Ding Y - Search Results

1

Promoter methylation is not associated with FLCN irregulation in lung cyst lesions of primary spontaneous pneumothorax.

Ding Y, Zou W, Zhu C, Min H, Ma D, Chen B, Ye M, Pan Y, Cao L, Wan Y, Zhu Q, Xia H, Zhang W, Feng Y, Gao Q, Yi L. Ding Y, et al. Mol Med Rep. 2015 Nov;12(5):7770-6. doi: 10.3892/mmr.2015.4341. Epub 2015 Sep 21. Mol Med Rep. 2015. PMID: 26398834

2

Influence of chromosome 22q11.2 microdeletion on postoperative calcium level after cardiac-correction surgery.

Shen L, Gu H, Wang D, Yang C, Xu Z, Jing H, Jiang Y, Ding Y, Hou H, Ge Z, Chen S, Mo X, Yi L. Shen L, et al. Among authors: ding y. Pediatr Cardiol. 2011 Oct;32(7):904-9. doi: 10.1007/s00246-011-0012-y. Epub 2011 Jun 16. Pediatr Cardiol. 2011. PMID: 21678063

3

Novel missense variants of ZFPM2/FOG2 identified in conotruncal heart defect patients do not impair interaction with GATA4.

Zhang W, Shen L, Deng Z, Ding Y, Mo X, Xu Z, Gao Q, Yi L. Zhang W, et al. Among authors: ding y. PLoS One. 2014 Jul 15;9(7):e102379. doi: 10.1371/journal.pone.0102379. eCollection 2014. PLoS One. 2014. PMID: 25025186 Free PMC article.

4

iTRAQ-based quantitative proteomic analysis of cervical cancer.

Ding Y, Yang M, She S, Min H, Xv X, Ran X, Wu Y, Wang W, Wang L, Yi L, Yang Y, Gao Q. Ding Y, et al. Int J Oncol. 2015 Apr;46(4):1748-58. doi: 10.3892/ijo.2015.2859. Epub 2015 Jan 29. Int J Oncol. 2015. PMID: 25633909

5

FLCN intragenic deletions in Chinese familial primary spontaneous pneumothorax.

Ding Y, Zhu C, Zou W, Ma D, Min H, Chen B, Ye M, Pan Y, Cao L, Wan Y, Zhang W, Meng L, Mei Y, Yang C, Chen S, Gao Q, Yi L. Ding Y, et al. Am J Med Genet A. 2015 May;167A(5):1125-33. doi: 10.1002/ajmg.a.36979. Epub 2015 Mar 21. Am J Med Genet A. 2015. PMID: 25807935

6

Does familial breast cancer and thymoma suggest a cancer syndrome? A family perspective.

Zhang X, Wang T, Wang W, Ding Y, Zhou L, Chen Q, Gao X, Wu Y, Mei Y, Jin Y, Gao Q, Yi L. Zhang X, et al. Among authors: ding y. Gene. 2015 Dec 1;573(2):333-7. doi: 10.1016/j.gene.2015.08.069. Epub 2015 Sep 4. Gene. 2015. PMID: 26344711

7

A rapid NGS strategy for comprehensive molecular diagnosis of Birt-Hogg-Dubé syndrome in patients with primary spontaneous pneumothorax.

Zhang X, Ma D, Zou W, Ding Y, Zhu C, Min H, Zhang B, Wang W, Chen B, Ye M, Cai M, Pan Y, Cao L, Wan Y, Jin Y, Gao Q, Yi L. Zhang X, et al. Among authors: ding y. Respir Res. 2016 May 27;17(1):64. doi: 10.1186/s12931-016-0377-9. Respir Res. 2016. PMID: 27229674 Free PMC article.

8

FLCN-regulated miRNAs suppressed reparative response in cells and pulmonary lesions of Birt-Hogg-Dubé syndrome.

Min H, Ma D, Zou W, Wu Y, Ding Y, Zhu C, Lin A, Song S, Liang Q, Chen B, Zhang B, Wan Y, Ye M, Pan Y, Wen Y, Yi L, Gao Q. Min H, et al. Among authors: ding y. Thorax. 2020 Jun;75(6):476-485. doi: 10.1136/thoraxjnl-2019-213225. Epub 2020 Mar 17. Thorax. 2020. PMID: 32184379 Free PMC article.

9

Inhibition of heat shock protein (HSP) 90 reverses signal transducer and activator of transcription (STAT) 3-mediated muscle wasting in cancer cachexia mice.

Niu M, Song S, Su Z, Wei L, Li L, Pu W, Zhao C, Ding Y, Wang J, Cao W, Gao Q, Wang H. Niu M, et al. Among authors: ding y. Br J Pharmacol. 2021 Nov;178(22):4485-4500. doi: 10.1111/bph.15625. Epub 2021 Aug 4. Br J Pharmacol. 2021. PMID: 34265073 Free article.

10

Minigene Assay as an Effective Molecular Diagnostic Strategy in Determining the Pathogenicity of Noncanonical Splice-Site Variants in FLCN.

Zhang X, Cai M, Ma Y, Chen J, Huang S, Cai M, Ding Y, Ma D, Gao Q, Hu X, Zhu C, Yi L. Zhang X, et al. Among authors: ding y. J Mol Diagn. 2023 Feb;25(2):110-120. doi: 10.1016/j.jmoldx.2022.10.005. Epub 2022 Nov 21. J Mol Diagn. 2023. PMID: 36410626 Free article.

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