Li M - Search Results

1

Detection of Mosaic Absence of Heterozygosity (AOH) Using Low-Pass Whole Genome Sequencing in Prenatal Diagnosis: A Preliminary Report.

Lü Y, Jiang Y, Zhou X, Hao N, Xu C, Guo R, Chang J, Li M, Zhang H, Zhou J, Zhang WV, Qi Q. Lü Y, et al. Among authors: li m. Diagnostics (Basel). 2023 Sep 9;13(18):2895. doi: 10.3390/diagnostics13182895. Diagnostics (Basel). 2023. PMID: 37761262 Free PMC article.

2

The Application of Optical Genome Mapping (OGM) in Severe Short Stature Caused by Duplication of 15q14q21.3.

Ke X, Yang H, Pan H, Jiang Y, Li M, Zhang H, Hao N, Zhu H. Ke X, et al. Among authors: li m. Genes (Basel). 2023 Apr 29;14(5):1016. doi: 10.3390/genes14051016. Genes (Basel). 2023. PMID: 37239376 Free PMC article.

3

Analysis of complex chromosomal rearrangement involving chromosome 6 via the integration of optical genomic mapping and molecular cytogenetic methodologies.

Hao N, Lou H, Li M, Zhang H, Chang J, Qi Q, Zhou X, Bai J, Guo J, Wang Y, Zhang Y, Jiang Y. Hao N, et al. Among authors: li m. J Hum Genet. 2024 Jan;69(1):3-11. doi: 10.1038/s10038-023-01197-3. Epub 2023 Oct 11. J Hum Genet. 2024. PMID: 37821671

4

Gene Analysis of Four Families with Severe Peripartum Cardiomyopathy Reveals Known Gene Mutations and Supports the Recent Call for Screening.

Li M, Yin K, Chen L, Chang J, Hao N. Li M, et al. Rev Cardiovasc Med. 2024 Nov 14;25(11):399. doi: 10.31083/j.rcm2511399. eCollection 2024 Nov. Rev Cardiovasc Med. 2024. PMID: 39618871 Free PMC article.

5

The SARS-CoV-2 receptor ACE2 expression of maternal-fetal interface and fetal organs by single-cell transcriptome study.

Li M, Chen L, Zhang J, Xiong C, Li X. Li M, et al. Among authors: li x. PLoS One. 2020 Apr 16;15(4):e0230295. doi: 10.1371/journal.pone.0230295. eCollection 2020. PLoS One. 2020. PMID: 32298273 Free PMC article.

6

The homozygous variant c.245G > A/p.G82D in PNPLA2 is associated with arrhythmogenic cardiomyopathy phenotypic manifestations.

Rao M, Guo G, Li M, Chen S, Chen K, Chen X, Song J, Hu S. Rao M, et al. Among authors: li m. Clin Genet. 2019 Dec;96(6):532-540. doi: 10.1111/cge.13642. Epub 2019 Oct 23. Clin Genet. 2019. PMID: 31525260

7

Selection of reference genes for gene expression studies in heart failure for left and right ventricles.

Li M, Rao M, Chen K, Zhou J, Song J. Li M, et al. Gene. 2017 Jul 15;620:30-35. doi: 10.1016/j.gene.2017.04.006. Epub 2017 Apr 5. Gene. 2017. PMID: 28390990

8

MiR-1-3p that correlates with left ventricular function of HCM can serve as a potential target and differentiate HCM from DCM.

Li M, Chen X, Chen L, Chen K, Zhou J, Song J. Li M, et al. J Transl Med. 2018 Jun 9;16(1):161. doi: 10.1186/s12967-018-1534-3. J Transl Med. 2018. PMID: 29885652 Free PMC article.

9

Novel SFTSV Phylogeny Reveals New Reassortment Events and Migration Routes.

Wu X, Li M, Zhang Y, Liang B, Shi J, Fang Y, Su Z, Li M, Zhang W, Xu L, Wang J, Wu Q, Tang S, Wang H, Zhang T, Peng C, Zheng X, Deng F, Shen S. Wu X, et al. Among authors: li m. Virol Sin. 2021 Apr;36(2):300-310. doi: 10.1007/s12250-020-00289-0. Epub 2020 Sep 22. Virol Sin. 2021. PMID: 32960400 Free PMC article.

10

Vitamin D receptor restricts T helper 2-biased inflammation in the heart.

Song J, Chen X, Cheng L, Rao M, Chen K, Zhang N, Meng J, Li M, Liu ZQ, Yang PC. Song J, et al. Among authors: li m. Cardiovasc Res. 2018 May 1;114(6):870-879. doi: 10.1093/cvr/cvy034. Cardiovasc Res. 2018. PMID: 29444238

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