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 (71-80 of 115) with videos related to

Pageof 12
Sort By:
The Journal of Investigative Dermatology|May 19, 2016
Semidominant Inheritance in Olmsted SyndromeXu Cao, Huijun Wang, Yanhong Li, et al.
The Journal of Investigative Dermatology|February 12, 2014
New and recurrent SERPINB7 mutations in seven Chinese patients with Nagashima-type palmoplantar keratosisJinghua Yin, Guiwen Xu, Huijun Wang, et al.
The British Journal of Dermatology|October 4, 2025
Gain-of-function variants in IRF6 cause hidradenitis suppurativa, ectodermal dysplasia and deafness syndromeZeqiao Zhang, Gaolei Zhang, Yaxuan Lv, et al.
The Journal of Investigative Dermatology|March 6, 2021
Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular KeratinocytesZhongya Song, Xi Chen, Qian Zhao, et al.
Experimental Dermatology|February 22, 2023
Biallelic mutations in LSS in autosomal-recessive mutilating palmoplantar keratodermaShengru Zhou, Xingyuan Jiang, Yuhao Zhu, et al.
Biochemical and Biophysical Research Communications|October 6, 2009
Erythromelalgia mutation L823R shifts activation and inactivation of threshold sodium channel Nav1.7 to hyperpolarized potentialsAngelika Lampert, Sulayman D Dib-Hajj, Emmanuella M Eastman, et al.
The Journal of Investigative Dermatology|January 23, 2022
KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes AlopeciaJun Cui, Qian Zhao, Zhongya Song, et al.
The British Journal of Dermatology|February 8, 2026
A recurrent variant in two patients with EMP2-nEDDYunran Peng, Nicole Cesarato, Tsenka Tomova-Simitchieva, et al.
The Journal of Investigative Dermatology|July 23, 2013
Mutation in AQP5, encoding aquaporin 5, causes palmoplantar keratoderma Bothnia typeXu Cao, Jinghua Yin, Huijun Wang, et al.
The British Journal of Dermatology|July 1, 2026
Recurrent and novel GLTP variants in five patients with nonsyndromic epidermal differentiation disorder: phenotypic and genotypic expansionZeqiao Zhang, Chao Yang, Xingyuan Jiang, et al.
Pageof 12

Showing results (71-80 of 115) with videos related to

Sort By:
Pageof 12
The Journal of Investigative Dermatology|May 19, 2016
Semidominant Inheritance in Olmsted SyndromeXu Cao, Huijun Wang, Yanhong Li, et al.
The Journal of Investigative Dermatology|February 12, 2014
New and recurrent SERPINB7 mutations in seven Chinese patients with Nagashima-type palmoplantar keratosisJinghua Yin, Guiwen Xu, Huijun Wang, et al.
The British Journal of Dermatology|October 4, 2025
Gain-of-function variants in IRF6 cause hidradenitis suppurativa, ectodermal dysplasia and deafness syndromeZeqiao Zhang, Gaolei Zhang, Yaxuan Lv, et al.
The Journal of Investigative Dermatology|March 6, 2021
Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular KeratinocytesZhongya Song, Xi Chen, Qian Zhao, et al.
Experimental Dermatology|February 22, 2023
Biallelic mutations in LSS in autosomal-recessive mutilating palmoplantar keratodermaShengru Zhou, Xingyuan Jiang, Yuhao Zhu, et al.
Biochemical and Biophysical Research Communications|October 6, 2009
Erythromelalgia mutation L823R shifts activation and inactivation of threshold sodium channel Nav1.7 to hyperpolarized potentialsAngelika Lampert, Sulayman D Dib-Hajj, Emmanuella M Eastman, et al.
The Journal of Investigative Dermatology|January 23, 2022
KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes AlopeciaJun Cui, Qian Zhao, Zhongya Song, et al.
The British Journal of Dermatology|February 8, 2026
A recurrent variant in two patients with EMP2-nEDDYunran Peng, Nicole Cesarato, Tsenka Tomova-Simitchieva, et al.
The Journal of Investigative Dermatology|July 23, 2013
Mutation in AQP5, encoding aquaporin 5, causes palmoplantar keratoderma Bothnia typeXu Cao, Jinghua Yin, Huijun Wang, et al.
The British Journal of Dermatology|July 1, 2026
Recurrent and novel GLTP variants in five patients with nonsyndromic epidermal differentiation disorder: phenotypic and genotypic expansionZeqiao Zhang, Chao Yang, Xingyuan Jiang, et al.
Pageof 12