Zhang F - Search Results

1

Disruption in ACTL7A causes acrosomal ultrastructural defects in human and mouse sperm as a novel male factor inducing early embryonic arrest.

Xin A, Qu R, Chen G, Zhang L, Chen J, Tao C, Fu J, Tang J, Ru Y, Chen Y, Peng X, Shi H, Zhang F, Sun X. Xin A, et al. Among authors: zhang l, zhang f. Sci Adv. 2020 Aug 28;6(35):eaaz4796. doi: 10.1126/sciadv.aaz4796. eCollection 2020 Aug. Sci Adv. 2020. PMID: 32923619 Free PMC article.

2

Joint utilization of genetic analysis and semi-cloning technology reveals a digenic etiology of Müllerian anomalies.

Wang L, Zhang Y, Fu X, Dong S, Tang S, Zhang N, Song C, Yang N, Zhang L, Wang H, Shi H, Jin L, Zhang F, Li J, Hua K. Wang L, et al. Among authors: zhang n, zhang l, zhang f, zhang y. Cell Res. 2020 Jan;30(1):91-94. doi: 10.1038/s41422-019-0243-7. Epub 2019 Oct 18. Cell Res. 2020. PMID: 31628433 Free PMC article. No abstract available.

3

Increased TBX6 gene dosages induce congenital cervical vertebral malformations in humans and mice.

Ren X, Yang N, Wu N, Xu X, Chen W, Zhang L, Li Y, Du RQ, Dong S, Zhao S, Chen S, Jiang LP, Wang L, Zhang J, Wu Z, Jin L, Qiu G, Lupski JR, Shi J, Zhang F, Liu P. Ren X, et al. Among authors: zhang l, zhang f, zhang j. J Med Genet. 2020 Jun;57(6):371-379. doi: 10.1136/jmedgenet-2019-106333. Epub 2019 Dec 30. J Med Genet. 2020. PMID: 31888956 Free PMC article.

4

Haploinsufficiency in non-homologous end joining factor 1 induces ovarian dysfunction in humans and mice.

Li G, Yang X, Wang L, Pan Y, Chen S, Shang L, Zhang Y, Wu Y, Zhou Z, Chen Q, Zhang X, Zhang L, Wang Y, Li J, Jin L, Wu Y, Zhang X, Zhang F. Li G, et al. Among authors: zhang l, zhang f, zhang x, zhang y. J Med Genet. 2022 Jun;59(6):579-588. doi: 10.1136/jmedgenet-2020-107398. Epub 2021 Apr 22. J Med Genet. 2022. PMID: 33888552

5

Modified strict sperm morphology threshold aids in the clinical selection of conventional in vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI).

Zhu Y, Zhang F, Cheng H, Sun XX, Jiang F. Zhu Y, et al. Among authors: zhang f. Asian J Androl. 2022 Jan-Feb;24(1):62-66. doi: 10.4103/aja.aja_45_21. Asian J Androl. 2022. PMID: 34135171 Free PMC article.

6

Homozygous Variant in KASH5 Causes Premature Ovarian Insufficiency by Disordered Meiotic Homologous Pairing.

Zhang Q, Tao C, Gao S, Li S, Xu B, Ke H, Wang Y, Zhang F, Qin Y, Zhang L, Guo T. Zhang Q, et al. Among authors: zhang l, zhang f. J Clin Endocrinol Metab. 2022 Aug 18;107(9):2589-2597. doi: 10.1210/clinem/dgac368. J Clin Endocrinol Metab. 2022. PMID: 35708642

7

FISH analysis of numerical chromosomal abnormalities in the sperm of robertsonian translocation der(13; 14)(q10;q10) carriers.

Zhu S, Zhu Y, Zhang F, Wu J, Chen Y, Sun Y, Fu J, Wu J, Xiao M, Zhang S, Zhou J, Lei C, Jiang F. Zhu S, et al. Among authors: zhang s, zhang f. Front Genet. 2022 Sep 27;13:1010568. doi: 10.3389/fgene.2022.1010568. eCollection 2022. Front Genet. 2022. PMID: 36238152 Free PMC article.

8

The use of frozen embryos and frozen sperm have complementary IVF outcomes: a retrospective analysis in couples experiencing IVF/Donor and IVF/Husband.

Zhu Y, Zhang F, Chen H, Sun X, Jiang F. Zhu Y, et al. Among authors: zhang f. BMC Pregnancy Childbirth. 2022 Oct 18;22(1):776. doi: 10.1186/s12884-022-05088-x. BMC Pregnancy Childbirth. 2022. PMID: 36258180 Free PMC article.

9

Novo pathogenic variations of NLRP7 increasing the risk of gestational trophoblastic neoplasia.

Tao C, Zhu T, Tang S, Lu J, Lin X, Li X, Liu X, Pang Y, Zhao H, Liang J, Zhang F, Lu X, Zhang L. Tao C, et al. Among authors: zhang l, zhang f. Clin Genet. 2023 Apr;103(4):498-500. doi: 10.1111/cge.14288. Epub 2022 Dec 30. Clin Genet. 2023. PMID: 36544392

10

Deficiency of MFSD6L, an acrosome membrane protein, causes oligoasthenoteratozoospermia in humans and mice.

Zhou D, Wu H, Wang L, Wang X, Tang S, Zhou Y, Wang J, Wu B, Tang J, Zhou X, Tian S, Liu S, Lv M, He X, Jin L, Shi H, Zhang F, Cao Y, Liu C. Zhou D, et al. Among authors: zhang f. J Genet Genomics. 2024 Oct;51(10):1007-1019. doi: 10.1016/j.jgg.2024.06.008. Epub 2024 Jun 21. J Genet Genomics. 2024. PMID: 38909778

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