Lei K - Search Results

1

A novel 1-bp deletion mutation and extremely skewed X-chromosome inactivation causing severe X-linked hypohidrotic ectodermal dysplasia in a Chinese girl.

Lei K, Zhang Y, Dong Z, Sun Y, Yi Z, Chen Z. Lei K, et al. Clin Exp Dermatol. 2018 Jan;43(1):60-62. doi: 10.1111/ced.13241. Epub 2017 Sep 22. Clin Exp Dermatol. 2018. PMID: 28940425 No abstract available.

2

[A case with 8q22.2q22.3 deletion syndrome].

Lei K, Zhang Y, Sun Y, Yuan SY. Lei K, et al. Zhonghua Er Ke Za Zhi. 2020 Jan 2;58(1):56-57. doi: 10.3760/cma.j.issn.0578-1310.2020.01.014. Zhonghua Er Ke Za Zhi. 2020. PMID: 31905479 Chinese.

3

[A study of clinical and genetic characteristics of a Leber hereditary optic neuropathy family with the heteroplasmic m.14484T>C mutation].

Sun Y, Lei K, Xu ZL, Geng Y. Sun Y, et al. Among authors: lei k. Zhonghua Yan Ke Za Zhi. 2018 Jul 11;54(7):526-534. doi: 10.3760/cma.j.issn.0412-4081.2018.07.012. Zhonghua Yan Ke Za Zhi. 2018. PMID: 29996615 Chinese.

4

Case report: genetic analysis of a child with 18q deletion syndrome and developmental dysplasia of the hip.

Yu S, Wang C, Lei K, Leng X, Zhang L, Tian F, Chen Z. Yu S, et al. Among authors: lei k. BMC Med Genomics. 2022 Sep 19;15(1):199. doi: 10.1186/s12920-022-01345-2. BMC Med Genomics. 2022. PMID: 36123715 Free PMC article.

5

[Dynamic analysis of junctional sequences of T cell receptor (TCR) delta and gamma gene rearrangement in childhood with acute lymphoblastic leukemia].

Lu J, Gu R, Lei K, Wang X, Sun L, Pang X, Li X, Dong Z. Lu J, et al. Among authors: lei k. Zhonghua Xue Ye Xue Za Zhi. 2000 Jun;21(6):301-4. Zhonghua Xue Ye Xue Za Zhi. 2000. PMID: 11876997 Chinese.

6

Epstein-Barr virus infection and type I interferon signature in patients with systemic lupus erythematosus.

Han L, Zhang Y, Wang Q, Xin M, Yang K, Lei K, Sun M. Han L, et al. Among authors: lei k. Lupus. 2018 Jan 1:961203317753069. doi: 10.1177/0961203317753069. Online ahead of print. Lupus. 2018. PMID: 29338588

7

[Establishment of An Animal Model of Acute B Lymphoblastic Leukemia with Minimal Residual Disease].

Jin XF, Wang LZ, Lei K, Dong ZY, Zhong R, Zhao H, Sun LR. Jin XF, et al. Among authors: lei k. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2022 Apr;30(2):381-385. doi: 10.19746/j.cnki.issn.1009-2137.2022.02.010. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2022. PMID: 35395967 Chinese.

8

Gonadal dysgenesis in Turner syndrome with Y-chromosome mosaicism: Two case reports.

Leng XF, Lei K, Li Y, Tian F, Yao Q, Zheng QM, Chen ZH. Leng XF, et al. Among authors: lei k. World J Clin Cases. 2020 Nov 26;8(22):5737-5743. doi: 10.12998/wjcc.v8.i22.5737. World J Clin Cases. 2020. PMID: 33344568 Free PMC article.

9

[Changes of plasma concentration of soluble intercellular adhesion molecule-1 and vascular endothelial growth factor in children with Henoch-Schoenlein purpura].

Zhang QY, Liu W, Lei K, Dong Z. Zhang QY, et al. Among authors: lei k. Zhonghua Er Ke Za Zhi. 2004 Jun;42(6):454-5. Zhonghua Er Ke Za Zhi. 2004. PMID: 15265435 Chinese. No abstract available.

10

Mannan-binding lectin promotes keratinocyte to produce CXCL1 and enhances neutrophil infiltration at the early stages of psoriasis.

Zeng J, Chen X, Lei K, Wang D, Lin L, Wang Y, Li Y, Liu Y, Zhang L, Zuo D, Sun L. Zeng J, et al. Among authors: lei k. Exp Dermatol. 2019 Sep;28(9):1017-1024. doi: 10.1111/exd.13995. Epub 2019 Aug 13. Exp Dermatol. 2019. PMID: 31260126

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