Pathogenetic sequence for aneurysm revealed in mice underexpressing fibrillin-1 (Q24651261)

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12 November 2019

title

Pathogenetic sequence for aneurysm revealed in mice underexpressing fibrillin-1 (English)

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1

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author name string

S Y Lee

2

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12 November 2019

B Gayraud

3

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K Andrikopoulos

4

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S D Shapiro

5

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T Bunton

6

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N J Biery

7

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H C Dietz

8

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L Y Sakai

9

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F Ramirez

10

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12 November 2019

language of work or name

English

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publication date

1 March 1999

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

12 November 2019

published in

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volume

96

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issue

7

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12 November 2019

page(s)

3819-3823

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Elastin is an essential determinant of arterial morphogenesis

12 November 2019

cites work

1 reference

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Latent transforming growth factor-beta binding protein domains involved in activation and transglutaminase-dependent cross-linking of latent transforming growth factor-beta

7 April 2017

1 reference

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Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

7 April 2017

1 reference

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Hydrolysis of a broad spectrum of extracellular matrix proteins by human macrophage elastase

7 April 2017

1 reference

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Spontaneous calcification of arteries and cartilage in mice lacking matrix GLA protein

7 April 2017

1 reference

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Latent transforming growth factor-beta 1 and its binding protein are components of extracellular matrix microfibrils

7 April 2017

1 reference

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Developmental expression of fibrillin genes suggests heterogeneity of extracellular microfibrils

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22378

Targeted mutation in the col5a2 gene reveals a regulatory role for type V collagen during matrix assembly

7 April 2017

1 reference

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Derivation of completely cell culture-derived mice from early-passage embryonic stem cells

7 April 2017

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Overexpression of transforming growth factor beta1 in arterial endothelium causes hyperplasia, apoptosis, and cartilaginous metaplasia

7 April 2017

1 reference

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Long-range disruption of gene expression by a selectable marker cassette

28 September 2017

1 reference

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Fibrillln mutations in Marfan syndrome and related phenotypes

28 September 2017

1 reference

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Metalloelastase is required for macrophage-mediated proteolysis and matrix invasion in mice

28 September 2017

1 reference

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Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders

28 September 2017

1 reference

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Marfan's syndrome and other microfibrillar diseases

28 September 2017

1 reference

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Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S.

28 September 2017

1 reference

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Targetting of the gene encoding fibrillin-1 recapitulates the vascular aspect of Marfan syndrome.

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073/PNAS.96.7.3819

Fibrillin-1 in Human Cartilage: Developmental Expression and Formation of Special Banded Fibers

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073/PNAS.96.7.3819

Genetic determination of cartilaginous metaplasia in mouse aorta.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073/PNAS.96.7.3819

THE ROLE OF THE MATRIX IN AORTIC CALCIFICATION

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10097121

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Immunohistochemistry of matrix metalloproteinases and their inhibitors in thoracic aortic aneurysms and aortic valves of patients with Marfan's syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10097121

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Homeotic transformations of murine vertebrae and concomitant alteration of Hox codes induced by retinoic acid

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10097121

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.96.7.3819

2 references

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12 November 2019

ADS bibcode

1999PNAS...96.3819P

0 references

1 reference

2 references

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12 November 2019

PubMed publication ID

10097121

2 references