Li M - Search Results

1

A novel germline mutation in SDHA identified in a rare case of gastrointestinal stromal tumor complicated with renal cell carcinoma.

Jiang Q, Zhang Y, Zhou YH, Hou YY, Wang JY, Li JL, Li M, Tong HX, Lu WQ. Jiang Q, et al. Among authors: li jl, li m. Int J Clin Exp Pathol. 2015 Oct 1;8(10):12188-97. eCollection 2015. Int J Clin Exp Pathol. 2015. PMID: 26722403 Free PMC article.

2

Three novel mutations in GPNMB in two pedigrees with amyloidosis cutis dyschromica.

Wang J, Li Y, Xing L, Zhao M, Zhang S, Li Z, Yao Z, Li M. Wang J, et al. Among authors: li y, li z, li m. Br J Dermatol. 2019 Dec;181(6):1327-1329. doi: 10.1111/bjd.18260. Epub 2019 Sep 1. Br J Dermatol. 2019. PMID: 31260093 No abstract available.

3

A novel MBTPS2 start codon mutation causes a mild ichthyosis follicularis with atrichia and photophobia phenotype.

Chen F, Wang J, Yao Z, Li M. Chen F, et al. Among authors: li m. Clin Exp Dermatol. 2020 Jun;45(4):505-507. doi: 10.1111/ced.14114. Epub 2019 Oct 24. Clin Exp Dermatol. 2020. PMID: 31646662 No abstract available.

4

Clinicopathological and molecular characteristics of abdominal desmoid tumors in the Chinese population: A single-center report of 15 cases.

Wang J, Jia N, Lin Q, Huang Y, Li J, Jiang Q, Liu W, Xu J, Hou Y, Liu J, Li M, Lu W, Zhou Y, Zhang Y, Tong H. Wang J, et al. Among authors: li j, li m. Oncol Lett. 2019 Dec;18(6):6443-6450. doi: 10.3892/ol.2019.11038. Epub 2019 Nov 1. Oncol Lett. 2019. PMID: 31807167 Free PMC article.

5

Next-generation sequencing through multi-gene panel testing for diagnosis of hereditary ichthyosis in Chinese.

Cheng R, Liang J, Li Y, Zhang J, Ni C, Yu H, Kong X, Li M, Yao Z. Cheng R, et al. Among authors: li y, li m. Clin Genet. 2020 May;97(5):770-778. doi: 10.1111/cge.13704. Epub 2020 Feb 9. Clin Genet. 2020. PMID: 31953843

6

Novel mutations in Chinese hypotrichosis simplex patients associated with LSS gene.

Hua S, Ding Y, Zhang J, Qian Q, Li M. Hua S, et al. Among authors: li m. J Dermatol. 2021 Mar;48(3):408-412. doi: 10.1111/1346-8138.15697. Epub 2020 Nov 22. J Dermatol. 2021. PMID: 33222230

7

Quantitative assessment of the influence of tumor necrosis factor alpha polymorphism with gastritis and gastric cancer risk.

Li M, Wang Y, Gu Y. Li M, et al. Tumour Biol. 2014 Feb;35(2):1495-502. doi: 10.1007/s13277-013-1206-0. Epub 2013 Sep 27. Tumour Biol. 2014. PMID: 24072494

8

Quantitative assessment of the influence of common variation rs16892766 at 8q23.3 with colorectal adenoma and cancer susceptibility.

Li M, Gu Y. Li M, et al. Mol Genet Genomics. 2015 Apr;290(2):461-9. doi: 10.1007/s00438-014-0928-z. Epub 2014 Oct 8. Mol Genet Genomics. 2015. PMID: 25293934

9

Coinheritance of generalized pustular psoriasis and familial Behçet-like autoinflammatory syndrome with variants in IL36RN and TNFAIP3 in the heterozygous state.

Liang J, Zhang H, Guo Y, Yang K, Ni C, Yu H, Kong X, Li M, Lu Z, Yao Z. Liang J, et al. Among authors: li m. J Dermatol. 2019 Oct;46(10):907-910. doi: 10.1111/1346-8138.15034. Epub 2019 Jul 29. J Dermatol. 2019. PMID: 31353537

10

The first case of a mosaic superficial epidermolytic ichthyosis diagnosed by Ultra-Deep Sequence.

Li Y, Cheng R, Liang J, Yao Z, Li M. Li Y, et al. Among authors: li m. Mol Genet Genomic Med. 2020 Nov;8(11):e1457. doi: 10.1002/mgg3.1457. Epub 2020 Sep 2. Mol Genet Genomic Med. 2020. PMID: 32881395 Free PMC article.

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