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Identification of genetic modifiers of murine hepatic β-glucocerebrosidase activity.
Durán A, Rebolledo-Jaramillo B, Olguin V, Rojas-Herrera M, Las Heras M, Calderón JF, Zanlungo S, Priestman DA, Platt FM, Klein AD. Durán A, et al. Among authors: priestman da. Biochem Biophys Rep. 2021 Aug 18;28:101105. doi: 10.1016/j.bbrep.2021.101105. eCollection 2021 Dec. Biochem Biophys Rep. 2021. PMID: 34458595 Free PMC article.
Implications for invariant natural killer T cell ligands due to the restricted presence of isoglobotrihexosylceramide in mammals.
Speak AO, Salio M, Neville DC, Fontaine J, Priestman DA, Platt N, Heare T, Butters TD, Dwek RA, Trottein F, Exley MA, Cerundolo V, Platt FM. Speak AO, et al. Among authors: priestman da. Proc Natl Acad Sci U S A. 2007 Apr 3;104(14):5971-6. doi: 10.1073/pnas.0607285104. Epub 2007 Mar 19. Proc Natl Acad Sci U S A. 2007. PMID: 17372214 Free PMC article.
Amyotrophic lateral sclerosis and denervation alter sphingolipids and up-regulate glucosylceramide synthase.
Henriques A, Croixmarie V, Priestman DA, Rosenbohm A, Dirrig-Grosch S, D'Ambra E, Huebecker M, Hussain G, Boursier-Neyret C, Echaniz-Laguna A, Ludolph AC, Platt FM, Walther B, Spedding M, Loeffler JP, Gonzalez De Aguilar JL. Henriques A, et al. Among authors: priestman da. Hum Mol Genet. 2015 Dec 20;24(25):7390-405. doi: 10.1093/hmg/ddv439. Epub 2015 Oct 19. Hum Mol Genet. 2015. PMID: 26483191 Free PMC article.
A novel approach to analyze lysosomal dysfunctions through subcellular proteomics and lipidomics: the case of NPC1 deficiency.
Tharkeshwar AK, Trekker J, Vermeire W, Pauwels J, Sannerud R, Priestman DA, Te Vruchte D, Vints K, Baatsen P, Decuypere JP, Lu H, Martin S, Vangheluwe P, Swinnen JV, Lagae L, Impens F, Platt FM, Gevaert K, Annaert W. Tharkeshwar AK, et al. Among authors: priestman da. Sci Rep. 2017 Jan 30;7:41408. doi: 10.1038/srep41408. Sci Rep. 2017. PMID: 28134274 Free PMC article.
62 results