Resultados de procura - Eranga N. Vithana

Limitar resultados
  1. 1
    Ion Transport Function of SLC4A11 in Corneal Endothelium

    Ion Transport Function of SLC4A11 in Corneal Endothelium por Supriya S. Jalimarada, Diego G. Ogando, Eranga N. Vithana, Joseph A. Bonanno

    Publicado 2013
    Ligazón do recurso
    Artigo
    Engadir a favoritos
    Gardado en:
  2. 2
    SLC4A11 is an EIPA-sensitive Na<sup>+</sup> permeable pH<sub>i</sub> regulator

    SLC4A11 is an EIPA-sensitive Na<sup>+</sup> permeable pH<sub>i</sub> regulator por Diego G. Ogando, Supriya S. Jalimarada, Wenlin Zhang, Eranga N. Vithana, Joseph A. Bonanno

    Publicado 2013
    Ligazón do recurso
    Artigo
    Engadir a favoritos
    Gardado en:
  3. 3
    Oligomerization of SLC4A11 protein and the severity of FECD and CHED2 corneal dystrophies caused by<i>SLC4A11</i>mutations

    Oligomerization of SLC4A11 protein and the severity of FECD and CHED2 corneal dystrophies caused by<i>SLC4A11</i>mutations por Gonzalo L. Vilas, Sampath K. Loganathan, Anita Quon, Periasamy Sundaresan, Eranga N. Vithana, Joseph R. Casey

    Publicado 2011
    Ligazón do recurso
    Artigo
    Engadir a favoritos
    Gardado en:
  4. 4
    Transethnic Replication of Association of CTG18.1 Repeat Expansion of<i>TCF4</i>Gene With Fuchs' Corneal Dystrophy in Chinese Implies Common Causal Variant

    Transethnic Replication of Association of CTG18.1 Repeat Expansion of<i>TCF4</i>Gene With Fuchs' Corneal Dystrophy in Chinese Implies Common Causal Variant por Chao Xing, Xin Gong, Imran Hussain, Chiea Chuen Khor, Donald Tan, Tin Aung, Jodhbir S. Mehta, Eranga N. Vithana, V. Vinod Mootha

    Publicado 2014
    Ligazón do recurso
    Artigo
    Engadir a favoritos
    Gardado en:
  5. 5
    Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases

    Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases por Gonzalo L. Vilas, Sampath K. Loganathan, Jun Liu, Andri K. Riau, James D. Young, Jodhbir S. Mehta, Eranga N. Vithana, Joseph R. Casey

    Publicado 2013
    Ligazón do recurso
    Artigo
    Engadir a favoritos
    Gardado en:
  6. 6
    Alpha-B Crystallin Gene (CRYAB) Mutation Causes Dominant Congenital Posterior Polar Cataract in Humans

    Alpha-B Crystallin Gene (CRYAB) Mutation Causes Dominant Congenital Posterior Polar Cataract in Humans por Vanita Berry, Peter J. Francis, M. Ashwin Reddy, Dean Collyer, Eranga N. Vithana, Ian Mackay, Gary Dawson, Alisoun H. Carey, Anthony T. Moore, Shomi S. Bhattacharya, Roy A. Quinlan

    Publicado 2001
    Ligazón do recurso Ligazón do recurso
    Artigo
    Engadir a favoritos
    Gardado en:
  7. 7
    SPARC Deficiency Results in Improved Surgical Survival in a Novel Mouse Model of Glaucoma Filtration Surgery

    SPARC Deficiency Results in Improved Surgical Survival in a Novel Mouse Model of Glaucoma Filtration Surgery por Li‐Fong Seet, Roseline Su, Veluchamy A. Barathi, Wing Sum Lee, Rebekah Poh, Yee M. Heng, Ed Manser, Eranga N. Vithana, Tin Aung, Matt Weaver, E. Helene Sage, Tina Wong

    Publicado 2010
    Ligazón do recurso Ligazón do recurso
    Artigo
    Engadir a favoritos
    Gardado en:
  8. 8
    Missense mutations in the sodium borate cotransporter SLC4A11 cause late-onset Fuchs corneal dystrophya

    Missense mutations in the sodium borate cotransporter SLC4A11 cause late-onset Fuchs corneal dystrophya por S. Amer Riazuddin, Eranga N. Vithana, Li Fong Seet, Yangjian Liu, Amr Al‐Saif, Li Wei Koh, Yee M. Heng, Tin Aung, Danielle N. Meadows, Allen O. Eghrari, John D. Gottsch, Nicholas Katsanis

    Publicado 2010
    Ligazón do recurso
    Artigo
    Engadir a favoritos
    Gardado en:
  9. 9
    A Human Homolog of Yeast Pre-mRNA Splicing Gene, PRP31, Underlies Autosomal Dominant Retinitis Pigmentosa on Chromosome 19q13.4 (RP11)

