Du Q - Search Results

1

The detection and significance of cystic fibrosis transmembrane conductance regulator gene promoter mutations in Chinese patients with congenital bilateral absence of the vas deferens.

Bai S, Du Q, Liu X, Tong Y, Wu B. Bai S, et al. Among authors: du q. Gene. 2018 Sep 25;672:64-71. doi: 10.1016/j.gene.2018.05.108. Epub 2018 Jun 1. Gene. 2018. PMID: 29864494

2

[Intracytoplasmic sperm injection for obstructive azoospermia].

Du Q, Yang DL, Pan BC, He LX, Wang XX, Song YS, Wu B. Du Q, et al. Zhonghua Nan Ke Xue. 2010 Oct;16(10):922-4. Zhonghua Nan Ke Xue. 2010. PMID: 21243758 Chinese.

3

[Alternate-day oral tadalafil for erectile dysfunction with no successful intercourse at the baseline].

Du Q, Li ZT, Xing X, Pan BC, Song YS, Wu B. Du Q, et al. Zhonghua Nan Ke Xue. 2012 Jan;18(1):93-5. Zhonghua Nan Ke Xue. 2012. PMID: 22295857 Chinese.

4

[Detection of the mutation of all the exons of the CFTR gene in Chinese men with congenital bilateral absence of the vas deferens].

Du Q, Fang YY, Pan YF, Pan BC, Song YS, Wu B. Du Q, et al. Zhonghua Nan Ke Xue. 2012 Nov;18(11):999-1003. Zhonghua Nan Ke Xue. 2012. PMID: 23214250 Chinese.

5

[Oral tadalafil on alternate days for erectile dysfunction that fails to respond to on-demand sildenafil: a report of 15 cases].

Du Q, Gu LX, Miao Y, Xing X, Pan BC, Song YS, Wu B. Du Q, et al. Zhonghua Nan Ke Xue. 2013 Apr;19(4):337-9. Zhonghua Nan Ke Xue. 2013. PMID: 23678714 Chinese.

6

The CFTR M470V, intron 8 poly-T, and 8 TG-repeats detection in Chinese males with congenital bilateral absence of the vas deferens.

Du Q, Li Z, Pan Y, Liu X, Pan B, Wu B. Du Q, et al. Biomed Res Int. 2014;2014:689185. doi: 10.1155/2014/689185. Epub 2014 Jan 8. Biomed Res Int. 2014. PMID: 24551851 Free PMC article.

7

Persistent Müllerian duct syndrome in an assisted reproductive patient: a novel variant impairs the biosynthesis and secretion of anti-Müllerian hormone (AMH).

Du Q, Qiu C, Zhang L, Wang QY, Hong K, Liu XL. Du Q, et al. Asian J Androl. 2023;25(4):534-536. doi: 10.4103/aja202299. Asian J Androl. 2023. PMID: 36629155 Free PMC article. No abstract available.

8

A novel AMH variant at the prehelix loop impairs the binding to AMHR2 and causes persistent Müllerian duct syndrome.

Du Q, Qiu C, Zhang YY, Shang XJ, Liu XL. Du Q, et al. Asian J Androl. 2024 Mar 1;26(2):222-224. doi: 10.4103/aja202362. Epub 2023 Oct 24. Asian J Androl. 2024. PMID: 37902848 Free PMC article. No abstract available.

9

Prenatal risk assessment of Xp21.1 duplication involving the DMD gene by optical genome mapping.

Zhang Y, Du Q, Gao H, Pan Y, Liu N, Qiu C, Liu X. Zhang Y, et al. Among authors: du q. Life Sci Alliance. 2024 Aug 8;7(11):e202402780. doi: 10.26508/lsa.202402780. Print 2024 Nov. Life Sci Alliance. 2024. PMID: 39117454 Free PMC article.

10

[Semen expulsion under the ureterocystoscope].

Du Q, Wu B, Zou BL, Li ZT, Yang DL, Pan BC. Du Q, et al. Zhonghua Nan Ke Xue. 2014 Apr;20(4):334-7. Zhonghua Nan Ke Xue. 2014. PMID: 24873160 Chinese.

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