Hua R - Search Results

1

CALR3 defects disrupt sperm-zona pellucida binding in humans: new insights into male factor fertilization failure and relevant clinical therapeutic approaches.

Gao Y, Xue R, Guo R, Yang F, Sha X, Li Y, Hua R, Li G, Shen Q, Li K, Liu W, Xu Y, Zhou P, Wei Z, Zhang Z, Cao Y, He X, Wu H. Gao Y, et al. Among authors: hua r. Hum Reprod. 2024 Nov 1;39(11):2608-2617. doi: 10.1093/humrep/deae205. Hum Reprod. 2024. PMID: 39237102

2

ACROSIN deficiency causes total fertilization failure in humans by preventing the sperm from penetrating the zona pellucida.

Hua R, Xue R, Liu Y, Li Y, Sha X, Li K, Gao Y, Shen Q, Lv M, Xu Y, Zhang Z, He X, Cao Y, Wu H. Hua R, et al. Hum Reprod. 2023 Jun 1;38(6):1213-1223. doi: 10.1093/humrep/dead059. Hum Reprod. 2023. PMID: 37004249

3

Loss of DRC1 function leads to multiple morphological abnormalities of the sperm flagella and male infertility in human and mouse.

Zhang J, He X, Wu H, Zhang X, Yang S, Liu C, Liu S, Hua R, Zhou S, Zhao S, Hu F, Zhang J, Liu W, Cheng H, Gao Y, Zhang F, Cao Y, Liu M. Zhang J, et al. Among authors: hua r. Hum Mol Genet. 2021 Oct 13;30(21):1996-2011. doi: 10.1093/hmg/ddab171. Hum Mol Genet. 2021. PMID: 34169321 Free PMC article.

4

A homozygous loss-of-function mutation in FBXO43 causes human non-obstructive azoospermia.

Wu H, Zhang X, Shen Q, Liu Y, Gao Y, Wang G, Lv M, Hua R, Xu Y, Zhou P, Wei Z, Tao F, He X, Cao Y, Liu M. Wu H, et al. Among authors: hua r. Clin Genet. 2022 Jan;101(1):55-64. doi: 10.1111/cge.14069. Epub 2021 Oct 11. Clin Genet. 2022. PMID: 34595750

5

Bi-allelic variants in human TCTE1/DRC5 cause asthenospermia and male infertility.

Zhou S, Wu H, Zhang J, He X, Liu S, Zhou P, Hua R, Cao Y, Liu M. Zhou S, et al. Among authors: hua r. Eur J Hum Genet. 2022 Jun;30(6):721-729. doi: 10.1038/s41431-022-01095-w. Epub 2022 Apr 7. Eur J Hum Genet. 2022. PMID: 35388187 Free PMC article.

6

Homozygous missense mutation in CCDC155 disrupts the transmembrane distribution of CCDC155 and SUN1, resulting in non-obstructive azoospermia and premature ovarian insufficiency in humans.

Wu H, Zhang X, Hua R, Li Y, Cheng L, Li K, Liu Y, Gao Y, Shen Q, Wang G, Lv M, Xu Y, He X, Cao Y, Liu M. Wu H, et al. Among authors: hua r. Hum Genet. 2022 Nov;141(11):1795-1809. doi: 10.1007/s00439-022-02459-4. Epub 2022 May 19. Hum Genet. 2022. PMID: 35587281

7

Biallelic loss-of-function mutations in SEPTIN4 (C17ORF47), encoding a conserved annulus protein, cause thin midpiece spermatozoa and male infertility in humans.

Wang G, Zhu X, Gao Y, Lv M, Li K, Tang D, Wu H, Xu C, Geng H, Shen Q, Zha X, Duan Z, Zhang J, Hua R, Tao F, Zhou P, Wei Z, Cao Y, Guo R, He X. Wang G, et al. Among authors: hua r. Hum Mutat. 2022 Dec;43(12):2079-2090. doi: 10.1002/humu.24475. Epub 2022 Oct 2. Hum Mutat. 2022. PMID: 36135717

8

Bi-allelic human TEKT3 mutations cause male infertility with oligoasthenoteratozoospermia owing to acrosomal hypoplasia and reduced progressive motility.

Liu Y, Li Y, Meng L, Li K, Gao Y, Lv M, Guo R, Xu Y, Zhou P, Wei Z, He X, Cao Y, Wu H, Tan Y, Hua R. Liu Y, et al. Among authors: hua r. Hum Mol Genet. 2023 May 5;32(10):1730-1740. doi: 10.1093/hmg/ddad013. Hum Mol Genet. 2023. PMID: 36708031

9

DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath.

Wu H, Liu Y, Li Y, Li K, Xu C, Gao Y, Lv M, Guo R, Xu Y, Zhou P, Wei Z, Hua R, He X, Cao Y. Wu H, et al. Among authors: hua r. Cell Death Dis. 2023 Feb 15;14(2):127. doi: 10.1038/s41419-023-05653-y. Cell Death Dis. 2023. PMID: 36792588 Free PMC article.

10

A metabolomic perspective on the mechanisms by which environmental pollutants and lifestyle lead to male infertility.

Yang W, Hua R, Cao Y, He X. Yang W, et al. Among authors: hua r. Andrology. 2024 May;12(4):719-739. doi: 10.1111/andr.13530. Epub 2023 Oct 10. Andrology. 2024. PMID: 37815095 Review.

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