Ion Transport Function of SLC4A11 in Corneal Endothelium

nork Jalimarada, Supriya S., Ogando, Diego G., Vithana, Eranga N., Bonanno, Joseph A.
Argitaratua 2013

Differential expression of the Slc4 bicarbonate transporter family in murine corneal endothelium and cell culture

nork Shei, William, Liu, Jun, Htoon, Hla M., Aung, Tin, Vithana, Eranga N.
Argitaratua 2013

SLC4A11 is an EIPA-sensitive Na(+) permeable pH(i) regulator

nork Ogando, Diego G., Jalimarada, Supriya S., Zhang, Wenlin, Vithana, Eranga N., Bonanno, Joseph A.
Argitaratua 2013

Identification of a novel mutation in the NTF4 gene that causes primary open-angle glaucoma in a Chinese population

nork Vithana, Eranga N., Nongpiur, Monisha E., Venkataraman, Divya, Chan, Stephanie H., Mavinahalli, Jagadeesh, Aung, Tin
Argitaratua 2010

Analysis of conjunctival fibroblasts from a proband with Schnyder corneal dystrophy

nork Mehta, Jodhbir S., Vithana, Eranga N., Venkataraman, Divya, Venkatraman, Anandalakshmi, Poh, Rebekah, Beuerman, Roger W., Aung, Tin, Tan, Donald T.H.
Argitaratua 2008

Association of peripheral anterior synechiae with anterior segment parameters in eyes with primary angle closure glaucoma

nork Loo, Yunhua, Tun, Tin A., Vithana, Eranga N., Perera, Shamira A., Husain, Rahat, Wong, Tina T., Aung, Tin, Nongpiur, Monisha E.
Argitaratua izan da Sci Rep (2021)

Association of LOXL1 polymorphisms with pseudoexfoliation in the Chinese

nork Lee, Kelvin Y.C., Ho, Su Ling, Thalamuthu, Anbupalam, Venkatraman, Anandalakshmi, Venkataraman, Divya, Pek, Don C.K., Aung, Tin, Vithana, Eranga N.
Argitaratua 2009

Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases

nork Vilas, Gonzalo L., Loganathan, Sampath K., Liu, Jun, Riau, Andri K., Young, James D., Mehta, Jodhbir S., Vithana, Eranga N., Casey, Joseph R.
Argitaratua 2013

Transethnic Replication of Association of CTG18.1 Repeat Expansion of TCF4 Gene With Fuchs' Corneal Dystrophy in Chinese Implies Common Causal Variant

nork Xing, Chao, Gong, Xin, Hussain, Imran, Khor, Chiea-Chuen, Tan, Donald T. H., Aung, Tin, Mehta, Jodhbir S., Vithana, Eranga N., Mootha, V. Vinod
Argitaratua izan da Invest Ophthalmol Vis Sci (2014)

Association of Common SIX6 Polymorphisms With Peripapillary Retinal Nerve Fiber Layer Thickness: The Singapore Chinese Eye Study

nork Cheng, Ching-Yu, Allingham, R. Rand, Aung, Tin, Tham, Yih-Chung, Hauser, Michael A., Vithana, Eranga N., Khor, Chiea Chuen, Wong, Tien Yin
Argitaratua izan da Invest Ophthalmol Vis Sci (2015)

Muscarinic cholinergic receptor (M(2)) plays a crucial role in the development of myopia in mice

nork Barathi, Veluchamy A., Kwan, Jia Lin, Tan, Queenie S. W., Weon, Sung Rhan, Seet, Li Fong, Goh, Liang Kee, Vithana, Eranga N., Beuerman, Roger W.
Argitaratua 2013

Depletion of SLC4A11 Causes Cell Death by Apoptosis in an Immortalized Human Corneal Endothelial Cell Line

nork Liu, Jun, Seet, Li-Fong, Koh, Li Wei, Venkatraman, Anandalakshmi, Venkataraman, Divya, Mohan, Rajiv R., Praetorius, Jeppe, Bonanno, Joseph A., Aung, Tin, Vithana, Eranga N.
Argitaratua 2012

