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Articles published in PLoS Genet

Retrieve available abstracts of 27 articles:
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Single Articles

    May 2024
  1. MAJOCHA MR, Jackson DE, Ha NH, Amin R, et al
    Resf1 is a compound G4 quadruplex-associated tumor suppressor for triple negative breast cancer.
    PLoS Genet. 2024;20:e1011236.
    PubMed     Abstract available

    February 2024
  2. SCOTT TG, Sathyan KM, Gioeli D, Guertin MJ, et al
    TRPS1 modulates chromatin accessibility to regulate estrogen receptor alpha (ER) binding and ER target gene expression in luminal breast cancer cells.
    PLoS Genet. 2024;20:e1011159.
    PubMed     Abstract available

    November 2023
  3. CARPENTER MA, Temiz NA, Ibrahim MA, Jarvis MC, et al
    Mutational impact of APOBEC3A and APOBEC3B in a human cell line and comparisons to breast cancer.
    PLoS Genet. 2023;19:e1011043.
    PubMed     Abstract available

    September 2023
  4. WANG J, Chen Y, Zou Q
    Inferring gene regulatory network from single-cell transcriptomes with graph autoencoder model.
    PLoS Genet. 2023;19:e1010942.
    PubMed     Abstract available

  5. SAHU S, Sullivan TL, Mitrophanov AY, Galloux M, et al
    Saturation genome editing of 11 codons and exon 13 of BRCA2 coupled with chemotherapeutic drug response accurately determines pathogenicity of variants.
    PLoS Genet. 2023;19:e1010940.
    PubMed     Abstract available

    August 2023
  6. KUMPULA TA, Vorimo S, Mattila TT, O'Gorman L, et al
    Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibility.
    PLoS Genet. 2023;19:e1010889.
    PubMed     Abstract available

  7. DIABATE M, Islam MM, Nagy G, Banerjee T, et al
    DNA repair function scores for 2172 variants in the BRCA1 amino-terminus.
    PLoS Genet. 2023;19:e1010739.
    PubMed     Abstract available

    July 2023
  8. LIU W, Deng W, Chen M, Dong Z, et al
    A statistical framework to identify cell types whose genetically regulated proportions are associated with complex diseases.
    PLoS Genet. 2023;19:e1010825.
    PubMed     Abstract available

    January 2023
  9. FERRANDO L, Vingiani A, Garuti A, Vernieri C, et al
    ESR1 gene amplification and MAP3K mutations are selected during adjuvant endocrine therapies in relapsing Hormone Receptor-positive, HER2-negative breast cancer (HR+ HER2- BC).
    PLoS Genet. 2023;19:e1010563.
    PubMed     Abstract available

  10. WASHINGTON-HUGHES CL, Roy S, Seneviratne HK, Karuppagounder SS, et al
    Atp7b-dependent choroid plexus dysfunction causes transient copper deficit and metabolic changes in the developing mouse brain.
    PLoS Genet. 2023;19:e1010558.
    PubMed     Abstract available

    November 2022
  11. CAMPAGNA L, Mo Z, Siepel A, Uy JAC, et al
    Selective sweeps on different pigmentation genes mediate convergent evolution of island melanism in two incipient bird species.
    PLoS Genet. 2022;18:e1010474.
    PubMed     Abstract available

    September 2022
  12. LUONG TT, Li Z, Priedigkeit N, Parker PS, et al
    Hrq1/RECQL4 regulation is critical for preventing aberrant recombination during DNA intrastrand crosslink repair and is upregulated in breast cancer.
    PLoS Genet. 2022;18:e1010122.
    PubMed     Abstract available

    August 2022
  13. GAGLIANI EK, Gutzwiller LM, Kuang Y, Odaka Y, et al
    A Drosophila Su(H) model of Adams-Oliver Syndrome reveals cofactor titration as a mechanism underlying developmental defects.
    PLoS Genet. 2022;18:e1010335.
    PubMed     Abstract available

    June 2022
  14. SANCHEZ VC, Yang HH, Craig-Lucas A, Dubois W, et al
    Host CLIC4 expression in the tumor microenvironment is essential for breast cancer metastatic competence.
    PLoS Genet. 2022;18:e1010271.
    PubMed     Abstract available

