Zhu MM - Search Results

1

Micheliolide ameliorates severe acute pancreatitis in mice through potentiating Nrf2-mediated anti-inflammation and anti-oxidation effects.

Wu CY, Wang KQ, Qin YY, Wang HW, Wu MM, Zhu XD, Lu XY, Zhu MM, Lu CS, Hu QQ. Wu CY, et al. Among authors: zhu mm. Int Immunopharmacol. 2024 Dec 25;143(Pt 2):113490. doi: 10.1016/j.intimp.2024.113490. Epub 2024 Oct 29. Int Immunopharmacol. 2024. PMID: 39467351

2

Identification of a novel intronic variant in COL4A2 gene associated with fetal severe cerebral encephalomalacia and subdural hemorrhage.

Sun RY, Xu Y, Huang QQ, Hu SS, Xu HZ, Luo YZ, Zhu T, Sun JH, Gong YJ, Zhu MM, Wang HW, Pan JY, Lu CS, Wang D. Sun RY, et al. Among authors: zhu mm. BMC Med Genomics. 2024 Sep 30;17(1):238. doi: 10.1186/s12920-024-02012-4. BMC Med Genomics. 2024. PMID: 39350129 Free PMC article.

3

Novel compound heterozygous SUCLG1 variants may contribute to mitochondria DNA depletion syndrome-9.

Chen YM, Chen W, Xu Y, Lu CS, Zhu MM, Sun RY, Wang Y, Chen Y, Shi J, Wang D. Chen YM, et al. Among authors: zhu mm. Mol Genet Genomic Med. 2022 Sep;10(9):e2010. doi: 10.1002/mgg3.2010. Epub 2022 Jun 28. Mol Genet Genomic Med. 2022. PMID: 35762302 Free PMC article.

4

[Analysis of phenotype and genetic variant in a family with Shprintzen-Goldberg syndrome].

Shi J, Sun J, Chen Y, Zhu M, Wang Q, Lu C, Wang D. Shi J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Jul 10;39(7):703-707. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35810425 Chinese.

5

[Genetic analysis of a Chinese pedigree with 6q26q27 microduplication and 15q26.3 microdeletion].

Wang D, Lu C, Shi J, Chen Y, Zhu M, Wang Q, Ruan M. Wang D, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023 Jun 10;40(6):733-736. doi: 10.3760/cma.j.cn511374-20211027-00852. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2023. PMID: 37212012 Chinese.

6

A novel chromosome 2q24.3-q32.1 microdeletion in a fetus with multiple malformations.

Zhu M, Wang Y, Guan L, Lu C, Sun R, Chen Y, Shi J, Zhu Y, Wang D. Zhu M, et al. J Clin Lab Anal. 2022 Aug;36(8):e24602. doi: 10.1002/jcla.24602. Epub 2022 Jul 12. J Clin Lab Anal. 2022. PMID: 35819063 Free PMC article.

7

[Analysis of PROC gene variant in a Chinese pedigree affected with hereditary protein C deficiency].

Chen Y, Shi J, Huang X, Sheng A, Lu C, Zhu M, Wang Q, Wang M, Wang D. Chen Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Nov 10;39(11):1233-1237. doi: 10.3760/cma.j.cn511374-20210809-00661. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 36317209 Chinese.

8

Metabolomics profiling of maternal and umbilical cord blood in normoglycemia macrosomia.

Zhu M, Sun R, Jin L, Yu D, Huang X, Zhu T, Gong Y, Chen Y, Shi J, Wang Q, Lu C, Wang D. Zhu M, et al. J Matern Fetal Neonatal Med. 2023 Dec;36(2):2270761. doi: 10.1080/14767058.2023.2270761. Epub 2023 Oct 17. J Matern Fetal Neonatal Med. 2023. PMID: 37848386 Free article.

9

Heterozygous pathogenic variants in CWF19L1 in a Chinese family with spinocerebellar ataxia, autosomal recessive 17.

Ruan M, Wang H, Zhu M, Sun R, Shi J, Wang Q, Chen Y, Wang Y, Wang D. Ruan M, et al. J Clin Lab Anal. 2022 Dec;36(12):e24767. doi: 10.1002/jcla.24767. Epub 2022 Nov 10. J Clin Lab Anal. 2022. PMID: 36357319 Free PMC article.

10

Identification and functional characteristics of a novel splicing heterozygote variant of COL2A1 associated with Stickler syndrome type I.

Gong Y, Zhu W, Zhu M, Chen D, Wu S, Hu S, Luo Y, Jiang Y, Zhu T, Wang D. Gong Y, et al. Front Genet. 2024 Jul 10;15:1308737. doi: 10.3389/fgene.2024.1308737. eCollection 2024. Front Genet. 2024. PMID: 39050257 Free PMC article.

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