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Journal Abstract Search

316 related items for PubMed ID: 35551387

  • 1. Bi-allelic variants in KCNU1 cause impaired acrosome reactions and male infertility.
    Liu R, Yan Z, Fan Y, Qu R, Chen B, Li B, Wu L, Wu H, Mu J, Zhao L, Wang W, Dong J, Zeng Y, Li Q, Wang L, Sang Q, Zhang Z, Kuang Y.
    Hum Reprod; 2022 Jun 30; 37(7):1394-1405. PubMed ID: 35551387
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  • 2. Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia.
    Wang W, Su L, Meng L, He J, Tan C, Yi D, Cheng D, Zhang H, Lu G, Du J, Lin G, Zhang Q, Tu C, Tan YQ.
    Hum Reprod; 2023 Jul 05; 38(7):1399-1411. PubMed ID: 37192818
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  • 3. IQUB deficiency causes male infertility by affecting the activity of p-ERK1/2/RSPH3.
    Zhang Z, Zhou H, Deng X, Zhang R, Qu R, Mu J, Liu R, Zeng Y, Chen B, Wang L, Sang Q, Bao S.
    Hum Reprod; 2023 Jan 05; 38(1):168-179. PubMed ID: 36355624
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  • 7. Novel bi-allelic variants in ACTL7A are associated with male infertility and total fertilization failure.
    Wang J, Zhang J, Sun X, Lin Y, Cai L, Cui Y, Liu J, Liu M, Yang X.
    Hum Reprod; 2021 Nov 18; 36(12):3161-3169. PubMed ID: 34727571
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  • 8. Loss of SPACA1 function causes autosomal recessive globozoospermia by damaging the acrosome-acroplaxome complex.
    Chen P, Saiyin H, Shi R, Liu B, Han X, Gao Y, Ye X, Zhang X, Sun Y.
    Hum Reprod; 2021 Aug 18; 36(9):2587-2596. PubMed ID: 34172998
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  • 9. Biallelic variants in IQCN cause sperm flagellar assembly defects and male infertility.
    Li Q, Wang Y, Zheng W, Guo J, Zhang S, Gong F, Lu GX, Lin G, Dai J.
    Hum Reprod; 2023 Jul 05; 38(7):1390-1398. PubMed ID: 37140151
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  • 10. Deletion of ACTRT1 is associated with male infertility as sperm acrosomal ultrastructural defects and fertilization failure in human.
    Zhang Q, Jin H, Long S, Tang X, Li J, Liu W, Han W, Liao H, Fu T, Huang G, Chen S, Lin T.
    Hum Reprod; 2024 May 02; 39(5):880-891. PubMed ID: 38414365
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  • 11. 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.
    Hum Reprod; 2023 Jun 01; 38(6):1213-1223. PubMed ID: 37004249
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  • 16. Whole-exome sequencing of a cohort of infertile men reveals novel causative genes in teratozoospermia that are chiefly related to sperm head defects.
    Li Y, Wang Y, Wen Y, Zhang T, Wang X, Jiang C, Zheng R, Zhou F, Chen D, Yang Y, Shen Y.
    Hum Reprod; 2021 Dec 27; 37(1):152-177. PubMed ID: 34791246
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  • 18. A homozygous variant in TBPL2 was identified in women with oocyte maturation defects and infertility.
    Yang P, Chen T, Wu K, Hou Z, Zou Y, Li M, Zhang X, Xu J, Zhao H.
    Hum Reprod; 2021 Jun 18; 36(7):2011-2019. PubMed ID: 33893736
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  • 20. 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.
    Hum Reprod; 2024 Nov 01; 39(11):2608-2617. PubMed ID: 39237102
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