Lin G - Search Results

1

Coronavirus: A possible cause of reduced male fertility.

Huang C, Ji X, Zhou W, Huang Z, Peng X, Fan L, Lin G, Zhu W. Huang C, et al. Among authors: lin g. Andrology. 2021 Jan;9(1):80-87. doi: 10.1111/andr.12907. Epub 2020 Oct 11. Andrology. 2021. PMID: 32960504 Free PMC article. Review.

2

A rare polypyrimidine tract mutation in the androgen receptor gene results in complete androgen insensitivity syndrome.

Yuan SM, Huang H, Tu CF, Du J, Xu DB, Lin G, Lu GX, Tan YQ. Yuan SM, et al. Among authors: lin g. Asian J Androl. 2018 May-Jun;20(3):308-310. doi: 10.4103/aja.aja_32_17. Asian J Androl. 2018. PMID: 28857053 Free PMC article. No abstract available.

3

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. Among authors: lin g. 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

4

Phenotypic and molecular characteristics of androgen insensitivity syndrome patients.

Yuan SM, Zhang YN, Du J, Li W, Tu CF, Meng LL, Lin G, Lu GX, Tan YQ. Yuan SM, et al. Among authors: lin g. Asian J Androl. 2018 Sep-Oct;20(5):473-478. doi: 10.4103/aja.aja_17_18. Asian J Androl. 2018. PMID: 29785970 Free PMC article.

5

Generation of NERCe003-A-3, a p53 compound heterozygous mutation human embryonic stem cell line, by CRISPR/Cas9 editing.

Li Y, Huang C, Zha L, Kong M, Yang Q, Zhu Y, Peng Y, Ouyang Q, Lu G, Lin G, Zhou D. Li Y, et al. Among authors: lin g. Stem Cell Res. 2019 Jan;34:101371. doi: 10.1016/j.scr.2018.101371. Epub 2018 Dec 17. Stem Cell Res. 2019. PMID: 30658254 Free article.

6

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: lin g. 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.

7

The role of total chromosomal disomy in human spermatozoa as a predictor of the outcome of pre-implantation genetic screening.

Jiang S, Peng X, Gong F, Huang C, Peng Y, Long X, Lin G, Zhu W. Jiang S, et al. Among authors: lin g. Fertil Steril. 2020 Jun;113(6):1196-1204.e1. doi: 10.1016/j.fertnstert.2020.02.004. Epub 2020 May 13. Fertil Steril. 2020. PMID: 32416980 Free 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. Among authors: lin g. 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

Patients with acephalic spermatozoa syndrome linked to novel TSGA10/PMFBP1 variants have favorable pregnancy outcomes from intracytoplasmic sperm injection.

Liu G, Xing X, Zhang H, Zhu W, Lin G, Lu G, Li W. Liu G, et al. Among authors: lin g. Clin Genet. 2021 Sep;100(3):334-339. doi: 10.1111/cge.14007. Epub 2021 Jun 21. Clin Genet. 2021. PMID: 34089195

10

CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis.

Wang W, Tian S, Nie H, Tu C, Liu C, Li Y, Li D, Yang X, Meng L, Hu T, Zhang Q, Du J, Fan L, Lu G, Lin G, Zhang F, Tan YQ. Wang W, et al. Among authors: lin g. Hum Mol Genet. 2021 Nov 16;30(23):2240-2254. doi: 10.1093/hmg/ddab185. Hum Mol Genet. 2021. PMID: 34231842

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