Wang Y - Search Results

1

MicroRNA-195-5p suppresses glucose uptake and proliferation of human bladder cancer T24 cells by regulating GLUT3 expression.

Fei X, Qi M, Wu B, Song Y, Wang Y, Li T. Fei X, et al. Among authors: wang y. FEBS Lett. 2012 Feb 17;586(4):392-7. doi: 10.1016/j.febslet.2012.01.006. Epub 2012 Jan 16. FEBS Lett. 2012. PMID: 22265971 Free article.

2

Identification of immediate early gene X-1 as a cellular target gene of hcmv-mir-UL148D.

Wang YP, Qi Y, Huang YJ, Qi ML, Ma YP, He R, Ji YH, Sun ZR, Ruan Q. Wang YP, et al. Int J Mol Med. 2013 Apr;31(4):959-66. doi: 10.3892/ijmm.2013.1271. Epub 2013 Feb 6. Int J Mol Med. 2013. PMID: 23403649

3

A new small supernumerary marker chromosome involving 14pter → q12 in a child with severe neurodevelopmental retardation: case report and literature review.

Qi M, Zhao Y, Wang Y, Li T. Qi M, et al. Among authors: wang y. Gene. 2013 Dec 1;531(2):457-61. doi: 10.1016/j.gene.2013.08.084. Epub 2013 Sep 5. Gene. 2013. PMID: 24013083 Review.

4

Two novel mutations in the BCKDHB gene (R170H, Q346R) cause the classic form of maple syrup urine disease (MSUD).

Wang YP, Qi ML, Li TT, Zhao YJ. Wang YP, et al. Gene. 2012 Apr 25;498(1):112-5. doi: 10.1016/j.gene.2012.01.082. Epub 2012 Feb 3. Gene. 2012. PMID: 22326532

5

Contactin‑associated protein‑like 2 expression in SH‑SY5Y cells is upregulated by a FOXP2 mutant with a shortened poly‑glutamine tract.

Zhao Y, Liu X, Sun H, Wang Y, Yang W, Ma H. Zhao Y, et al. Among authors: wang y. Mol Med Rep. 2015 Dec;12(6):8162-8. doi: 10.3892/mmr.2015.4483. Epub 2015 Oct 23. Mol Med Rep. 2015. PMID: 26497390

6

Three novel CYP17A1 gene mutations (A82D, R125X, and C442R) found in combined 17α-hydroxylase/17,20-lyase deficiency.

Wang YP, Li J, Li JX, Zhao YJ, Zhang DY. Wang YP, et al. Metabolism. 2011 Oct;60(10):1386-91. doi: 10.1016/j.metabol.2011.03.008. Epub 2011 May 6. Metabolism. 2011. PMID: 21550081

7

[The investigation of the relationship between the phenotypes of 46, XX males and the SRY gene].

Wang YP, Zhao YJ, Ruan Q, Ji YH, Hao MG, Jiang WH. Wang YP, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Feb;26(1):95-7. doi: 10.3760/cma.j.issn.1003-9406.2009.01.022. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19199262 Chinese.

8

Chromosome 13q deletion syndrome involving 13q31‑qter: A case report.

Wang YP, Wang DJ, Niu ZB, Cui WT. Wang YP, et al. Mol Med Rep. 2017 Jun;15(6):3658-3664. doi: 10.3892/mmr.2017.6425. Epub 2017 Apr 3. Mol Med Rep. 2017. PMID: 28393221 Free PMC article.

9

Evaluation of non-invasive prenatal testing to detect chromosomal aberrations in a Chinese cohort.

Cui W, Liu X, Zhang Y, Wang Y, Chu G, He R, Zhao Y. Cui W, et al. Among authors: wang y. J Cell Mol Med. 2019 Nov;23(11):7873-7878. doi: 10.1111/jcmm.14614. Epub 2019 Aug 27. J Cell Mol Med. 2019. PMID: 31454164 Free PMC article.

10

Association between FOXP2 gene and speech sound disorder in Chinese population.

Zhao Y, Ma H, Wang Y, Gao H, Xi C, Hua T, Zhao Y, Qiu G. Zhao Y, et al. Among authors: wang y. Psychiatry Clin Neurosci. 2010 Oct;64(5):565-73. doi: 10.1111/j.1440-1819.2010.02123.x. Psychiatry Clin Neurosci. 2010. PMID: 20923434 Free article.

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