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Zhimiao Lin

Showing results (101-110 of 115) with videos related to

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Patient Preference and Adherence|January 15, 2021
Visit Adherence of Mild to Moderate Psoriasis Patients: A Mobile-Based Randomized StudyYi Zhao, Gang Wang, Wenqiong Ni, et al.
The British Journal of Dermatology|May 25, 2026
Loss-of-function variants in EPHX3 cause nonsyndromic epidermal differentiation disordersKunlun Lv, Karina M Forde, Amanda T Moon, et al.
Human Molecular Genetics|August 30, 2014
Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndromeHuijun Wang, Xu Cao, Zhimiao Lin, et al.
The British Journal of Dermatology|November 24, 2025
Safety and efficacy of stapokibart, an anti-IL-4Rα monoclonal antibody, in children aged 6-11 years with moderate-to-severe atopic dermatitis: An open-label, single-arm phase 1b/2a trialMutong Zhao, Zigang Xu, Liming Wu, et al.
Human Molecular Genetics|September 16, 2015
Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndromeHuijun Wang, Xu Cao, Zhimiao Lin, et al.
American Journal of Human Genetics|October 16, 2012
Loss-of-function mutations in HOXC13 cause pure hair and nail ectodermal dysplasiaZhimiao Lin, Quan Chen, Lei Shi, et al.
American Journal of Human Genetics|March 13, 2012
Exome sequencing reveals mutations in TRPV3 as a cause of Olmsted syndromeZhimiao Lin, Quan Chen, Mingyang Lee, et al.
Cell|August 16, 2025
Fibroblast bioelectric signaling drives hair growthDaoming Chen, Zhou Yu, Wenbo Wu, et al.
JAMA Dermatology|January 14, 2026
De Novo Germline L858R EGFR Variants and Generalized Acanthosis NigricansXingyuan Jiang, Mark Y Jeng, Zhou Yang, et al.
Nature Genetics|November 8, 2016
Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragilityZhimiao Lin, Shuo Li, Cheng Feng, et al.
Pageof 12

Showing results (101-110 of 115) with videos related to

Sort By:
Pageof 12
Patient Preference and Adherence|January 15, 2021
Visit Adherence of Mild to Moderate Psoriasis Patients: A Mobile-Based Randomized StudyYi Zhao, Gang Wang, Wenqiong Ni, et al.
The British Journal of Dermatology|May 25, 2026
Loss-of-function variants in EPHX3 cause nonsyndromic epidermal differentiation disordersKunlun Lv, Karina M Forde, Amanda T Moon, et al.
Human Molecular Genetics|August 30, 2014
Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndromeHuijun Wang, Xu Cao, Zhimiao Lin, et al.
The British Journal of Dermatology|November 24, 2025
Safety and efficacy of stapokibart, an anti-IL-4Rα monoclonal antibody, in children aged 6-11 years with moderate-to-severe atopic dermatitis: An open-label, single-arm phase 1b/2a trialMutong Zhao, Zigang Xu, Liming Wu, et al.
Human Molecular Genetics|September 16, 2015
Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndromeHuijun Wang, Xu Cao, Zhimiao Lin, et al.
American Journal of Human Genetics|October 16, 2012
Loss-of-function mutations in HOXC13 cause pure hair and nail ectodermal dysplasiaZhimiao Lin, Quan Chen, Lei Shi, et al.
American Journal of Human Genetics|March 13, 2012
Exome sequencing reveals mutations in TRPV3 as a cause of Olmsted syndromeZhimiao Lin, Quan Chen, Mingyang Lee, et al.
Cell|August 16, 2025
Fibroblast bioelectric signaling drives hair growthDaoming Chen, Zhou Yu, Wenbo Wu, et al.
JAMA Dermatology|January 14, 2026
De Novo Germline L858R EGFR Variants and Generalized Acanthosis NigricansXingyuan Jiang, Mark Y Jeng, Zhou Yang, et al.
Nature Genetics|November 8, 2016
Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragilityZhimiao Lin, Shuo Li, Cheng Feng, et al.
Pageof 12