Wu Y - Search Results

1

Rare variants in FANCJ induce premature ovarian insufficiency in humans and mice.

Yang X, Ren S, Yang J, Pan Y, Zhou Z, Chen Q, Fang Y, Shang L, Zhang F, Zhang X, Wu Y. Yang X, et al. Among authors: wu y. J Genet Genomics. 2024 Feb;51(2):252-255. doi: 10.1016/j.jgg.2023.03.013. Epub 2023 Apr 14. J Genet Genomics. 2024. PMID: 37062450 No abstract available.

2

Breast cancer metastasis suppressor 1 modulates SIRT1-dependent p53 deacetylation through interacting with DBC1.

Liu X, Ehmed E, Li B, Dou J, Qiao X, Jiang W, Yang X, Qiao S, Wu Y. Liu X, et al. Among authors: wu y. Am J Cancer Res. 2016 Jun 1;6(6):1441-9. eCollection 2016. Am J Cancer Res. 2016. PMID: 27429856 Free PMC article.

3

Characterization of DAPK1 as a novel transcriptional target of BRMS1.

Qiao X, Yang X, Zhou Y, Mei X, Dou J, Xie W, Li G, Wang Y, Qiao S, Hu J, Wu Y. Qiao X, et al. Among authors: wu y. Int J Oncol. 2017 May;50(5):1760-1766. doi: 10.3892/ijo.2017.3930. Epub 2017 Mar 23. Int J Oncol. 2017. PMID: 28339067

4

Knockdown of calponin 2 suppressed cell growth in gastric cancer cells.

Hu J, Xie W, Shang L, Yang X, Li Q, Xu M, Dou J, Zhou Y, Niu W, Wu Y. Hu J, et al. Among authors: wu y. Tumour Biol. 2017 Jul;39(7):1010428317706455. doi: 10.1177/1010428317706455. Tumour Biol. 2017. PMID: 28714360 Free article.

5

Knockdown of ZNF233 suppresses hepatocellular carcinoma cell proliferation and tumorigenesis.

Xie W, Qiao X, Shang L, Dou J, Yang X, Qiao S, Wu Y. Xie W, et al. Among authors: wu y. Gene. 2018 Dec 30;679:179-185. doi: 10.1016/j.gene.2018.08.070. Epub 2018 Sep 1. Gene. 2018. PMID: 30179682

6

BRMS1 participates in regulating cell sensitivity to DNA interstrand crosslink damage by interacting with FANCI.

Dou J, Zhou Y, Liu X, Qiao X, Yang X, Xie W, Qiao S, Wu Y. Dou J, et al. Among authors: wu y. Oncol Rep. 2019 Jan;41(1):552-558. doi: 10.3892/or.2018.6816. Epub 2018 Oct 24. Oncol Rep. 2019. PMID: 30365131

7

Whole-exome sequencing reveals SALL4 variants in premature ovarian insufficiency: an update on genotype-phenotype correlations.

Wang Q, Li D, Cai B, Chen Q, Li C, Wu Y, Jin L, Wang X, Zhang X, Zhang F. Wang Q, et al. Among authors: wu y. Hum Genet. 2019 Jan;138(1):83-92. doi: 10.1007/s00439-018-1962-4. Epub 2019 Jan 2. Hum Genet. 2019. PMID: 30603774

8

Noncoding rare variants of TBX6 in congenital anomalies of the kidney and urinary tract.

Dong S, Wang C, Li X, Shen Q, Fu X, Wu M, Song C, Yang N, Wu Y, Wang H, Jin L, Xu H, Zhang F. Dong S, et al. Among authors: wu y, wu m. Mol Genet Genomics. 2019 Apr;294(2):493-500. doi: 10.1007/s00438-018-1522-6. Epub 2019 Jan 2. Mol Genet Genomics. 2019. PMID: 30604070

9

Rare variants in FANCA induce premature ovarian insufficiency.

Yang X, Zhang X, Jiao J, Zhang F, Pan Y, Wang Q, Chen Q, Cai B, Tang S, Zhou Z, Chen S, Yin H, Fu W, Luo Y, Li D, Li G, Shang L, Yang J, Jin L, Shi Q, Wu Y. Yang X, et al. Among authors: wu y. Hum Genet. 2019 Dec;138(11-12):1227-1236. doi: 10.1007/s00439-019-02059-9. Epub 2019 Sep 18. Hum Genet. 2019. PMID: 31535215 Free PMC article.

10

Rare deleterious BUB1B variants induce premature ovarian insufficiency and early menopause.

Chen Q, Ke H, Luo X, Wang L, Wu Y, Tang S, Li J, Jin L, Zhang F, Qin Y, Chen X. Chen Q, et al. Among authors: wu y. Hum Mol Genet. 2020 Sep 29;29(16):2698-2707. doi: 10.1093/hmg/ddaa153. Hum Mol Genet. 2020. PMID: 32716490

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