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Journal Abstract Search

143 related items for PubMed ID: 37640479

  • 1. A variant in sperm-specific glycolytic enzyme enolase 4 (ENO4) causes human male infertility.
    Nawaz S, Hussain S, Bilal M, Syed N, Liaqat K, Ullah I, Akil AA, Fakhro KA, Ahmad W.
    J Gene Med; 2024 Jan; 26(1):e3583. PubMed ID: 37640479
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  • 2. Disruption of a spermatogenic cell-specific mouse enolase 4 (eno4) gene causes sperm structural defects and male infertility.
    Nakamura N, Dai Q, Williams J, Goulding EH, Willis WD, Brown PR, Eddy EM.
    Biol Reprod; 2013 Apr; 88(4):90. PubMed ID: 23446454
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  • 3. Biallelic mutations in ARMC12 cause asthenozoospermia and multiple midpiece defects in humans and mice.
    Liu W, Wei X, Liu X, Chen G, Zhang X, Liang X, Isachenko V, Sha Y, Wang Y.
    J Med Genet; 2023 Feb; 60(2):154-162. PubMed ID: 35534203
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  • 4. Deficiency in AK9 causes asthenozoospermia and male infertility by destabilising sperm nucleotide homeostasis.
    Sha Y, Liu W, Li S, Osadchuk LV, Chen Y, Nie H, Gao S, Xie L, Qin W, Zhou H, Li L.
    EBioMedicine; 2023 Oct; 96():104798. PubMed ID: 37713809
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  • 5. Genetic underpinnings of asthenozoospermia.
    Tu C, Wang W, Hu T, Lu G, Lin G, Tan YQ.
    Best Pract Res Clin Endocrinol Metab; 2020 Dec; 34(6):101472. PubMed ID: 33191078
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  • 6. A homozygous ARMC3 splicing variant causes asthenozoospermia and flagellar disorganization in a consanguineous family.
    Rahim F, Tao L, Khan K, Ali I, Zeb A, Khan I, Dil S, Abbas T, Hussain A, Zubair M, Zhang H, Hui M, Khan MA, Shah W, Shi Q.
    Clin Genet; 2024 Oct; 106(4):437-447. PubMed ID: 39221575
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  • 8. 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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  • 13. ADGB variants cause asthenozoospermia and male infertility.
    Qu R, Zhang Z, Wu L, Li Q, Mu J, Zhao L, Yan Z, Wang W, Zeng Y, Liu R, Dong J, Li Q, Sun X, Wang L, Sang Q, Chen B, Kuang Y.
    Hum Genet; 2023 Jun 05; 142(6):735-748. PubMed ID: 36995441
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  • 14. A novel CCDC39 mutation causes multiple morphological abnormalities of the flagella in a primary ciliary dyskinesia patient.
    Chen D, Liang Y, Li J, Zhang X, Zheng R, Wang X, Zhang H, Shen Y.
    Reprod Biomed Online; 2021 Nov 05; 43(5):920-930. PubMed ID: 34674941
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  • 15. ADCY10 frameshift variant leading to severe recessive asthenozoospermia and segregating with absorptive hypercalciuria.
    Akbari A, Pipitone GB, Anvar Z, Jaafarinia M, Ferrari M, Carrera P, Totonchi M.
    Hum Reprod; 2019 Jun 04; 34(6):1155-1164. PubMed ID: 31119281
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  • 16. In Silico Analysis of CatSper Family Genes and APOB Gene Regulation in Male Infertility.
    Maurya S, Bhoi NR, Kesari KK, Roychoudhury S, Kumar D.
    Adv Exp Med Biol; 2022 Jun 04; 1391():323-332. PubMed ID: 36472830
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  • 18. Metabolic Dysregulation and Sperm Motility in Male Infertility.
    Maurya S, Kesari KK, Roychoudhury S, Kolleboyina J, Jha NK, Jha SK, Sharma A, Kumar A, Rathi B, Kumar D.
    Adv Exp Med Biol; 2022 Jun 04; 1358():257-273. PubMed ID: 35641874
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