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271 related items for PubMed ID: 17110443

  • 1. Alanine-glyoxylate aminotransferase-deficient mice, a model for primary hyperoxaluria that responds to adenoviral gene transfer.
    Salido EC, Li XM, Lu Y, Wang X, Santana A, Roy-Chowdhury N, Torres A, Shapiro LJ, Roy-Chowdhury J.
    Proc Natl Acad Sci U S A; 2006 Nov 28; 103(48):18249-54. PubMed ID: 17110443
    [Abstract] [Full Text] [Related]

  • 2. Differential expression of liver and kidney proteins in a mouse model for primary hyperoxaluria type I.
    Hernández-Fernaud JR, Salido E.
    FEBS J; 2010 Nov 28; 277(22):4766-74. PubMed ID: 20977670
    [Abstract] [Full Text] [Related]

  • 3. Phenotypic correction of a mouse model for primary hyperoxaluria with adeno-associated virus gene transfer.
    Salido E, Rodriguez-Pena M, Santana A, Beattie SG, Petry H, Torres A.
    Mol Ther; 2011 May 28; 19(5):870-5. PubMed ID: 21119625
    [Abstract] [Full Text] [Related]

  • 4. Generation of a Primary Hyperoxaluria Type 1 Disease Model Via CRISPR/Cas9 System in Rats.
    Zheng R, Fang X, He L, Shao Y, Guo N, Wang L, Liu M, Li D, Geng H.
    Curr Mol Med; 2018 May 28; 18(7):436-447. PubMed ID: 30539697
    [Abstract] [Full Text] [Related]

  • 5. Generation and characterization of a novel rat model of primary hyperoxaluria type 1 with a nonsense mutation in alanine-glyoxylate aminotransferase gene.
    Li Y, Zheng R, Xu G, Huang Y, Li Y, Li D, Geng H.
    Am J Physiol Renal Physiol; 2021 Mar 01; 320(3):F475-F484. PubMed ID: 33491567
    [Abstract] [Full Text] [Related]

  • 6. Systemic Alanine Glyoxylate Aminotransferase mRNA Improves Glyoxylate Metabolism in a Mouse Model of Primary Hyperoxaluria Type 1.
    Kukreja A, Lasaro M, Cobaugh C, Forbes C, Tang JP, Gao X, Martin-Higueras C, Pey AL, Salido E, Sobolov S, Subramanian RR.
    Nucleic Acid Ther; 2019 Apr 01; 29(2):104-113. PubMed ID: 30676254
    [Abstract] [Full Text] [Related]

  • 7. Enteric oxalate elimination is induced and oxalate is normalized in a mouse model of primary hyperoxaluria following intestinal colonization with Oxalobacter.
    Hatch M, Gjymishka A, Salido EC, Allison MJ, Freel RW.
    Am J Physiol Gastrointest Liver Physiol; 2011 Mar 01; 300(3):G461-9. PubMed ID: 21163900
    [Abstract] [Full Text] [Related]

  • 8. Effect of alanine supplementation on oxalate synthesis.
    Wood KD, Freeman BL, Killian ME, Lai WS, Assimos D, Knight J, Fargue S.
    Biochim Biophys Acta Mol Basis Dis; 2021 Jan 01; 1867(1):165981. PubMed ID: 33002578
    [Abstract] [Full Text] [Related]

  • 9. Correction of hyperoxaluria by liver repopulation with hepatocytes in a mouse model of primary hyperoxaluria type-1.
    Jiang J, Salido EC, Guha C, Wang X, Moitra R, Liu L, Roy-Chowdhury J, Roy-Chowdhury N.
    Transplantation; 2008 May 15; 85(9):1253-60. PubMed ID: 18475180
    [Abstract] [Full Text] [Related]

  • 10. Primary hyperoxaluria type 1: update and additional mutation analysis of the AGXT gene.
    Williams EL, Acquaviva C, Amoroso A, Chevalier F, Coulter-Mackie M, Monico CG, Giachino D, Owen T, Robbiano A, Salido E, Waterham H, Rumsby G.
    Hum Mutat; 2009 Jun 15; 30(6):910-7. PubMed ID: 19479957
    [Abstract] [Full Text] [Related]

