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Articles published in
PLoS Genet
    January 2023
  1. 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.
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  2. 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.
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    November 2022
  3. 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.
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    September 2022
  4. 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.
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    August 2022
  5. 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.
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    June 2022
  6. 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.
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  7. 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.
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    May 2022
  8. 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.
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    April 2022
  9. 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.
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    March 2022
  10. 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.
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    February 2022
  11. 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.
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    January 2022
  12. 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.
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    December 2021
  13. 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.
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  14. 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.
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    November 2021
  15. 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.
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    September 2021
  16. FRITSCHE LG, Ma Y, Zhang D, Salvatore M, et al
    On cross-ancestry cancer polygenic risk scores.
    PLoS Genet. 2021;17:e1009670.
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    August 2021
  17. 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.
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    June 2021
  18. 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.
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  19. 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.
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