242 related articles for article (PubMed ID: 12737622)
41. Allele-specific characterization of alanine: glyoxylate aminotransferase variants associated with primary hyperoxaluria.
Lage MD; Pittman AM; Roncador A; Cellini B; Tucker CL
PLoS One; 2014; 9(4):e94338. PubMed ID: 24718375
[TBL] [Abstract][Full Text] [Related]
42. S81L and G170R mutations causing Primary Hyperoxaluria type I in homozygosis and heterozygosis: an example of positive interallelic complementation.
Montioli R; Roncador A; Oppici E; Mandrile G; Giachino DF; Cellini B; Borri Voltattorni C
Hum Mol Genet; 2014 Nov; 23(22):5998-6007. PubMed ID: 24990153
[TBL] [Abstract][Full Text] [Related]
43. The N-terminal extension is essential for the formation of the active dimeric structure of liver peroxisomal alanine:glyoxylate aminotransferase.
Montioli R; Fargue S; Lewin J; Zamparelli C; Danpure CJ; Borri Voltattorni C; Cellini B
Int J Biochem Cell Biol; 2012 Mar; 44(3):536-46. PubMed ID: 22198249
[TBL] [Abstract][Full Text] [Related]
44. Novel mutations of the AGXT gene causing primary hyperoxaluria type 1.
Yuen YP; Lai CK; Tong GM; Wong PN; Wong FK; Mak SK; Lo KY; Wong AK; Tong SF; Chan YW; Lam CW
J Nephrol; 2004; 17(3):436-40. PubMed ID: 15365967
[TBL] [Abstract][Full Text] [Related]
45. Molecular etiology of primary hyperoxaluria type 1: new directions for treatment.
Danpure CJ
Am J Nephrol; 2005; 25(3):303-10. PubMed ID: 15961951
[TBL] [Abstract][Full Text] [Related]
46. Molecular aetiology of primary hyperoxaluria type 1.
Danpure CJ
Nephron Exp Nephrol; 2004; 98(2):e39-44. PubMed ID: 15499210
[TBL] [Abstract][Full Text] [Related]
47. 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; 10(10):2227-36. PubMed ID: 26161999
[TBL] [Abstract][Full Text] [Related]
48. Identification of 5 novel mutations in the AGXT gene.
Basmaison O; Rolland MO; Cochat P; Bozon D
Hum Mutat; 2000 Jun; 15(6):577. PubMed ID: 10862087
[TBL] [Abstract][Full Text] [Related]
49. Crystal structure of alanine:glyoxylate aminotransferase and the relationship between genotype and enzymatic phenotype in primary hyperoxaluria type 1.
Zhang X; Roe SM; Hou Y; Bartlam M; Rao Z; Pearl LH; Danpure CJ
J Mol Biol; 2003 Aug; 331(3):643-52. PubMed ID: 12899834
[TBL] [Abstract][Full Text] [Related]
50. [Primary hiperoxaluria: a new mutation in gen AGXT (R197Q) cause of neonatal convulsions].
Guevara-Campos J; Riverol D; González-Guevara L; Tinedo R
Invest Clin; 2008 Dec; 49(4):553-60. PubMed ID: 19245173
[TBL] [Abstract][Full Text] [Related]
51. Partial deletion of the AGXT gene (EX1_EX7del): A new genotype in hyperoxaluria type 1.
Nogueira PK; Vuong TS; Bouton O; Maillard A; Marchand M; Rolland MO; Cochat P; Bozon D
Hum Mutat; 2000 Apr; 15(4):384-5. PubMed ID: 10737993
[TBL] [Abstract][Full Text] [Related]
52. A glycine-to-glutamate substitution abolishes alanine:glyoxylate aminotransferase catalytic activity in a subset of patients with primary hyperoxaluria type 1.
Purdue PE; Lumb MJ; Allsop J; Minatogawa Y; Danpure CJ
Genomics; 1992 May; 13(1):215-8. PubMed ID: 1349575
[TBL] [Abstract][Full Text] [Related]
53. Use of polymer conjugates for the intraperoxisomal delivery of engineered human alanine:glyoxylate aminotransferase as a protein therapy for primary hyperoxaluria type I.
Roncador A; Oppici E; Talelli M; Pariente AN; Donini M; Dusi S; Voltattorni CB; Vicent MJ; Cellini B
Nanomedicine; 2017 Apr; 13(3):897-907. PubMed ID: 27993722
[TBL] [Abstract][Full Text] [Related]
54. Reconstruction of human hepatocyte glyoxylate metabolic pathways in stably transformed Chinese-hamster ovary cells.
Behnam JT; Williams EL; Brink S; Rumsby G; Danpure CJ
Biochem J; 2006 Mar; 394(Pt 2):409-16. PubMed ID: 16309382
[TBL] [Abstract][Full Text] [Related]
55. The AGT gene in Africa: a distinctive minor allele haplotype, a polymorphism (V326I), and a novel PH1 mutation (A112D) in Black Africans.
Coulter-Mackie MB; Tung A; Henderson HE; Toone JR; Applegarth DA
Mol Genet Metab; 2003 Jan; 78(1):44-50. PubMed ID: 12559847
[TBL] [Abstract][Full Text] [Related]
56. 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; 277(22):4766-74. PubMed ID: 20977670
[TBL] [Abstract][Full Text] [Related]
57. 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; 1864(9):1195-1205. PubMed ID: 27179589
[TBL] [Abstract][Full Text] [Related]
58. Primary hyperoxalurias: disorders of glyoxylate detoxification.
Salido E; Pey AL; Rodriguez R; Lorenzo V
Biochim Biophys Acta; 2012 Sep; 1822(9):1453-64. PubMed ID: 22446032
[TBL] [Abstract][Full Text] [Related]
59. Protein homeostasis defects of alanine-glyoxylate aminotransferase: new therapeutic strategies in primary hyperoxaluria type I.
Pey AL; Albert A; Salido E
Biomed Res Int; 2013; 2013():687658. PubMed ID: 23956997
[TBL] [Abstract][Full Text] [Related]
60. Evolution of alanine:glyoxylate aminotransferase intracellular targeting: structural and functional analysis of the guinea pig gene.
Birdsey GM; Danpure CJ
Biochem J; 1998 Apr; 331 ( Pt 1)(Pt 1):49-60. PubMed ID: 9512461
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]