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Articles published in PLoS Genet

Retrieve available abstracts of 14 articles:
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Single Articles

    August 2017
  1. MOUSAS A, Ntritsos G, Chen MH, Song C, et al
    Rare coding variants pinpoint genes that control human hematological traits.
    PLoS Genet. 2017;13:e1006925.
    PubMed     Text format     Abstract available

  2. LEO PJ, Madeleine MM, Wang S, Schwartz SM, et al
    Defining the genetic susceptibility to cervical neoplasia-A genome-wide association study.
    PLoS Genet. 2017;13:e1006866.
    PubMed     Text format     Abstract available

    July 2017
  3. SCOTT CA, Marsden AN, Rebagliati MR, Zhang Q, et al
    Nuclear/cytoplasmic transport defects in BBS6 underlie congenital heart disease through perturbation of a chromatin remodeling protein.
    PLoS Genet. 2017;13:e1006936.
    PubMed     Text format     Abstract available

    April 2017
  4. PENNER-GOEKE S, Lichtensztejn Z, Neufeld M, Ali JL, et al
    The temporal dynamics of chromosome instability in ovarian cancer cell lines and primary patient samples.
    PLoS Genet. 2017;13:e1006707.
    PubMed     Text format     Abstract available

  5. LI S, Garcia M, Gewiss RL, Winuthayanon W, et al
    Crucial role of estrogen for the mammalian female in regulating semen coagulation and liquefaction in vivo.
    PLoS Genet. 2017;13:e1006743.
    PubMed     Text format     Abstract available

    August 2016
  6. RUMP A, Benet-Pages A, Schubert S, Kuhlmann JD, et al
    Identification and Functional Testing of ERCC2 Mutations in a Multi-national Cohort of Patients with Familial Breast- and Ovarian Cancer.
    PLoS Genet. 2016;12:e1006248.
    PubMed     Text format     Abstract available

    July 2016
  7. FOX BA, Sanders KL, Rommereim LM, Guevara RB, et al
    Secretion of Rhoptry and Dense Granule Effector Proteins by Nonreplicating Toxoplasma gondii Uracil Auxotrophs Controls the Development of Antitumor Immunity.
    PLoS Genet. 2016;12:e1006189.
    PubMed     Text format     Abstract available

    June 2016
  8. THOUVENOT P, Ben Yamin B, Fourriere L, Lescure A, et al
    Functional Assessment of Genetic Variants with Outcomes Adapted to Clinical Decision-Making.
    PLoS Genet. 2016;12:e1006096.
    PubMed     Text format     Abstract available

  9. ZHAO B, Pritchard JR
    Inherited Disease Genetics Improves the Identification of Cancer-Associated Genes.
    PLoS Genet. 2016;12:e1006081.
    PubMed     Text format     Abstract available

    April 2016
  10. NAKAOKA H, Gurumurthy A, Hayano T, Ahmadloo S, et al
    Allelic Imbalance in Regulation of ANRIL through Chromatin Interaction at 9p21 Endometriosis Risk Locus.
    PLoS Genet. 2016;12:e1005893.
    PubMed     Text format     Abstract available

    March 2016
  11. HILL T, Schlotterer C, Betancourt AJ
    Hybrid Dysgenesis in Drosophila simulans Associated with a Rapid Invasion of the P-Element.
    PLoS Genet. 2016;12:e1005920.
    PubMed     Text format     Abstract available

    February 2016
  12. MAKINEN N, Aavikko M, Heikkinen T, Taipale M, et al
    Exome Sequencing of Uterine Leiomyosarcomas Identifies Frequent Mutations in TP53, ATRX, and MED12.
    PLoS Genet. 2016;12:e1005850.
    PubMed     Text format     Abstract available

    January 2016
  13. SOUKARIEH O, Gaildrat P, Hamieh M, Drouet A, et al
    Exonic Splicing Mutations Are More Prevalent than Currently Estimated and Can Be Predicted by Using In Silico Tools.
    PLoS Genet. 2016;12:e1005756.
    PubMed     Text format     Abstract available

  14. HALABI NM, Martinez A, Al-Farsi H, Mery E, et al
    Preferential Allele Expression Analysis Identifies Shared Germline and Somatic Driver Genes in Advanced Ovarian Cancer.
    PLoS Genet. 2016;12:e1005755.
    PubMed     Text format     Abstract available

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