Showing results (71-80 of 100) with videos related to

Sort By:
Pageof 10
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.
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.
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