(Q44188680)

30 November 2017

title

BIGH3 (TGFBI) Arg124 mutations influence the amyloid conversion of related peptides in vitro (English)

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30 November 2017

author name string

Clair-Florent Schmitt-Bernard

1

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30 November 2017

Alain Chavanieu

2

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30 November 2017

Gudrun Herrada

3

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30 November 2017

Guy Subra

4

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30 November 2017

Bernard Arnaud

5

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30 November 2017

Jacques G Demaille

6

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30 November 2017

Bernard Calas

7

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30 November 2017

Angel Argilés

8

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30 November 2017

language of work or name

English

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publication date

1 November 2002

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30 November 2017

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30 November 2017

volume

269

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30 November 2017

issue

21

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30 November 2017

page(s)

5149-5156

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Kerato-epithelin mutations in four 5q31-linked corneal dystrophies

30 November 2017

cites work

1 reference

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cDNA cloning and sequence analysis of beta ig-h3, a novel gene induced in a human adenocarcinoma cell line after treatment with transforming growth factor-beta

21 January 2018

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Identification of motifs for cell adhesion within the repeated domains of transforming growth factor-beta-induced gene, betaig-h3.

21 January 2018

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Mutation hot spots in 5q31-linked corneal dystrophies

21 January 2018

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A new L527R mutation of the betaIGH3 gene in patients with lattice corneal dystrophy with deep stromal opacities

21 January 2018

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A kerato-epithelin (betaig-h3) mutation in lattice corneal dystrophy type IIIA

21 January 2018

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Heterogeneity in granular corneal dystrophy: identification of three causative mutations in the TGFBI (BIGH3) gene-lessons for corneal amyloidogenesis

21 January 2018

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Fluorometric determination of amyloid fibrils in vitro using the fluorescent dye, thioflavin T1.

21 January 2018

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Apolipoprotein E inhibits the depolymerization of beta 2-microglobulin-related amyloid fibrils at a neutral pH.

21 January 2018

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Amyloid deposits and amyloidosis. The beta-fibrilloses (first of two parts).

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Amyloid deposits and amyloidosis: the beta-fibrilloses (second of two parts).

21 January 2018

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Deposits and proteoglycan changes in primary and recurrent granular dystrophy of the cornea.

21 January 2018

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Transforming growth factor-beta induced protein, betaIG-H3, is present in degraded form and altered localization in lattice corneal dystrophy type I.

21 January 2018

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Lattice corneal dystrophy

21 January 2018

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Leu518Pro mutation of the beta ig-h3 gene causes lattice corneal dystrophy type I

21 January 2018

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A novel mutation at codon 124 (R124L) in the BIGH3 gene is associated with a superficial variant of granular corneal dystrophy

21 January 2018

1 reference

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In vitro creation of amyloid fibrils from native and Arg124Cys mutated betaIGH3((110-131)) peptides, and its relevance for lattice corneal amyloid dystrophy type I

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1432-1033.2002.03205.X

An FT-IR study of the beta-amyloid conformation: standardization of aggregation grade

21 January 2018

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Amyloid and non-amyloid forms of 5q31-linked corneal dystrophy resulting from kerato-epithelin mutations at Arg-124 are associated with abnormal turnover of the protein

21 January 2018

1 reference

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Amyloidosis due to a mutation of the gelsolin gene in an American family with lattice corneal dystrophy type II

21 January 2018

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21 January 2018

Identifiers

DOI

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30 November 2017

1 reference