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Journal Abstract Search

145 related items for PubMed ID: 27720751

  • 1. Effects of interface mutations on the dimerization of alanine glyoxylate aminotransferase and implications in the mistargeting of the pathogenic variants F152I and I244T.
    Dindo M, Montioli R, Busato M, Giorgetti A, Cellini B, Borri Voltattorni C.
    Biochimie; 2016 Dec; 131():137-148. PubMed ID: 27720751
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  • 2. Human liver peroxisomal alanine:glyoxylate aminotransferase: Different stability under chemical stress of the major allele, the minor allele, and its pathogenic G170R variant.
    Cellini B, Lorenzetto A, Montioli R, Oppici E, Voltattorni CB.
    Biochimie; 2010 Dec; 92(12):1801-11. PubMed ID: 20713123
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  • 3. Misfolding caused by the pathogenic mutation G47R on the minor allele of alanine:glyoxylate aminotransferase and chaperoning activity of pyridoxine.
    Montioli R, Oppici E, Dindo M, Roncador A, Gotte G, Cellini B, Borri Voltattorni C.
    Biochim Biophys Acta; 2015 Oct; 1854(10 Pt A):1280-9. PubMed ID: 26149463
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  • 4. Molecular Insight into the Synergism between the Minor Allele of Human Liver Peroxisomal Alanine:Glyoxylate Aminotransferase and the F152I Mutation.
    Cellini B, Montioli R, Paiardini A, Lorenzetto A, Voltattorni CB.
    J Biol Chem; 2009 Mar 27; 284(13):8349-58. PubMed ID: 19155213
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  • 5. Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I.
    Cellini B, Montioli R, Paiardini A, Lorenzetto A, Maset F, Bellini T, Oppici E, Voltattorni CB.
    Proc Natl Acad Sci U S A; 2010 Feb 16; 107(7):2896-901. PubMed ID: 20133649
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  • 6. Functional synergism between the most common polymorphism in human alanine:glyoxylate aminotransferase and four of the most common disease-causing mutations.
    Lumb MJ, Danpure CJ.
    J Biol Chem; 2000 Nov 17; 275(46):36415-22. PubMed ID: 10960483
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  • 7. 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 17; 1832(12):2277-88. PubMed ID: 24055001
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  • 8. Biochemical analyses are instrumental in identifying the impact of mutations on holo and/or apo-forms and on the region(s) of alanine:glyoxylate aminotransferase variants associated with primary hyperoxaluria type I.
    Oppici E, Montioli R, Lorenzetto A, Bianconi S, Borri Voltattorni C, Cellini B.
    Mol Genet Metab; 2012 Jan 17; 105(1):132-40. PubMed ID: 22018727
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  • 10. Human wild-type alanine:glyoxylate aminotransferase and its naturally occurring G82E variant: functional properties and physiological implications.
    Cellini B, Bertoldi M, Montioli R, Paiardini A, Borri Voltattorni C.
    Biochem J; 2007 Nov 15; 408(1):39-50. PubMed ID: 17696873
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  • 12. Overexpression of human alanine:glyoxylate aminotransferase in Escherichia coli: renaturation from guanidine-HCl and affinity for pyridoxal phosphate co-factor.
    Coulter-Mackie MB, Lian Q, Wong SG.
    Protein Expr Purif; 2005 May 15; 41(1):18-26. PubMed ID: 15802217
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  • 17. Interaction of pyridoxal 5'-phosphate with tryptophan-139 at the subunit interface of dimeric D-amino acid transaminase.
    Martinez del Pozo A, van Ophem PW, Ringe D, Petsko G, Soda K, Manning JM.
    Biochemistry; 1996 Feb 20; 35(7):2112-6. PubMed ID: 8652553
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  • 19. Dimerization misalignment in human glutamate-oxaloacetate transaminase variants is the primary factor for PLP release.
    Lee J, Gokey T, Ting D, He ZH, Guliaev AB.
    PLoS One; 2018 Feb 20; 13(9):e0203889. PubMed ID: 30208107
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  • 20. Caenorhabditis elegans AGXT-1 is a mitochondrial and temperature-adapted ortholog of peroxisomal human AGT1: New insights into between-species divergence in glyoxylate metabolism.
    Mesa-Torres N, Calvo AC, Oppici E, Titelbaum N, Montioli R, Miranda-Vizuete A, Cellini B, Salido E, Pey AL.
    Biochim Biophys Acta; 2016 Sep 20; 1864(9):1195-1205. PubMed ID: 27179589
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