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by Cheng, Ching-Yu and Yamashiro, Kenji and Jia Chen, Li and Ahn, Jeeyun and Huang, Lulin and Huang, Lvzhen and Cheung, Chui Ming G and Miyake, Masahiro and Cackett, Peter D and Yeo, Ian Y and Laude, Augustinus and Mathur, Ranjana and Pang, Junxiong and Sim, Kar Seng and Koh, Adrian H and Chen, Peng and Lee, Shu Yen and Wong, Doric and Chan, Choi Mun and Loh, Boon Kwang and Sun, Yaoyao and Davila, Sonia and Nakata, Isao and Nakanishi, Hideo and Akagi-Kurashige, Yumiko and Gotoh, Norimoto and Tsujikawa, Akitaka and Matsuda, Fumihiko and Mori, Keisuke and Yoneya, Shin and Sakurada, Yoichi and Iijima, Hiroyuki and Iida, Tomohiro and Honda, Shigeru and Lai, Timothy Yuk Yau and Tam, Pancy Oi Sin and Chen, Haoyu and Tang, Shibo and Ding, Xiaoyan and Wen, Feng and Lu, Fang and Zhang, Xiongze and Shi, Yi and Zhao, Peiquan and Zhao, Bowen and Sang, Jinghong and Gong, Bo and Dorajoo, Rajkumar and Yuan, Jian-Min and Koh, Woon-Puay and Van Dam, Rob M and Friedlander, Yechiel and Lin, Ying and Hibberd, Martin L and Foo, Jia Nee and Wang, Ningli and Wong, Chang Hua and Tan, Gavin S and Park, Sang Jun and Bhargava, Mayuri and Gopal, Lingam and Naing, Thet and Liao, Jiemin and Guan Ong, Peng and Mitchell, Paul and Zhou, Peng and Xie, Xuefeng and Liang, Jinlong and Mei, Junpu and Jin, Xin and Saw, Seang-Mei and Ozaki, Mineo and Mizoguchi, Takanori and Kurimoto, Yasuo and Woo, Se Joon and Chung, Hum and Yu, Hyeong-Gon and Shin, Joo Young and Park, Dong Ho and Kim, In Taek and Chang, Woohyok and Sagong, Min and Lee, Sang-Joon and Kim, Hyun Woong and Lee, Ji Eun and Li, Yi and Liu, Jianjun and Teo, Yik Ying and Heng, Chew Kiat and Lim, Tock Han and Yang, Suk-Kyun and Song, Kyuyoung and Vithana, Eranga N and Aung, Tin and Bei, Jin Xin and Zeng, Yi Xin and Tai, E. Shyong and Li, Xiao Xin and Yang, Zhenglin and Park, Kyu-Hyung and ...
Nature Communications, ISSN 2041-1723, 01/2015, Volume 6, Issue 1, p. 6063
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 06/2011, Volume 88, Issue 6, pp. 805 - 813
Journal Article
Genetics in medicine : official journal of the American College of Medical Genetics, ISSN 1098-3600, 04/2019, Volume 21, Issue 10, pp. 2345 - 2354
Primary open-angle glaucoma (POAG) is the leading cause of irreversible blindness worldwide and mutations in known genes can only explain 5-6% of POAG. This... 
Journal Article
Molecular Vision, ISSN 1090-0535, 01/2009, Volume 15, pp. 89 - 98
Purpose To evaluate the individual and interactive effects of polymorphisms in the myocilin (MYOC), optineurin (OPTN), WD repeat domain 36 (WDR36), and... 
Journal Article
DISEASE MARKERS, ISSN 0278-0240, 2019, Volume 2019, pp. 5820537 - 5
Purpose. To study the roles of sequence alterations in the optineurin (OPTN) gene-coding region in normal-tension glaucoma (NTG) among Chinese patients.... 
