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For: Tu C, Wang W, Hu T, Lu G, Lin G, Tan YQ. Genetic underpinnings of asthenozoospermia. Best Pract Res Clin Endocrinol Metab 2020;34:101472. [PMID: 33191078 DOI: 10.1016/j.beem.2020.101472] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Li N, Dong X, Fu S, Wang X, Li H, Song G, Huang D. C-Type Natriuretic Peptide (CNP) Could Improve Sperm Motility and Reproductive Function of Asthenozoospermia. IJMS 2022;23:10370. [DOI: 10.3390/ijms231810370] [Reference Citation Analysis]
2 Li J, Xu J, Yang T, Chen J, Li F, Shen B, Fan C. Genome-wide methylation analyses of human sperm unravel novel differentially methylated regions in asthenozoospermia. Epigenomics 2022. [PMID: 36004499 DOI: 10.2217/epi-2022-0122] [Reference Citation Analysis]
3 Liu Z, Wang C, Ni F, Yang F, Wei H, Li T, Wang J, Wang B. Novel compound heterozygous variants of DNAH17 in a Chinese infertile man with multiple morphological abnormalities of sperm flagella. Andrologia 2022;:e14553. [PMID: 35932098 DOI: 10.1111/and.14553] [Reference Citation Analysis]
4 Zhou S, Wu H, Zhang J, He X, Liu S, Zhou P, Hua R, Cao Y, Liu M. Bi-allelic variants in human TCTE1/DRC5 cause asthenospermia and male infertility. Eur J Hum Genet 2022;30:721-9. [PMID: 35388187 DOI: 10.1038/s41431-022-01095-w] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
5 Liu W, Wei X, Liu X, Chen G, Zhang X, Liang X, Isachenko V, Sha Y, Wang Y. Biallelic mutations in ARMC12 cause asthenozoospermia and multiple midpiece defects in humans and mice. J Med Genet 2022:jmedgenet-2021-108137. [PMID: 35534203 DOI: 10.1136/jmedgenet-2021-108137] [Reference Citation Analysis]
6 Tan C, Meng L, Lv M, He X, Sha Y, Tang D, Tan Y, Hu T, He W, Tu C, Nie H, Zhang H, Du J, Lu G, Fan LQ, Cao Y, Lin G, Tan YQ. Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice. Am J Hum Genet 2022;109:157-71. [PMID: 34932939 DOI: 10.1016/j.ajhg.2021.11.022] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
7 Gao Y, Wu H, Xu Y, Shen Q, Xu C, Geng H, Lv M, Tan Q, Li K, Tang D, Song B, Zhou P, Wei Z, He X, Cao Y. Novel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease. Hum Mutat 2021. [PMID: 34923715 DOI: 10.1002/humu.24322] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
8 Lei C, Yang D, Wang R, Ding S, Wang L, Guo T, Luo H. DRC1 deficiency caused primary ciliary dyskinesia and MMAF in a Chinese patient. J Hum Genet 2021. [PMID: 34815526 DOI: 10.1038/s10038-021-00985-z] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
9 Giaccagli MM, Gómez-Elías MD, Herzfeld JD, Marín-Briggiler CI, Cuasnicú PS, Cohen DJ, Da Ros VG. Capacitation-Induced Mitochondrial Activity Is Required for Sperm Fertilizing Ability in Mice by Modulating Hyperactivation. Front Cell Dev Biol 2021;9:767161. [PMID: 34765607 DOI: 10.3389/fcell.2021.767161] [Reference Citation Analysis]
10 Wei X, Sha Y, Wei Z, Zhu X, He F, Zhang X, Liu W, Wang Y, Lu Z. Bi-allelic mutations in DNAH7 cause asthenozoospermia by impairing the integrality of axoneme structure. Acta Biochim Biophys Sin (Shanghai) 2021;53:1300-9. [PMID: 34476482 DOI: 10.1093/abbs/gmab113] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Wu B, Yu X, Liu C, Wang L, Huang T, Lu G, Chen ZJ, Li W, Liu H. Essential Role of CFAP53 in Sperm Flagellum Biogenesis. Front Cell Dev Biol 2021;9:676910. [PMID: 34124066 DOI: 10.3389/fcell.2021.676910] [Reference Citation Analysis]