Xiang M - Search Results

1

Unraveling the Impact of the PROCA1 Mutation in Male Infertility: Incorporating Whole Exome Sequencing in Teratozoospermia Patients and Analyzing Proca1 Knockout Mice.

Zheng N, Shen Y, Wang Y, Xiang M, Yu K, Zhang J, Zha X, Duan Z, Wang F, Zhu F, Cao Y. Zheng N, et al. Among authors: xiang m. Reprod Sci. 2024 Jun 12. doi: 10.1007/s43032-024-01624-6. Online ahead of print. Reprod Sci. 2024. PMID: 38867036

2

A novel homozygous missense mutation of PMFBP1 causes acephalic spermatozoa syndrome.

Lu M, Kong S, Xiang M, Wang Y, Zhang J, Duan Z, Zha X, Wang F, Cao Y, Zhu F. Lu M, et al. Among authors: xiang m. J Assist Reprod Genet. 2021 Apr;38(4):949-955. doi: 10.1007/s10815-021-02075-7. Epub 2021 Jan 23. J Assist Reprod Genet. 2021. PMID: 33484382 Free PMC article.

3

A homozygous missense mutation in TBPL2 is associated with oocyte maturation arrest and degeneration.

Wang Y, Xiang M, Yu Z, Hao Y, Xu Q, Kong S, Wang F, Shi X, Song G, Cao Y, Huang L, Zhu F. Wang Y, et al. Among authors: xiang m. Clin Genet. 2021 Sep;100(3):324-328. doi: 10.1111/cge.13993. Epub 2021 May 13. Clin Genet. 2021. PMID: 33966269

4

Novel Mutation and Deletion in SUN5 Cause Male Infertility with Acephalic Spermatozoa Syndrome.

Xiang M, Wang Y, Wang K, Kong S, Lu M, Zhang J, Duan Z, Zha X, Shi X, Wang F, Cao Y, Zhu F. Xiang M, et al. Reprod Sci. 2022 Feb;29(2):646-651. doi: 10.1007/s43032-021-00665-5. Epub 2021 Jun 22. Reprod Sci. 2022. PMID: 34159570

5

Pathogenesis of acephalic spermatozoa syndrome caused by splicing mutation and de novo deletion in TSGA10.

Xiang M, Wang Y, Xu W, Zheng N, Zhang J, Duan Z, Zha X, Shi X, Wang F, Cao Y, Zhu F. Xiang M, et al. J Assist Reprod Genet. 2021 Oct;38(10):2791-2799. doi: 10.1007/s10815-021-02295-x. Epub 2021 Aug 18. J Assist Reprod Genet. 2021. PMID: 34409526 Free PMC article.

6

A novel homozygous missense mutation in AK7 causes multiple morphological anomalies of the flagella and oligoasthenoteratozoospermia.

Xiang M, Wang Y, Xu W, Zheng N, Deng H, Zhang J, Duan Z, Zha X, Zhang W, Song G, Shi X, Wang F, Cao Y, Zhu F. Xiang M, et al. J Assist Reprod Genet. 2022 Jan;39(1):261-266. doi: 10.1007/s10815-021-02363-2. Epub 2021 Dec 2. J Assist Reprod Genet. 2022. PMID: 34854019 Free PMC article.

7

Genetic pathogenesis of acephalic spermatozoa syndrome: past, present, and future.

Wang Y, Xiang MF, Zheng N, Cao YX, Zhu FX. Wang Y, et al. Asian J Androl. 2022 May-Jun;24(3):231-237. doi: 10.4103/aja202198. Asian J Androl. 2022. PMID: 35074941 Free PMC article. Review.

8

Loss of PMFBP1 Disturbs Mouse Spermatogenesis by Downregulating HDAC3 Expression.

Xu W, Yao Z, Li Y, Wang K, Kong S, Wang Y, Xiang M, Zhu F, Wang F, Zhang H. Xu W, et al. Among authors: xiang m. J Assist Reprod Genet. 2023 Aug;40(8):1865-1879. doi: 10.1007/s10815-023-02874-0. Epub 2023 Jul 10. J Assist Reprod Genet. 2023. PMID: 37423931 Free PMC article.

9

Novel and recurrent hemizygous variants in BCORL1 cause oligoasthenoteratozoospermia by interfering transcription.

Wang Y, Xiang M, Zhou Y, Zheng N, Zhang J, Zha X, Duan Z, Wang F, Zhang Y, Wang Z, Cao Y, Zhu F. Wang Y, et al. Among authors: xiang m. Andrology. 2024 Aug 27. doi: 10.1111/andr.13743. Online ahead of print. Andrology. 2024. PMID: 39189935

10

A homozygous loss-of-function mutation in CEP250 is associated with acephalic spermatozoa syndrome in humans.

Xiang M, Wang Y, Jiao Y, Guo R, Zheng N, Yu K, Zhu X, Hu P, Zhang J, Zha X, Duan Z, Wang F, Cao Y, Zhu F. Xiang M, et al. Andrology. 2024 Dec 26. doi: 10.1111/andr.13827. Online ahead of print. Andrology. 2024. PMID: 39726222

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