Yang Y - Search Results

1

Three new founder mutations in Chinese patients with Nagashima-type palmoplantar keratoderma.

Liu J, Chen Z, Hu L, Song Z, Mo R, Tsang LS, Liu Y, Huang X, Gong Z, Xiang R, Lin Z, Yang Y. Liu J, et al. Among authors: yang y. Br J Dermatol. 2022 Dec;187(6):1043-1045. doi: 10.1111/bjd.21835. Epub 2022 Sep 7. Br J Dermatol. 2022. PMID: 35976164 No abstract available.

2

A case of Hailey-Hailey disease in an infant with a new ATP2C1 gene mutation.

Xu Z, Zhang L, Xiao Y, Li L, Lin Z, Yang Y, Ma L. Xu Z, et al. Among authors: yang y. Pediatr Dermatol. 2011 Mar-Apr;28(2):165-8. doi: 10.1111/j.1525-1470.2010.01088.x. Pediatr Dermatol. 2011. PMID: 20403116

3

Novel and founder variants of SERPINA12 in Chinese patients with autosomal recessive palmoplantar keratoderma.

Liu Y, Tan Y, Liu J, Song Z, Hu L, Mo R, Chen Z, Yang Y. Liu Y, et al. Among authors: yang y. Br J Dermatol. 2022 Aug;187(2):267-270. doi: 10.1111/bjd.21064. Epub 2022 May 6. Br J Dermatol. 2022. PMID: 35199331

4

Structural basis of TRPV3 inhibition by an antagonist.

Fan J, Hu L, Yue Z, Liao D, Guo F, Ke H, Jiang D, Yang Y, Lei X. Fan J, et al. Among authors: yang y. Nat Chem Biol. 2023 Jan;19(1):81-90. doi: 10.1038/s41589-022-01166-5. Epub 2022 Oct 27. Nat Chem Biol. 2023. PMID: 36302896

5

Investigation of Nagashima-type palmoplantar keratoderma in China: A cross-sectional study of 234 patients.

Liu J, Chen Z, Hu L, Song Z, Mo R, Tsang LS, Liu Y, Huang X, Gong Z, Lin Z, Yang Y. Liu J, et al. Among authors: yang y. J Dermatol. 2023 Mar;50(3):375-382. doi: 10.1111/1346-8138.16621. Epub 2022 Nov 1. J Dermatol. 2023. PMID: 36317385

6

Clinicopathologic and trichoscopic features of keratosis follicularis spinulosa decalvans: A case series study.

Lan X, Qiao R, Sun J, Song H, Gao M, Mo R, Song Z, Yang Y, Jiang Y. Lan X, et al. Among authors: yang y. J Dermatol. 2024 Feb;51(2):253-260. doi: 10.1111/1346-8138.17026. Epub 2023 Dec 12. J Dermatol. 2024. PMID: 38087855

7

Potential digenic inheritance of SERPINB7 and SERPINA12 variants in Chinese patients with Nagashima-type palmoplantar keratosis.

Liu Y, Liu J, Chen Y, Mo R, Xiang R, Song Z, Yang Y, Chen Z. Liu Y, et al. Among authors: yang y. Br J Dermatol. 2024 Jun 20;191(1):136-138. doi: 10.1093/bjd/ljae134. Br J Dermatol. 2024. PMID: 38529670 No abstract available.

8

Novel variant in WNT10A caused short anagen hair syndrome in a Chinese pedigree.

Mo R, Chen Z, Yang Y, Jiang Y. Mo R, et al. Among authors: yang y. J Eur Acad Dermatol Venereol. 2024 Nov;38(11):e976-e978. doi: 10.1111/jdv.20035. Epub 2024 Apr 23. J Eur Acad Dermatol Venereol. 2024. PMID: 38650486 No abstract available.

9

Novel compound heterozygous MPDU1 variants causing congenital disorders of glycosylation presenting with erythrokeratodermia variabilis.

Wei Z, Mo R, Yang Y, Chen Z. Wei Z, et al. Among authors: yang y. J Dermatol. 2024 Jun 3. doi: 10.1111/1346-8138.17321. Online ahead of print. J Dermatol. 2024. PMID: 38831602 No abstract available.

10

[Clinical and genetic characteristics of a patient with dyskeratosis congenita].

Li JG, Li Y, Lin ZM, Ma ZH, Li JH, Liu R, Shi XD, Yang Y, Wang TY. Li JG, et al. Among authors: yang y. Zhonghua Er Ke Za Zhi. 2009 Nov;47(11):867-70. Zhonghua Er Ke Za Zhi. 2009. PMID: 20079002 Chinese.

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