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

por Wang, Wei, Jiang, Jin, Zhu, Yanan, Li, Jinyu, Jin, Chongfei, Shentu, Xingchao, Yao, Ke
Publicado 2010

A detailed phenotypic assessment of individuals affected by MFRP-related oculopathy

por Mukhopadhyay, Rajarshi, Sergouniotis, Panagiotis I., Mackay, Donna S., Day, Alexander C., Wright, Genevieve, Devery, Sophie, Leroy, Bart P., Robson, Anthony G., Holder, Graham E., Li, Zheng, Webster, Andrew R.
Publicado 2010

TGFBI gene mutation analysis in a Chinese pedigree of Reis-Bücklers corneal dystrophy

por Ma, Ke, Liu, Guo, Yang, Yin, Yu, Man, Sui, Ruifang, Yu, Wenhan, Chen, Xiaoming, Deng, Yinping, Yan, Naihong, Cao, Guiqun, Liu, Xuyang
Publicado 2010

Candidate gene study to investigate the genetic determinants of normal variation in central corneal thickness

por Dimasi, David P., Burdon, Kathryn P., Hewitt, Alex W., Savarirayan, Ravi, Healey, Paul R., Mitchell, Paul, Mackey, David A., Craig, Jamie E.
Publicado 2010

Microscopic mammalian retinal pigment epithelium lesions induce widespread proliferation with differences in magnitude between center and periphery

por Lundh von Leithner, Peter, Ciurtin, Coziana, Jeffery, Glen
Publicado 2010

Absence of PITX3 mutation in a Tunisian family with congenital cataract and mental retardation

por Chograni, Manèl, Chaabouni, Myriam, Chelly, Imen, Helayem, Mohamed Bechir, Chaabouni-Bouhamed, Habiba
Publicado 2010

Effects of (-)-epigallocatechin gallate on RPE cell migration and adhesion

por Chan, Chi-Ming, Huang, Jheng-Hua, Chiang, Han-Sun, Wu, Wen-Bin, Lin, Hsin-Huang, Hong, Jing-Yin, Hung, Chi-Feng
Publicado 2010

Assessment of SNPs associated with the human glucocorticoid receptor in primary open-angle glaucoma and steroid responders

por Fingert, John H., Alward, Wallace L., Wang, Kai, Yorio, Thomas, Clark, Abbot F.
Publicado 2010

Enhanced survival in vitro of human corneal endothelial cells using mouse embryonic stem cell conditioned medium

por Lu, Xiaoyan, Chen, Dong, Liu, Zhiping, Li, Chaoyang, Liu, Ying, Zhou, Jin, Wan, Pengxia, Mou, Yong-gao, Wang, Zhichong
Publicado 2010

Aquaporin expression in blood-retinal barrier cells during experimental autoimmune uveitis

por Motulsky, Elie, Koch, Philippe, Janssens, Sarah, Liénart, Maité, Vanbellinghen, Anne-Marie, Bolaky, Nargis, Chan, Chi-Chao, Caspers, Laure, Martin-Martinez, Maria-Dolores, Xu, Heping, Delporte, Christine, Willermain, François
Publicado 2010

An association between BPDE-like DNA adduct levels and CYP1A1 and GSTM1 polymorphisma in pterygium

por Tung, Jai-Nien, Wu, Heng-Hsiung, Chiang, Chun-Chi, Tsai, Yi-Yu, Chou, Ming-Chih, Lee, Huei, Cheng, Ya-Wen
Publicado 2010

Characterization and functional expression of the natriuretic peptide system in human lens epithelial cells

por Cammarata, Patrick R., Braun, Brittany, Dimitrijevich, Slobodan D., Pack, Jessica
Publicado 2010

All-trans retinoic acid regulates the expression of the extracellular matrix protein fibulin-1 in the guinea pig sclera and human scleral fibroblasts

por Li, Chuanxu, McFadden, Sally A., Morgan, Ian, Cui, Dongmei, Hu, Jianmin, Wan, Wenjuan, Zeng, Junwen
Publicado 2010

Expression of transient receptor potential vanilloid channels TRPV5 and TRPV6 in retinal pigment epithelium

por Kennedy, Brian G., Torabi, Asad J., Kurzawa, Rafal, Echtenkamp, Stephen F., Mangini, Nancy J.
Publicado 2010

A novel mutation of PAX6 in Chinese patients with new clinical features of Peters’ anomaly

por Jia, Xiuhua, Guo, Xiangming, Jia, Xiaoyun, Xiao, Xueshan, Li, Shiqiang, Zhang, Qingjiong
Publicado 2010

Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1

por Yasmeen, Afshan, Riazuddin, S. Amer, Kaul, Haiba, Mohsin, Sadia, Khan, Mohsin, Qazi, Zaheeruddin A., Nasir, Idrees A., Zafar, Ahmad U., Khan, Shaheen N., Husnain, Tayyab, Akram, Javed, Hejtmancik, J. Fielding, Riazuddin, Sheikh
Publicado 2010

Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathy

por Meyer, Esther, Michaelides, Michel, Tee, Louise J., Robson, Anthony G., Rahman, Fatimah, Pasha, Shanaz, Luxon, Linda M., Moore, Anthony T., Maher, Eamonn R.
Publicado 2010

Alterations in ZENK and glucagon RNA transcript expression during increased ocular growth in chickens

por Ashby, Regan, Kozulin, Peter, Megaw, Pam L., Morgan, Ian G.
Publicado 2010

Pterygium and genetic polymorphisms of the DNA repair enzymes XRCC1, XPA, and XPD

por Chiang, Chun-Chi, Tsai, Yi-Yu, Bau, Da-Tian, Cheng, Ya-Wen, Tseng, Sung-Huei, Wang, Rou-Fen, Tsai, Fuu-Jen
Publicado 2010

Major LOXL1 risk allele is reversed in exfoliation glaucoma in a black South African population

por Williams, Susan E.I., Whigham, Benjamin T., Liu, Yutao, Carmichael, Trevor R., Qin, Xuejun, Schmidt, Silke, Ramsay, Michele, Hauser, Michael A., Allingham, R. Rand
Publicado 2010