(Q34494982)

2 August 2017

title

The truncated prelamin A in Hutchinson-Gilford progeria syndrome alters segregation of A-type and B-type lamin homopolymers (English)

1 reference

2 August 2017

1 reference

Erwan Delbarre

1

1 reference

2 August 2017

Marc Tramier

2

1 reference

2 August 2017

Maïté Coppey-Moisan

3

1 reference

2 August 2017

Claire Gaillard

4

1 reference

2 August 2017

Jean-Claude Courvalin

5

1 reference

2 August 2017

Brigitte Buendia

6

1 reference

2 August 2017

publication date

15 February 2006

1 reference

2 August 2017

published in

Human Molecular Genetics

1 reference

2 August 2017

volume

15

1 reference

2 August 2017

issue

7

1 reference

2 August 2017

page(s)

1113-1122

1 reference

Nuclear lamins: their structure, assembly, and interactions

2 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Nuclear pore complexes form immobile networks and have a very low turnover in live mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Lamins: building blocks or regulators of gene expression?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Defective prelamin A processing and muscular and adipocyte alterations in Zmpste24 metalloproteinase-deficient mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Functional aspects of polyisoprenoid protein substituents: roles in protein-protein interaction and trafficking

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Prelamin A, Zmpste24, misshapen cell nuclei, and progeria--new evidence suggesting that protein farnesylation could be important for disease pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Zmpste24 deficiency in mice causes spontaneous bone fractures, muscle weakness, and a prelamin A processing defect.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Prelamin A endoproteolytic processing in vitro by recombinant Zmpste24

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

The role of the head and tail domain in lamin structure and assembly: analysis of bacterially expressed chicken lamin A and truncated B2 lamins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

The stability of the nuclear lamina polymer changes with the composition of lamin subtypes according to their individual binding strengths

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Protein-protein interactions between human nuclear lamins expressed in yeast

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Nuclear envelope, nuclear lamina, and inherited disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Lamin a truncation in Hutchinson-Gilford progeria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Blocking protein farnesyltransferase improves nuclear shape in fibroblasts from humans with progeroid syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Incomplete processing of mutant lamin A in Hutchinson-Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Inhibiting farnesylation reverses the nuclear morphology defect in a HeLa cell model for Hutchinson-Gilford progeria syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Blocking protein farnesyltransferase improves nuclear blebbing in mouse fibroblasts with a targeted Hutchinson-Gilford progeria syndrome mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Reversal of the cellular phenotype in the premature aging disease Hutchinson-Gilford progeria syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Nuclear lamins A and B1: different pathways of assembly during nuclear envelope formation in living cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Head and/or CaaX domain deletions of lamin proteins disrupt preformed lamin A and C but not lamin B structure in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

The nuclear envelope lamina is reversibly depolymerized during mitosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

A carboxyl-terminal interaction of lamin B1 is dependent on the CAAX endoprotease Rce1 and carboxymethylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

The lamin CxxM motif promotes nuclear membrane growth

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Intranuclear membrane structure formations by CaaX-containing nuclear proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Prenylated prelamin A interacts with Narf, a novel nuclear protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Genomic instability in laminopathy-based premature aging

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Accelerated ageing in mice deficient in Zmpste24 protease is linked to p53 signalling activation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Aging of Hutchinson-Gilford progeria syndrome fibroblasts is characterised by hyperproliferation and increased apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Expression of a mutant lamin A that causes Emery-Dreifuss muscular dystrophy inhibits in vitro differentiation of C2C12 myoblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Biochemistry, mutagenesis, and oligomerization of DsRed, a red fluorescent protein from coral

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Analysis of DsRed Mutants. Space around the fluorophore accelerates fluorescence development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Identification of different emitting species in the red fluorescent protein DsRed by means of ensemble and single-molecule spectroscopy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Picosecond-hetero-FRET microscopy to probe protein-protein interactions in live cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

Low-intensity two-dimensional imaging of fluorescence lifetimes in living cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL026

21 January 2018

Identifiers

DOI

10.1093/HMG/DDL026

1 reference

release_k536jwmzhvfclfiw6rtinnoy7m

2 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/k536jwmzhvfclfiw6rtinnoy7m

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference