Mingfei Xiang
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Explore the profile of Mingfei Xiang including associated specialties, affiliations and a list of published articles.
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10
Citations
32
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Recent Articles
1.
Zhang T, Xiang M, Yin H, Dan J, Zu R, Rao L, et al.
Sci Rep
. 2025 Jan;
15(1):1131.
PMID: 39775021
The aim of this study was to investigate the role of platelet indicators in the susceptibility of ABO blood groups to lung adenocarcinoma. This was a multicenter retrospective cohort analysis....
2.
Xiang M, Wang Y, Jiao Y, Guo R, Zheng N, Yu K, et al.
Andrology
. 2024 Dec;
PMID: 39726222
Background: The presence of predominantly headless sperm in semen is a hallmark of acephalic spermatozoa syndrome, which is primarily caused by gene mutations in humans. Purpose: To identify genetic causes...
3.
Wang Y, Xiang M, Zhou Y, Zheng N, Zhang J, Zha X, et al.
Andrology
. 2024 Aug;
PMID: 39189935
Background: Oligoasthenoteratozoospermia (OAT) is a common cause of male infertility, of which the causes remain largely unknown. Recently, BCORL1 was identified as a contributor to male infertility from non-obstructive azoospermia...
4.
Zheng N, Shen Y, Wang Y, Xiang M, Yu K, Zhang J, et al.
Reprod Sci
. 2024 Jun;
PMID: 38867036
In the world, about 15% of couples are infertile, and nearly half of all infertility was caused by men. A large number of genetic mutations are thought to affect spermatogenesis...
5.
Xu W, Yao Z, Li Y, Wang K, Kong S, Wang Y, et al.
J Assist Reprod Genet
. 2023 Jul;
40(8):1865-1879.
PMID: 37423931
Purpose: Polyamine modulating factor 1 binding protein (PMFBP1) acts as a scaffold protein for the maintenance of sperm structure. The aim of this study was further to identify the new...
6.
Xiang M, Wang Y, Xu W, Zheng N, Deng H, Zhang J, et al.
J Assist Reprod Genet
. 2021 Dec;
39(1):261-266.
PMID: 34854019
Purpose: To identify the genetic causes of multiple morphological anomalies of the flagella (MMAF) and oligoasthenoteratozoospermia (OAT). Methods: Whole-exome sequencing (WES) was performed on the proband to identify pathogenic mutation...
7.
Xiang M, Wang Y, Xu W, Zheng N, Zhang J, Duan Z, et al.
J Assist Reprod Genet
. 2021 Aug;
38(10):2791-2799.
PMID: 34409526
Purpose: To identify the genetic causes for acephalic spermatozoa syndrome. Methods: Whole-exome sequencing was performed on the proband from a non-consanguineous to identify pathogenic mutations for acephalic spermatozoa syndrome. Quantitative...
8.
Xiang M, Wang Y, Wang K, Kong S, Lu M, Zhang J, et al.
Reprod Sci
. 2021 Jun;
29(2):646-651.
PMID: 34159570
Acephalic spermatozoa syndrome (ASS) is a severe form of teratozoospermia, previous studies have shown that SUN5 mutations are the major cause of acephalic spermatozoa syndrome. This study is to identify...
9.
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, et al.
Clin Genet
. 2021 May;
100(3):324-328.
PMID: 33966269
The genetic causes in most of patients with oocyte maturation arrest remain largely unknown. In this study, we identified a homozygous missense mutation (c.895T>C; p.C299R) in TBPL2 (TATA box binding...
10.
Lu M, Kong S, Xiang M, Wang Y, Zhang J, Duan Z, et al.
J Assist Reprod Genet
. 2021 Jan;
38(4):949-955.
PMID: 33484382
Purpose: To identify the pathogenic mutation in PMFBP1 leading to acephalic spermatozoa syndrome. Methods: Sanger sequencing was used to screen for mutations in the known pathogenic genes SUN5 and PMFBP1...