Sökresultat - Jiao, Xiaodong

Polymorphism rs7278468 is associated with Age-related cataract through decreasing transcriptional activity of the CRYAA promoter av Ma, Xiaoyin, Jiao, Xiaodong, Ma, Zhiwei, Hejtmancik, J. Fielding

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Association and interaction of myopia with SNP markers rs13382811 and rs6469937 at ZFHX1B and SNTB1 in Han Chinese and European populations av Li, Jiali, Jiao, Xiaodong, Zhang, Qingjiong, Hejtmancik, J. Fielding

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Functional non-coding polymorphism in an EPHA2 promoter PAX2 binding site modifies expression and alters the MAPK and AKT pathways av Ma, Xiaoyin, Ma, Zhiwei, Jiao, Xiaodong, Hejtmancik, J. Fielding

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Autosomal Recessive Familial Exudative Vitreoretinopathy Is Associated with Mutations in LRP5 av Jiao, Xiaodong, Ventruto, Valerio, Trese, Michael T., Shastry, Barkur S., Hejtmancik, J. Fielding

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Lack of phenotypic effect of triallelic variation in SPATA7 in a family with Leber congenital amaurosis resulting from CRB1 mutations av Li, Lin, Xiao, Xueshan, Li, Shiqiang, Jiao, Xiaodong, Hejtmancik, J. Fielding, Zhang, Qingjiong

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A novel LRAT mutation affecting splicing in a family with early onset retinitis pigmentosa av Chen, Yabin, Huang, Li, Jiao, Xiaodong, Riazuddin, Sheikh, Amer Riazuddin, S., Fielding Hetmancik, J.

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Changes in DNA methylation hallmark alterations in chromatin accessibility and gene expression for eye lens differentiation av Disatham, Joshua, Brennan, Lisa, Jiao, Xiaodong, Ma, Zhiwei, Hejtmancik, J. Fielding, Kantorow, Marc

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Mutations in ASCC3L1 on 2q11.2 Are Associated with Autosomal Dominant Retinitis Pigmentosa in a Chinese Family av Li, Ningdong, Mei, Han, MacDonald, Ian M., Jiao, XiaoDong, Hejtmancik, J. Fielding

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ADAM-17 is a poor prognostic indicator for patients with hilar cholangiocarcinoma and is regulated by FoxM1 av Jiao, Xiaodong, Yu, Wenlong, Qian, Jianxin, Chen, Ying, Wei, Peilian, Fang, Wenzheng, Yu, Guanzhen

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Association of markers at chromosome 15q14 in Chinese patients with moderate to high myopia av Jiao, Xiaodong, Wang, Panfeng, Li, Shiqiang, Li, Anren, Guo, Xiangming, Zhang, Qingjiong, Hejtmancik, J. Fielding

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Analysis of RP2 and RPGR Mutations in Five X-Linked Chinese Families with Retinitis Pigmentosa av Jiang, Jingjing, Wu, Xiaofei, Shen, Di, Dong, Lijin, Jiao, Xiaodong, Hejtmancik, J. Fielding, Li, Ningdong

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Novel SIL1 mutations in consanguineous Pakistani families mapping to chromosomes 5q31 av Riazuddin, S. Amer, Amiri-Kordestani, Laleh, Kaul, Haiba, Butt, Tariq, Jiao, Xiaodong, Riazuddin, Sheikh, Hejtmancik, J. Fielding

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CDKN2B Polymorphism Is Associated with Primary Open-Angle Glaucoma (POAG) in the Afro-Caribbean Population of Barbados, West Indies av Cao, Dan, Jiao, Xiaodong, Liu, Xing, Hennis, Anselm, Leske, M. Cristina, Nemesure, Barbara, Hejtmancik, J. Fielding

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The EPHA2 gene is associated with cataracts linked to chromosome 1p av Shiels, Alan, Bennett, Thomas M., Knopf, Harry L.S., Maraini, Giovanni, Li, Anren, Jiao, Xiaodong, Hejtmancik, J. Fielding

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Reply to Liu et al.: Differential effects of chromosome 2p16.3 variants on glaucoma in African derived populations av Zhang, Kang, Jiao, Xiaodong, Chen, Yuhong, Yang, Zhenglin, Hennis, Anselm, Nemesure, Barbara, Hoh, Josephine, Hejtmancik, J. Fielding

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Increased SNAT1 is a marker of human osteosarcoma and potential therapeutic target av Wang, Miaomiao, Liu, Ying, Fang, Wenzheng, Liu, Ke, Jiao, Xiaodong, Wang, Zhan, Wang, Jiejun, Zang, Yuan-Sheng

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Thyroid hormone receptor beta mutations alter photoreceptor development and function in Danio rerio (zebrafish) av Deveau, Ciana, Jiao, Xiaodong, Suzuki, Sachihiro C., Krishnakumar, Asha, Yoshimatsu, Takeshi, Hejtmancik, J Fielding, Nelson, Ralph F.

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Novel compound heterozygous mutations in CYP1B1 identified in a Chinese family with developmental glaucoma av Cai, Suping, Zhang, Daren, Jiao, Xiaodong, Wang, Tingting, Fan, Mengjie, Wang, Yun, Hejtmancik, James Fielding, Liu, Xuyang

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Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11 av Jiao, Xiaodong, Sultana, Afia, Garg, Prashant, Ramamurthy, Balasubramanya, Vemuganti, Geeta K, Gangopadhyay, Nibaran, Hejtmancik, J Fielding, Kannabiran, Chitra

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Detection of Variants in 15 Genes in 87 Unrelated Chinese Patients with Leber Congenital Amaurosis av Li, Lin, Xiao, Xueshan, Li, Shiqiang, Jia, Xiaoyun, Wang, Panfeng, Guo, Xiangming, Jiao, Xiaodong, Zhang, Qingjiong, Hejtmancik, J. Fielding

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