Dai M - Search Results

1

Revealing diverse alternative splicing variants of the highly homologous SMN1 and SMN2 genes by targeted long-read sequencing.

Dai M, Xu Y, Sun Y, Xiao B, Ying X, Liu Y, Jiang W, Zhang J, Liu X, Ji X. Dai M, et al. Mol Genet Genomics. 2022 Jul;297(4):1039-1048. doi: 10.1007/s00438-022-01874-6. Epub 2022 May 25. Mol Genet Genomics. 2022. PMID: 35612622

2

Identifying occult maternal malignancies from 1.93 million pregnant women undergoing noninvasive prenatal screening tests.

Ji X, Li J, Huang Y, Sung PL, Yuan Y, Liu Q, Chen Y, Ju J, Zhou Y, Huang S, Chen F, Han Y, Yuan W, Fan C, Zhao Q, Wu H, Feng S, Liu W, Li Z, Chen J, Chen M, Yao H, Zeng L, Ma T, Fan S, Zhang J, Yuen KY, Cheng SH, Chik IWS, Liu NT, Zhu J, Lin S, Cao J, Tong S, Shan Z, Li W, Hekmat MR, Garshasbi M, Suela J, Torres Y, Cigudosa JC, Ruiz FJP, Rodríguez L, García M, Bernik J, Traven E, Reš U, Tul N, Tseng CF, Zhao D, Sun L, Pan Q, Shen L, Dai M, Wang Y, Wang J, Yang H, Yin Y, Duan T, Zhu B, Choolani M, Jin X, Chen Y, Mao M. Ji X, et al. Among authors: dai m. Genet Med. 2019 Oct;21(10):2293-2302. doi: 10.1038/s41436-019-0510-5. Epub 2019 Apr 12. Genet Med. 2019. PMID: 30976098 Free article.

3

Prenatal diagnosis of methylmalonic aciduria from amniotic fluid using genetic and biochemical approaches.

Ji X, Wang H, Ye J, Qiu W, Zhang H, Liang L, Xiao B, Dai M, Xu Y, Chen T, Xu F, Chen Y, Ye W, Gu X, Wang L, Han L. Ji X, et al. Among authors: dai m. Prenat Diagn. 2019 Oct;39(11):993-997. doi: 10.1002/pd.5519. Epub 2019 Aug 5. Prenat Diagn. 2019. PMID: 31278756

4

[Diagnosis of two cases from one family with Joubert syndrome caused by novel mutations of TCTN1 gene by whole exome sequencing].

Wang H, Jiang W, Dai M, Xiao B, Xu Y, Sun Y, Liu Y, Ying X, Sun Y, Wei W, Ji X. Wang H, et al. Among authors: dai m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jul 10;36(7):686-689. doi: 10.3760/cma.j.issn.1003-9406.2019.07.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31302911 Chinese.

5

Identification of novel SMN1 subtle mutations using an allelic-specific RT-PCR.

Xu Y, Xiao B, Liu Y, Qu XX, Dai MY, Ying XM, Jiang WT, Zhang JM, Liu XQ, Chen YW, Ji X. Xu Y, et al. Neuromuscul Disord. 2020 Mar;30(3):219-226. doi: 10.1016/j.nmd.2019.11.010. Epub 2019 Dec 25. Neuromuscul Disord. 2020. PMID: 32169315

6

Biochemical and genetic approaches to the prenatal diagnosis of propionic acidemia in 78 pregnancies.

Dai M, Xiao B, Zhang H, Ye J, Qiu W, Zhu H, Wang L, Liang L, Zhan X, Ji W, Wang Y, Yu Y, Gu X, Han L. Dai M, et al. Orphanet J Rare Dis. 2020 Oct 7;15(1):276. doi: 10.1186/s13023-020-01539-w. Orphanet J Rare Dis. 2020. PMID: 33028371 Free PMC article.

7

Erratum to "Identification of novel SMN1 subtle mutations using an allelic-specific RT-PCR" [Neuromuscular Disorders, 30(3) 2020, 219-226].

Xu Y, Xiao B, Liu Y, Qu XX, Dai MY, Ying XM, Jiang WT, Zhang JM, Liu XQ, Chen YW, Ji X. Xu Y, et al. Neuromuscul Disord. 2021 Jan;31(1):e1. doi: 10.1016/j.nmd.2020.11.006. Epub 2020 Dec 1. Neuromuscul Disord. 2021. PMID: 33277158 No abstract available.

8

Multi-omics analyses of G6PD deficiency variants in Chinese population.

Ji H, Chen J, Huang P, Feng Z, Hu W, Dai M, Sun X, Jin X, Chen G, Ning G, Li L, Wang W, Cao Y. Ji H, et al. Among authors: dai m. J Genet Genomics. 2024 Jan;51(1):100-104. doi: 10.1016/j.jgg.2023.08.008. Epub 2023 Sep 2. J Genet Genomics. 2024. PMID: 37666358 No abstract available.

9

The ChinaMAP reference panel for the accurate genotype imputation in Chinese populations.

Li L, Huang P, Sun X, Wang S, Xu M, Liu S, Feng Z, Zhang Q, Wang X, Zheng X, Dai M, Bi Y, Ning G, Cao Y, Wang W. Li L, et al. Among authors: dai m. Cell Res. 2021 Dec;31(12):1308-1310. doi: 10.1038/s41422-021-00564-z. Epub 2021 Sep 6. Cell Res. 2021. PMID: 34489580 Free PMC article. No abstract available.

10

Altered Inflammatory Pathway but Unaffected Liver Fibrosis in Mouse Models of Nonalcoholic Steatohepatitis Involving Interleukin-1 Receptor-Associated Kinase 1 Knockout.

Lei Y, Yang T, Shan A, Di W, Dai M, Nan J, Liu D, Cao Y, Jiang X. Lei Y, et al. Among authors: dai m. Med Sci Monit. 2020 Nov 18;26:e926187. doi: 10.12659/MSM.926187. Med Sci Monit. 2020. PMID: 33203828 Free PMC article.

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