Wang W - Search Results

1

Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice.

Tu C, Cong J, Zhang Q, He X, Zheng R, Yang X, Gao Y, Wu H, Lv M, Gu Y, Lu S, Liu C, Tian S, Meng L, Wang W, Tan C, Nie H, Li D, Zhang H, Gong F, Hu L, Lu G, Xu W, Lin G, Zhang F, Cao Y, Tan YQ. Tu C, et al. Among authors: wang w. Am J Hum Genet. 2021 Aug 5;108(8):1466-1477. doi: 10.1016/j.ajhg.2021.06.010. Epub 2021 Jul 7. Am J Hum Genet. 2021. PMID: 34237282 Free PMC article.

2

Insight on multiple morphological abnormalities of sperm flagella in male infertility: what is new?

Wang WL, Tu CF, Tan YQ. Wang WL, et al. Asian J Androl. 2020 May-Jun;22(3):236-245. doi: 10.4103/aja.aja_53_19. Asian J Androl. 2020. PMID: 31210147 Free PMC article. Review.

3

Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations.

Wang W, Tu C, Nie H, Meng L, Li Y, Yuan S, Zhang Q, Du J, Wang J, Gong F, Fan L, Lu GX, Lin G, Tan YQ. Wang W, et al. Among authors: wang j. J Med Genet. 2019 Nov;56(11):750-757. doi: 10.1136/jmedgenet-2019-106031. Epub 2019 Aug 14. J Med Genet. 2019. PMID: 31413122 Free PMC article.

4

Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD.

Tu C, Nie H, Meng L, Wang W, Li H, Yuan S, Cheng D, He W, Liu G, Du J, Gong F, Lu G, Lin G, Zhang Q, Tan YQ. Tu C, et al. Among authors: wang w. Hum Genet. 2020 Feb;139(2):257-271. doi: 10.1007/s00439-020-02110-0. Epub 2020 Jan 16. Hum Genet. 2020. PMID: 31942643

5

An M1AP homozygous splice-site mutation associated with severe oligozoospermia in a consanguineous family.

Tu C, Wang Y, Nie H, Meng L, Wang W, Li Y, Li D, Zhang H, Lu G, Lin G, Tan YQ, Du J. Tu C, et al. Among authors: wang w, wang y. Clin Genet. 2020 May;97(5):741-746. doi: 10.1111/cge.13712. Epub 2020 Feb 10. Clin Genet. 2020. PMID: 32017041

6

A homozygous RPL10L missense mutation associated with male factor infertility and severe oligozoospermia.

Tu C, Meng L, Nie H, Yuan S, Wang W, Du J, Lu G, Lin G, Tan YQ. Tu C, et al. Among authors: wang w. Fertil Steril. 2020 Mar;113(3):561-568. doi: 10.1016/j.fertnstert.2019.10.029. Epub 2020 Feb 25. Fertil Steril. 2020. PMID: 32111475 Free article.

7

Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia.

Wang Y, Tu C, Nie H, Meng L, Li D, Wang W, Zhang H, Lu G, Lin G, Tan YQ, Du J. Wang Y, et al. Among authors: wang w. J Assist Reprod Genet. 2020 Apr;37(4):811-820. doi: 10.1007/s10815-020-01735-4. Epub 2020 Mar 13. J Assist Reprod Genet. 2020. PMID: 32170493 Free PMC article.

8

A novel homozygous frameshift mutation in MNS1 associated with severe oligoasthenoteratozoospermia in humans.

Li Y, Wang WL, Tu CF, Meng LL, Hu TY, Du J, Lin G, Nie HC, Tan YQ. Li Y, et al. Asian J Androl. 2021 Mar-Apr;23(2):197-204. doi: 10.4103/aja.aja_56_20. Asian J Androl. 2021. PMID: 33037173 Free PMC article.

9

Genetic underpinnings of asthenozoospermia.

Tu C, Wang W, Hu T, Lu G, Lin G, Tan YQ. Tu C, et al. Among authors: wang w. Best Pract Res Clin Endocrinol Metab. 2020 Dec;34(6):101472. doi: 10.1016/j.beem.2020.101472. Epub 2020 Nov 6. Best Pract Res Clin Endocrinol Metab. 2020. PMID: 33191078 Review.

10

TDRD7 participates in lens development and spermiogenesis by mediating autophagosome maturation.

Tu C, Li H, Liu X, Wang Y, Li W, Meng L, Wang W, Li Y, Li D, Du J, Lu G, Lin G, Tan YQ. Tu C, et al. Among authors: wang w, wang y. Autophagy. 2021 Nov;17(11):3848-3864. doi: 10.1080/15548627.2021.1894058. Epub 2021 Mar 3. Autophagy. 2021. PMID: 33618632 Free PMC article.

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