(Q34480435)

2 August 2017

Progressive vascular smooth muscle cell defects in a mouse model of Hutchinson-Gilford progeria syndrome (English)

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2 August 2017

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19

Francis S Collins

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Frank D Kolodgie

6

object named as

Frank Kolodgie

1 reference

2 August 2017

16

Renu Virmani

1 reference

2 August 2017

7

Brian C Capell

1 reference

2 August 2017

17

Thomas N Wight

1 reference

2 August 2017

4

Michelle Olive

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2 August 2017

3

Michael R Erdos

1 reference

2 August 2017

9

Dina Faddah

1 reference

2 August 2017

14

Santhi Ganesh

1 reference

2 August 2017

11

Hedwig Avallone

1 reference

2 August 2017

15

Leslie B Gordon

1 reference

2 August 2017

Renee Varga

1

1 reference

2 August 2017

Maria Eriksson

2

1 reference

2 August 2017

Ingrid Harten

5

1 reference

2 August 2017

Jun Cheng

8

1 reference

2 August 2017

Stacie Perkins

10

1 reference

2 August 2017

Hong San

12

1 reference

2 August 2017

Xuan Qu

13

1 reference

2 August 2017

Elizabeth G Nabel

18

1 reference

2 August 2017

language of work or name

English

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publication date

21 February 2006

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

2 August 2017

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2 August 2017

103

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2 August 2017

3250-3255

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2 August 2017

9

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

2 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

LMNA mutations in progeroid syndromes.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

The nuclear lamina comes of age.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

LMNA mutation in a 45 year old Japanese subject with Hutchinson-Gilford progeria syndrome.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

Zinc metalloproteinase, ZMPSTE24, is mutated in mandibuloacral dysplasia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

Lamin a truncation in Hutchinson-Gilford progeria.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

A highly efficient recombineering-based method for generating conditional knockout mutations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

Isolated allogeneic bone marrow-derived mesenchymal cells engraft and stimulate growth in children with osteogenesis imperfecta: Implications for cell therapy of bone

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

Nuclear lamins: building blocks of nuclear architecture

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

Smooth muscle cell depletion and collagen types in progeric arteries

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

A highly efficient Escherichia coli-based chromosome engineering system adapted for recombinogenic targeting and subcloning of BAC DNA

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

Impaired vascular contractility and blood pressure homeostasis in the smooth muscle alpha-actin null mouse

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

Cardiovascular abnormalities in progeria. Case report and review of the literature.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

The Hutchinson-Gilford progeria syndrome. Report of 4 cases and review of the literature

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

A progeroid syndrome in mice is caused by defects in A-type lamins

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1413943

Morphological evaluation of proteoglycans in cells and tissues

27 October 2018

1 reference

12 December 2020

Hutchinson-Gilford progeria syndrome: a pathologic study

1 reference

12 December 2020

Morphological predictors of restenosis after coronary stenting in humans

1 reference

12 December 2020

LMNA mutations in atypical Werner's syndrome

1 reference

12 December 2020

Histological and ultrastructural features of atherosclerosis in progeria

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.0600012103

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2 August 2017

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1 reference

2 August 2017

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