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Journal of Dermatological Science|September 23, 2021
Amyloidosis cutis dyschromica cases caused by GPNMB mutations with different inheritance patternsWen Qin, Huijun Wang, Weilong Zhong, et al.
Journal of Dermatological Science|March 1, 2025
A signal peptide variant in SLURP1 with dominant-negative effect causes progressive symmetric erythrokeratodermiaZhuoqing Gong, Yunran Peng, Sisi Zhao, et al.
European Journal of Dermatology : EJD|July 17, 2024
Unilateral focal palmoplantar keratoderma associated with a postzygotic variant in PIK3CA and activation of the PI3K/AKT/mTOR pathwayZhuoqing Gong, Sha Peng, Huijun Wang, et al.
The Journal of Dermatology|June 22, 2021
Novel pathogenic variants in the RECQL4 gene causing Rothmund-Thomson syndrome in three Chinese patientsYingzi Zhang, Wen Qin, Huijun Wang, et al.
The British Journal of Dermatology|January 23, 2023
Variants in KLK11, affecting signal peptide cleavage of kallikrein-related peptidase 11, cause an autosomal-dominant cornification disorderZhuoqing Gong, Shangzhi Dai, Xingyuan Jiang, et al.
Pediatric Dermatology|April 21, 2010
A case of Hailey-Hailey disease in an infant with a new ATP2C1 gene mutationZhe Xu, Lixin Zhang, Yuanyuan Xiao, et al.
European Journal of Dermatology : EJD|August 28, 2024
Symmetrical acral keratoderma associated with new variants in the filaggrin geneWanting Luo, Qiaoyun Lu, Yangyang Jiang, et al.
Frontiers in Cellular and Infection Microbiology|June 10, 2025
A novel loss-of-function variant in STAT1 causes Mendelian susceptibility to mycobacterial diseaseKunlun Lv, Zhuoqing Gong, Yiting Fu, et al.
Molecular Pain|February 10, 2018
TRPV1 gain-of-function mutation impairs pain and itch sensations in miceLina Duo, Linghan Hu, Naxi Tian, et al.
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