(Q52192356)

26 April 2018

title

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

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26 April 2018

L Pereira

1

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author name string

K Andrikopoulos

2

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26 April 2018

J Tian

3

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26 April 2018

S Y Lee

4

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D R Keene

5

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26 April 2018

R Ono

6

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26 April 2018

D P Reinhardt

7

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26 April 2018

L Y Sakai

8

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26 April 2018

N J Biery

9

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26 April 2018

T Bunton

10

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26 April 2018

H C Dietz

11

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26 April 2018

F Ramirez

12

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26 April 2018

language of work or name

English

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publication date

1 October 1997

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26 April 2018

published in

Nature Genetics

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26 April 2018

volume

17

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26 April 2018

page(s)

218-222

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26 April 2018

issue

2

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26 April 2018

https://scigraph.springernature.com/pub.10.1038/ng1097-218

exact match

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cites work

Fibrillin, a new 350-kD glycoprotein, is a component of extracellular microfibrils

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-218

Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-218

Fibrillln mutations in Marfan syndrome and related phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-218

Structure and expression of fibrillin-2, a novel microfibrillar component preferentially located in elastic matrices

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-218

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-218

Developmental expression of fibrillin genes suggests heterogeneity of extracellular microfibrils

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-218

Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, congenital contractural arachnodactyly

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-218

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-218

Fibrillin-1: organization in microfibrils and structural properties

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-218

Marfan's syndrome and other microfibrillar diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-218

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-218

7 January 2021

Genomic organization of the sequence coding for fibrillin, the defective gene product in Marfan syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-218

7 January 2021

Targeted deletion of 5'HS2 of the murine beta-globin LCR reveals that it is not essential for proper regulation of the beta-globin locus.

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-218

7 January 2021

Immunohistologic abnormalities of the microfibrillar-fiber system in the Marfan syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-218

7 January 2021

Supravalvular aortic stenosis associated with a deletion disrupting the elastin gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-218

7 January 2021

Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-218

7 January 2021

Fibrillin-1 in human cartilage: developmental expression and formation of special banded fibers.

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-218

7 January 2021

Fibrillin: monomers and microfibrils

1 reference

https://api.crossref.org/works/10.1038%2FNG1097-218

7 January 2021

Identifiers

DOI

10.1038/NG1097-218

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26 April 2018

Dimensions Publication ID

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1 reference

26 April 2018