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

Zhimiao Lin

Showing results (91-100 of 115) with videos related to

Pageof 12
Sort By:
Gene|April 22, 2015
Exome sequencing reveals novel BCS1L mutations in siblings with hearing loss and hypotrichosisJie Zhang, Lina Duo, Zhimiao Lin, et al.
The British Journal of Dermatology|March 15, 2024
Loss-of-function variants in GLMN are associated with generalized skin hyperpigmentation with or without glomuvenous malformationXingyuan Jiang, Chao Yang, Zhaoyang Wang, et al.
The Journal of Investigative Dermatology|December 12, 2018
Gain-of-Function Mutations in TRPM4 Activation Gate Cause Progressive Symmetric ErythrokeratodermiaHuijun Wang, Zhe Xu, Bo Hyun Lee, et al.
The British Journal of Dermatology|August 17, 2022
Three new founder mutations in Chinese patients with Nagashima-type palmoplantar keratodermaJuan Liu, Zhiming Chen, Linghan Hu, et al.
Journal of the American Academy of Dermatology|August 25, 2024
A combination therapy with secukinumab and dupilumab in Netherton syndrome: A prospective pilot studyTaoming Liu, Manman Tang, Jiao Liu, et al.
Nature Biomedical Engineering|July 27, 2023
Detection of low-frequency mutations in clinical samples by increasing mutation abundance via the excision of wild-type sequencesWei Chen, Haiqi Xu, Shenbin Dai, et al.
The British Journal of Dermatology|July 15, 2024
A gain-of-function variant in SREBF1 causes generalized skin hyperpigmentation with congenital cataractsHuijun Wang, Yuan Wu, Jennifer A Bassetti, et al.
The Journal of Investigative Dermatology|August 16, 2020
Genotype‒Phenotype Correlation of TRPV3-Related Olmsted SyndromeWeilong Zhong, Linghan Hu, Xu Cao, et al.
The Journal of Allergy and Clinical Immunology|November 16, 2013
CARD9 mutations linked to subcutaneous phaeohyphomycosis and TH17 cell deficienciesXiaowen Wang, Wenyan Wang, Zhimiao Lin, et al.
Dermatologic Therapy|September 26, 2018
Efficacy, safety, and cost-effectiveness of all-trans retinoic acid/Clobetasol Propionate Compound Ointment in the treatment of mild to moderate psoriasis vulgaris: A randomized, single-blind, multicenter clinical trialLixin Xia, Ruoyu Li, Yun Wang, et al.
Pageof 12

Showing results (91-100 of 115) with videos related to

Sort By:
Pageof 12
Gene|April 22, 2015
Exome sequencing reveals novel BCS1L mutations in siblings with hearing loss and hypotrichosisJie Zhang, Lina Duo, Zhimiao Lin, et al.
The British Journal of Dermatology|March 15, 2024
Loss-of-function variants in GLMN are associated with generalized skin hyperpigmentation with or without glomuvenous malformationXingyuan Jiang, Chao Yang, Zhaoyang Wang, et al.
The Journal of Investigative Dermatology|December 12, 2018
Gain-of-Function Mutations in TRPM4 Activation Gate Cause Progressive Symmetric ErythrokeratodermiaHuijun Wang, Zhe Xu, Bo Hyun Lee, et al.
The British Journal of Dermatology|August 17, 2022
Three new founder mutations in Chinese patients with Nagashima-type palmoplantar keratodermaJuan Liu, Zhiming Chen, Linghan Hu, et al.
Journal of the American Academy of Dermatology|August 25, 2024
A combination therapy with secukinumab and dupilumab in Netherton syndrome: A prospective pilot studyTaoming Liu, Manman Tang, Jiao Liu, et al.
Nature Biomedical Engineering|July 27, 2023
Detection of low-frequency mutations in clinical samples by increasing mutation abundance via the excision of wild-type sequencesWei Chen, Haiqi Xu, Shenbin Dai, et al.
The British Journal of Dermatology|July 15, 2024
A gain-of-function variant in SREBF1 causes generalized skin hyperpigmentation with congenital cataractsHuijun Wang, Yuan Wu, Jennifer A Bassetti, et al.
The Journal of Investigative Dermatology|August 16, 2020
Genotype‒Phenotype Correlation of TRPV3-Related Olmsted SyndromeWeilong Zhong, Linghan Hu, Xu Cao, et al.
The Journal of Allergy and Clinical Immunology|November 16, 2013
CARD9 mutations linked to subcutaneous phaeohyphomycosis and TH17 cell deficienciesXiaowen Wang, Wenyan Wang, Zhimiao Lin, et al.
Dermatologic Therapy|September 26, 2018
Efficacy, safety, and cost-effectiveness of all-trans retinoic acid/Clobetasol Propionate Compound Ointment in the treatment of mild to moderate psoriasis vulgaris: A randomized, single-blind, multicenter clinical trialLixin Xia, Ruoyu Li, Yun Wang, et al.
Pageof 12