Qian YQ - Search Results

1

Comprehensive genetic diagnosis of patients with Duchenne/Becker muscular dystrophy (DMD/BMD) and pathogenicity analysis of splice site variants in the DMD gene.

Yang YM, Yan K, Liu B, Chen M, Wang LY, Huang YZ, Qian YQ, Sun YX, Li HG, Dong MY. Yang YM, et al. Among authors: qian yq. J Zhejiang Univ Sci B. 2019 Sept.;20(9):753-765. doi: 10.1631/jzus.B1800541. J Zhejiang Univ Sci B. 2019. PMID: 31379145 Free PMC article.

2

Superovulation Induced Changes of Lipid Metabolism in Ovaries and Embryos and Its Probable Mechanism.

Wang LY, Wang N, Le F, Li L, Lou HY, Liu XZ, Zheng YM, Qian YQ, Chen YL, Jiang XH, Huang HF, Jin F. Wang LY, et al. Among authors: qian yq. PLoS One. 2015 Jul 13;10(7):e0132638. doi: 10.1371/journal.pone.0132638. eCollection 2015. PLoS One. 2015. PMID: 26167919 Free PMC article.

3

Identification of novel PKD1 and PKD2 mutations in a Chinese population with autosomal dominant polycystic kidney disease.

Liu B, Chen SC, Yang YM, Yan K, Qian YQ, Zhang JY, Hu YT, Dong MY, Jin F, Huang HF, Xu CM. Liu B, et al. Among authors: qian yq. Sci Rep. 2015 Dec 3;5:17468. doi: 10.1038/srep17468. Sci Rep. 2015. PMID: 26632257 Free PMC article.

4

Corrigendum: Identification of novel PKD1 and PKD2 mutations in a Chinese population with autosomal dominant polycystic kidney disease.

Liu B, Chen SC, Yang YM, Yan K, Qian YQ, Zhang JY, Hu YT, Dong MY, Jin F, Huang HF, Xu CM. Liu B, et al. Among authors: qian yq. Sci Rep. 2016 Feb 23;6:21578. doi: 10.1038/srep21578. Sci Rep. 2016. PMID: 26902268 Free PMC article. No abstract available.

5

XCI-escaping gene KDM5C contributes to ovarian development via downregulating miR-320a.

Sun YX, Zhang YX, Zhang D, Xu CM, Chen SC, Zhang JY, Ruan YC, Chen F, Zhang RJ, Qian YQ, Liu YF, Jin LY, Yu TT, Xu HY, Luo YQ, Liu XM, Sun F, Sheng JZ, Huang HF. Sun YX, et al. Among authors: qian yq. Hum Genet. 2017 Feb;136(2):227-239. doi: 10.1007/s00439-016-1752-9. Epub 2016 Nov 28. Hum Genet. 2017. PMID: 27896428

6

Detection of fetal duplication 16p11.2q12.1 by next-generation sequencing of maternal plasma and invasive diagnosis.

Chen M, Fu XY, Luo YQ, Qian YQ, Pan L, Wang LY, Dong MY. Chen M, et al. Among authors: qian yq. J Matern Fetal Neonatal Med. 2019 Jan;32(1):38-45. doi: 10.1080/14767058.2017.1369947. Epub 2017 Sep 7. J Matern Fetal Neonatal Med. 2019. PMID: 28882078

7

[Detection of cell-free fetal DNA in maternal plasma for noninvasive prenatal screening of fetal chromosomal aneuploidies in women of advanced maternal age].

Zhu H, Miao Z, Qian Y, Li H, Jin J, He J, Dong M. Zhu H, et al. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2017 May 25;46(3):256-261. doi: 10.3785/j.issn.1008-9292.2017.06.05. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2017. PMID: 29039166 Free PMC article. Chinese.

8

[Single nucleotide polymorphism-array in genetic analysis of chorionic villi from early spontaneous miscarriages].

Sun Y, Luo Y, Qian Y, Dong M, Jin F. Sun Y, et al. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2017 May 25;46(3):262-267. doi: 10.3785/j.issn.1008-9292.2017.06.06. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2017. PMID: 29039167 Free PMC article. Chinese.

9

[Research progress on the safety of offsprings conceived by assisted reproductive technology].

Wang L, Qian Y, Jin F. Wang L, et al. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2017 May 25;46(3):279-284. doi: 10.3785/j.issn.1008-9292.2017.06.09. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2017. PMID: 29039170 Free PMC article. Review. Chinese.

10

[Advances in the application of high-throughput sequencing in clinical genetics].

Qian Y, Wang L, Luo Y, Yan K, Dong M, Jin F. Qian Y, et al. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2017 May 25;46(3):334-337. doi: 10.3785/j.issn.1008-9292.2017.06.18. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2017. PMID: 29039179 Free PMC article. Chinese. No abstract available.

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