MEDICINE, RESEARCH & EXPERIMENTAL | PATHOLOGY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ASSOCIATION | GENETICS & HEREDITY | Glaucoma | Polymerase chain reaction | Change detection | Exons | Amino acids | Mutation | Deoxyribonucleic acid--DNA
Journal Article
Genome Biology, ISSN 1474-7596, 02/2002, Volume 3, Issue 2, pp. reports2009 - reports2009
Y.F. Leung's Functional Genomics website is a portal of up-to-date annotated links to databases, software, analysis materials and protocols for functional... 
Journal Article
by Cheng, Ching-Yu and Yamashiro, Kenji and Jia Chen, Li and Ahn, Jeeyun and Huang, Lulin and Huang, Lvzhen and Cheung, Chui Ming G and Miyake, Masahiro and Cackett, Peter D and Yeo, Ian Y and Laude, Augustinus and Mathur, Ranjana and Pang, Junxiong and Sim, Kar Seng and Koh, Adrian H and Chen, Peng and Lee, Shu Yen and Wong, Doric and Chan, Choi Mun and Loh, Boon Kwang and Sun, Yaoyao and Davila, Sonia and Nakata, Isao and Nakanishi, Hideo and Akagi-Kurashige, Yumiko and Gotoh, Norimoto and Tsujikawa, Akitaka and Matsuda, Fumihiko and Mori, Keisuke and Yoneya, Shin and Sakurada, Yoichi and Iijima, Hiroyuki and Iida, Tomohiro and Honda, Shigeru and Lai, Timothy Yuk Yau and Tam, Pancy Oi Sin and Chen, Haoyu and Tang, Shibo and Ding, Xiaoyan and Wen, Feng and Lu, Fang and Zhang, Xiongze and Shi, Yi and Zhao, Peiquan and Zhao, Bowen and Sang, Jinghong and Gong, Bo and Dorajoo, Rajkumar and Yuan, Jian-Min and Koh, Woon-Puay and van Dam, Rob M and Friedlander, Yechiel and Lin, Yin and Hibberd, Martin L and Foo, Jia Nee and Wang, Ningli and Wong, Chang Hua and Tan, Gavin S and Park, Sang Jun and Bhargava, Mayuri and Gopal, Lingam and Naing, Thet and Liao, Jiemin and Ong, Peng Guan and Mitchell, Paul and Zhou, Peng and Xie, Xuefeng and Liang, Jinlong and Mei, Junpu and Jin, Xin and Saw, Seang-Mei and Ozaki, Mineo and Mizoguchi, Takinori and Kurimoto, Yasuo and Woo, Se Joon and Chung, Hum and Yu, Hyeong-Gon and Shin, Joo Young and Park, Dong Ho and Kim, In Taek and Chang, Woohyok and Sagong, Min and Lee, Sang-Joon and Kim, Hyun Woong and Lee, Ji Eun and Li, Yi and Liu, Jianjun and Teo, Yik Ying and Heng, Chew Kiat and Lim, Tock Han and Yang, Suk-Kyun and Song, Kyuyoung and Vithana, Eranga N and Aung, Tin and Bei, Jin Xin and Zeng, Yi Xin and Tai, E. Shyong and Li, Xiao Xin and Yang, Zhenglin and Park, Kyu-Hyung and ...
Nature Communications, ISSN 2041-1723, 11/2015, Volume 6, Issue 1
Journal Article
Molecular Vision, ISSN 1090-0535, 11/2007, Volume 13, Issue 236-37, pp. 2096 - 2104
Purpose: To investigate a novel deletion variant of gamma D-crystallin (CRYGD) identified in a Chinese family with nuclear congenital cataract. Methods: A... 
ACULEIFORM CATARACT | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENE CRYGD | MISSENSE MUTATION | OPHTHALMOLOGY | DIFFERENTIATION | CHINESE FAMILY | LENS | DENUCLEATION | SOLUBILITY
Journal Article
Molecular Vision, ISSN 1090-0535, 2009, Volume 15, Issue 119-20, pp. 1127 - 1138
Purpose: To investigate the clinical features and molecular basis of inherited cataract-microcornea caused by an alpha A-crystallin gene (CRYAA) mutation in a... 
