Xie M - Search Results

1

[A large-scale retrospective analysis of copy number variations in single center using ACMG-ClinGen latest guidelines].

Zhang Y, Xue J, Yan L, Liu Y, Zhuang D, Xie M, Chen Y, An Y, Shen Y, Li H. Zhang Y, et al. Among authors: xie m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Aug 10;39(8):814-818. doi: 10.3760/cma.j.cn511374-20210519-00429. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35929928 Chinese.

2

22q11.2 recurrent copy number variation-related syndrome: a retrospective analysis of our own microarray cohort and a systematic clinical overview of ClinGen curation.

Xue J, Shen R, Xie M, Liu Y, Zhang Y, Gong L, Li H. Xue J, et al. Among authors: xie m. Transl Pediatr. 2021 Dec;10(12):3273-3281. doi: 10.21037/tp-21-560. Transl Pediatr. 2021. PMID: 35070841 Free PMC article.

3

[Variation analysis of EPG5 gene in a Vici syndrome family].

Yan L, Cai Y, Liu Y, Han C, Huo Y, Xie M, Xue J, Li H. Yan L, et al. Among authors: xie m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Feb 10;39(2):189-193. doi: 10.3760/cma.j.cn511374-20210216-00131. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35076917 Chinese.

4

Antley-Bixler syndrome arising from compound heterozygotes in the P450 oxidoreductase gene: a case report.

Li H, Zhao A, Xie M, Chen L, Wu H, Shen Y, Wang H. Li H, et al. Among authors: xie m. Transl Pediatr. 2021 Dec;10(12):3309-3318. doi: 10.21037/tp-21-499. Transl Pediatr. 2021. PMID: 35070845 Free PMC article.

5

A Novel Missense Variant in the Gene PPP2R5D Causes a Rare Neurodevelopmental Disorder with Increased Phenotype.

Yan L, Shen R, Cao Z, Han C, Zhang Y, Liu Y, Yang X, Xie M, Li H. Yan L, et al. Among authors: xie m. Biomed Res Int. 2021 Feb 11;2021:6661860. doi: 10.1155/2021/6661860. eCollection 2021. Biomed Res Int. 2021. Retraction in: Biomed Res Int. 2023 Nov 29;2023:9781948. doi: 10.1155/2023/9781948 PMID: 33628804 Free PMC article. Retracted. Clinical Trial.

6

[Advance in clinical research on Antley-Bixler syndrome].

Xie M, Wang H, Chen L, Li H, Li H. Xie M, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Apr 10;35(2):280-283. doi: 10.3760/cma.j.issn.1003-9406.2018.02.031. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29653011 Review. Chinese.

7

Aneuploid abortion correlates positively with MAD1 overexpression and miR-125b down-regulation.

Zhao J, Li H, Chen G, Du L, Xu P, Zhang X, Xie M, Cao T, Li H. Zhao J, et al. Among authors: xie m. Mol Cytogenet. 2021 Apr 26;14(1):22. doi: 10.1186/s13039-021-00538-1. Mol Cytogenet. 2021. PMID: 33902659 Free PMC article.

8

HOXA11-AS: a novel regulator in human cancer proliferation and metastasis.

Xue JY, Huang C, Wang W, Li HB, Sun M, Xie M. Xue JY, et al. Among authors: xie m. Onco Targets Ther. 2018 Jul 27;11:4387-4393. doi: 10.2147/OTT.S166961. eCollection 2018. Onco Targets Ther. 2018. PMID: 30100744 Free PMC article. Review.

9

The long intergenic non-protein coding RNA 707 promotes proliferation and metastasis of gastric cancer by interacting with mRNA stabilizing protein HuR.

Xie M, Ma T, Xue J, Ma H, Sun M, Zhang Z, Liu M, Liu Y, Ju S, Wang Z, De W. Xie M, et al. Cancer Lett. 2019 Feb 28;443:67-79. doi: 10.1016/j.canlet.2018.11.032. Epub 2018 Nov 29. Cancer Lett. 2019. PMID: 30502359

10

[Application of next-generation sequencing technology for genetic diagnosis of Duchenne muscular dystrophy].

Liu MJ, Xie M, Mao J, Li H, Yan WH, Chen Y. Liu MJ, et al. Among authors: xie m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Jun;29(3):249-54. doi: 10.3760/cma.j.issn.1003-9406.2012.03.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22678781 Chinese.

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