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Articles published in PLoS Genet

Retrieve available abstracts of 12 articles:
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    July 2017
  1. KLAR J, Piontek J, Milatz S, Tariq M, et al
    Altered paracellular cation permeability due to a rare CLDN10B variant causes anhidrosis and kidney damage.
    PLoS Genet. 2017;13:e1006897.
    PubMed     Text format     Abstract available

    June 2017
  2. KAWAZU M, Kojima S, Ueno T, Totoki Y, et al
    Integrative analysis of genomic alterations in triple-negative breast cancer in association with homologous recombination deficiency.
    PLoS Genet. 2017;13:e1006853.
    PubMed     Text format     Abstract available

    March 2017
  3. HOFFMAN JD, Graff RE, Emami NC, Tai CG, et al
    Cis-eQTL-based trans-ethnic meta-analysis reveals novel genes associated with breast cancer risk.
    PLoS Genet. 2017;13:e1006690.
    PubMed     Text format     Abstract available

  4. STRICKER TP, Brown CD, Bandlamudi C, McNerney M, et al
    Robust stratification of breast cancer subtypes using differential patterns of transcript isoform expression.
    PLoS Genet. 2017;13:e1006589.
    PubMed     Text format     Abstract available

    February 2017
  5. HAGENAARS SP, Hill WD, Harris SE, Ritchie SJ, et al
    Genetic prediction of male pattern baldness.
    PLoS Genet. 2017;13:e1006594.
    PubMed     Text format     Abstract available

  6. EVANS JM, Noorai RE, Tsai KL, Starr-Moss AN, et al
    Beyond the MHC: A canine model of dermatomyositis shows a complex pattern of genetic risk involving novel loci.
    PLoS Genet. 2017;13:e1006604.
    PubMed     Text format     Abstract available

    January 2017
  7. KASPAREK P, Ileninova Z, Zbodakova O, Kanchev I, et al
    KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype.
    PLoS Genet. 2017;13:e1006566.
    PubMed     Text format     Abstract available

    September 2016
  8. MAIR B, Konopka T, Kerzendorfer C, Sleiman K, et al
    Gain- and Loss-of-Function Mutations in the Breast Cancer Gene GATA3 Result in Differential Drug Sensitivity.
    PLoS Genet. 2016;12:e1006279.
    PubMed     Text format     Abstract available

    August 2016
  9. 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

    June 2016
  10. 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

    January 2016
  11. MANTERE T, Winqvist R, Kauppila S, Grip M, et al
    Targeted Next-Generation Sequencing Identifies a Recurrent Mutation in MCPH1 Associating with Hereditary Breast Cancer Susceptibility.
    PLoS Genet. 2016;12:e1005816.
    PubMed     Text format     Abstract available

  12. FARAJI F, Hu Y, Yang HH, Lee MP, et al
    Post-transcriptional Control of Tumor Cell Autonomous Metastatic Potential by CCR4-NOT Deadenylase CNOT7.
    PLoS Genet. 2016;12:e1005820.
    PubMed     Text format     Abstract available

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