the chromatin-binding region regulates chromosome association of LAP2alpha

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Roles of LAP2 proteins in nuclear assembly and DNA replication: truncated LAP2beta proteins alter lamina assembly, envelope formation, nuclear size, and DNA replication efficiency in Xenopus laevis extracts

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

GOR method for predicting protein secondary structure from amino acid sequence.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

The nuclear lamina and its functions in the nucleus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Three distinct human thymopoietins are derived from alternatively spliced mRNAs

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Structure and mapping of the human thymopoietin (TMPO) gene and relationship of human TMPO beta to rat lamin-associated polypeptide 2

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Intermediate filaments: novel assembly models and exciting new functions for nuclear lamins

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Improvements in protein secondary structure prediction by an enhanced neural network

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Aging and nuclear organization: lamins and progeria

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Nuclear membrane proteins with potential disease links found by subtractive proteomics

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Natural history of dilated cardiomyopathy due to lamin A/C gene mutations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Ubiquitous expression of a cloned murine thymopoietin cDNA.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Functional diversity of LAP2alpha and LAP2beta in postmitotic chromosome association is caused by an alpha-specific nuclear targeting domain

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Distinct functions of the unique C terminus of LAP2alpha in cell proliferation and nuclear assembly

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Lco1 is a novel widely expressed lamin-binding protein in the nuclear interior.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

The nuclear envelope, muscular dystrophy and gene expression

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

How do mutations in lamins A and C cause disease?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Proteins that bind A-type lamins: integrating isolated clues

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20250

7 January 2021

Identifiers

DOI

10.1002/HUMU.20250

1 reference

25 April 2018

PubMed ID

16247757

1 reference

25 April 2018