Zhang QJ - Search Results

1

Sperm flagellar 2 (SPEF2) is essential for sperm flagellar assembly in humans.

Li DY, Yang XX, Tu CF, Wang WL, Meng LL, Lu GX, Tan YQ, Zhang QJ, Du J. Li DY, et al. Among authors: zhang qj. Asian J Androl. 2022 Jul-Aug;24(4):359-366. doi: 10.4103/aja202154. Asian J Androl. 2022. PMID: 34755699 Free PMC article.

2

Knocking down Wnt9a mRNA levels increases cellular proliferation.

Xiang Y, Lin G, Zhang Q, Tan Y, Lu G. Xiang Y, et al. Mol Biol Rep. 2008 Jun;35(2):73-9. doi: 10.1007/s11033-007-9055-9. Epub 2007 Mar 10. Mol Biol Rep. 2008. PMID: 17351820

3

Borealin is differentially expressed in ES cells and is essential for the early development of embryonic cells.

Zhang Q, Lin G, Gu Y, Peng J, Nie Z, Huang Y, Lu G. Zhang Q, et al. Mol Biol Rep. 2009 Mar;36(3):603-9. doi: 10.1007/s11033-008-9220-9. Epub 2008 Mar 3. Mol Biol Rep. 2009. PMID: 18311593

4

[Common mutations of congenital adrenal hyperplasia are also the hotspots for new mutations].

Zhang Q, Li W, Li S, Tang W, Li L, Lu G. Zhang Q, et al. Nan Fang Yi Ke Da Xue Xue Bao. 2012 May;32(5):669-72. Nan Fang Yi Ke Da Xue Xue Bao. 2012. PMID: 22588921 Chinese.

5

Physiological oxygen prevents frequent silencing of the DLK1-DIO3 cluster during human embryonic stem cells culture.

Xie P, Sun Y, Ouyang Q, Hu L, Tan Y, Zhou X, Xiong B, Zhang Q, Yuan D, Pan Y, Liu T, Liang P, Lu G, Lin G. Xie P, et al. Stem Cells. 2014 Feb;32(2):391-401. doi: 10.1002/stem.1558. Stem Cells. 2014. PMID: 24123616 Free article.

6

[Paramyotonia congenita caused by a novel mutation of SCN4A gene in a Chinese family].

Li W, Chen Q, Zhang Q, Li X, Du J. Li W, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Apr;33(2):131-4. doi: 10.3760/cma.j.issn.1003-9406.2016.02.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27060299 Chinese.

7

[Evaluation of performance of five bioinformatics software for the prediction of missense mutations].

Chen Q, Dai C, Zhang Q, Du J, Li W. Chen Q, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Oct;33(5):625-8. doi: 10.3760/cma.j.issn.1003-9406.2016.05.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27577208 Chinese.

8

[Analysis of FOXL2 gene mutations in 5 families affected with blepharophimosis, ptosis and epicanthus inversus syndrome].

Yang X, Li W, Du J, Yuan S, He W, Zhang Q, Zhong C, Lu G, Tan Y. Yang X, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Jun 10;34(3):342-346. doi: 10.3760/cma.j.issn.1003-9406.2017.03.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28604951 Chinese.

9

Long-read sequencing identified a causal structural variant in an exome-negative case and enabled preimplantation genetic diagnosis.

Miao H, Zhou J, Yang Q, Liang F, Wang D, Ma N, Gao B, Du J, Lin G, Wang K, Zhang Q. Miao H, et al. Hereditas. 2018 Sep 28;155:32. doi: 10.1186/s41065-018-0069-1. eCollection 2018. Hereditas. 2018. PMID: 30279644 Free PMC article.

10

Novel mutations of PKD genes in Chinese patients suffering from autosomal dominant polycystic kidney disease and seeking assisted reproduction.

He WB, Xiao WJ, Tan YQ, Zhao XM, Li W, Zhang QJ, Zhong CG, Li XR, Hu L, Lu GX, Lin G, Du J. He WB, et al. Among authors: zhang qj. BMC Med Genet. 2018 Oct 17;19(1):186. doi: 10.1186/s12881-018-0693-7. BMC Med Genet. 2018. PMID: 30333007 Free PMC article.

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