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Articles published in PLoS Genet

Retrieve available abstracts of 24 articles:
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Single Articles


    February 2021
  1. GUAN Y, Keeney S, Jain D, Wang PJ, et al
    yama, a mutant allele of Mov10l1, disrupts retrotransposon silencing and piRNA biogenesis.
    PLoS Genet. 2021;17:e1009265.
    PubMed     Abstract available


  2. APREA I, Raidt J, Hoben IM, Loges NT, et al
    Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility.
    PLoS Genet. 2021;17:e1009306.
    PubMed     Abstract available


    December 2020
  3. LI W, Liang J, Outeda P, Turner S, et al
    A genetic screen in Drosophila reveals an unexpected role for the KIP1 ubiquitination-promoting complex in male fertility.
    PLoS Genet. 2020;16:e1009217.
    PubMed     Abstract available


    September 2020
  4. WANG YY, Ke CC, Chen YL, Lin YH, et al
    Deficiency of the Tbc1d21 gene causes male infertility with morphological abnormalities of the sperm mitochondria and flagellum in mice.
    PLoS Genet. 2020;16:e1009020.
    PubMed     Abstract available


    August 2020
  5. OURA S, Kazi S, Savolainen A, Nozawa K, et al
    Cfap97d1 is important for flagellar axoneme maintenance and male mouse fertility.
    PLoS Genet. 2020;16:e1008954.
    PubMed     Abstract available


    June 2020
  6. KOTHANDAPANI A, Lewis SR, Noel JL, Zacharski A, et al
    GLI3 resides at the intersection of hedgehog and androgen action to promote male sex differentiation.
    PLoS Genet. 2020;16:e1008810.
    PubMed     Abstract available


    May 2020
  7. HILTPOLD M, Niu G, Kadri NK, Crysnanto D, et al
    Activation of cryptic splicing in bovine WDR19 is associated with reduced semen quality and male fertility.
    PLoS Genet. 2020;16:e1008804.
    PubMed     Abstract available


    April 2020
  8. ABRAMS EW, Fuentes R, Marlow FL, Kobayashi M, et al
    Molecular genetics of maternally-controlled cell divisions.
    PLoS Genet. 2020;16:e1008652.
    PubMed     Abstract available


    January 2020
  9. MOROHOSHI A, Miyata H, Shimada K, Nozawa K, et al
    Nexin-Dynein regulatory complex component DRC7 but not FBXL13 is required for sperm flagellum formation and male fertility in mice.
    PLoS Genet. 2020;16:e1008585.
    PubMed     Abstract available


    October 2019
  10. CAPALBO A, Valero RA, Jimenez-Almazan J, Pardo PM, et al
    Optimizing clinical exome design and parallel gene-testing for recessive genetic conditions in preconception carrier screening: Translational research genomic data from 14,125 exomes.
    PLoS Genet. 2019;15:e1008409.
    PubMed     Abstract available


    August 2019
  11. GOMEZ-H L, Felipe-Medina N, Condezo YB, Garcia-Valiente R, et al
    The PSMA8 subunit of the spermatoproteasome is essential for proper meiotic exit and mouse fertility.
    PLoS Genet. 2019;15:e1008316.
    PubMed     Abstract available


  12. MOYE AR, Bedoni N, Cunningham JG, Sanzhaeva U, et al
    Mutations in ARL2BP, a protein required for ciliary microtubule structure, cause syndromic male infertility in humans and mice.
    PLoS Genet. 2019;15:e1008315.
    PubMed     Abstract available


    February 2019
  13. GOBE C, Elzaiat M, Meunier N, Andre M, et al
    Dual role of DMXL2 in olfactory information transmission and the first wave of spermatogenesis.
    PLoS Genet. 2019;15:e1007909.
    PubMed     Abstract available


  14. LAURINYECZ B, Vedelek V, Kovacs AL, Szilasi K, et al
    Sperm-Leucylaminopeptidases are required for male fertility as structural components of mitochondrial paracrystalline material in Drosophila melanogaster sperm.
    PLoS Genet. 2019;15:e1007987.
    PubMed     Abstract available


    August 2018
  15. GREY C, Baudat F, de Massy B
    PRDM9, a driver of the genetic map.
    PLoS Genet. 2018;14:e1007479.
    PubMed     Abstract available


  16. TA-SHMA A, Hjeij R, Perles Z, Dougherty GW, et al
    Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility.
    PLoS Genet. 2018;14:e1007602.
    PubMed     Abstract available


    May 2018
  17. FUNIKOV SY, Kulikova DA, Krasnov GS, Rezvykh AP, et al
    Spontaneous gain of susceptibility suggests a novel mechanism of resistance to hybrid dysgenesis in Drosophila virilis.
    PLoS Genet. 2018;14:e1007400.
    PubMed     Abstract available


    March 2018
  18. MANTEROLA M, Brown TM, Oh MY, Garyn C, et al
    BRDT is an essential epigenetic regulator for proper chromatin organization, silencing of sex chromosomes and crossover formation in male meiosis.
    PLoS Genet. 2018;14:e1007209.
    PubMed     Abstract available


    November 2017
  19. DUNLEAVY JEM, Okuda H, O'Connor AE, Merriner DJ, et al
    Katanin-like 2 (KATNAL2) functions in multiple aspects of haploid male germ cell development in the mouse.
    PLoS Genet. 2017;13:e1007078.
    PubMed     Abstract available


    August 2017
  20. JAIN D, Meydan C, Lange J, Claeys Bouuaert C, et al
    rahu is a mutant allele of Dnmt3c, encoding a DNA methyltransferase homolog required for meiosis and transposon repression in the mouse male germline.
    PLoS Genet. 2017;13:e1006964.
    PubMed     Abstract available


  21. SKOV L, Schierup MH
    Analysis of 62 hybrid assembled human Y chromosomes exposes rapid structural changes and high rates of gene conversion.
    PLoS Genet. 2017;13:e1006834.
    PubMed     Abstract available


    May 2017
  22. SHARMA V, Pandey AK, Kumar A, Misra S, et al
    Functional male accessory glands and fertility in Drosophila require novel ecdysone receptor.
    PLoS Genet. 2017;13:e1006788.
    PubMed     Abstract available


    April 2017
  23. WANG YY, Lin YH, Wu YN, Chen YL, et al
    Loss of SLC9A3 decreases CFTR protein and causes obstructed azoospermia in mice.
    PLoS Genet. 2017;13:e1006715.
    PubMed     Abstract available


    March 2017
  24. SHEN YR, Wang HY, Kuo YC, Shih SC, et al
    SEPT12 phosphorylation results in loss of the septin ring/sperm annulus, defective sperm motility and poor male fertility.
    PLoS Genet. 2017;13:e1006631.
    PubMed     Abstract available


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