C. Jin

发表

Characterization of a novel mutation in the CRYBB2 gene associated with autosomal dominant congenital posterior subcapsular cataract in a Chinese family

K. Yao, Jinyu Li, C. Jin, 2011, Molecular vision.

Correlation of the recurrent FBN1 mutation (c.364C>T) with a unique phenotype in a Chinese patient with Marfan syndrome

Renyi Wu, K. Yao, C. Jin, 2008, Japanese Journal of Ophthalmology.

Novel FBN1 mutations associated with predominant ectopia lentis and marfanoid habitus in Chinese patients.

Renyi Wu, Xiajing Tang, K. Yao, 2007, Molecular vision.

A Chinese family with progressive childhood cataracts and IVS3+1G>A CRYBA3/A1 mutations

K. Yao, Jinyu Li, C. Jin, 2010, Molecular vision.

A nonsense mutation in CRYGC associated with autosomal dominant congenital nuclear cataract in a Chinese family

Renyi Wu, K. Yao, C. Jin, 2008, Molecular vision.

A recurrent PAX6 mutation is associated with aniridia and congenital progressive cataract in a Chinese family

K. Yao, Jinyu Li, C. Jin, 2012, Molecular vision.

Molecular Analysis and Phenotypic Study in 14 Chinese Families with Bietti Crystalline Dystrophy

Zhaoan Su, X. Fang, Jinfu Yin, 2014, PloS one.

Bromfenac Sodium 0.1%, Fluorometholone 0.1% and Dexamethasone 0.1% for Control of Ocular Inflammation and Prevention of Cystoid Macular Edema after Phacoemulsification

K. Yao, Wen Xu, Peiqing Chen, 2013, Ophthalmologica.

Successful Diagnosis and Treatment of a Single Case of Bilateral Necrotizing Keratitis following Femtosecond-LASIK

Xiuming Jin, Yabo Yang, K. Yao, 2014, Ocular immunology and inflammation.

A novel mutation in the major intrinsic protein (MIP) associated with autosomal dominant congenital cataracts in a Chinese family

K. Yao, Jinyu Li, C. Jin, 2010, Molecular vision.

Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani Families

P. Sieving, Shaheen N. Khan, S. Riazuddin, 2017, Investigative ophthalmology & visual science.

Noncoding variation of the gene for ferritin light chain in hereditary and age-related cataract

J. Hejtmancik, Wenmin Sun, T. Bennett, 2013, Molecular vision.

Apoptosis of lens epithelial cells induced by high concentration of glucose is associated with a decrease in caveolin-1 levels

K. Yao, C. Jin, Zhiyong Zhang, 2009, Molecular vision.

Identification of a novel frameshift mutation in PITX2 gene in a Chinese family with Axenfeld-Rieger syndrome

Xiaolan Fang, C. Jin, Su-juan Zhao, 2014, Journal of Zhejiang University SCIENCE B.

Identification of a MIP mutation that activates a cryptic acceptor splice site in the 3′ untranslated region

K. Yao, C. Jin, Wei Wang, 2010, Molecular vision.

Different-sized incisions for phacoemulsification in age-related cataract.

Xue Wang, K. Yao, Wen Xu, 2017, The Cochrane database of systematic reviews.

AIPL1 implicated in the pathogenesis of two cases of autosomal recessive retinal degeneration

P. Sieving, S. Riazuddin, X. Jiao, 2014, Molecular vision.

[Clinical evaluation on the coaxial 1.8 mm microincision cataract surgery].

K. Yao, C. Jin, Wei Wang, 2011, [Zhonghua yan ke za zhi] Chinese journal of ophthalmology.

A novel GJA3 mutation associated with congenital nuclear pulverulent and posterior polar cataract in a chinese family

K. Yao, C. Jin, Wei Wang, 2011, Human mutation.

Identification of a novel splice-site mutation in MIP in a Chinese congenital cataract family

K. Xia, Renyi Wu, Xiajing Tang, 2009, Molecular vision.