Liu Y - Search Results

1

The genomic architectures of tumour-adjacent tissues, plasma and saliva reveal evolutionary underpinnings of relapse in head and neck squamous cell carcinoma.

Wu P, Xie C, Yang L, Liu Y, Zeng J, Li X, Fang X, Fan Y, Zhao S, Kuang N, Xuan T, Xia X, Yi X, Huang Y, Yu Z, Tang Y. Wu P, et al. Among authors: liu y. Br J Cancer. 2021 Sep;125(6):854-864. doi: 10.1038/s41416-021-01464-0. Epub 2021 Jul 6. Br J Cancer. 2021. PMID: 34230611 Free PMC article.

2

Down-Regulation of MiR-181c-5p Promotes Epithelial-to-Mesenchymal Transition in Laryngeal Squamous Cell Carcinoma via Targeting SERPINE1.

Li X, Wu P, Tang Y, Fan Y, Liu Y, Fang X, Wang W, Zhao S. Li X, et al. Among authors: liu y. Front Oncol. 2020 Dec 21;10:544476. doi: 10.3389/fonc.2020.544476. eCollection 2020. Front Oncol. 2020. PMID: 33680908 Free PMC article.

3

N6-methyladenosine modification of circCUX1 confers radioresistance of hypopharyngeal squamous cell carcinoma through caspase1 pathway.

Wu P, Fang X, Liu Y, Tang Y, Wang W, Li X, Fan Y. Wu P, et al. Among authors: liu y. Cell Death Dis. 2021 Mar 19;12(4):298. doi: 10.1038/s41419-021-03558-2. Cell Death Dis. 2021. PMID: 33741902 Free PMC article.

4

Antifibrotic Role of Nintedanib in Tracheal Stenosis After a Tracheal Wound.

Fan Y, Li X, Fang X, Liu Y, Zhao S, Yu Z, Tang Y, Wu P. Fan Y, et al. Among authors: liu y. Laryngoscope. 2021 Sep;131(9):E2496-E2505. doi: 10.1002/lary.29618. Epub 2021 May 17. Laryngoscope. 2021. PMID: 34000066

5

New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing.

Li W, Mei L, Chen H, Cai X, Liu Y, Men M, Liu XZ, Yan D, Ling J, Feng Y. Li W, et al. Among authors: liu y, liu xz. Neural Plast. 2019 Feb 27;2019:7143458. doi: 10.1155/2019/7143458. eCollection 2019. Neural Plast. 2019. PMID: 30936914 Free PMC article.

6

A rapid improved multiplex ligation detection reaction method for the identification of gene mutations in hereditary hearing loss.

Liu Y, Hu C, Liu C, Liu D, Mei L, He C, Jiang L, Wu H, Chen H, Feng Y. Liu Y, et al. Among authors: liu c, liu d. PLoS One. 2019 Apr 11;14(4):e0215212. doi: 10.1371/journal.pone.0215212. eCollection 2019. PLoS One. 2019. PMID: 30973918 Free PMC article.

7

Next-generation sequencing-based mutation analysis of genes associated with enlarged vestibular aqueduct in Chinese families.

Liu Y, Wen J, Sang S, Mei L, He C, Jiang L, Huang S, Feng Y. Liu Y, et al. Eur Arch Otorhinolaryngol. 2020 Dec;277(12):3331-3339. doi: 10.1007/s00405-020-06050-3. Epub 2020 May 23. Eur Arch Otorhinolaryngol. 2020. PMID: 32447495

8

Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China.

Wu H, Feng Y, Jiang L, Pan Q, Liu Y, Liu C, He C, Chen H, Liu X, Hu C, Hu Y, Mei L. Wu H, et al. Among authors: liu y, liu x, liu c. PLoS One. 2016 Mar 28;11(3):e0151909. doi: 10.1371/journal.pone.0151909. eCollection 2016. PLoS One. 2016. PMID: 27018795 Free PMC article.

9

[Study of gene mutation and pathogenetic mechanism for a family with Waardenburg syndrome].

Chen H, Liao X, Liu Y, He C, Zhang H, Jiang L, Feng Y, Mei L. Chen H, et al. Among authors: liu y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Aug 10;34(4):471-475. doi: 10.3760/cma.j.issn.1003-9406.2017.04.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28777840 Chinese.

10

Exome sequencing identifies a novel missense mutation of WFS1 as the cause of non-syndromic low-frequency hearing loss in a Chinese family.

Niu Z, Feng Y, Hu Z, Li J, Sun J, Chen H, He C, Wang X, Jiang L, Liu Y, Cai X, Wang L, Cai Y, Liu X, Mei L. Niu Z, et al. Among authors: liu y, liu x. Int J Pediatr Otorhinolaryngol. 2017 Sep;100:1-7. doi: 10.1016/j.ijporl.2017.06.008. Epub 2017 Jun 15. Int J Pediatr Otorhinolaryngol. 2017. PMID: 28802351

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