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Journal Abstract Search

219 related items for PubMed ID: 22729392

  • 1. Primary hyperoxaluria type III--a model for studying perturbations in glyoxylate metabolism.
    Belostotsky R, Pitt JJ, Frishberg Y.
    J Mol Med (Berl); 2012 Dec; 90(12):1497-504. PubMed ID: 22729392
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  • 2. Primary hyperoxaluria type III gene HOGA1 (formerly DHDPSL) as a possible risk factor for idiopathic calcium oxalate urolithiasis.
    Monico CG, Rossetti S, Belostotsky R, Cogal AG, Herges RM, Seide BM, Olson JB, Bergstrahl EJ, Williams HJ, Haley WE, Frishberg Y, Milliner DS.
    Clin J Am Soc Nephrol; 2011 Sep; 6(9):2289-95. PubMed ID: 21896830
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  • 3. 4-Hydroxyproline metabolism and glyoxylate production: A target for substrate depletion in primary hyperoxaluria?
    Coulter-Mackie MB.
    Kidney Int; 2006 Dec; 70(11):1891-3. PubMed ID: 17130820
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  • 5. Mitochondrial hydroxyproline metabolism: implications for primary hyperoxaluria.
    Knight J, Holmes RP.
    Am J Nephrol; 2005 Dec; 25(2):171-5. PubMed ID: 15849464
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  • 10. Regulation of human 4-hydroxy-2-oxoglutarate aldolase by pyruvate and α-ketoglutarate: implications for primary hyperoxaluria type-3.
    Huang A, Burke J, Bunker RD, Mok YF, Griffin MD, Baker EN, Loomes KM.
    Biochem J; 2019 Nov 15; 476(21):3369-3383. PubMed ID: 31696211
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  • 11. Folding Defects Leading to Primary Hyperoxaluria.
    Oppici E, Dindo M, Conter C, Borri Voltattorni C, Cellini B.
    Handb Exp Pharmacol; 2018 Nov 15; 245():313-343. PubMed ID: 29071511
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  • 12. Structural and biochemical studies of human 4-hydroxy-2-oxoglutarate aldolase: implications for hydroxyproline metabolism in primary hyperoxaluria.
    Riedel TJ, Johnson LC, Knight J, Hantgan RR, Holmes RP, Lowther WT.
    PLoS One; 2011 Nov 15; 6(10):e26021. PubMed ID: 21998747
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  • 15. Cellular degradation of 4-hydroxy-2-oxoglutarate aldolase leads to absolute deficiency in primary hyperoxaluria type 3.
    MacDonald JR, Huang AD, Loomes KM.
    FEBS Lett; 2016 May 15; 590(10):1467-76. PubMed ID: 27096395
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  • 18. Glyoxylate reductase: Definitive identification in human liver mitochondria, its importance for the compartment-specific detoxification of glyoxylate.
    Garrelfs SF, Chornyi S, Te Brinke H, Ruiter J, Groothoff J, Wanders RJA.
    J Inherit Metab Dis; 2024 Mar 15; 47(2):280-288. PubMed ID: 38200664
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  • 19. Oxalate metabolism in thiamine-deficient rats.
    Sidhu H, Gupta R, Thind SK, Nath R.
    Ann Nutr Metab; 1987 Mar 15; 31(6):354-61. PubMed ID: 3426152
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  • 20. HOGA1 gene pathogenic variants in primary hyperoxaluria type III: Spectrum of pathogenic sequence variants, and phenotypic association.
    Abid A, Raza A, Aziz T, Khaliq S.
    Hum Mutat; 2022 Dec 15; 43(12):1757-1779. PubMed ID: 36259736
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