GGT by Pubmed references

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2008 Mitsunori Ikeda Biol. Pharm. Bull. Characterization of peroxisomal targeting signals on alanine: glyoxylate aminotransferase.[Pubmed]
2008 Mariarita Bertoldi Biochim. Biophys. Acta Reactions of human liver peroxisomal alanine:glyoxylate aminotransferase with beta-chloro-L-alanine and L-cysteine: spectroscopic and kinetic analysis.[Pubmed]
2006 Danpure Danpure Biochim. Biophys. Acta Primary hyperoxaluria type 1: AGT mistargeting highlights the fundamental differences between the peroxisomal and mitochondrial protein import pathways.[Pubmed]
2006 Marinus Groothoff Mol. Genet. Metab. High incidence of hyperoxaluria in generalized peroxisomal disorders.[Pubmed]
2006 Yang Salido Proc. Natl. Acad. Sci. U.S.A. Alanine-glyoxylate aminotransferase-deficient mice, a model for primary hyperoxaluria that responds to adenoviral gene transfer.[Pubmed]
2005 Huber Huber J. Biol. Chem. Peroxisomal import of human alanine:glyoxylate aminotransferase requires ancillary targeting information remote from its C terminus.[Pubmed]
2004 Danpure Danpure Nephron Exp. Nephrol. Molecular aetiology of primary hyperoxaluria type 1.[Pubmed]
2004 Caldwell Caldwell Hum. Genet. Diet and the frequency of the alanine:glyoxylate aminotransferase Pro11Leu polymorphism in different human populations.[Pubmed]
2004 Martha Baker Am. J. Physiol., Cell Physiol. Glycolate and glyoxylate metabolism in HepG2 cells.[Pubmed]
2004 Gill Danpure Molecular aetiology of primary hyperoxaluria and its implications for clinical management.[Pubmed]
2003 Daisuke Igarashi Plant J. Identification of photorespiratory glutamate:glyoxylate aminotransferase (GGAT) gene in Arabidopsis.[Pubmed]
2003 Liepman Liepman Plant Physiol. Alanine aminotransferase homologs catalyze the glutamate:glyoxylate aminotransferase reaction in peroxisomes of Arabidopsis.[Pubmed]
2003 Xiaoxuan Zhang J. Mol. Biol. Crystal structure of alanine:glyoxylate aminotransferase and the relationship between genotype and enzymatic phenotype in primary hyperoxaluria type 1.[Pubmed]
2003 Tatsuya Takayama J. Am. Soc. Nephrol. Control of oxalate formation from L-hydroxyproline in liver mitochondria.[Pubmed]
2003 A Santana Proc. Natl. Acad. Sci. U.S.A. Primary hyperoxaluria type 1 in the Canary Islands: a conformational disease due to I244T mutation in the P11L-containing alanine:glyoxylate aminotransferase.[Pubmed]
2003 Lumb Lumb Biochem. J. Correction of an enzyme trafficking defect in hereditary kidney stone disease in vitro.[Pubmed]
2003 Xiaoxuan Danpure Biochim. Biophys. Acta Alanine:glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting in human hereditary kidney stone disease.[Pubmed]
2002 Youichiro Fukao Plant Cell Physiol. Proteomic analysis of leaf peroxisomal proteins in greening cotyledons of Arabidopsis thaliana.[Pubmed]
2002 Holbrook Holbrook J. Biol. Chem. Molecular basis for the dual mitochondrial and cytosolic localization of alanine:glyoxylate aminotransferase in amphibian liver cells.[Pubmed]
2001 Liepman Liepman Plant J. Peroxisomal alanine : glyoxylate aminotransferase (AGT1) is a photorespiratory enzyme with multiple substrates in Arabidopsis thaliana.[Pubmed]
2000 Knott Knott Biochem. J. The peroxisomal targeting sequence type 1 receptor, Pex5p, and the peroxisomal import efficiency of alanine:glyoxylate aminotransferase.[Pubmed]
2000 T Oda Cell Biochem. Biophys. Peroxisomal and mitochondrial targeting of serine:pyruvate/alanine:glyoxylate aminotransferase in rat liver.[Pubmed]
2000 T Oda J. Biochem. Mitochondrial targeting signal-induced conformational change and repression of the peroxisomal targeting signal of the precursor for rat liver serine:pyruvate/alanine:glyoxylate aminotransferase.[Pubmed]
2000 Lumb Lumb J. Biol. Chem. Functional synergism between the most common polymorphism in human alanine:glyoxylate aminotransferase and four of the most common disease-causing mutations.[Pubmed]
