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Lejin Wang

Showing results (11-20 of 24) with videos related to

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Mitochondrion|April 29, 2008
T14484C and T14502C in the mitochondrial ND6 gene are associated with Leber's hereditary optic neuropathy in a Chinese familyShirong Zhang, Lejin Wang, Yansheng Hao, et al.
Biomed Research International|February 27, 2019
Modified Posterior Scleral Reinforcement as a Treatment for High Myopia in Children and Its Therapeutic EffectZequn Miao, Luojia Li, Xiaoli Meng, et al.
Molecular Vision|January 21, 2012
A new novel mutation in FBN1 causes autosomal dominant Marfan syndrome in a Chinese familyJiamei Dong, Juan Bu, Wei Du, et al.
ACS Omega|September 21, 2020
Ultrathin and Robust Micro-Nano Composite Coating for Implantable Pressure Sensor EncapsulationJialin Yao, Wenjiang Qiang, Hao Wei, et al.
Investigative Ophthalmology & Visual Science|May 24, 2020
FRMD7 Mutations Disrupt the Interaction with GABRA2 and May Result in Infantile Nystagmus SyndromeLei Jiang, Yulei Li, Kangjuan Yang, et al.
Journal of Human Genetics|May 23, 2007
Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestationJing Yu Liu, Xiang Ren, Xiufeng Yang, et al.
Frontiers in Cell and Developmental Biology|November 30, 2020
p.His16Arg of STXBP1 (MUNC18-1) Associated With Syntaxin 3B Causes Autosomal Dominant Congenital NystagmusYulei Li, Lei Jiang, Lejin Wang, et al.
Molecular Vision|October 30, 2008
Identification of a genetic locus for autosomal dominant infantile cataract on chromosome 20p12.1-p11.23 in a Chinese familyShirong Zhang, Mugen Liu, Jia Mei Dong, et al.
Ophthalmic Genetics|June 15, 2018
A novel deletion downstream of the PAX6 gene identified in a Chinese family with congenital aniridiaXiaoqi Liu, Yaqi Wu, Zequn Miao, et al.
Eye and Vision (London, England)|December 9, 2020
The critical role of m<sup>6</sup>A methylation in the pathogenesis of Graves' ophthalmopathyLi Zhu, Siyan Li, Shikun He, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Mitochondrion|April 29, 2008
T14484C and T14502C in the mitochondrial ND6 gene are associated with Leber's hereditary optic neuropathy in a Chinese familyShirong Zhang, Lejin Wang, Yansheng Hao, et al.
Biomed Research International|February 27, 2019
Modified Posterior Scleral Reinforcement as a Treatment for High Myopia in Children and Its Therapeutic EffectZequn Miao, Luojia Li, Xiaoli Meng, et al.
Molecular Vision|January 21, 2012
A new novel mutation in FBN1 causes autosomal dominant Marfan syndrome in a Chinese familyJiamei Dong, Juan Bu, Wei Du, et al.
ACS Omega|September 21, 2020
Ultrathin and Robust Micro-Nano Composite Coating for Implantable Pressure Sensor EncapsulationJialin Yao, Wenjiang Qiang, Hao Wei, et al.
Investigative Ophthalmology & Visual Science|May 24, 2020
FRMD7 Mutations Disrupt the Interaction with GABRA2 and May Result in Infantile Nystagmus SyndromeLei Jiang, Yulei Li, Kangjuan Yang, et al.
Journal of Human Genetics|May 23, 2007
Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestationJing Yu Liu, Xiang Ren, Xiufeng Yang, et al.
Frontiers in Cell and Developmental Biology|November 30, 2020
p.His16Arg of STXBP1 (MUNC18-1) Associated With Syntaxin 3B Causes Autosomal Dominant Congenital NystagmusYulei Li, Lei Jiang, Lejin Wang, et al.
Molecular Vision|October 30, 2008
Identification of a genetic locus for autosomal dominant infantile cataract on chromosome 20p12.1-p11.23 in a Chinese familyShirong Zhang, Mugen Liu, Jia Mei Dong, et al.
Ophthalmic Genetics|June 15, 2018
A novel deletion downstream of the PAX6 gene identified in a Chinese family with congenital aniridiaXiaoqi Liu, Yaqi Wu, Zequn Miao, et al.
Eye and Vision (London, England)|December 9, 2020
The critical role of m<sup>6</sup>A methylation in the pathogenesis of Graves' ophthalmopathyLi Zhu, Siyan Li, Shikun He, et al.
Pageof 3