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Scholar Results 1 - 10 of about 101 related to Yoo: Development of a DNA chip for the diagnosis of the most common corneal dystrophies caused.... (0.13 sec) 

Development of a DNA chip for the diagnosis of the most common corneal dystrophies caused …


SY Yoo, TI Kim, SY Lee, EK Kim, KC Keum, … - British Journal of Ophthalmology, 2007 - bjo.bmj.com
Results: Direct sequencing of exons 4 and 12 of the βigh3 gene in the patients'
genome showed that β-aCDs could be mainly classified into five types:
homozygotic Avellino corneal dystrophy (ACD), heterozygotic ACD, ...
Cited by 6 - Related articles - BL Direct - All 5 versions

BIGH3 mutation in a Bangladeshi family with a variable phenotype of LCDI


MF El-Ashry, MMA El-Aziz, LA Ficker, AJ … - Eye, 2004 - nature.com
Methods Molecular genetic analysis was performed on DNA extracted from all
members of the family. Exons of BIGH3gene were amplified by polymerase chain
reaction. Gene mutation and polymorphisms were identified by heteroduplex ...
Cited by 6 - Related articles - All 4 versions

Lattice corneal dystrophy type I without typical lattice lines: role of mutational analysis


S Yoshida, A Yoshida, S Nakao, A Emori, T … - American journal of ophthalmology, 2004 - Elsevier
The patient had diffuse opacification of the central corneal stroma but without
lattice lines and corneal epithelial erosions bilaterally. Molecular genetic
analysis identified a lattice corneal dystrophy I–associated heterozygous ...
Cited by 13 - Related articles - All 10 versions

Journal List> J Korean Ophthalmol Soc> v. 49 (8); Aug 2008


WK Kim, SY Yoo, BJ Ha, SW Kim, SY Lee, TI … - J Korean Ophthalmol Soc, 2008 - synapse.koreamed.org
J Korean Ophthalmol Soc. 2008 Aug;49(8):1220-1225. Published online 2008 August
20. doi: 10.3341/jkos.2008.49.8.1220. ... 1 Department of Ophthalmology, Yonsei
University College of Medicine, Seoul, Korea.
Related articles - Cached

A Simple DNA Chip for Diagnosis of Most Common Corneal Dystrophies Caused by ßigh3 …


SYY Tae-im Kim, SYLEK Kim, KCKNC Yoo, … - Frontiers in the Convergence of Bioscience and …, 2007 - ieeexplore.ieee.org
Abstract The aim of this study is to develop and evaluate a rapid diagnostic DNA
chip to detect most common betaigh3 mutations which cause corneal dystrophies
(CDs). Recent studies have shown that LASIK can worsen the CDs, and thus ...
Related articles

正常及饥饿大鼠胃壁组织基因表达谱的研究


邵莉, 王晓, 李荣英, 朱鋐达, 宋怀东, 陈名道 - 上海交通大学学报: 医学版, 2008 - cqvip.com
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充值中心; 论文翻译. 登录 注册 帮助. 维普资讯 ...
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A Simple DNA Chip for Diagnosis of Most Common Corneal Dystrophies Caused by βigh3 …


SY Yoo, T Kim, SY Lee, EK Kim, KC Keum, … - Proceedings of the 2007 Frontiers in the Convergence …, 2007 - doi.ieeecomputersociety.org
The aim of this study is to develop and evaluate a rapid diagnostic DNA chip to
detect most common βigh3 mutations which cause corneal dystrophies (CDs).
Recent studies have shown that LASIK can worsen the CDs, and thus initial ...
Related articles - All 2 versions

[PDF] Applications of DNA microarray in disease diagnostics


SM Yoo, HC Jong, SY Lee, NC Yoo - J. Microbiol. Biotechnol, 2009 - mbel.kaist.ac.kr
1 Department of Chemical and Biomolecular Engineering (BK21 Program), BioProcess
Engineering Research Center, Center for Systems and Synthetic Biotechnology, and
Institute for the BioCentury, KAIST, Daejeon 305-701, Korea 2 Department of ...
Cited by 1 - Related articles - View as HTML - All 2 versions

JC viral DNA chip allows geographical localization of unidentified cadavers for rapid …


H Ikegaya, H Iwase, PJ Saukko, T Akutsu, K … - Forensic Science International: Genetics, 2008 - Elsevier
Many countries are facing problems of human identification due to recent
increases in the number of unidentified cadavers following large-scale
disasters, such as those resulting from the Indonesian tsunami and ...
Cited by 2 - Related articles - All 8 versions

Corneal amyloidosis caused by Leu518Pro mutation of βig-h3 gene


K Hirano, Y Hotta, K Fujiki, A Kanai - British Journal of Ophthalmology, 2000 - bjo.bmj.com
RESULTS All the affected members were clinically diagnosed as having LCDI, and
the pedigree indicated an autosomal dominant inheritance. A heterozygous single
base pair transition (CTG to CCG, leucine to proline) was detected in codon ...
Cited by 20 - Related articles - BL Direct - All 7 versions


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