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The fibrillins
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
10216958
retrieved
28 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
The fibrillins
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10216958
retrieved
28 July 2017
author
Lygia Veiga Pereira
object named as
L Pereira
series ordinal
2
0 references
author name string
F Ramirez
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
10216958
retrieved
28 July 2017
publication date
1 February 1999
1 reference
stated in
Europe PubMed Central
PubMed ID
10216958
retrieved
28 July 2017
published in
International Journal of Biochemistry & Cell Biology
1 reference
stated in
Europe PubMed Central
PubMed ID
10216958
retrieved
28 July 2017
volume
31
1 reference
stated in
Europe PubMed Central
PubMed ID
10216958
retrieved
28 July 2017
page(s)
255-259
1 reference
stated in
Europe PubMed Central
PubMed ID
10216958
retrieved
28 July 2017
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
10216958
retrieved
28 July 2017
cites work
Fibrillin, a new 350-kD glycoprotein, is a component of extracellular microfibrils
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-2725%2898%2900109-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-2725%2898%2900109-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Developmental expression of fibrillin genes suggests heterogeneity of extracellular microfibrils
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-2725%2898%2900109-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-2725%2898%2900109-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, congenital contractural arachnodactyly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-2725%2898%2900109-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fibrillln mutations in Marfan syndrome and related phenotypes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-2725%2898%2900109-5
retrieved
7 January 2021
based on heuristic
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Solution structure of a pair of calcium-binding epidermal growth factor-like domains: implications for the Marfan syndrome and other genetic disorders
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-2725%2898%2900109-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fibrillin-containing microfibrils: structure and function in health and disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-2725%2898%2900109-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Solution structure of the transforming growth factor beta-binding protein-like module, a domain associated with matrix fibrils
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-2725%2898%2900109-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in FBN1 disrupts profibrillin processing and results in isolated skeletal features of the Marfan syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-2725%2898%2900109-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fibrillin-1: organization in microfibrils and structural properties
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-2725%2898%2900109-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Targetting of the gene encoding fibrillin-1 recapitulates the vascular aspect of Marfan syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-2725%2898%2900109-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Elastin is an essential determinant of arterial morphogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-2725%2898%2900109-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1357-2725(98)00109-5
1 reference
stated in
Europe PubMed Central
PubMed ID
10216958
retrieved
28 July 2017
PubMed ID
10216958
1 reference
stated in
Europe PubMed Central
PubMed ID
10216958
retrieved
28 July 2017
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