Liu X - Search Results

1

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: liu x. 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

2

Evaluation of CMV and KAP promoters for driving the expression of human CYP4F2 in transgenic mice.

Lai G, Liu X, Wu J, Liu H, Zhao Y. Lai G, et al. Among authors: liu x, liu h. Int J Mol Med. 2012 Jan;29(1):107-12. doi: 10.3892/ijmm.2011.787. Epub 2011 Sep 1. Int J Mol Med. 2012. PMID: 21887457

3

[Genetic diagnosis of Duchenne/Becker muscular dystrophy by MLPA].

Zhang Y, Liu X, He R, Ma H, Zhao Y. Zhang Y, et al. Among authors: liu x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Jun;31(3):338-43. doi: 10.3760/cma.j.issn.1003-9406.2014.03.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 24928015 Chinese.

4

Alteration of epoxyeicosatrienoic acids in the liver and kidney of cytochrome P450 4F2 transgenic mice.

Zhang B, Lai G, Liu X, Zhao Y. Zhang B, et al. Among authors: liu x. Mol Med Rep. 2016 Dec;14(6):5739-5745. doi: 10.3892/mmr.2016.5962. Epub 2016 Nov 23. Mol Med Rep. 2016. PMID: 27878278

5

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: liu x. 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.

6

Genetic subtypes and phenotypic characteristics of 110 patients with Prader-Willi syndrome.

Zhang L, Liu X, Zhao Y, Wang Q, Zhang Y, Gao H, Zhang B, Cui W, Zhao Y. Zhang L, et al. Among authors: liu x. Ital J Pediatr. 2022 Jul 23;48(1):121. doi: 10.1186/s13052-022-01319-1. Ital J Pediatr. 2022. PMID: 35870983 Free PMC article.

7

Novel Germline KIT Variants in Families With Severe Piebaldism: Case Series and Literature Review.

Zhang Y, Gao H, Zhang L, Zhao Y, Qiu C, Liu X. Zhang Y, et al. Among authors: liu x. J Clin Lab Anal. 2024 Jun;38(11-12):e25073. doi: 10.1002/jcla.25073. Epub 2024 Jun 17. J Clin Lab Anal. 2024. PMID: 38887855 Free PMC article. Review.

8

A microdeletion of chromosome 9q33.3 encompasses the entire LMX1B gene in a Chinese family with nail patella syndrome.

Jiang S, Zhang J, Huang D, Zhang Y, Liu X, Wang Y, He R, Zhao Y. Jiang S, et al. Among authors: liu x. Int J Mol Sci. 2014 Nov 5;15(11):20158-68. doi: 10.3390/ijms151120158. Int J Mol Sci. 2014. PMID: 25380522 Free PMC article.

9

Nonsense suppression induced readthrough of a novel PAX6 mutation in patient-derived cells of congenital aniridia.

Liu X, Zhang Y, Zhang B, Gao H, Qiu C. Liu X, et al. Mol Genet Genomic Med. 2020 May;8(5):e1198. doi: 10.1002/mgg3.1198. Epub 2020 Mar 3. Mol Genet Genomic Med. 2020. PMID: 32125788 Free PMC article.

10

Overexpression of cytochrome P450 4F2 in mice increases 20-hydroxyeicosatetraenoic acid production and arterial blood pressure.

Liu X, Zhao Y, Wang L, Yang X, Zheng Z, Zhang Y, Chen F, Liu H. Liu X, et al. Among authors: liu h. Kidney Int. 2009 Jun;75(12):1288-1296. doi: 10.1038/ki.2009.67. Epub 2009 Mar 11. Kidney Int. 2009. PMID: 19279555 Free article.

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