BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

219 related articles for article (PubMed ID: 30413389)

  • 1. Dissociation of globotriaosylceramide and impaired endothelial function in α-galactosidase-A deficient EA.hy926 cells.
    Kaissarian N; Kang J; Shu L; Ferraz MJ; Aerts JM; Shayman JA
    Mol Genet Metab; 2018 Dec; 125(4):338-344. PubMed ID: 30413389
    [TBL] [Abstract][Full Text] [Related]  

  • 2. α-galactosidase A deficiency promotes von Willebrand factor secretion in models of Fabry disease.
    Kang JJ; Kaissarian NM; Desch KC; Kelly RJ; Shu L; Bodary PF; Shayman JA
    Kidney Int; 2019 Jan; 95(1):149-159. PubMed ID: 30470436
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Globotriaosylsphingosine accumulation and not alpha-galactosidase-A deficiency causes endothelial dysfunction in Fabry disease.
    Namdar M; Gebhard C; Studiger R; Shi Y; Mocharla P; Schmied C; Brugada P; Lüscher TF; Camici GG
    PLoS One; 2012; 7(4):e36373. PubMed ID: 22558451
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Endothelial nitric oxide synthase uncoupling and microvascular dysfunction in the mesentery of mice deficient in α-galactosidase A.
    Kang JJ; Shu L; Park JL; Shayman JA; Bodary PF
    Am J Physiol Gastrointest Liver Physiol; 2014 Jan; 306(2):G140-6. PubMed ID: 24232002
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Distributions of Globotriaosylceramide Isoforms, and Globotriaosylsphingosine and Its Analogues in an α-Galactosidase A Knockout Mouse, a Model of Fabry Disease.
    Sueoka H; Aoki M; Tsukimura T; Togawa T; Sakuraba H
    PLoS One; 2015; 10(12):e0144958. PubMed ID: 26661087
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Globotriaosylceramide induces lysosomal degradation of endothelial KCa3.1 in fabry disease.
    Choi S; Kim JA; Na HY; Cho SE; Park S; Jung SC; Suh SH
    Arterioscler Thromb Vasc Biol; 2014 Jan; 34(1):81-9. PubMed ID: 24158513
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Caveolin-associated accumulation of globotriaosylceramide in the vascular endothelium of alpha-galactosidase A null mice.
    Shu L; Shayman JA
    J Biol Chem; 2007 Jul; 282(29):20960-7. PubMed ID: 17535804
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Vascular dysfunction in the alpha-galactosidase A-knockout mouse is an endothelial cell-, plasma membrane-based defect.
    Park JL; Whitesall SE; D'Alecy LG; Shu L; Shayman JA
    Clin Exp Pharmacol Physiol; 2008 Oct; 35(10):1156-63. PubMed ID: 18565198
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pathogenesis and Molecular Mechanisms of Anderson-Fabry Disease and Possible New Molecular Addressed Therapeutic Strategies.
    Tuttolomondo A; Simonetta I; Riolo R; Todaro F; Di Chiara T; Miceli S; Pinto A
    Int J Mol Sci; 2021 Sep; 22(18):. PubMed ID: 34576250
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Differences in cleavage of globotriaosylceramide and its derivatives accumulated in organs of young Fabry mice following enzyme replacement therapy.
    Kodama T; Tsukimura T; Kawashima I; Sato A; Sakuraba H; Togawa T
    Mol Genet Metab; 2017; 120(1-2):116-120. PubMed ID: 27756537
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Glucosylceramide synthase inhibition with lucerastat lowers globotriaosylceramide and lysosome staining in cultured fibroblasts from Fabry patients with different mutation types.
    Welford RWD; Mühlemann A; Garzotti M; Rickert V; Groenen PMA; Morand O; Üçeyler N; Probst MR
    Hum Mol Genet; 2018 Oct; 27(19):3392-3403. PubMed ID: 29982630
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Endothelial Dysfunction in Fabry Disease Is Related to Glycocalyx Degradation.
    Pollmann S; Scharnetzki D; Manikowski D; Lenders M; Brand E
    Front Immunol; 2021; 12():789142. PubMed ID: 34917096
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Decreased nitric oxide bioavailability in a mouse model of Fabry disease.
    Shu L; Park JL; Byun J; Pennathur S; Kollmeyer J; Shayman JA
    J Am Soc Nephrol; 2009 Sep; 20(9):1975-85. PubMed ID: 19628671
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Enhanced thrombospondin-1 causes dysfunction of vascular endothelial cells derived from Fabry disease-induced pluripotent stem cells.
    Do HS; Park SW; Im I; Seo D; Yoo HW; Go H; Kim YH; Koh GY; Lee BH; Han YM
    EBioMedicine; 2020 Feb; 52():102633. PubMed ID: 31981984
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Variations in the GLA gene correlate with globotriaosylceramide and globotriaosylsphingosine analog levels in urine and plasma.
    Ferreira S; Auray-Blais C; Boutin M; Lavoie P; Nunes JP; Martins E; Garman S; Oliveira JP
    Clin Chim Acta; 2015 Jul; 447():96-104. PubMed ID: 26070511
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular basis for high renal cell sensitivity to the cytotoxic effects of shigatoxin-1: upregulation of globotriaosylceramide expression.
    Hughes AK; Ergonul Z; Stricklett PK; Kohan DE
    J Am Soc Nephrol; 2002 Sep; 13(9):2239-45. PubMed ID: 12191968
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Plasma globotriaosylsphingosine as a biomarker of Fabry disease.
    Togawa T; Kodama T; Suzuki T; Sugawara K; Tsukimura T; Ohashi T; Ishige N; Suzuki K; Kitagawa T; Sakuraba H
    Mol Genet Metab; 2010 Jul; 100(3):257-61. PubMed ID: 20409739
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Differential involvement of COX1 and COX2 in the vasculopathy associated with the alpha-galactosidase A-knockout mouse.
    Park JL; Shu L; Shayman JA
    Am J Physiol Heart Circ Physiol; 2009 Apr; 296(4):H1133-40. PubMed ID: 19202000
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular basis for globotriaosylceramide regulation and enzyme uptake in immortalized aortic endothelial cells from Fabry mice.
    Meng XL; Day TS; McNeill N; Ashcraft P; Frischmuth T; Cheng SH; Liu ZP; Shen JS; Schiffmann R
    J Inherit Metab Dis; 2016 May; 39(3):447-455. PubMed ID: 26960552
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A comprehensive testing algorithm for the diagnosis of Fabry disease in males and females.
    Stiles AR; Zhang H; Dai J; McCaw P; Beasley J; Rehder C; Koeberl DD; McDonald M; Bali DS; Young SP
    Mol Genet Metab; 2020 Jul; 130(3):209-214. PubMed ID: 32418857
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.