Zhou XY - Search Results

1

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

2

ACOX2 deficiency in primary malignant cardiac tumors.

Zhou X, Wang H. Zhou X, et al. Proc Natl Acad Sci U S A. 2017 May 2;114(18):E3590-E3591. doi: 10.1073/pnas.1701212114. Epub 2017 Apr 11. Proc Natl Acad Sci U S A. 2017. PMID: 28400508 Free PMC article. No abstract available.

3

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.

4

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.

5

Combined effects of FH (E404D) and ACOX2 (R409H) cause metabolic defects in primary cardiac malignant tumor.

Zhou X, Xu M, Zeng W, Chen Z, Lu G, Gong Y, Finnell RH, Xiao H, Qiao B, Wang H. Zhou X, et al. Cell Death Discov. 2018 Jul 23;4:18. doi: 10.1038/s41420-018-0072-3. eCollection 2018. Cell Death Discov. 2018. PMID: 30062063 Free PMC article.

6

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

7

Bi-Allelic Mutations in NUP205 and NUP210 Are Associated With Abnormal Cardiac Left-Right Patterning.

Chen W, Zhang Y, Yang S, Shi Z, Zeng W, Lu Z, Zhou X. Chen W, et al. Circ Genom Precis Med. 2019 Jul;12(7):e002492. doi: 10.1161/CIRCGEN.119.002492. Epub 2019 Jul 15. Circ Genom Precis Med. 2019. PMID: 31306055 No abstract available.

8

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.

9

Biallelic loss of function NEK3 mutations deacetylate α-tubulin and downregulate NUP205 that predispose individuals to cilia-related abnormal cardiac left-right patterning.

Zhang Y, Chen W, Zeng W, Lu Z, Zhou X. Zhang Y, et al. Cell Death Dis. 2020 Nov 23;11(11):1005. doi: 10.1038/s41419-020-03214-1. Cell Death Dis. 2020. PMID: 33230144 Free PMC article.

10

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.

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