  • 11. [From gene to disease; primary hyperoxaluria type I caused by mutations in the AGXT gene].
    van Woerden CS, Groothof JW, Wanders RJ, Waterham HR, Wijburg FR.
    Ned Tijdschr Geneeskd; 2006 Jul 29; 150(30):1669-72. PubMed ID: 16922352
    [Abstract] [Full Text] [Related]

  • 12. A Putative Mutation Hotspot of the AGXT Gene Associated with Primary Hyperoxaluria Type 1 in the Chinese Population.
    Li X, Gu J, Yang Y, Li J, Li Y.
    Tohoku J Exp Med; 2018 Dec 29; 246(4):233-241. PubMed ID: 30541997
    [Abstract] [Full Text] [Related]

  • 13. Primary hyperoxaluria type 1 in the Canary Islands: a conformational disease due to I244T mutation in the P11L-containing alanine:glyoxylate aminotransferase.
    Santana A, Salido E, Torres A, Shapiro LJ.
    Proc Natl Acad Sci U S A; 2003 Jun 10; 100(12):7277-82. PubMed ID: 12777626
    [Abstract] [Full Text] [Related]

  • 14. Gly161 mutations associated with Primary Hyperoxaluria Type I induce the cytosolic aggregation and the intracellular degradation of the apo-form of alanine:glyoxylate aminotransferase.
    Oppici E, Roncador A, Montioli R, Bianconi S, Cellini B.
    Biochim Biophys Acta; 2013 Dec 10; 1832(12):2277-88. PubMed ID: 24055001
    [Abstract] [Full Text] [Related]

  • 15. Molecular aetiology of primary hyperoxaluria type 1.
    Danpure CJ.
    Nephron Exp Nephrol; 2004 Dec 10; 98(2):e39-44. PubMed ID: 15499210
    [Abstract] [Full Text] [Related]

  • 16. Mutation spectrum of primary hyperoxaluria type 1 in Tunisia: implication for diagnosis in North Africa.
    Nagara M, Tiar A, Ben Halim N, Ben Rhouma F, Messaoud O, Bouyacoub Y, Kefi R, Hassayoun S, Zouari N, Ben Ammar MS, Abdelhak S, Chemli J.
    Gene; 2013 Sep 15; 527(1):316-20. PubMed ID: 23810941
    [Abstract] [Full Text] [Related]

  • 17. Primary hyperoxalurias: disorders of glyoxylate detoxification.
    Salido E, Pey AL, Rodriguez R, Lorenzo V.
    Biochim Biophys Acta; 2012 Sep 15; 1822(9):1453-64. PubMed ID: 22446032
    [Abstract] [Full Text] [Related]

  • 18. CRISPR/Cas9-mediated metabolic pathway reprogramming in a novel humanized rat model ameliorates primary hyperoxaluria type 1.
    Zheng R, Li Y, Wang L, Fang X, Zhang J, He L, Yang L, Li D, Geng H.
    Kidney Int; 2020 Oct 15; 98(4):947-957. PubMed ID: 32464217
    [Abstract] [Full Text] [Related]

  • 19. Identification of compound heterozygous patients with primary hyperoxaluria type 1: clinical evaluations and in silico investigations.
    Kanoun H, Jarraya F, Maalej B, Lahiani A, Mahfoudh H, Makni F, Hachicha J, Fakhfakh F.
    BMC Nephrol; 2017 Oct 02; 18(1):303. PubMed ID: 28969594
    [Abstract] [Full Text] [Related]

  • 20. Identification of a novel AGXT gene mutation in primary hyperoxaluria after kidney transplantation failure.
    M'dimegh S, Omezzine A, Hamida-Rebai MB, Aquaviva-Bourdain C, M'barek I, Sahtout W, Zellama D, Souche G, Achour A, Abroug S, Bouslama A.
    Transpl Immunol; 2016 Nov 02; 39():60-65. PubMed ID: 27568336
    [Abstract] [Full Text] [Related]

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