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Journal Abstract Search

197 related items for PubMed ID: 31794008

  • 1. Cycloserine enantiomers are reversible inhibitors of human alanine:glyoxylate aminotransferase: implications for Primary Hyperoxaluria type 1.
    Dindo M, Grottelli S, Annunziato G, Giardina G, Pieroni M, Pampalone G, Faccini A, Cutruzzolà F, Laurino P, Costantino G, Cellini B.
    Biochem J; 2019 Dec 23; 476(24):3751-3768. PubMed ID: 31794008
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  • 2. 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 23; 1832(12):2277-88. PubMed ID: 24055001
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  • 4. Correlation between the molecular effects of mutations at the dimer interface of alanine-glyoxylate aminotransferase leading to primary hyperoxaluria type I and the cellular response to vitamin B6.
    Dindo M, Oppici E, Dell'Orco D, Montone R, Cellini B.
    J Inherit Metab Dis; 2018 Mar 23; 41(2):263-275. PubMed ID: 29110180
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  • 7. The Chaperoning Activity of Amino-oxyacetic Acid on Folding-Defective Variants of Human Alanine:Glyoxylate Aminotransferase Causing Primary Hyperoxaluria Type I.
    Oppici E, Montioli R, Dindo M, Maccari L, Porcari V, Lorenzetto A, Chellini S, Voltattorni CB, Cellini B.
    ACS Chem Biol; 2015 Oct 16; 10(10):2227-36. PubMed ID: 26161999
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  • 10. Four of the most common mutations in primary hyperoxaluria type 1 unmask the cryptic mitochondrial targeting sequence of alanine:glyoxylate aminotransferase encoded by the polymorphic minor allele.
    Fargue S, Lewin J, Rumsby G, Danpure CJ.
    J Biol Chem; 2013 Jan 25; 288(4):2475-84. PubMed ID: 23229545
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  • 11. Biochemical and cellular effects of a novel missense mutation of the AGXT gene associated with Primary Hyperoxaluria Type 1.
    Gatticchi L, Dindo M, Pampalone G, Conter C, Cellini B, Takayama T.
    Biochem Biophys Res Commun; 2023 Feb 19; 645():118-123. PubMed ID: 36682331
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  • 12. Crystal structure of the S187F variant of human liver alanine: glyoxylate [corrected] aminotransferase associated with primary hyperoxaluria type I and its functional implications.
    Oppici E, Fodor K, Paiardini A, Williams C, Voltattorni CB, Wilmanns M, Cellini B.
    Proteins; 2013 Aug 19; 81(8):1457-65. PubMed ID: 23589421
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  • 14. Natural and Unnatural Compounds Rescue Folding Defects of Human Alanine: Glyoxylate Aminotransferase Leading to Primary Hyperoxaluria Type I.
    Oppici E, Montioli R, Dindo M, Cellini B.
    Curr Drug Targets; 2016 Aug 19; 17(13):1482-91. PubMed ID: 26931357
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  • 20. Multiple mechanisms of action of pyridoxine in primary hyperoxaluria type 1.
    Fargue S, Rumsby G, Danpure CJ.
    Biochim Biophys Acta; 2013 Oct 19; 1832(10):1776-83. PubMed ID: 23597595
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