2000 I Kerckaert Virchows Arch. Hepatic peroxisomes in isolated hyperpipecolic acidaemia: evidence supporting its classification as a single peroxisomal enzyme deficiency.[Pubmed]
1999 T Xue J. Biol. Chem. Flux of the L-serine metabolism in rabbit, human, and dog livers. Substantial contributions of both mitochondrial and peroxisomal serine:pyruvate/alanine:glyoxylate aminotransferase.[Pubmed]
1999 Lumb Lumb J. Biol. Chem. Effect of N-terminal alpha-helix formation on the dimerization and intracellular targeting of alanine:glyoxylate aminotransferase.[Pubmed]
1998 Birdsey Birdsey Biochem. J. Evolution of alanine:glyoxylate aminotransferase intracellular targeting: structural and functional analysis of the guinea pig gene.[Pubmed]
1997 Leiper Leiper Clin. Chim. Acta A unique molecular basis for enzyme mistargeting in primary hyperoxaluria type 1.[Pubmed]
1997 Danpure Danpure Bioessays Variable peroxisomal and mitochondrial targeting of alanine: glyoxylate aminotransferase in mammalian evolution and disease.[Pubmed]
1997 M Espeel Microsc. Res. Tech. Biogenesis of peroxisomes in fetal liver.[Pubmed]
1996 Oatey Oatey Ann. N. Y. Acad. Sci. Context dependency of the PTS1 motif in human alanine: glyoxylate aminotransferase 1.[Pubmed]
1996 K Lhotta Nephrol. Dial. Transplant. Primary hyperoxaluria type 1 caused by peroxisome-to-mitochondrion mistargeting of alanine: glyoxylate aminotransferase.[Pubmed]
1996 Leiper Leiper J. Cell Biol. Inhibition of alanine:glyoxylate aminotransferase 1 dimerization is a prerequisite for its peroxisome-to-mitochondrion mistargeting in primary hyperoxaluria type 1.[Pubmed]
1996 C Eyskens Kidney Int. Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: a novel type of primary hyperoxaluria.[Pubmed]
1996 Oatey Oatey Eur. J. Biochem. Molecular basis of the variable mitochondrial and peroxisomal localisation of alanine-glyoxylate aminotransferase.[Pubmed]
1996 T Oda Biochem. Biophys. Res. Commun. In vitro association with peroxisomes and conformational change of peroxisomal serine:pyruvate/alanine:glyoxylate aminotransferase in rat and human livers.[Pubmed]
1995 T Funai J. Biochem. Fidelity of translation initiation of mRNA for the precursor of rat mitochondrial serine:pyruvate/alanine:glyoxylate aminotransferase.[Pubmed]
1995 A Motley J. Cell Biol. Mammalian alanine/glyoxylate aminotransferase 1 is imported into peroxisomes via the PTS1 translocation pathway. Increased degeneracy and context specificity of the mammalian PTS1 motif and implications for the peroxisome-to-mitochondrion mistargeting of AGT in primary hyperoxaluria type 1.[Pubmed]
1995 M Espeel J. Inherit. Metab. Dis. Immunocytochemical localization of peroxisomal proteins in human liver and kidney.[Pubmed]
1995 Danpure Danpure Nephrol. Dial. Transplant. Advances in the enzymology and molecular genetics of primary hyperoxaluria type 1. Prospects for gene therapy.[Pubmed]
1994 Lumb Lumb Eur. J. Biochem. Molecular evolution of alanine/glyoxylate aminotransferase 1 intracellular targeting. Analysis of the feline gene.[Pubmed]
1994 H Mandel J. Pediatr. A new type of peroxisomal disorder with variable expression in liver and fibroblasts.[Pubmed]
1994 M Schrader Eur. J. Cell Biol. Heterogeneity of peroxisomes in human hepatoblastoma cell line HepG2. Evidence of distinct subpopulations.[Pubmed]
1994 G Danpure Hum. Genet. Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine:glyoxylate aminotransferase gene.[Pubmed]
1994 P Danpure J. Inherit. Metab. Dis. Primary hyperoxaluria type 1: genotypic and phenotypic heterogeneity.[Pubmed]
1993 K Nishiyama J. Cell Biol. ATP-dependent degradation of a mutant serine: pyruvate/alanine:glyoxylate aminotransferase in a primary hyperoxaluria type 1 case.[Pubmed]
