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Zimeng Ye

Showing results (11-20 of 38) with videos related to

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Cold Spring Harbor Molecular Case Studies|September 30, 2021
Somatic <i>IDH1</i> variant (p.R132C) in an adult male with Maffucci syndromeNatasha J Brown, Zimeng Ye, Chloe Stutterd, et al.
Ophthalmic Genetics|August 4, 2016
Association between SKIV2L polymorphism rs429608 and age-related macular degeneration: A meta-analysisPing Shuai, Zimeng Ye, Yuping Liu, et al.
Molecular Genetics & Genomic Medicine|March 7, 2019
Mutation screening in the FBN1 gene responsible for Marfan syndrome and related disorder in Chinese familiesBo Gong, Lan Yang, Qingwei Wang, et al.
Science China. Life Sciences|June 14, 2024
Identification of LRRC46 as a novel candidate gene for high myopiaLingxi Jiang, Chao Dai, Yao Wei, et al.
Ophthalmic Genetics|January 14, 2017
Evaluation of genome-wide susceptibility loci for high myopia in a Han Chinese populationFang Li, Zimeng Ye, Yaru Zhai, et al.
Ophthalmic Genetics|April 6, 2016
Association of IGF1 and IGF1R gene polymorphisms with high myopia in a Han Chinese populationPu Wang, Xiaoqi Liu, Zimeng Ye, et al.
Epilepsy Research|July 12, 2019
Somatic mutation: The hidden genetics of brain malformations and focal epilepsiesZimeng Ye, Lara McQuillan, Annapurna Poduri, et al.
Molecular Medicine Reports|June 15, 2018
A novel APC mutation identified in a large Chinese family with familial adenomatous polyposis and a brief literature reviewMinghui Pang, Yijun Liu, Xiaolin Hou, et al.
Gene|June 23, 2015
Identification of a novel MYOC mutation in a Chinese family with primary open-angle glaucomaYin Yang, Yi Shi, Xiaofang Huang, et al.
Human Genome Variation|June 23, 2016
A novel deleterious mutation in the COMP gene that causes pseudoachondroplasiaHuaichao Luo, Sisi Yu, Ying Lin, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Cold Spring Harbor Molecular Case Studies|September 30, 2021
Somatic <i>IDH1</i> variant (p.R132C) in an adult male with Maffucci syndromeNatasha J Brown, Zimeng Ye, Chloe Stutterd, et al.
Ophthalmic Genetics|August 4, 2016
Association between SKIV2L polymorphism rs429608 and age-related macular degeneration: A meta-analysisPing Shuai, Zimeng Ye, Yuping Liu, et al.
Molecular Genetics & Genomic Medicine|March 7, 2019
Mutation screening in the FBN1 gene responsible for Marfan syndrome and related disorder in Chinese familiesBo Gong, Lan Yang, Qingwei Wang, et al.
Science China. Life Sciences|June 14, 2024
Identification of LRRC46 as a novel candidate gene for high myopiaLingxi Jiang, Chao Dai, Yao Wei, et al.
Ophthalmic Genetics|January 14, 2017
Evaluation of genome-wide susceptibility loci for high myopia in a Han Chinese populationFang Li, Zimeng Ye, Yaru Zhai, et al.
Ophthalmic Genetics|April 6, 2016
Association of IGF1 and IGF1R gene polymorphisms with high myopia in a Han Chinese populationPu Wang, Xiaoqi Liu, Zimeng Ye, et al.
Epilepsy Research|July 12, 2019
Somatic mutation: The hidden genetics of brain malformations and focal epilepsiesZimeng Ye, Lara McQuillan, Annapurna Poduri, et al.
Molecular Medicine Reports|June 15, 2018
A novel APC mutation identified in a large Chinese family with familial adenomatous polyposis and a brief literature reviewMinghui Pang, Yijun Liu, Xiaolin Hou, et al.
Gene|June 23, 2015
Identification of a novel MYOC mutation in a Chinese family with primary open-angle glaucomaYin Yang, Yi Shi, Xiaofang Huang, et al.
Human Genome Variation|June 23, 2016
A novel deleterious mutation in the COMP gene that causes pseudoachondroplasiaHuaichao Luo, Sisi Yu, Ying Lin, et al.
Pageof 4