Zhang MT - Search Results

1

LIFGO: A modular laser-induced fluorescence detection system based on plug-in blocks.

Zhang MT, Peng YM, Pan JZ, Fang XX, Li HY, Zhang XY, Liao YC, Yao JK, Wu ML, Yao YY, Fang Q. Zhang MT, et al. Among authors: zhang xy. Talanta. 2022 Mar 1;239:123063. doi: 10.1016/j.talanta.2021.123063. Epub 2021 Nov 25. Talanta. 2022. PMID: 34890938

2

[Germinal mosaicism for partial deletion of the Dystrophin gene in a family affected with Duchenne muscular dystrophy].

Xiao H, Zhang Z, Li T, Zhang Q, Guo Q, Wu D, Wang H, Zhang M, Gao Y, Liao S. Xiao H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Oct 10;36(10):1015-1018. doi: 10.3760/cma.j.issn.1003-9406.2019.10.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31598949 Chinese.

3

[Genetic analysis of a child with atypical Williams-Beuren syndrome presenting as supravalvular aortic stenosis].

Wu D, Zhang M, Gao Y, Huo X, Xiao H, Zhang Q, Kang B, Wang X, Liao S. Wu D, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Apr 10;37(4):475-478. doi: 10.3760/cma.j.issn.1003-9406.2020.04.028. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32219841 Chinese.

4

[Genetic analysis of a pedigree with atypical partial 4q trisomy].

Zhang Q, Wu D, Zhang M, Zhang X, Xiao H, Gao Y, Li X, Wang F, Zhang X, Yan F, Liao S. Zhang Q, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Dec 10;38(12):1245-1249. doi: 10.3760/cma.j.cn511374-20200913-00667. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34839517 Chinese.

5

[Genetic diagnosis of a child with aortic stenosis and thumb aplasia].

Wu D, Hou Q, Li T, Wang X, Huo X, Gao Y, Zhang M, Ding X, Yang Y, Liao S. Wu D, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Aug 10;35(4):531-534. doi: 10.3760/cma.j.issn.1003-9406.2018.04.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30098250 Chinese.

6

[Genetic diagnosis of a child with Smith-Magenis syndrome].

Gao Y, Wu D, Huo X, Zhang M, Hou Q, Wang H, Liao S. Gao Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jul 10;36(7):724-726. doi: 10.3760/cma.j.issn.1003-9406.2019.07.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31302921 Chinese.

7

A gonadal mosaicism novel KMT2D mutation identified by haplotype construction and clone sequencing strategy.

Guo L, Zhang M, Gao Y, Qin L, Xia H, Liu L, Wang H. Guo L, et al. Clin Chim Acta. 2022 Jun 1;531:197-203. doi: 10.1016/j.cca.2022.04.008. Epub 2022 Apr 11. Clin Chim Acta. 2022. PMID: 35421397

8

HNRNPC mediated m⁶A methylation of 5-methyltetrahydrofolate-homocysteine methyltransferase and involved in the occurrence of RSA.

Zhang M, Huang N, Gao Y, Feng Z, Kang B, Guo H, Jiang J, Liao S, Wang H. Zhang M, et al. J Reprod Immunol. 2023 Dec;160:104160. doi: 10.1016/j.jri.2023.104160. Epub 2023 Oct 4. J Reprod Immunol. 2023. PMID: 37857158

9

A novel mutation within intron 17 of the CUL7 gene results in appearance of premature termination codon.

Guo L, Feng Z, Jin X, Yin S, Zhang M, Gao Y, Zhang B, Wang H, Liu L. Guo L, et al. Clin Chim Acta. 2020 Aug;507:23-30. doi: 10.1016/j.cca.2020.04.008. Epub 2020 Apr 9. Clin Chim Acta. 2020. PMID: 32278698

10

Leptin receptor neurons in the ventral premammillary nucleus modulate emotion-induced insomnia.

Yuan XS, Xiang Z, Jiang JB, Yuan F, Zhang MT, Zhang KY, Chen ZY, Qu WM, Li WS, Huang ZL. Yuan XS, et al. Among authors: zhang mt. Cell Discov. 2024 Jun 4;10(1):59. doi: 10.1038/s41421-024-00676-x. Cell Discov. 2024. PMID: 38830876 No abstract available.

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