Molecular analysis of CHX10 and MFRP in Chinese subjects with primary angle closure glaucoma and short axial length eyes

nork Aung, Tin, Lim, Marcus C.C., Wong, Tina T.L., Thalamuthu, Anbupalam, Yong, Victor H.K., Venkataraman, Divya, Venkatraman, Anandalakshmi, Chew, Paul T.K., Vithana, Eranga N.
Argitaratua 2008

Lens Status Influences the Association between CFH Polymorphisms and Age-Related Macular Degeneration: Findings from Two Population-Based Studies in Singapore

nork Wong, Chee Wai, Liao, Jiemin, Cheung, Gemmy C., Khor, Chiea Chuen, Vithana, Eranga N., Wang, Jie Jin, Mitchell, Paul, Aung, Tin, Wong, Tien Y., Cheng, Ching-Yu
Argitaratua izan da PLoS One (2015)

SPARC Deficiency Results in Improved Surgical Survival in a Novel Mouse Model of Glaucoma Filtration Surgery

nork Seet, Li-Fong, Su, Roseline, Barathi, V. A., Lee, Wing Sum, Poh, Rebekah, Heng, Yee Meng, Manser, Ed, Vithana, Eranga N., Aung, Tin, Weaver, Matt, Sage, E. Helene, Wong, Tina T.
Argitaratua 2010

Missense mutations in the sodium borate co-transporter SLC4A11 cause late onset Fuchs corneal dystrophy

nork Riazuddin, S. Amer, Vithana, Eranga N., Seet, Li-Fong, Liu, Yangjian, Al-Saif, Amr, Koh, Li Wei, Heng, Yee Meng, Aung, Tin, Meadows, Danielle N., Eghrari, Allen O., Gottsch, John D., Katsanis, Nicholas
Argitaratua 2010

Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus

nork Hauser, Michael A., Aboobakar, Inas F., Liu, Yutao, Miura, Shiroh, Whigham, Benjamin T., Challa, Pratap, Wheeler, Joshua, Williams, Andrew, Santiago-Turla, Cecelia, Qin, Xuejun, Rautenbach, Robyn M., Ziskind, Ari, Ramsay, Michèle, Uebe, Steffen, Song, Lingyun, Safi, Alexias, Vithana, Eranga N., Mizoguchi, Takanori, Nakano, Satoko, Kubota, Toshiaki, Hayashi, Ken, Manabe, Shin-ichi, Kazama, Shigeyasu, Mori, Yosai, Miyata, Kazunori, Yoshimura, Nagahisa, Reis, Andre, Crawford, Gregory E., Pasutto, Francesca, Carmichael, Trevor R., Williams, Susan E. I., Ozaki, Mineo, Aung, Tin, Khor, Chiea-Chuen, Stamer, W. Daniel, Ashley-Koch, Allison E., Allingham, R. Rand
Argitaratua izan da Hum Mol Genet (2015)

Common variants in SOX-2 and congenital cataract genes contribute to age-related nuclear cataract

nork Yonova-Doing, Ekaterina, Zhao, Wanting, Igo, Robert P., Wang, Chaolong, Sundaresan, Periasamy, Lee, Kristine E., Jun, Gyungah R., Alves, Alexessander Couto, Chai, Xiaoran, Chan, Anita S. Y., Lee, Mei Chin, Fong, Allan, Tan, Ava G., Khor, Chiea Chuen, Chew, Emily Y., Hysi, Pirro G., Fan, Qiao, Chua, Jacqueline, Chung, Jaeyoon, Liao, Jiemin, Colijn, Johanna M., Burdon, Kathryn P., Fritsche, Lars G., Swift, Maria K., Hilmy, Maryam H., Chee, Miao Ling, Tedja, Milly, Bonnemaijer, Pieter W. M., Gupta, Preeti, Tan, Queenie S., Li, Zheng, Vithana, Eranga N., Ravindran, Ravilla D., Chee, Soon-Phaik, Shi, Yuan, Liu, Wenting, Su, Xinyi, Sim, Xueling, Shen, Yang, Wang, Ya Xing, Li, Hengtong, Tham, Yih-Chung, Teo, Yik Ying, Aung, Tin, Small, Kerrin S., Mitchell, Paul, Jonas, Jost B., Wong, Tien Yin, Fletcher, Astrid E., Klaver, Caroline C. W., Klein, Barbara E. K., Wang, Jie Jin, Iyengar, Sudha K., Hammond, Christopher J., Cheng, Ching-Yu
Argitaratua izan da Commun Biol (2020)

Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

nork Iglesias, Adriana I., Mishra, Aniket, Vitart, Veronique, Bykhovskaya, Yelena, Höhn, René, Springelkamp, Henriët, Cuellar-Partida, Gabriel, Gharahkhani, Puya, Bailey, Jessica N. Cooke, Willoughby, Colin E., Li, Xiaohui, Yazar, Seyhan, Nag, Abhishek, Khawaja, Anthony P., Polašek, Ozren, Siscovick, David, Mitchell, Paul, Tham, Yih Chung, Haines, Jonathan L., Kearns, Lisa S., Hayward, Caroline, Shi, Yuan, van Leeuwen, Elisabeth M., Taylor, Kent D., Bonnemaijer, Pieter, Rotter, Jerome I., Martin, Nicholas G., Zeller, Tanja, Mills, Richard A., Souzeau, Emmanuelle, Staffieri, Sandra E., Jonas, Jost B., Schmidtmann, Irene, Boutin, Thibaud, Kang, Jae H., Lucas, Sionne E. M., Wong, Tien Yin, Beutel, Manfred E., Wilson, James F., Uitterlinden, André G., Vithana, Eranga N., Foster, Paul J., Hysi, Pirro G., Hewitt, Alex W., Khor, Chiea Chuen, Pasquale, Louis R., Montgomery, Grant W., Klaver, Caroline C. W., Aung, Tin, Pfeiffer, Norbert, Mackey, David A., Hammond, Christopher J., Cheng, Ching-Yu, Craig, Jamie E., Rabinowitz, Yaron S., Wiggs, Janey L., Burdon, Kathryn P., van Duijn, Cornelia M., MacGregor, Stuart
Argitaratua izan da Nat Commun (2018)

Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma

nork Shiga, Yukihiro, Akiyama, Masato, Nishiguchi, Koji M, Sato, Kota, Shimozawa, Nobuhiro, Takahashi, Atsushi, Momozawa, Yukihide, Hirata, Makoto, Matsuda, Koichi, Yamaji, Taiki, Iwasaki, Motoki, Tsugane, Shoichiro, Oze, Isao, Mikami, Haruo, Naito, Mariko, Wakai, Kenji, Yoshikawa, Munemitsu, Miyake, Masahiro, Yamashiro, Kenji, Kashiwagi, Kenji, Iwata, Takeshi, Mabuchi, Fumihiko, Takamoto, Mitsuko, Ozaki, Mineo, Kawase, Kazuhide, Aihara, Makoto, Araie, Makoto, Yamamoto, Tetsuya, Kiuchi, Yoshiaki, Nakamura, Makoto, Ikeda, Yasuhiro, Sonoda, Koh-Hei, Ishibashi, Tatsuro, Nitta, Koji, Iwase, Aiko, Shirato, Shiroaki, Oka, Yoshitaka, Satoh, Mamoru, Sasaki, Makoto, Fuse, Nobuo, Suzuki, Yoichi, Cheng, Ching-Yu, Khor, Chiea Chuen, Baskaran, Mani, Perera, Shamira, Aung, Tin, Vithana, Eranga N, Cooke Bailey, Jessica N, Kang, Jae H, Pasquale, Louis R, Haines, Jonathan L, Wiggs, Janey L, Burdon, Kathryn P, Gharahkhani, Puya, Hewitt, Alex W, Mackey, David A, MacGregor, Stuart, Craig, Jamie E, Allingham, R Rand, Hauser, Micheal, Ashaye, Adeyinka, Budenz, Donald L, Akafo, Stephan, Williams, Susan E I, Kamatani, Yoichiro, Nakazawa, Toru, Kubo, Michiaki
Argitaratua izan da Hum Mol Genet (2018)