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Plos One|May 26, 2016
Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger CamptodactylyHao Deng, Sheng Deng, Hongbo Xu, et al.Indian Journal of Biochemistry & Biophysics|April 30, 2014
Identification of a GJA3 mutation in a Chinese family with congenital nuclear cataract using exome sequencingYi Guo, Lamei Yuan, Junhui Yi, et al.Investigative Ophthalmology & Visual Science|June 27, 2015
Unique Variants in OPN1LW Cause Both Syndromic and Nonsyndromic X-Linked High Myopia Mapped to MYP1Jiali Li, Bei Gao, Liping Guan, et al.Human Genetics|June 19, 2014
Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencingYan Xu, Liping Guan, Tao Shen, et al.Investigative Ophthalmology & Visual Science|May 11, 2013
Comprehensive mutation analysis by whole-exome sequencing in 41 Chinese families with Leber congenital amaurosisYabin Chen, Qingyan Zhang, Tao Shen, et al.BMC Medical Genomics|March 19, 2021
Genome-wide association study identifies new loci associated with risk of HBV infection and disease progressionZheng Zeng, Hankui Liu, Huifang Xu, et al.Frontiers in Plant Science|January 23, 2018
Comparative Transcriptome and Microscopy Analyses Provide Insights into Flat Shape Formation in Peach (Prunus persica)Jian Guo, Ke Cao, Yong Li, et al.Journal of Tissue Engineering and Regenerative Medicine|July 24, 2010
Biological safety of human skin-derived stem cells after long-term in vitro cultureLiping Guan, Jie Yu, Ling Zhong, et al.Cellular Signalling|October 23, 2025
APC/C coactivators Cdh1 and Cdc20: Mechanistic insights into cancer progression and therapeutic opportunitiesYaqi Zhang, Haoyi Wang, Kaifan Li, et al.Plos Genetics|October 31, 2017
A trehalose biosynthetic enzyme doubles as an osmotic stress sensor to regulate bacterial morphogenesisXiming Chen, Lizhe An, Xiaochuan Fan, et al.Pageof 10