Wang Y - Search Results

1

Artemisia Argyi essential oil ameliorates acetaminophen-induced hepatotoxicity via CYP2E1 and γ-glutamyl cycle reprogramming.

Cui W, Cao Q, Liu L, Yin X, Wang X, Zhao Y, Wang Y, Wei B, Xu X, Tang Y. Cui W, et al. Among authors: wang x, wang y. Phytomedicine. 2024 Dec;135:156106. doi: 10.1016/j.phymed.2024.156106. Epub 2024 Sep 29. Phytomedicine. 2024. PMID: 39366156

2

Exploring the mechanisms of Guizhifuling pills in the treatment of coronary spastic angina based on network pharmacology combined with molecular docking.

Xu S, Cui W, Zhang X, Song W, Wang Y, Zhao Y. Xu S, et al. Among authors: wang y. Medicine (Baltimore). 2024 Jul 19;103(29):e39014. doi: 10.1097/MD.0000000000039014. Medicine (Baltimore). 2024. PMID: 39029023 Free PMC article.

3

Eupatilin inhibits EGF-induced JB6 cell transformation by targeting PI3K.

Li F, Tao Y, Qiao Y, Li K, Jiang Y, Cao C, Ren S, Chang X, Wang X, Wang Y, Xie Y, Dong Z, Zhao J, Liu K. Li F, et al. Among authors: wang x, wang y. Int J Oncol. 2016 Sep;49(3):1148-54. doi: 10.3892/ijo.2016.3600. Epub 2016 Jul 4. Int J Oncol. 2016. PMID: 27573489

4

Proton pump inhibitors and increased reporting odds of renal neoplasms: FAERS-based adverse event data mining and analysis.

Song W, Shi L, Wang Y, Zhang Z. Song W, et al. Among authors: wang y. Expert Opin Drug Saf. 2022 May;21(5):707-713. doi: 10.1080/14740338.2022.2020245. Epub 2021 Dec 29. Expert Opin Drug Saf. 2022. PMID: 34915780

5

HPDL mutations identified by exome sequencing are associated with infant neurodevelopmental disorders.

Wang Y, Zheng X, Feng C, Fan X, Liu L, Guo P, Lei Z, Mei S. Wang Y, et al. Mol Genet Genomic Med. 2022 Oct;10(10):e2025. doi: 10.1002/mgg3.2025. Epub 2022 Aug 19. Mol Genet Genomic Med. 2022. PMID: 35985664 Free PMC article.

6

[Clinical characteristics and genetic analysis of a Chinese pedigree affected with mitochondrial DNA depletion syndrome due to compound heterozygous variants of RRM2B gene].

Wang Y, Zheng X, Wang X, Zhang X, Guo P, Liu L, Mei S. Wang Y, et al. Among authors: wang x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Jan 10;39(1):26-30. doi: 10.3760/cma.j.cn511374-20201116-00799. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 34964961 Chinese.

7

A novel variant in UBE3A in a family with multigenerational intellectual disability and developmental delay.

Zhao X, Zheng Y, Wang L, Wang Y, Mei S, Kong X. Zhao X, et al. Among authors: wang l, wang y. Mol Genet Genomic Med. 2022 Apr;10(4):e1883. doi: 10.1002/mgg3.1883. Epub 2022 Feb 28. Mol Genet Genomic Med. 2022. PMID: 35225435 Free PMC article.

8

[Clinical and genetic analysis of two rare male patients with Rett syndrome].

Zheng X, Liu L, Wang Y, Wang Y, Wang H, Du Y, Gao L, Zhang Y, Mei S. Zheng X, et al. Among authors: wang h, wang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 May 10;39(5):488-493. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35598263 Chinese.

9

[Isolation and characterization of dendritic cells from normal human esophageal mucosa].

Wang CL, Ning HB, Wang YH, Zhang LF, Li JC. Wang CL, et al. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2012 Jul;28(7):733-4, 737. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2012. PMID: 22768865 Chinese.

10

Epimutation of MMACHC compound to a genetic mutation in cblC cases.

Zhang X, Chen Q, Song Y, Guo P, Wang Y, Luo S, Zhang Y, Zhou C, Li D, Chen Y, Wei H. Zhang X, et al. Among authors: wang y. Mol Genet Genomic Med. 2021 Jun;9(6):e1625. doi: 10.1002/mgg3.1625. Epub 2021 May 12. Mol Genet Genomic Med. 2021. PMID: 33982424 Free PMC article.

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