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Articles published in
PLoS Genet
    May 2024
  1. DENNIS M, Hurley A, Bray N, Cordero C, et al
    Her2 amplification, Rel-A, and Bach1 can influence APOBEC3A expression in breast cancer cells.
    PLoS Genet. 2024;20:e1011293.
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  2. 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.
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  3. GOMEZ ACUNA LI, Flyamer I, Boyle S, Friman ET, et al
    Transcription decouples estrogen-dependent changes in enhancer-promoter contact frequencies and spatial proximity.
    PLoS Genet. 2024;20:e1011277.
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    February 2024
  4. 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.
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    November 2023
  5. 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.
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    September 2023
  6. WANG J, Chen Y, Zou Q
    Inferring gene regulatory network from single-cell transcriptomes with graph autoencoder model.
    PLoS Genet. 2023;19:e1010942.
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  7. 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.
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    August 2023
  8. 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.
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  9. 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.
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    July 2023
  10. 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.
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    January 2023
  11. 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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  12. 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
  13. 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
  14. 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
  15. 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
  16. 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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  17. 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
  18. 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
  19. 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
  20. 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
  21. 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
  22. 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
  23. 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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  24. 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
  25. 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
  26. 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
  27. 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
  28. 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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  29. 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.
    >> Share


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