These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

180 related items for PubMed ID: 30785396

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. UbiA prenyltransferase domain-containing protein-1 modulates HMG-CoA reductase degradation to coordinate synthesis of sterol and nonsterol isoprenoids.
    Schumacher MM, Jun DJ, Johnson BM, DeBose-Boyd RA.
    J Biol Chem; 2018 Jan 05; 293(1):312-323. PubMed ID: 29167270
    [Abstract] [Full Text] [Related]

  • 3. Schnyder corneal dystrophy-associated UBIAD1 is defective in MK-4 synthesis and resists autophagy-mediated degradation.
    Jun DJ, Schumacher MM, Hwang S, Kinch LN, Grishin NV, DeBose-Boyd RA.
    J Lipid Res; 2020 May 05; 61(5):746-757. PubMed ID: 32188638
    [Abstract] [Full Text] [Related]

  • 4. Geranylgeranyl-regulated transport of the prenyltransferase UBIAD1 between membranes of the ER and Golgi.
    Schumacher MM, Jun DJ, Jo Y, Seemann J, DeBose-Boyd RA.
    J Lipid Res; 2016 Jul 05; 57(7):1286-99. PubMed ID: 27121042
    [Abstract] [Full Text] [Related]

  • 5. Schnyder corneal dystrophy-associated UBIAD1 mutations cause corneal cholesterol accumulation by stabilizing HMG-CoA reductase.
    Jiang SY, Tang JJ, Xiao X, Qi W, Wu S, Jiang C, Hong J, Xu J, Song BL, Luo J.
    PLoS Genet; 2019 Jul 05; 15(7):e1008289. PubMed ID: 31323021
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. The UBIAD1 prenyltransferase links menaquinone-4 [corrected] synthesis to cholesterol metabolic enzymes.
    Nickerson ML, Bosley AD, Weiss JS, Kostiha BN, Hirota Y, Brandt W, Esposito D, Kinoshita S, Wessjohann L, Morham SG, Andresson T, Kruth HS, Okano T, Dean M.
    Hum Mutat; 2013 Feb 29; 34(2):317-29. PubMed ID: 23169578
    [Abstract] [Full Text] [Related]

  • 11. Posttranslational Regulation of HMG CoA Reductase, the Rate-Limiting Enzyme in Synthesis of Cholesterol.
    Schumacher MM, DeBose-Boyd RA.
    Annu Rev Biochem; 2021 Jun 20; 90():659-679. PubMed ID: 34153214
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Clinical diversity in patients with Schnyder corneal dystrophy-a novel and known UBIAD1 pathogenic variants.
    Sarosiak A, Udziela M, Ścieżyńska A, Oziębło D, Wawrzynowska A, Szaflik JP, Ołdak M.
    Graefes Arch Clin Exp Ophthalmol; 2018 Nov 20; 256(11):2127-2134. PubMed ID: 30084067
    [Abstract] [Full Text] [Related]

  • 18. Schnyder corneal dystrophy and associated phenotypes caused by novel and recurrent mutations in the UBIAD1 gene.
    Evans CJ, Dudakova L, Skalicka P, Mahelkova G, Horinek A, Hardcastle AJ, Tuft SJ, Liskova P.
    BMC Ophthalmol; 2018 Sep 17; 18(1):250. PubMed ID: 30223810
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.