Analysis of TGFBI gene mutations in Chinese patients with corneal dystrophies and review of the literature
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Investigation of the influence of Arg555Trp and Thr538Pro TGFBI mutations on C-terminal cleavage and cell endoplasmic reticulum stress.Comparison of two phenotypically distinct lattice corneal dystrophies caused by mutations in the transforming growth factor beta induced (TGFBI) geneTGFBI Gene Mutation Analysis of Clinically Diagnosed Granular Corneal Dystrophy Patients Prior to PTK: A Pilot Study from Eastern China.Phenotype-genotype correlations in patients with TGFBI-linked corneal dystrophies in Taiwan.TGFBI gene mutations in a Korean population with corneal dystrophyGenotype-phenotype correlation of TGFBI corneal dystrophies in Polish patients.First identification of a triple corneal dystrophy association: keratoconus, epithelial basement membrane corneal dystrophy and fuchs' endothelial corneal dystrophyFibril Core of Transforming Growth Factor Beta-Induced Protein (TGFBIp) Facilitates Aggregation of Corneal TGFBIp.An Arg124His mutation in TGFBI associated to Avellino corneal dystrophy in a Chinese pedigree.Targeted pituitary overexpression of pituitary adenylate-cyclase activating polypeptide alters postnatal sexual maturation in male miceUncovering the profile of mutations of transforming growth factor beta-induced gene in Chinese corneal dystrophy patients.Early Events in the Amyloid Formation of the A546T Mutant of Transforming Growth Factor β-Induced Protein in Corneal Dystrophies Compared to the Nonfibrillating R555W and R555Q MutantsThe Human Eye Proteome Project: perspectives on an emerging proteome.Chinese family with atypical granular corneal dystrophy type I caused by the typical R555W mutation in TGFBI.TGFBI and CHST6 gene analysis in Chinese stromal corneal dystrophies.Effect of position-specific single-point mutations and biophysical characterization of amyloidogenic peptide fragments identified from lattice corneal dystrophy patientsVortex Pattern of Corneal Deposits in Granular Corneal Dystrophy Associated With the p.(Arg555Trp) Mutation in TGFBI.
P2860
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P2860
Analysis of TGFBI gene mutations in Chinese patients with corneal dystrophies and review of the literature
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Analysis of TGFBI gene mutatio ...... s and review of the literature
@ast
Analysis of TGFBI gene mutatio ...... s and review of the literature
@en
type
label
Analysis of TGFBI gene mutatio ...... s and review of the literature
@ast
Analysis of TGFBI gene mutatio ...... s and review of the literature
@en
prefLabel
Analysis of TGFBI gene mutatio ...... s and review of the literature
@ast
Analysis of TGFBI gene mutatio ...... s and review of the literature
@en
P2093
P2860
P921
P1433
P1476
Analysis of TGFBI gene mutatio ...... s and review of the literature
@en
P2093
Binliang Zhu
Chuanbao Li
Dinggou Huang
Juhua Yang
Mingshe Weng
Xiaoli Han
P2860
P304
P5008
P577
2010-06-30T00:00:00Z