Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Lulin Huang

Showing results (31-40 of 81) with videos related to

Pageof 9
Sort By:
BMC Medical Genetics|June 28, 2017
Association study of candidate genes for susceptibility to Kashin-Beck disease in a Tibetan populationZhengfu Tai, Lulin Huang, Fang Lu, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|August 11, 2025
D-glucuronyl C5-Epimerase Binds to EGFR to Suppress Kidney FibrosisXiaoqi Jing, Jun Wu, Jingru Ning, 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.
Elife|September 12, 2024
Dysfunction of Calcyphosine-Like gene impairs retinal angiogenesis through the MYC axis and is associated with familial exudative vitreoretinopathyWenjing Liu, Shujin Li, Mu Yang, et al.
Plos One|September 24, 2013
Association study of polymorphisms in selenoprotein genes and Kashin-Beck disease and serum selenium/iodine concentration in a Tibetan populationLulin Huang, Yi Shi, Fang Lu, et al.
Plos One|March 18, 2014
Exome sequencing analysis identifies compound heterozygous mutation in ABCA4 in a Chinese family with Stargardt diseaseYu Zhou, Siyu Tao, Hui Chen, et al.
Human Molecular Genetics|May 5, 2018
A splicing mutation in aryl hydrocarbon receptor associated with retinitis pigmentosaYu Zhou, Shujin Li, Lulin Huang, et al.
Human Molecular Genetics|June 23, 2018
A splicing mutation in aryl hydrocarbon receptor associated with retinitis pigmentosaYu Zhou, Shujin Li, Lulin Huang, et al.
Genetic Testing and Molecular Biomarkers|May 4, 2021
Whole-Exome Sequencing Identified <i>DLG1</i> as a Candidate Gene for Familial Exudative VitreoretinopathyShanshan Zhang, Xiao Li, Wenjing Liu, et al.
Scientific Reports|May 18, 2017
Mutation screening in genes known to be responsible for Retinitis Pigmentosa in 98 Small Han Chinese FamiliesLulin Huang, Qi Zhang, Xin Huang, et al.
Pageof 9

Showing results (31-40 of 81) with videos related to

Sort By:
Pageof 9
BMC Medical Genetics|June 28, 2017
Association study of candidate genes for susceptibility to Kashin-Beck disease in a Tibetan populationZhengfu Tai, Lulin Huang, Fang Lu, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|August 11, 2025
D-glucuronyl C5-Epimerase Binds to EGFR to Suppress Kidney FibrosisXiaoqi Jing, Jun Wu, Jingru Ning, 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.
Elife|September 12, 2024
Dysfunction of Calcyphosine-Like gene impairs retinal angiogenesis through the MYC axis and is associated with familial exudative vitreoretinopathyWenjing Liu, Shujin Li, Mu Yang, et al.
Plos One|September 24, 2013
Association study of polymorphisms in selenoprotein genes and Kashin-Beck disease and serum selenium/iodine concentration in a Tibetan populationLulin Huang, Yi Shi, Fang Lu, et al.
Plos One|March 18, 2014
Exome sequencing analysis identifies compound heterozygous mutation in ABCA4 in a Chinese family with Stargardt diseaseYu Zhou, Siyu Tao, Hui Chen, et al.
Human Molecular Genetics|May 5, 2018
A splicing mutation in aryl hydrocarbon receptor associated with retinitis pigmentosaYu Zhou, Shujin Li, Lulin Huang, et al.
Human Molecular Genetics|June 23, 2018
A splicing mutation in aryl hydrocarbon receptor associated with retinitis pigmentosaYu Zhou, Shujin Li, Lulin Huang, et al.
Genetic Testing and Molecular Biomarkers|May 4, 2021
Whole-Exome Sequencing Identified <i>DLG1</i> as a Candidate Gene for Familial Exudative VitreoretinopathyShanshan Zhang, Xiao Li, Wenjing Liu, et al.
Scientific Reports|May 18, 2017
Mutation screening in genes known to be responsible for Retinitis Pigmentosa in 98 Small Han Chinese FamiliesLulin Huang, Qi Zhang, Xin Huang, et al.
Pageof 9