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Wenmin Sun

Showing results (41-50 of 95) with videos related to

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American Journal of Ophthalmology|September 28, 2021
Severe Exudative Vitreoretinopathy as a Common Feature for CTNNB1, KIF11 and NDP Variants Plus Sector Degeneration for KIF11Junxing Yang, Xueshan Xiao, Shiqiang Li, et al.
Molecular Vision|March 10, 2016
Exome sequencing identified null mutations in LOXL3 associated with early-onset high myopiaJiali Li, Bei Gao, Xueshan Xiao, et al.
Journal of Medical Genetics|December 22, 2018
Biallelic mutations in <i>USP45,</i> encoding a deubiquitinating enzyme, are associated with Leber congenital amaurosisZhen Yi, Jiamin Ouyang, Wenmin Sun, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|August 5, 2019
Rare variants in novel and known genes associated with primary angle closure glaucoma based on whole exome sequencing of 549 probandsWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Investigative Ophthalmology & Visual Science|January 15, 2015
Evaluation of 12 myopia-associated genes in Chinese patients with high myopiaJiali Li, Dan Jiang, Xueshan Xiao, et al.
Human Molecular Genetics|January 29, 2019
CPSF1 mutations are associated with early-onset high myopia and involved in retinal ganglion cell axon projectionJiamin Ouyang, Wenmin Sun, Xueshan Xiao, et al.
Frontiers in Public Health|July 18, 2019
Perspectives on the Training of Chinese Primary Health Care Physicians to Reduce Chronic Illnesses and Their BurdenWenmin Sun, Yang Li, Yiting Hu, et al.
Investigative Ophthalmology & Visual Science|December 20, 2014
Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencingDan Jiang, Jiali Li, Xueshan Xiao, et al.
Human Genetics|June 8, 2019
Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12-q13.3Xueshan Xiao, Wenmin Sun, Jiamin Ouyang, et al.
Molecular Genetics and Genomics : MGG|April 22, 2021
Pathogenicity evaluation and the genotype-phenotype analysis of OPA1 variantsXingyu Xu, Panfeng Wang, Xiaoyun Jia, et al.
Pageof 10

Showing results (41-50 of 95) with videos related to

Sort By:
Pageof 10
American Journal of Ophthalmology|September 28, 2021
Severe Exudative Vitreoretinopathy as a Common Feature for CTNNB1, KIF11 and NDP Variants Plus Sector Degeneration for KIF11Junxing Yang, Xueshan Xiao, Shiqiang Li, et al.
Molecular Vision|March 10, 2016
Exome sequencing identified null mutations in LOXL3 associated with early-onset high myopiaJiali Li, Bei Gao, Xueshan Xiao, et al.
Journal of Medical Genetics|December 22, 2018
Biallelic mutations in <i>USP45,</i> encoding a deubiquitinating enzyme, are associated with Leber congenital amaurosisZhen Yi, Jiamin Ouyang, Wenmin Sun, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|August 5, 2019
Rare variants in novel and known genes associated with primary angle closure glaucoma based on whole exome sequencing of 549 probandsWenmin Sun, Xueshan Xiao, Shiqiang Li, et al.
Investigative Ophthalmology & Visual Science|January 15, 2015
Evaluation of 12 myopia-associated genes in Chinese patients with high myopiaJiali Li, Dan Jiang, Xueshan Xiao, et al.
Human Molecular Genetics|January 29, 2019
CPSF1 mutations are associated with early-onset high myopia and involved in retinal ganglion cell axon projectionJiamin Ouyang, Wenmin Sun, Xueshan Xiao, et al.
Frontiers in Public Health|July 18, 2019
Perspectives on the Training of Chinese Primary Health Care Physicians to Reduce Chronic Illnesses and Their BurdenWenmin Sun, Yang Li, Yiting Hu, et al.
Investigative Ophthalmology & Visual Science|December 20, 2014
Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencingDan Jiang, Jiali Li, Xueshan Xiao, et al.
Human Genetics|June 8, 2019
Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12-q13.3Xueshan Xiao, Wenmin Sun, Jiamin Ouyang, et al.
Molecular Genetics and Genomics : MGG|April 22, 2021
Pathogenicity evaluation and the genotype-phenotype analysis of OPA1 variantsXingyu Xu, Panfeng Wang, Xiaoyun Jia, et al.
Pageof 10