INDIAN FAMILY | POPULATION | ZEBRAFISH HSP70 | STABILITY | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHICKEN LENS | OPHTHALMOLOGY | MICROPHTHALMIA | DOMINANT CONGENITAL CATARACT | CRYAA | CHAPERONE | PROTEINS
Journal Article
Investigative Ophthalmology & Visual Science, ISSN 0146-0404, 03/2003, Volume 44, Issue 3, p. 1012
Journal Article
Investigative ophthalmology & visual science, ISSN 0146-0404, 03/2003, Volume 44, Issue 3, p. 1012
Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 03/2003, Volume 44, Issue 3, pp. 1012 - 1015
PURPOSE. To investigate the coding exons of transforming growth factor (TGF)-beta-induced factor (TGIF) for mutations in Chinese patients with high myopia.... 
TRANSCRIPTIONAL COREPRESSOR TGIF | MAPS | HAPLOTYPES | SNPS | OPHTHALMOLOGY | PREVALENCE | PROMOTER | LOCUS | PROGRESSION | REFRACTION | CHILDREN
Journal Article
by Cheng, Ching-Yu and Yamashiro, Kenji and Chen, Li Jia and Ahn, Jeeyun and Huang, Lulin and Huang, Lvzhen and Cheung, Chui Ming G and Miyake, Masahiro and Cackett, Peter D and Yeo, Ian Y and Laude, Augustinus and Mathur, Ranjana and Pang, Junxiong and Sim, Kar Seng and Koh, Adrian H and Chen, Peng and Lee, Shu Yen and Wong, Doric and Chan, Choi Mun and Loh, Boon Kwang and Sun, Yaoyao and Davila, Sonia and Nakata, Isao and Nakanishi, Hideo and Akagi-Kurashige, Yumiko and Gotoh, Norimoto and Tsujikawa, Akitaka and Matsuda, Fumihiko and Mori, Keisuke and Yoneya, Shin and Sakurada, Yoichi and Iijima, Hiroyuki and Iida, Tomohiro and Honda, Shigeru and Lai, Timothy Yuk Yau and Tam, Pancy Oi Sin and Chen, Haoyu and Tang, Shibo and Ding, Xiaoyan and Wen, Feng and Lu, Fang and Zhang, Xiongze and Shi, Yi and Zhao, Peiquan and Zhao, Bowen and Sang, Jinghong and Gong, Bo and Dorajoo, Rajkumar and Yuan, Jian-Min and Koh, Woon-Puay and Van Dam, Rob M and Friedlander, Yechiel and Lin, Yin and Hibberd, Martin L and Foo, Jia Nee and Wang, Ningli and Wong, Chang Hua and Tan, Gavin S and Park, Sang Jun and Bhargava, Mayuri and Gopal, Lingam and Naing, Thet and Liao, Jiemin and Ong, Peng Guan and Mitchell, Paul and Zhou, Peng and Xie, Xuefeng and Liang, Jinlong and Mei, Junpu and Jin, Xin and Saw, Seang-Mei and Ozaki, Mineo and Mizoguchi, Takinori and Kurimoto, Yasuo and Woo, Se Joon and Chung, Hum and Yu, Hyeong-Gon and Shin, Joo Young and Park, Dong Ho and Kim, In Taek and Chang, Woohyok and Sagong, Min and Lee, Sang-Joon and Kim, Hyun Woong and Lee, Ji Eun and Li, Yi and Liu, Jianjun and Teo, Yik Ying and Heng, Chew Kiat and Lim, Tock Han and Yang, Suk-Kyun and Song, Kyuyoung and Vithana, Eranga N and Aung, Tin and Bei, Jin Xin and Zeng, Yi Xin and Tai, E. Shyong and Li, Xiao Xin and Yang, Zhenglin and Park, Kyu-Hyung and ...
Nature Communications, 2015, Volume 6, p. 6817
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 06/2011, Volume 88, Issue 6, p. 805
High myopia, which is extremely prevalent in the Chinese population, is one of the leading causes of blindness in the world. Genetic factors play a critical... 
Biological variation | Myopia | Genetics | Retina | Gene expression
Journal Article
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