Yang X - Search Results

1

Whole exome sequencing identified a rare WT1 loss-of-function variant in a non-syndromic POI patient.

Wang Y, Chen Q, Zhang F, Yang X, Shang L, Ren S, Pan Y, Zhou Z, Li G, Fang Y, Jin L, Wu Y, Zhang X. Wang Y, et al. Among authors: yang x. Mol Genet Genomic Med. 2022 Jan;10(1):e1820. doi: 10.1002/mgg3.1820. Epub 2021 Nov 29. Mol Genet Genomic Med. 2022. PMID: 34845858 Free PMC article.

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: yang x. 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: yang x. 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: yang x. 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: yang x. 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: yang x. Oncol Rep. 2019 Jan;41(1):552-558. doi: 10.3892/or.2018.6816. Epub 2018 Oct 24. Oncol Rep. 2019. PMID: 30365131

7

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: yang j. 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.

8

A heterozygous hypomorphic mutation of Fanca causes impaired follicle development and subfertility in female mice.

Pan Y, Yang X, Zhang F, Chen S, Zhou Z, Yin H, Ma H, Shang L, Yang J, Li G, Wang Y, Jin L, Shi Q, Wu Y. Pan Y, et al. Among authors: yang x, yang j. Mol Genet Genomics. 2021 Jan;296(1):103-112. doi: 10.1007/s00438-020-01730-5. Epub 2020 Oct 6. Mol Genet Genomics. 2021. PMID: 33025164

9

"Response to the letter to the editor "Concerns regarding the potentially causal role of FANCA heterozygous variants in human primary ovarian insufficiency"".

Yang X, Zhang F, Shi Q, Wu Y. Yang X, et al. Hum Genet. 2021 Apr;140(4):695-697. doi: 10.1007/s00439-020-02233-4. Epub 2020 Nov 11. Hum Genet. 2021. PMID: 33175223 No abstract available.

10

Haploinsufficiency in non-homologous end joining factor 1 induces ovarian dysfunction in humans and mice.

Li G, Yang X, Wang L, Pan Y, Chen S, Shang L, Zhang Y, Wu Y, Zhou Z, Chen Q, Zhang X, Zhang L, Wang Y, Li J, Jin L, Wu Y, Zhang X, Zhang F. Li G, et al. Among authors: yang x. J Med Genet. 2022 Jun;59(6):579-588. doi: 10.1136/jmedgenet-2020-107398. Epub 2021 Apr 22. J Med Genet. 2022. PMID: 33888552

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