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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

212 related items for PubMed ID: 34368857

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  • 7. Schnyder corneal dystrophy-associated UBIAD1 inhibits ER-associated degradation of HMG CoA reductase in mice.
    Jo Y, Hamilton JS, Hwang S, Garland K, Smith GA, Su S, Fuentes I, Neelam S, Thompson BM, McDonald JG, DeBose-Boyd RA.
    Elife; 2019 Feb 20; 8():. PubMed ID: 30785396
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  • 8. The prenyltransferase UBIAD1 is the target of geranylgeraniol in degradation of HMG CoA reductase.
    Schumacher MM, Elsabrouty R, Seemann J, Jo Y, DeBose-Boyd RA.
    Elife; 2015 Mar 05; 4():. PubMed ID: 25742604
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  • 16. Naturally occurring UBIAD1 mutations differentially affect menaquinone biosynthesis and vitamin K-dependent carboxylation.
    Chen X, Furukawa N, Jin DY, Liu Y, Stafford DW, Williams CM, Suhara Y, Tie JK.
    FEBS J; 2022 May 05; 289(9):2613-2627. PubMed ID: 34813684
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  • 17. Type 1 polyisoprenoid diphosphate phosphatase modulates geranylgeranyl-mediated control of HMG CoA reductase and UBIAD1.
    Elsabrouty R, Jo Y, Hwang S, Jun DJ, DeBose-Boyd RA.
    Elife; 2021 Nov 29; 10():. PubMed ID: 34842525
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  • 19. The gene for schnyder's crystalline corneal dystrophy maps to human chromosome 1p34.1-p36.
    Shearman AM, Hudson TJ, Andresen JM, Wu X, Sohn RL, Haluska F, Housman DE, Weiss JS.
    Hum Mol Genet; 1996 Oct 29; 5(10):1667-72. PubMed ID: 8894705
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