Genetic analysis of CHST6 and TGFBI in Turkish patients with corneal dystrophies: Five novel variations in CHST6. - Wikidata - awgldk - TriplyDB

Genetic analysis of CHST6 and TGFBI in Turkish patients with corneal dystrophies: Five novel variations in CHST6.

Genetic analysis of CHST6 and TGFBI in Turkish patients with corneal dystrophies: Five novel variations in CHST6.

http://www.wikidata.org/entity/Q37371325

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CHST6 mutation screening and endoplasmatic reticulum stress in macular corneal dystrophy.

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Genetic analysis of CHST6 and TGFBI in Turkish patients with corneal dystrophies: Five novel variations in CHST6.

http://www.wikidata.org/entity/Q37371325

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article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

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scientific article published on 26 October 2016

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vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Genetic analysis of CHST6 and ...... ive novel variations in CHST6.

@en

Genetic analysis of CHST6 and ...... ive novel variations in CHST6.

@nl

type

label

Genetic analysis of CHST6 and ...... ive novel variations in CHST6.

@en

Genetic analysis of CHST6 and ...... ive novel variations in CHST6.

@nl

prefLabel

Genetic analysis of CHST6 and ...... ive novel variations in CHST6.

@en

Genetic analysis of CHST6 and ...... ive novel variations in CHST6.

@nl

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Molecular Vision

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Genetic analysis of CHST6 and ...... ive novel variations in CHST6.

@en

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Fulya Yaylacioglu Tuncay

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Gülsüm Kayman Kurekci

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Ozge Tugce Pasaoglu

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Pervin Rukiye Dincer

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Rustu Fikret Akata

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Sezen Guntekin Ergun

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Human corneal GlcNac 6-O-sulfotransferase and mouse intestinal GlcNac 6-O-sulfotransferase both produce keratan sulfate

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

Corneal dystrophy-associated R124H mutation disrupts TGFBI interaction with Periostin and causes mislocalization to the lysosome

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

Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene

Truncating mutations in the carbohydrate sulfotransferase 6 gene (CHST6) result in macular corneal dystrophy

Novel mutations in the CHST6 gene associated with macular corneal dystrophy in southern India

Mutations in the CHST6 gene in patients with macular corneal dystrophy: immunohistochemical evidence of heterogeneity

Identification of novel mutations in the carbohydrate sulfotransferase gene (CHST6) causing macular corneal dystrophy

Novel mutations of the carbohydrate sulfotransferase-6 (CHST6) gene causing macular corneal dystrophy in India

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1267-1279

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scholarly article

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22

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2016-10-26T00:00:00Z

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5082643

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