Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome (Q24562621)

9

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Yosef Gruenbaum

7

object named as

Yosef Gruenbaum

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Leslie B Gordon

6

object named as

Leslie B Gordon

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author name string

Robert D Goldman

1

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Dale K Shumaker

2

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Michael R Erdos

3

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Maria Eriksson

4

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Anne E Goldman

5

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Satya Khuon

8

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Renée Varga

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

10

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language of work or name

English

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publication date

15 June 2004

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published in

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volume

101

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issue

24

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page(s)

8963-8

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cites work

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

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Pathway of incorporation of microinjected lamin A into the nuclear envelope

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Nuclear lamins: building blocks of nuclear architecture

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Structural analysis of emerin, an inner nuclear membrane protein mutated in X-linked Emery-Dreifuss muscular dystrophy

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

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Identification and characterization of a nuclear pore complex protein

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Protein kinase phosphorylation site sequences and consensus specificity motifs: tabulations

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Congenital Absence of Hair and Mammary Glands with Atrophic Condition of the Skin and its Appendages, in a Boy whose Mother had been almost wholly Bald from Alopecia Areata from the age of Six.

7 April 2017

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DNA polymerase clamp shows little turnover at established replication sites but sequential de novo assembly at adjacent origin clusters

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Incorporation of the nuclear pore basket protein nup153 into nuclear pore structures is dependent upon lamina assembly: evidence from cell-free extracts of Xenopus eggs

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Nuclear lamins: their structure, assembly, and interactions

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

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Dynamic properties of nuclear lamins: lamin B is associated with sites of DNA replication

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Maturation of nuclear lamin A involves a specific carboxy-terminal trimming, which removes the polyisoprenylation site from the precursor; implications for the structure of the nuclear lamina

27 September 2017

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Expression in Escherichia coli of human lamins A and C: influence of head and tail domains on assembly properties and paracrystal formation.

30 May 2018

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Hutchinson-Gilford syndrome.

30 May 2018

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The COPI complex functions in nuclear envelope breakdown and is recruited by the nucleoporin Nup153.

14 July 2018

1 reference

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

28 November 2018

1 reference

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

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15184648

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.0402943101

1 reference

ADS bibcode

2004PNAS..101.8963G

0 references

1 reference

1 reference

PubMed publication ID

15184648

1 reference