Functions and dysfunctions of the nuclear lamin Ig-fold domain in nuclear assembly, growth, and Emery-Dreifuss muscular dystrophy. (Q34081419)

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8 January 2020

title

Functions and dysfunctions of the nuclear lamin Ig-fold domain in nuclear assembly, growth, and Emery-Dreifuss muscular dystrophy (English)

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8 January 2020

author name string

Dale K Shumaker

1

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8 January 2020

Reynold I Lopez-Soler

2

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8 January 2020

Harald Herrmann

4

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8 January 2020

Timothy P Spann

6

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8 January 2020

Robert D Goldman

7

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8 January 2020

language of work or name

English

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publication date

14 October 2005

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Proceedings of the National Academy of Sciences of the United States of America

8 January 2020

published in

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8 January 2020

volume

102

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8 January 2020

issue

43

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8 January 2020

page(s)

15494-15499

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The nuclear lamina comes of age.

8 January 2020

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Alteration of nuclear lamin organization inhibits RNA polymerase II-dependent transcription

28 July 2018

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28 July 2018

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Tunicates have unusual nuclear lamins with a large deletion in the carboxyterminal tail domain

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

28 July 2018

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Nuclear envelope assembly in Xenopus extracts visualized by scanning EM reveals a transport-dependent 'envelope smoothing' event

28 July 2018

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Disruption of nuclear lamin organization alters the distribution of replication factors and inhibits DNA synthesis

28 July 2018

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Native chick laminin-4 containing the beta 2 chain (s-laminin) promotes motor axon growth

28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Characterization of the Hydra lamin and its gene: A molecular phylogeny of metazoan lamins

21 January 2018

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82nd ENMC international workshop, 5th international Emery-Dreifuss muscular dystrophy (EDMD) workshop, 1st Workshop of the MYO-CLUSTER project EUROMEN (European muscle envelope nucleopathies), 15-16 September 2000, Naarden, The Netherlands.

21 January 2018

1 reference

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The Ig-like structure of the C-terminal domain of lamin A/C, mutated in muscular dystrophies, cardiomyopathy, and partial lipodystrophy

21 January 2018

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Nuclear envelope disorganization in fibroblasts from lipodystrophic patients with heterozygous R482Q/W mutations in the lamin A/C gene

28 October 2018

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Meiotic breakdown of nuclear envelope in oocytes of Spisula solidissima involves phosphorylation and release of nuclear lamin

28 October 2018

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12 December 2020

Properties of lamin A mutants found in Emery-Dreifuss muscular dystrophy, cardiomyopathy and Dunnigan-type partial lipodystrophy

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12 December 2020

Nuclear envelope defects associated with LMNA mutations cause dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy

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12 December 2020

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

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12 December 2020

On the occurrence of a fibrous lamina on the inner aspect of the nuclear envelope in certain cells of vertebrates

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12 December 2020

Identification of protein phosphatase 1 as a mitotic lamin phosphatase

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12 December 2020

Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene

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12 December 2020

Nuclear reconstitution in vitro: stages of assembly around protein-free DNA

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12 December 2020

Identifiers

DOI

10.1073/PNAS.0507612102

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8 January 2020

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release_y7ga55lefjehfm4wmkezowms7q

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24 November 2022

mapped directly with Wikidata item

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8 January 2020

PubMed publication ID

16227433

1 reference