    A Human Homolog of Yeast Pre-mRNA Splicing Gene, PRP31, Underlies Autosomal Dominant Retinitis Pigmentosa on Chromosome 19q13.4 (RP11) por Eranga N. Vithana, Leen Abu‐Safieh, Maxine Allen, Alisoun H. Carey, Myrto Papaioannou, Christina Chakarova, Mai Al-Maghtheh, Neil D. Ebenezer, Catherine Willis, Anthony T. Moore, A.C. Bird, David M. Hunt, Shomi S. Bhattacharya

    Publicado 2001
    Ligazón do recurso
    Artigo
    Engadir a favoritos
    Gardado en:
  10. 10
    Novel<i>SLC4A11</i>mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2)

    Novel<i>SLC4A11</i>mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2) por Vedam L. Ramprasad, Neil D. Ebenezer, Tin Aung, Rama Rajagopal, Victor H. K. Yong, Stephen J. Tuft, Deepa Viswanathan, Mohamed F. El-Ashry, Petra Lišková, Donald Tan, Shomi S. Bhattacharya, Govindasamy Kumaramanickavel, Eranga N. Vithana

    Publicado 2007
    Ligazón do recurso Ligazón do recurso
    Artigo
    Engadir a favoritos
    Gardado en:
  11. 11
    SLC4A11 mutations in Fuchs endothelial corneal dystrophy

    SLC4A11 mutations in Fuchs endothelial corneal dystrophy por Eranga N. Vithana, Patricio E. Morgan, Vedam L. Ramprasad, Donald Tan, Victor H. K. Yong, Divya Venkataraman, Anandalakshmi Venkatraman, Gary Hin‐Fai Yam, Soumittra Nagasamy, Ricky W.K. Law, Rama Rajagopal, Chi Pui Pang, G. Kumaramanickevel, Joseph R. Casey, Tin Aung

    Publicado 2007
    Ligazón do recurso Ligazón do recurso
    Artigo
    Engadir a favoritos
    Gardado en:
  12. 12
    Evaluation of Generative Adversarial Networks for High-Resolution Synthetic Image Generation of Circumpapillary Optical Coherence Tomography Images for Glaucoma

    Evaluation of Generative Adversarial Networks for High-Resolution Synthetic Image Generation of Circumpapillary Optical Coherence Tomography Images for Glaucoma por Ashish Jith Sreejith Kumar, Rachel S. Chong, Jonathan G. Crowston, Jacqueline Chua, Inna Bujor, Rahat Husain, Eranga N. Vithana, Michaël J. A. Girard, Daniel Shu Wei Ting, Ching‐Yu Cheng, Tin Aung, Alina Popa‐Cherecheanu, Leopold Schmetterer, Damon Wing Kee Wong

    Publicado 2022
    Ligazón do recurso Ligazón do recurso
    Artigo
    Engadir a favoritos
    Gardado en:
  13. 13
    Mutations in HPRP3, a third member ofpre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa

    Mutations in HPRP3, a third member ofpre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa por Christina Chakarova, Matthew M. Hims, Hanno J. Bolz, Leen Abu‐Safieh, Reshma Patel, Myrto Papaioannou, Chris F. Inglehearn, T J Keen, Catherine Willis, Anthony T. Moore, Thomas Rosenberg, Andrew R. Webster, Alan C. Bird, Andreas Gal, David M. Hunt, Eranga N. Vithana, Shomi S. Bhattacharya

    Publicado 2002
    Ligazón do recurso
    Artigo
    Engadir a favoritos
    Gardado en:
  14. 14
    Determinants of diagnostic yield in a multi-ethnic Asian inherited retinal disease cohort

    Determinants of diagnostic yield in a multi-ethnic Asian inherited retinal disease cohort por Jane A. Lieviant, Choi Mun Chan, Yasmin Bylstra, Kanika Jain, Jing Xian Teo, Wan Wan Lim, Sylvia Kam, Tiffany N. Chao, N. Siew, Sonia Dávila, Eranga N. Vithana, Ranjana Mathur, Tien‐En Tan, Patrick Tan, Saumya S. Jamuar, Beau J. Fenner, Weng Khong Lim

    Publicado 2025
    Ligazón do recurso
    Artigo
    Engadir a favoritos
    Gardado en:
  15. 15
    Genome-Wide Association Studies Reveal Genetic Variants in CTNND2 for High Myopia in Singapore Chinese

    Genome-Wide Association Studies Reveal Genetic Variants in CTNND2 for High Myopia in Singapore Chinese por Yi‐Ju Li, Liang Kee Goh, Chiea Chuen Khor, Qiao Fan, Miao Yu, Siyu Han, Xueling Sim, Rick Twee‐Hee Ong, Tien Yin Wong, Eranga N. Vithana, Eric P.H. Yap, Hideo Nakanishi, Fumihiko Matsuda, Kyoko Ohno‐Matsui, Nagahisa Yoshimura, Mark Seielstad, E Shyong Tai, Terri L. Young, Seang‐Mei Saw

