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Articles published in PLoS Genet

Retrieve available abstracts of 9 articles:
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Single Articles


    December 2021
  1. ZHANG W, Wu C, Ni R, Yang Q, et al
    Formimidoyltransferase cyclodeaminase prevents the starvation-induced liver hepatomegaly and dysfunction through downregulating mTORC1.
    PLoS Genet. 2021;17:e1009980.
    PubMed     Abstract available


    June 2021
  2. KESHVARI S, Caruso M, Teakle N, Batoon L, et al
    CSF1R-dependent macrophages control postnatal somatic growth and organ maturation.
    PLoS Genet. 2021;17:e1009605.
    PubMed     Abstract available


  3. CRAIG AJ, Garcia-Lezana T, Ruiz de Galarreta M, Villacorta-Martin C, et al
    Transcriptomic characterization of cancer-testis antigens identifies MAGEA3 as a driver of tumor progression in hepatocellular carcinoma.
    PLoS Genet. 2021;17:e1009589.
    PubMed     Abstract available


    November 2020
  4. TCHEANDJIEU C, Aguirre M, Gustafsson S, Saha P, et al
    A phenome-wide association study of 26 mendelian genes reveals phenotypic expressivity of common and rare variants within the general population.
    PLoS Genet. 2020;16:e1008802.
    PubMed     Abstract available


    August 2020
  5. LI BT, Sun M, Li YF, Wang JQ, et al
    Disruption of the ERLIN-TM6SF2-APOB complex destabilizes APOB and contributes to non-alcoholic fatty liver disease.
    PLoS Genet. 2020;16:e1008955.
    PubMed     Abstract available


  6. WILSON MH, Rajan S, Danoff A, White RJ, et al
    A point mutation decouples the lipid transfer activities of microsomal triglyceride transfer protein.
    PLoS Genet. 2020;16:e1008941.
    PubMed     Abstract available


    May 2020
  7. LAU-CORONA D, Bae WK, Hennighausen L, Waxman DJ, et al
    Sex-biased genetic programs in liver metabolism and liver fibrosis are controlled by EZH1 and EZH2.
    PLoS Genet. 2020;16:e1008796.
    PubMed     Abstract available


    April 2020
  8. SETTY BA, Jinesh GG, Arnold M, Pettersson F, et al
    The genomic landscape of undifferentiated embryonal sarcoma of the liver is typified by C19MC structural rearrangement and overexpression combined with TP53 mutation or loss.
    PLoS Genet. 2020;16:e1008642.
    PubMed     Abstract available


  9. EMDIN CA, Haas ME, Khera AV, Aragam K, et al
    A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.
    PLoS Genet. 2020;16:e1008629.
    PubMed     Abstract available


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