These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 38909778)

  • 1. 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
    J Genet Genomics; 2024 Oct; 51(10):1007-1019. PubMed ID: 38909778
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Bi-allelic variants in chromatoid body protein TDRD6 cause spermiogenesis defects and severe oligoasthenoteratozoospermia in humans.
    Guo R; Wu H; Zhu X; Wang G; Hu K; Li K; Geng H; Xu C; Zu C; Gao Y; Tang D; Cao Y; He X
    J Med Genet; 2024 May; 61(6):553-565. PubMed ID: 38341271
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Galnt3 deficiency disrupts acrosome formation and leads to oligoasthenoteratozoospermia.
    Miyazaki T; Mori M; Yoshida CA; Ito C; Yamatoya K; Moriishi T; Kawai Y; Komori H; Kawane T; Izumi S; Toshimori K; Komori T
    Histochem Cell Biol; 2013 Feb; 139(2):339-54. PubMed ID: 23052838
    [TBL] [Abstract][Full Text] [Related]  

  • 4. CCDC157 is essential for sperm differentiation and shows oligoasthenoteratozoospermia-related mutations in men.
    Zheng H; Gong C; Li J; Hou J; Gong X; Zhu X; Deng H; Wu H; Zhang F; Shi Q; Zhou J; Shi B; Yang X; Xi Y
    J Cell Mol Med; 2024 Apr; 28(7):e18215. PubMed ID: 38509755
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations.
    Lv M; Liu C; Ma C; Yu H; Shao Z; Gao Y; Liu Y; Wu H; Tang D; Tan Q; Zhang J; Li K; Xu C; Geng H; Zhang J; Li H; Mao X; Ge L; Fu F; Zhong K; Xu Y; Tao F; Zhou P; Wei Z; He X; Zhang F; Cao Y
    Reprod Biol Endocrinol; 2022 Jan; 20(1):5. PubMed ID: 34980136
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Absence of Dpy19l2, a new inner nuclear membrane protein, causes globozoospermia in mice by preventing the anchoring of the acrosome to the nucleus.
    Pierre V; Martinez G; Coutton C; Delaroche J; Yassine S; Novella C; Pernet-Gallay K; Hennebicq S; Ray PF; Arnoult C
    Development; 2012 Aug; 139(16):2955-65. PubMed ID: 22764053
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Homozygous mutations in
    Cong J; Wang X; Amiri-Yekta A; Wang L; Kherraf ZE; Liu C; Cazin C; Tang S; Hosseini SH; Tian S; Daneshipour A; Wang J; Zhou Y; Zeng Y; Yang S; He X; Li J; Cao Y; Jin L; Ray PF; Zhang F
    J Med Genet; 2022 Jul; 59(7):710-718. PubMed ID: 34348960
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The impact of RABL2B gene (rs144944885) on human male infertility in patients with oligoasthenoteratozoospermia and immotile short tail sperm defects.
    Hosseini SH; Sadighi Gilani MA; Meybodi AM; Sabbaghian M
    J Assist Reprod Genet; 2017 Apr; 34(4):505-510. PubMed ID: 28138870
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Loss of perinuclear theca ACTRT1 causes acrosome detachment and severe male subfertility in mice.
    Zhang XZ; Wei LL; Zhang XH; Jin HJ; Chen SR
    Development; 2022 Jun; 149(12):. PubMed ID: 35616329
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Bi-allelic human TEKT3 mutations cause male infertility with oligoasthenoteratozoospermia owing to acrosomal hypoplasia and reduced progressive motility.
    Liu Y; Li Y; Meng L; Li K; Gao Y; Lv M; Guo R; Xu Y; Zhou P; Wei Z; He X; Cao Y; Wu H; Tan Y; Hua R
    Hum Mol Genet; 2023 May; 32(10):1730-1740. PubMed ID: 36708031
    [TBL] [Abstract][Full Text] [Related]  

  • 11. TENT5D disruption causes oligoasthenoteratozoospermia and male infertility.
    Sha Y; Liu W; Tang S; Zhang X; Xiao Z; Xiao Y; Deng H; Zhou H; Wei X
    Andrology; 2023 Sep; 11(6):1121-1131. PubMed ID: 36746179
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Homozygous
    Ye JW; Abbas T; Zhou JT; Chen J; Yang ML; Huang XH; Zhang H; Ma H; Ma A; Xu B; Murtaza G; Shi QH; Shi BL
    Zool Res; 2024 Sep; 45(5):1073-1087. PubMed ID: 39245651
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A mouse model of familial oligoasthenoteratozoospermia.
    Juneja SC; van Deursen JM
    Hum Reprod; 2005 Apr; 20(4):881-93. PubMed ID: 15705627
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 36(9):2587-2596. PubMed ID: 34172998
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Disruption in
    Jin HJ; Fan Y; Yang X; Dong Y; Zhang XZ; Geng XY; Yan Z; Wu L; Ma M; Li B; Lyu Q; Pan Y; Liu M; Kuang Y; Chen SR
    Elife; 2024 Apr; 13():. PubMed ID: 38573307
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Anandamide modulates human sperm motility: implications for men with asthenozoospermia and oligoasthenoteratozoospermia.
    Amoako AA; Marczylo TH; Marczylo EL; Elson J; Willets JM; Taylor AH; Konje JC
    Hum Reprod; 2013 Aug; 28(8):2058-66. PubMed ID: 23697839
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel homozygous missense TTC12 variant identified in an infertile Pakistani man with severe oligoasthenoteratozoospermia and primary ciliary dyskinesia.
    Ali I; Ali H; Unar A; Rahim F; Khan K; Dil S; Abbas T; Hussain A; Zeb A; Zubair M; Zhang H; Ma H; Jiang X; Khan MA; Xu B; Shah W; Shi Q
    Mol Genet Genomics; 2024 Jul; 299(1):69. PubMed ID: 38992144
    [TBL] [Abstract][Full Text] [Related]  

  • 18. CCDC28A deficiency causes sperm head defects, reduced sperm motility and male infertility in mice.
    Zhou H; Zhang Z; Qu R; Zhu H; Luo Y; Li Q; Mu J; Yu R; Zeng Y; Chen B; Sang Q; Wang L
    Cell Mol Life Sci; 2024 Apr; 81(1):174. PubMed ID: 38597936
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Biallelic
    Hu T; Meng L; Tan C; Luo C; He WB; Tu C; Zhang H; Du J; Nie H; Lu GX; Lin G; Tan YQ
    J Med Genet; 2023 Feb; 60(2):144-153. PubMed ID: 35387802
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cylicins are a structural component of the sperm calyx being indispensable for male fertility in mice and human.
    Schneider S; Kovacevic A; Mayer M; Dicke AK; Arévalo L; Koser SA; Hansen JN; Young S; Brenker C; Kliesch S; Wachten D; Kirfel G; Strünker T; Tüttelmann F; Schorle H
    Elife; 2023 Nov; 12():. PubMed ID: 38013430
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.