Zhou XY - Search Results

1

Low chorionic villous succinate accumulation associates with recurrent spontaneous abortion risk.

Wang XH, Xu S, Zhou XY, Zhao R, Lin Y, Cao J, Zang WD, Tao H, Xu W, Li MQ, Zhao SM, Jin LP, Zhao JY. Wang XH, et al. Among authors: zhou xy. Nat Commun. 2021 Jun 8;12(1):3428. doi: 10.1038/s41467-021-23827-0. Nat Commun. 2021. PMID: 34103526 Free PMC article.

2

Downregulation of lysyl oxidase and lysyl oxidase-like protein 2 suppressed the migration and invasion of trophoblasts by activating the TGF-β/collagen pathway in preeclampsia.

Xu XH, Jia Y, Zhou X, Xie D, Huang X, Jia L, Zhou Q, Zheng Q, Zhou X, Wang K, Jin LP. Xu XH, et al. Exp Mol Med. 2019 Feb 21;51(2):1-12. doi: 10.1038/s12276-019-0211-9. Exp Mol Med. 2019. PMID: 30804321 Free PMC article.

3

Natural killer cells: functional differences in recurrent spontaneous abortion†.

Hao F, Zhou X, Jin L. Hao F, et al. Biol Reprod. 2020 Mar 13;102(3):524-531. doi: 10.1093/biolre/ioz203. Biol Reprod. 2020. PMID: 31742319 Review.

4

Two sides of NNMT in alcoholic and non-alcoholic fatty liver development.

Zhang Y, Lu Z, Zeng W, Zhao J, Zhou X. Zhang Y, et al. J Hepatol. 2021 May;74(5):1250-1253. doi: 10.1016/j.jhep.2020.11.049. Epub 2020 Dec 16. J Hepatol. 2021. PMID: 33340570 No abstract available.

5

Biallelic DNAH9 mutations are identified in Chinese patients with defective left-right patterning and cilia-related complex congenital heart disease.

Chen W, Zhang Y, Shen L, Zhu J, Cai K, Lu Z, Zeng W, Zhao J, Zhou X. Chen W, et al. Hum Genet. 2022 Aug;141(8):1339-1353. doi: 10.1007/s00439-021-02426-5. Epub 2022 Jan 20. Hum Genet. 2022. PMID: 35050399

6

Acox2 is a regulator of lysine crotonylation that mediates hepatic metabolic homeostasis in mice.

Zhang Y, Chen Y, Zhang Z, Tao X, Xu S, Zhang X, Zurashvili T, Lu Z, Bayascas JR, Jin L, Zhao J, Zhou X. Zhang Y, et al. Cell Death Dis. 2022 Mar 29;13(3):279. doi: 10.1038/s41419-022-04725-9. Cell Death Dis. 2022. PMID: 35351852 Free PMC article.

7

Gestational palmitic acid suppresses embryonic GATA-binding protein 4 signaling and causes congenital heart disease.

Zhao R, Cao L, Gu WJ, Li L, Chen ZZ, Xiang J, Zhou ZY, Xu B, Zang WD, Zhou XY, Cao J, Sun K, Zhao JY. Zhao R, et al. Among authors: zhou zy, zhou xy. Cell Rep Med. 2023 Mar 21;4(3):100953. doi: 10.1016/j.xcrm.2023.100953. Epub 2023 Feb 20. Cell Rep Med. 2023. PMID: 36809766 Free PMC article.

8

A hypoxia-inducible factor 1α null splice variant lacking exon 10.

Zhou X, Zeng W, Peng R, Wang H. Zhou X, et al. Cell Death Dis. 2017 Jun 15;8(6):e2873. doi: 10.1038/cddis.2017.269. Cell Death Dis. 2017. PMID: 28617436 Free PMC article. No abstract available.

9

Mutations in the COPII vesicle component gene SEC24B are associated with human neural tube defects.

Yang XY, Zhou XY, Wang QQ, Li H, Chen Y, Lei YP, Ma XH, Kong P, Shi Y, Jin L, Zhang T, Wang HY. Yang XY, et al. Among authors: zhou xy. Hum Mutat. 2013 Aug;34(8):1094-101. doi: 10.1002/humu.22338. Epub 2013 May 13. Hum Mutat. 2013. PMID: 23592378

10

Rare mutations in apoptosis related genes APAF1, CASP9, and CASP3 contribute to human neural tube defects.

Zhou X, Zeng W, Li H, Chen H, Wei G, Yang X, Zhang T, Wang H. Zhou X, et al. Cell Death Dis. 2018 Jan 19;9(2):43. doi: 10.1038/s41419-017-0096-2. Cell Death Dis. 2018. PMID: 29352212 Free PMC article. No abstract available.

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