1993 P Danpure Am. J. Hum. Genet. Enzymological and mutational analysis of a complex primary hyperoxaluria type 1 phenotype involving alanine:glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting and intraperoxisomal aggregation.[Pubmed]
1993 Danpure Danpure Biochimie Primary hyperoxaluria type 1 and peroxisome-to-mitochondrion mistargeting of alanine:glyoxylate aminotransferase.[Pubmed]
1992 Purdue Purdue Eur. J. Biochem. Molecular evolution of alanine/glyoxylate aminotransferase 1 intracellular targeting. Analysis of the marmoset and rabbit genes.[Pubmed]
1992 A Katz Kidney Int. Success of kidney transplantation in oxalosis is unrelated to residual hepatic enzyme activity.[Pubmed]
1992 Watts Watts Adv. Enzyme Regul. Alanine glyoxylate aminotransferase deficiency: biochemical and molecular genetic lessons from the study of a human disease.[Pubmed]
1991 Wilson Wilson Biochem. Med. Metab. Biol. Structure-function relationships in the peroxisome: implications for human disease.[Pubmed]
1991 J Purdue Hum. Genet. An intronic duplication in the alanine: glyoxylate aminotransferase gene facilitates identification of mutations in compound heterozygote patients with primary hyperoxaluria type 1.[Pubmed]
1991 Danpure Danpure Am. J. Kidney Dis. Molecular and clinical heterogeneity in primary hyperoxaluria type 1.[Pubmed]
1990 T Ogawa J. Biol. Chem. Dimethylarginine:pyruvate aminotransferase in rats. Purification, properties, and identity with alanine:glyoxylate aminotransferase 2.[Pubmed]
1990 Y Takada Biochem. J. Human peroxisomal L-alanine: glyoxylate aminotransferase. Evolutionary loss of a mitochondrial targeting signal by point mutation of the initiation codon.[Pubmed]
1990 S Hayashi Biochem. Biophys. Res. Commun. Alanine: glyoxylate aminotransferase 1 is present in the peroxisomes of guinea pig kidney.[Pubmed]
1990 P Danpure J. Cell. Sci. Subcellular distribution of hepatic alanine:glyoxylate aminotransferase in various mammalian species.[Pubmed]
1990 Y Purdue J. Cell Biol. Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1.[Pubmed]
1988 Cooper Cooper J. Histochem. Cytochem. Immunocytochemical localization of human hepatic alanine: glyoxylate aminotransferase in control subjects and patients with primary hyperoxaluria type 1.[Pubmed]
1987 Wise Wise FEBS Lett. Immunological heterogeneity of hepatic alanine:glyoxylate aminotransferase in primary hyperoxaluria type 1.[Pubmed]
1987 R Wanders Clin. Chim. Acta Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndrome.[Pubmed]
1984 Y Takada Arch. Biochem. Biophys. The effect of vitamin B6 deficiency on alanine: glyoxylate aminotransferase isoenzymes in rat liver.[Pubmed]
1983 Titus Titus Plant Physiol. Purification and Characterization of Hydroxypyruvate Reductase from Cucumber Cotyledons.[Pubmed]
1982 Y Takada Comp. Biochem. Physiol., B Subcellular distribution, and physical and immunological properties of hepatic alanine: glyoxylate aminotransferase isoenzymes in different mammalian species.[Pubmed]
1978 T Noguchi Biochem. J. Purification and properties of peroxisomal pyruvate (glyoxylate) aminotransferase from rat liver.[Pubmed]
1978 T Noguchi Biochem. J. Subcellular distribution of pyruvate (glyoxylate) aminotransferases in rat liver.[Pubmed]
1976 B Hsieh J. Biol. Chem. Glyoxylate aminotransferase in peroxisomes from rat liver and kidney.[Pubmed]
0 J. Nephrol. The molecular basis of alanine: glyoxylate aminotransferase mistargeting: the most common single cause of primary hyperoxaluria type 1.[Pubmed]
0 Ultrastruct Pathol Cytoplasmic catalase and ghostlike peroxisomes in the liver from a child with atypical chondrodysplasia punctata.[Pubmed]
0 Am. J. Nephrol. Cellular transfection to deliver alanine-glyoxylate aminotransferase to hepatocytes: a rational gene therapy for primary hyperoxaluria-1 (PH-1).[Pubmed]
0 Mol. Genet. Metab. Genetic heterogeneity in primary hyperoxaluria type 1: impact on diagnosis.[Pubmed]