(Q43559273)

24 November 2017

A G1127S change in calcium-binding epidermal growth factor-like domain 13 of human fibrillin-1 causes short range conformational effects (English)

1 reference

24 November 2017

P Whiteman

1

1 reference

24 November 2017

R S Smallridge

2

1 reference

24 November 2017

V Knott

3

1 reference

24 November 2017

J J Cordle

4

1 reference

24 November 2017

A K Downing

5

1 reference

24 November 2017

P A Handford

6

1 reference

24 November 2017

language of work or name

English

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publication date

31 January 2001

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Journal of Biological Chemistry

24 November 2017

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24 November 2017

276

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24 November 2017

17156-17162

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24 November 2017

20

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Key residues involved in calcium-binding motifs in EGF-like domains

24 November 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

Ligand requirements for Ca2+ binding to EGF-like domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

Solution structure of a pair of calcium-binding epidermal growth factor-like domains: implications for the Marfan syndrome and other genetic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

Calcium stabilizes fibrillin-1 against proteolytic degradation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

Marfan Database (third edition): new mutations and new routines for the software

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

Haemophilia B: database of point mutations and short additions and deletions--eighth edition

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

Sequence, recombinant expression and tissue localization of two novel extracellular matrix proteins, fibulin-3 and fibulin-4

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

A Gly --> Ser change causes defective folding in vitro of calcium-binding epidermal growth factor-like domains from factor IX and fibrillin-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

NMR analysis of cbEGF domains gives new insights into the structural consequences of a P1148A substitution in fibrillin-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

EGF-like domain calcium affinity modulated by N-terminal domain linkage in human fibrillin-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

Mutations in calcium-binding epidermal growth factor modules render fibrillin-1 susceptible to proteolysis. A potential disease-causing mechanism in Marfan syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

Epidermal growth factor-like modules

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

Backbone dynamics of a cbEGF domain pair in the presence of calcium

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

Different susceptibilities of fibulin-1 and fibulin-2 to cleavage by matrix metalloproteinases and other tissue proteases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

Clustering of FBN2 mutations in patients with congenital contractural arachnodactyly indicates an important role of the domains encoded by exons 24 through 34 during human development

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

Defective calcium binding to fibrillin-1: consequence of an N2144S change for fibrillin-1 structure and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

Molecular effects of calcium binding mutations in Marfan syndrome depend on domain context

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M006547200

21 January 2018

Identifiers

DOI

10.1074/JBC.M006547200

1 reference

24 November 2017

1 reference