(Q35549134)

8 August 2017

title

Subcellular localization of SREBP1 depends on its interaction with the C-terminal region of wild-type and disease related A-type lamins (English)

1 reference

8 August 2017

author name string

Isabelle Duband-Goulet

1

1 reference

8 August 2017

Stephanie Woerner

2

1 reference

8 August 2017

Sylvaine Gasparini

3

1 reference

8 August 2017

Wikayatou Attanda

4

1 reference

8 August 2017

Emilie Kondé

5

1 reference

8 August 2017

Carine Tellier-Lebègue

6

1 reference

8 August 2017

Constantin T Craescu

7

1 reference

8 August 2017

Aurélie Gombault

8

1 reference

8 August 2017

Pascal Roussel

9

1 reference

8 August 2017

Nathalie Vadrot

10

1 reference

8 August 2017

Patrick Vicart

11

1 reference

8 August 2017

Cecilia Ostlund

12

1 reference

8 August 2017

Howard J Worman

13

1 reference

8 August 2017

Sophie Zinn-Justin

14

1 reference

8 August 2017

Brigitte Buendia

15

1 reference

8 August 2017

language of work or name

English

0 references

publication date

4 October 2011

1 reference

Experimental Cell Research

8 August 2017

published in

1 reference

8 August 2017

volume

317

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8 August 2017

issue

20

1 reference

8 August 2017

page(s)

2800-2813

1 reference

describes a project that uses

8 August 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3215798/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

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27 July 2018

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

27 July 2018

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HIV protease inhibitors block adipocyte differentiation independently of lamin A/C.

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Altered pre-lamin A processing is a common mechanism leading to lipodystrophy.

27 July 2018

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

27 July 2018

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27 July 2018

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A novel interaction between lamin A and SREBP1: implications for partial lipodystrophy and other laminopathies

27 July 2018

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Cyclin-dependent kinases govern formation and maintenance of the nucleolus

27 July 2018

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27 July 2018

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The SREBP pathway: regulation of cholesterol metabolism by proteolysis of a membrane-bound transcription factor

27 July 2018

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A direct role for sterol regulatory element binding protein in activation of 3-hydroxy-3-methylglutaryl coenzyme A reductase gene

27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

27 July 2018

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27 July 2018

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Filaments made from A- and B-type lamins differ in structure and organization.

27 July 2018

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SREBP1 interaction with prelamin A forms: a pathogenic mechanism for lipodystrophic laminopathies

26 September 2018

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Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy

26 September 2018

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Both lamin A and lamin C mutations cause lamina instability as well as loss of internal nuclear lamin organization.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3215798

Nuclear envelope alterations in fibroblasts from LGMD1B patients carrying nonsense Y259X heterozygous or homozygous mutation in lamin A/C gene

26 September 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3215798

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3215798

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

26 September 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3215798

26 September 2018

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2011.09.012

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

7 January 2021

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3215798

Laminopathy-inducing lamin A mutants can induce redistribution of lamin binding proteins into nuclear aggregates

26 September 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2011.09.012

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2011.09.012

Kinetic Studies of Fos·Jun·DNA Complex Formation: DNA Binding Prior to Dimerization†

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2011.09.012

Organization and modulation of nuclear lamina structure

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2011.09.012

inferred from DOI database lookup

7 January 2021

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21993218

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.YEXCR.2011.09.012

1 reference

8 August 2017

1 reference

8 August 2017

1 reference