  15. REYNISDOTTIR T, Anderson KJ, Boukas L, Bjornsson HT, et al
    Missense variants causing Wiedemann-Steiner syndrome preferentially occur in the KMT2A-CXXC domain and are accurately classified using AlphaFold2.
    PLoS Genet. 2022;18:e1010278.
    PubMed     Abstract available

    May 2022
  16. EAPEN AA, Parameswaran S, Forney C, Edsall LE, et al
    Epigenetic and transcriptional dysregulation in CD4+ T cells in patients with atopic dermatitis.
    PLoS Genet. 2022;18:e1009973.
    PubMed     Abstract available

    April 2022
  17. RALPH D, Nitschke Y, Levine MA, Caffet M, et al
    ENPP1 variants in patients with GACI and PXE expand the clinical and genetic heterogeneity of heritable disorders of ectopic calcification.
    PLoS Genet. 2022;18:e1010192.
    PubMed     Abstract available

    March 2022
  18. LEGRAND A, Guery C, Faugeroux J, Fontaine E, et al
    Comparative therapeutic strategies for preventing aortic rupture in a mouse model of vascular Ehlers-Danlos syndrome.
    PLoS Genet. 2022;18:e1010059.
    PubMed     Abstract available

    February 2022
  19. MYERS AN, Lawhon SD, Diesel AB, Bradley CW, et al
    An ancient haplotype containing antimicrobial peptide gene variants is associated with severe fungal skin disease in Persian cats.
    PLoS Genet. 2022;18:e1010062.
    PubMed     Abstract available

    January 2022
  20. HAYES BL, Robinson T, Kar S, Ruth KS, et al
    Do sex hormones confound or mediate the effect of chronotype on breast and prostate cancer? A Mendelian randomization study.
    PLoS Genet. 2022;18:e1009887.
    PubMed     Abstract available

    December 2021
  21. JEWELL BE, Xu A, Zhu D, Huang MF, et al
    Patient-derived iPSCs link elevated mitochondrial respiratory complex I function to osteosarcoma in Rothmund-Thomson syndrome.
    PLoS Genet. 2021;17:e1009971.
    PubMed     Abstract available

  22. GUILLON J, Coquelet H, Leman G, Toutain B, et al
    tRNA biogenesis and specific aminoacyl-tRNA synthetases regulate senescence stability under the control of mTOR.
    PLoS Genet. 2021;17:e1009953.
    PubMed     Abstract available

    November 2021
  23. MADSEN RR, Erickson EC, Rueda OM, Robin X, et al
    Positive correlation between transcriptomic stemness and PI3K/AKT/mTOR signaling scores in breast cancer, and a counterintuitive relationship with PIK3CA genotype.
    PLoS Genet. 2021;17:e1009876.
    PubMed     Abstract available

    September 2021
  24. FRITSCHE LG, Ma Y, Zhang D, Salvatore M, et al
    On cross-ancestry cancer polygenic risk scores.
    PLoS Genet. 2021;17:e1009670.
    PubMed     Abstract available

    August 2021
  25. AIDERUS A, Newberg JY, Guzman-Rojas L, Contreras-Sandoval AM, et al
    Transposon mutagenesis identifies cooperating genetic drivers during keratinocyte transformation and cutaneous squamous cell carcinoma progression.
    PLoS Genet. 2021;17:e1009094.
    PubMed     Abstract available

    June 2021
  26. POTTIE L, Van Gool W, Vanhooydonck M, Hanisch FG, et al
    Loss of zebrafish atp6v1e1b, encoding a subunit of vacuolar ATPase, recapitulates human ARCL type 2C syndrome and identifies multiple pathobiological signatures.
    PLoS Genet. 2021;17:e1009603.
    PubMed     Abstract available

  27. GUO L, Bloom J, Sykes S, Huang E, et al
    Genetics of white color and iridophoroma in "Lemon Frost" leopard geckos.
    PLoS Genet. 2021;17:e1009580.
    PubMed     Abstract available

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