Lin ZM - Search Results

1

Unique features of PTCH1 mutation spectrum in Chinese sporadic basal cell carcinoma.

Huang YS, Bu DF, Li XY, Ma ZH, Yang Y, Lin ZM, Lu FM, Tu P, Li H. Huang YS, et al. Among authors: lin zm. J Eur Acad Dermatol Venereol. 2013 Feb;27(2):235-41. doi: 10.1111/j.1468-3083.2012.04453.x. Epub 2012 Feb 7. J Eur Acad Dermatol Venereol. 2013. PMID: 22313357

2

SPINK5 gene mutation and decreased LEKTI activity in three Chinese patients with Netherton's syndrome.

Zhao Y, Ma ZH, Yang Y, Yang SX, Wu LS, Ding BL, Lin ZM, Wang AP, Bu DF, Tu P. Zhao Y, et al. Among authors: lin zm. Clin Exp Dermatol. 2007 Sep;32(5):564-7. doi: 10.1111/j.1365-2230.2007.02438.x. Epub 2007 Jul 2. Clin Exp Dermatol. 2007. PMID: 17608759

3

Four novel and two recurrent glycine substitution mutations in the COL7A1 gene in Chinese patients with epidermolysis bullosa pruriginosa.

Tang ZL, Lin ZM, Wang HJ, Chen Q, Xu XM, Ge HF, Yang Y. Tang ZL, et al. Among authors: lin zm. Clin Exp Dermatol. 2013 Mar;38(2):197-9. doi: 10.1111/ced.12061. Clin Exp Dermatol. 2013. PMID: 23397949 No abstract available.

4

New mutations in the PLEC gene in a Chinese patient with epidermolysis bullosa simplex with muscular dystrophy.

Chen Q, Lin ZM, Wang HJ, Zhang J, Yin JH, Yang Y. Chen Q, et al. Among authors: lin zm. Clin Exp Dermatol. 2013 Oct;38(7):792-4. doi: 10.1111/ced.12116. Epub 2013 Mar 18. Clin Exp Dermatol. 2013. PMID: 23496806 No abstract available.

5

A novel nonsense mutation in the CDSN gene underlying hypotrichosis simplex of the scalp in a Chinese family.

Yang SX, Yin JH, Lin ZM, Wang HJ, Ren YL, Zhang J, Li RY, Yang Y. Yang SX, et al. Among authors: lin zm. Clin Exp Dermatol. 2014 Jan;39(1):75-7. doi: 10.1111/ced.12168. Epub 2013 Jun 8. Clin Exp Dermatol. 2014. PMID: 23746069 No abstract available.

6

A new germline mutation in KIT associated with diffuse cutaneous mastocytosis in a Chinese family.

Wang HJ, Lin ZM, Zhang J, Yin JH, Yang Y. Wang HJ, et al. Among authors: lin zm. Clin Exp Dermatol. 2014 Mar;39(2):146-9. doi: 10.1111/ced.12225. Epub 2013 Dec 2. Clin Exp Dermatol. 2014. PMID: 24289326

7

Recurrent splice-site mutation in MBTPS2 underlying IFAP syndrome with Olmsted syndrome-like features in a Chinese patient.

Wang HJ, Tang ZL, Lin ZM, Dai LL, Chen Q, Yang Y. Wang HJ, et al. Among authors: lin zm. Clin Exp Dermatol. 2014 Mar;39(2):158-61. doi: 10.1111/ced.12248. Epub 2013 Dec 7. Clin Exp Dermatol. 2014. PMID: 24313295

8

A High-Performance FPGA PRNG Based on Multiple Deep-Dynamic Transformations.

Li S, Lin Z, Yang Y, Ning R. Li S, et al. Entropy (Basel). 2024 Aug 7;26(8):671. doi: 10.3390/e26080671. Entropy (Basel). 2024. PMID: 39202141 Free PMC article.

9

Recurrent duplication mutation in HRAS causing mild Costello syndrome in a Chinese patient.

Xu F, Wang HJ, Lin ZM, Yu B. Xu F, et al. Among authors: lin zm. Clin Exp Dermatol. 2015 Jun;40(4):404-7. doi: 10.1111/ced.12571. Epub 2015 Feb 10. Clin Exp Dermatol. 2015. PMID: 25677562

10

Clinical characteristics of re-positive COVID-19 patients in Huangshi, China: A retrospective cohort study.

Zhou J, Zhang J, Zhou J, Yi H, Lin Z, Liu Y, Zhu M, Wang H, Zhang W, Xu H, Jiang H, Xiang Z, Qu Z, Yang Y, Lu L, Guo S, Fu H, Adcock IM, Wei Y, Yao X. Zhou J, et al. PLoS One. 2020 Nov 4;15(11):e0241896. doi: 10.1371/journal.pone.0241896. eCollection 2020. PLoS One. 2020. PMID: 33147282 Free PMC article.

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