Tan Y - Search Results

1

[Paternal inheritance mediated by epigenetic changes in sperms].

Hu Y, Wang W, Tu C, Lin G, Hu L, Tan Y. Hu Y, et al. Among authors: tan y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2025 Jan 10;42(1):114-121. doi: 10.3760/cma.j.cn511374-20241107-00579. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2025. PMID: 39779345 Review. Chinese.

2

The dynamic changes of X chromosome inactivation during early culture of human embryonic stem cells.

Xie P, Ouyang Q, Leng L, Hu L, Cheng D, Tan Y, Lu G, Lin G. Xie P, et al. Among authors: tan y. Stem Cell Res. 2016 Jul;17(1):84-92. doi: 10.1016/j.scr.2016.05.011. Epub 2016 May 22. Stem Cell Res. 2016. PMID: 27262949 Free article.

3

[Genetic analysis of three families affected with split-hand/split-foot malformation].

He W, Lin G, Liang P, Cheng D, Hu X, Zhou L, Xiong B, Tan Y, Lu G, Li W. He W, et al. Among authors: tan y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Aug 10;34(4):476-480. doi: 10.3760/cma.j.issn.1003-9406.2017.04.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28777841 Chinese.

4

DMC1 mutation that causes human non-obstructive azoospermia and premature ovarian insufficiency identified by whole-exome sequencing.

He WB, Tu CF, Liu Q, Meng LL, Yuan SM, Luo AX, He FS, Shen J, Li W, Du J, Zhong CG, Lu GX, Lin G, Fan LQ, Tan YQ. He WB, et al. J Med Genet. 2018 Mar;55(3):198-204. doi: 10.1136/jmedgenet-2017-104992. Epub 2018 Jan 13. J Med Genet. 2018. PMID: 29331980

5

XRCC2 mutation causes premature ovarian insufficiency as well as non-obstructive azoospermia in humans.

Zhang YX, Li HY, He WB, Tu C, Du J, Li W, Lu GX, Lin G, Yang Y, Tan YQ. Zhang YX, et al. Among authors: tan yq. Clin Genet. 2019 Mar;95(3):442-443. doi: 10.1111/cge.13475. Epub 2018 Nov 29. Clin Genet. 2019. PMID: 30489636 No abstract available.

6

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.

7

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: tan yq. 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.

8

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. Hum Genet. 2020 Feb;139(2):257-271. doi: 10.1007/s00439-020-02110-0. Epub 2020 Jan 16. Hum Genet. 2020. PMID: 31942643

9

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: tan yq. Clin Genet. 2020 May;97(5):741-746. doi: 10.1111/cge.13712. Epub 2020 Feb 10. Clin Genet. 2020. PMID: 32017041

10

Genetic underpinnings of asthenozoospermia.

Tu C, Wang W, Hu T, Lu G, Lin G, Tan YQ. Tu C, et al. 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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

15,113 results

Search Page

Filters