BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

277 related articles for article (PubMed ID: 37140151)

  • 1. 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; 38(7):1390-1398. PubMed ID: 37140151
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Loss-of-function mutations in IQCN cause male infertility in humans and mice owing to total fertilization failure.
    Wang Y; Chen G; Tang Z; Mei X; Lin C; Kang J; Lian J; Lu J; Liu Y; Lan F; Huang W; Zhang D
    Mol Hum Reprod; 2023 Jun; 29(7):. PubMed ID: 37184908
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 38(7):1399-1411. PubMed ID: 37192818
    [TBL] [Abstract][Full Text] [Related]  

  • 4. IQCN disruption causes fertilization failure and male infertility due to manchette assembly defect.
    Dai J; Li Q; Zhou Q; Zhang S; Chen J; Wang Y; Guo J; Gu Y; Gong F; Tan Y; Lu G; Zheng W; Lin G
    EMBO Mol Med; 2022 Dec; 14(12):e16501. PubMed ID: 36321563
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel copy number variation in CATSPER2 causes idiopathic male infertility with normal semen parameters.
    Luo T; Chen HY; Zou QX; Wang T; Cheng YM; Wang HF; Wang F; Jin ZL; Chen Y; Weng SQ; Zeng XH
    Hum Reprod; 2019 Mar; 34(3):414-423. PubMed ID: 30629171
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 38(1):168-179. PubMed ID: 36355624
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 37(7):1394-1405. PubMed ID: 35551387
    [TBL] [Abstract][Full Text] [Related]  

  • 8. LRRC46 Accumulates at the Midpiece of Sperm Flagella and Is Essential for Spermiogenesis and Male Fertility in Mouse.
    Yin Y; Mu W; Yu X; Wang Z; Xu K; Wu X; Cai Y; Zhang M; Lu G; Chan WY; Ma J; Huang T; Liu H
    Int J Mol Sci; 2022 Jul; 23(15):. PubMed ID: 35955660
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic diagnosis, sperm phenotype and ICSI outcome in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellum.
    Ferreux L; Bourdon M; Chargui A; Schmitt A; Stouvenel L; Lorès P; Ray P; Lousqui J; Pocate-Cheriet K; Santulli P; Dulioust E; Toure A; Patrat C
    Hum Reprod; 2021 Oct; 36(11):2848-2860. PubMed ID: 34529793
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 36(12):3161-3169. PubMed ID: 34727571
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Effects of
    Olszewska M; Malcher A; Stokowy T; Pollock N; Berman AJ; Budkiewicz S; Kamieniczna M; Jackowiak H; Suszynska-Zajczyk J; Jedrzejczak P; Yatsenko AN; Kurpisz M
    Hum Reprod Open; 2024; 2024(2):hoae020. PubMed ID: 38650655
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders.
    Oud MS; Houston BJ; Volozonoka L; Mastrorosa FK; Holt GS; Alobaidi BKS; deVries PF; Astuti G; Ramos L; Mclachlan RI; O'Bryan MK; Veltman JA; Chemes HE; Sheth H
    Hum Reprod; 2021 Aug; 36(9):2597-2611. PubMed ID: 34089056
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 37(1):152-177. PubMed ID: 34791246
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 38(6):1213-1223. PubMed ID: 37004249
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Flagellar pH homeostasis mediated by Na+/H+ exchangers regulates human sperm functions through coupling with CatSper and KSper activation.
    Liang M; Ji N; Song J; Kang H; Zeng X
    Hum Reprod; 2024 Apr; 39(4):674-688. PubMed ID: 38366201
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 39(5):880-891. PubMed ID: 38414365
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Copy number variation of functional RBMY1 is associated with sperm motility: an azoospermia factor-linked candidate for asthenozoospermia.
    Yan Y; Yang X; Liu Y; Shen Y; Tu W; Dong Q; Yang D; Ma Y; Yang Y
    Hum Reprod; 2017 Jul; 32(7):1521-1531. PubMed ID: 28498920
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fertilization defects in sperm from Cysteine-rich secretory protein 2 (Crisp2) knockout mice: implications for fertility disorders.
    Brukman NG; Miyata H; Torres P; Lombardo D; Caramelo JJ; Ikawa M; Da Ros VG; Cuasnicú PS
    Mol Hum Reprod; 2016 Apr; 22(4):240-51. PubMed ID: 26786179
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Depolarization of sperm membrane potential is a common feature of men with subfertility and is associated with low fertilization rate at IVF.
    Brown SG; Publicover SJ; Mansell SA; Lishko PV; Williams HL; Ramalingam M; Wilson SM; Barratt CL; Sutton KA; Da Silva SM
    Hum Reprod; 2016 Jun; 31(6):1147-57. PubMed ID: 27052499
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Bi-allelic variants in
    Meng GQ; Wang Y; Luo C; Tan YM; Li Y; Tan C; Tu C; Zhang QJ; Hu L; Zhang H; Meng LL; Liu CY; Deng L; Lu GX; Lin G; Du J; Tan YQ; Sha Y; Wang L; He WB
    Hum Reprod Open; 2024; 2024(1):hoae003. PubMed ID: 38312775
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.