    Publicado 2010
    Ligazón do recurso
    Artigo
    Engadir a favoritos
    Gardado en:
  16. 16
    Association of variants in FRAP1 and PDGFRA with corneal curvature in Asian populations from Singapore

    Association of variants in FRAP1 and PDGFRA with corneal curvature in Asian populations from Singapore por Siyu Han, Peng Chen, Qiao Fan, Chiea Chuen Khor, Xueling Sim, Wan-Ting Tay, Rick Twee‐Hee Ong, Chen Suo, Liang-Kee Goh, Raghavan Lavanya, Yingfeng Zheng, Renyi Wu, Mark Seielstad, Eranga N. Vithana, Jianjun Liu, Kee‐Seng Chia, Jeannette Jen-Mai Lee, E Shyong Tai, Tien Yin Wong, Tin Aung, Yik‐Ying Teo, Seang‐Mei Saw

    Publicado 2011
    Ligazón do recurso Ligazón do recurso
    Artigo
    Engadir a favoritos
    Gardado en:
  17. 17
    Identification of four novel variants that influence central corneal thickness in multi-ethnic Asian populations

    Identification of four novel variants that influence central corneal thickness in multi-ethnic Asian populations por Belinda K. Cornes, Chiea Chuen Khor, Monisha E. Nongpiur, Liang Xu, Wan-Ting Tay, Yingfeng Zheng, Raghavan Lavanya, Yang Li, Renyi Wu, Xueling Sim, Ya Xing Wang, Peng Chen, Yik Ying Teo, Kee‐Seng Chia, Mark Seielstad, Jianjun Liu, Martin L. Hibberd, Ching‐Yu Cheng, Seang‐Mei Saw, E Shyong Tai, Jost B. Jonas, Eranga N. Vithana, Tien Yin Wong, Tin Aung

    Publicado 2011
    Ligazón do recurso Ligazón do recurso
    Artigo
    Engadir a favoritos
    Gardado en:
  18. 18
    Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area

    Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area por Chiea Chuen Khor, Wishal D. Ramdas, Eranga N. Vithana, Belinda K. Cornes, Xueling Sim, Wan-Ting Tay, Seang‐Mei Saw, Yingfeng Zheng, Raghavan Lavanya, Renyi Wu, Jie Jin Wang, Paul Mitchell, André G. Uitterlinden, Fernando Rivadeneira, Yik‐Ying Teo, Kee‐Seng Chia, Mark Seielstad, Martin L. Hibberd, Johannes R. Vingerling, Caroline C. W. Klaver, Nomdo M. Jansonius, E Shyong Tai, Tien Yin Wong, Cornelia M. van Duijn, Tin Aung

    Publicado 2011
    Ligazón do recurso
    Artigo
    Engadir a favoritos
    Gardado en:
  19. 19
    Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia

    Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia por Chiea Chuen Khor, Masahiro Miyake, Li Jia Chen, Yi Shi, Veluchamy A. Barathi, Qiao Fan, Isao Nakata, Kenji Yamashiro, Xin Zhou, Pancy O. S. Tam, Ching‐Yu Cheng, E Shyong Tai, Eranga N. Vithana, Tin Aung, Yik-Ying Teo, Tien Yin Wong, Muka Moriyama, Kyoko Ohno-Matsui, Manabu Mochizuki, Fumihiko Matsuda, Rita Y.Y. Yong, Eric P.H. Yap, Zhenglin Yang, Chi Pui Pang, Seang‐Mei Saw, Nagahisa Yoshimura

    Publicado 2013
    Ligazón do recurso Ligazón do recurso
    Revisão
    Engadir a favoritos
    Gardado en:
  20. 20
    Genetic Variants on Chromosome 1q41 Influence Ocular Axial Length and High Myopia

    Genetic Variants on Chromosome 1q41 Influence Ocular Axial Length and High Myopia por Qiao Fan, Veluchamy A. Barathi, Ching‐Yu Cheng, Xin Zhou, Akira Meguro, Isao Nakata, Chiea Chuen Khor, Liang-Kee Goh, Yi‐Ju Li, Wan'e Lim, Candice Ho, Felicia Hawthorne, Yingfeng Zheng, Daniel Chua, Hidetoshi Inoko, Kenji Yamashiro, Kyoko Ohno-Matsui, Keitaro Matsuo, Fumihiko Matsuda, Eranga N. Vithana, Mark Seielstad, Nobuhisa Mizuki, Roger W. Beuerman, E Shyong Tai, Nagahisa Yoshimura, Tin Aung, Terri L. Young, Tien Yin Wong, Yik-Ying Teo, Seang‐Mei Saw

    Publicado 2012
    Ligazón do recurso Ligazón do recurso
    Revisão
    Engadir a favoritos
    Gardado en:

Ferramentas de procura: