| YEAR | FIRST AUTHOR | JOURNAL | TITLE |
|---|---|---|---|
| 2009 | Barbara Cellini | J. Biol. Chem. | Molecular Insight into the Synergism between the Minor Allele of Human Liver Peroxisomal Alanine:Glyoxylate Aminotransferase and the F152I Mutation.[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] |
| 2008 | Barbara Cellini | Protein Pept. Lett. | Construction, purification and characterization of untagged human liver alanine-glyoxylate aminotransferase expressed in Escherichia coli.[Pubmed] |
| 2008 | Mitsunori Ikeda | Biol. Pharm. Bull. | Characterization of peroxisomal targeting signals on alanine: glyoxylate aminotransferase.[Pubmed] |
| 2008 | Stefan Timm | Plant Cell | A cytosolic pathway for the conversion of hydroxypyruvate to glycerate during photorespiration in Arabidopsis.[Pubmed] |
| 2008 | Itsara Cousins | Plant Physiol. | Peroxisomal malate dehydrogenase is not essential for photorespiration in Arabidopsis but its absence causes an increase in the stoichiometry of photorespiratory CO2 release.[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] |
| 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] |
| 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 | Lumb Lumb | Biochem. J. | Correction of an enzyme trafficking defect in hereditary kidney stone disease in vitro.[Pubmed] |
| 2003 | Daisuke Igarashi | Plant J. | Identification of photorespiratory glutamate:glyoxylate aminotransferase (GGAT) gene in Arabidopsis.[Pubmed] |
| 2003 | Xiaoxuan Danpure | Biochim. Biophys. Acta | Alanine:glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting in human hereditary kidney stone disease.[Pubmed] |
| 2003 | Liepman Liepman | Plant Physiol. | Alanine aminotransferase homologs catalyze the glutamate:glyoxylate aminotransferase reaction in peroxisomes of Arabidopsis.[Pubmed] |
| 2003 | Tatsuya Takayama | J. Am. Soc. Nephrol. | Control of oxalate formation from L-hydroxyproline in liver mitochondria.[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 | 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] |
| 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] |
| 2002 | Takuji Mizuno | Histochem. Cell Biol. | Analyses in transfected cells and in vitro of a putative peroxisomal targeting signal of rat liver serine:pyruvate aminotransferase.[Pubmed] |
| 2001 | Liepman Liepman | Plant J. | Peroxisomal alanine : glyoxylate aminotransferase (AGT1) is a photorespiratory enzyme with multiple substrates in Arabidopsis thaliana.[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 | T Oda | Cell Biochem. Biophys. | Peroxisomal and mitochondrial targeting of serine:pyruvate/alanine:glyoxylate aminotransferase in rat liver.[Pubmed] |
| 2000 | I Kerckaert | Virchows Arch. | Hepatic peroxisomes in isolated hyperpipecolic acidaemia: evidence supporting its classification as a single peroxisomal enzyme deficiency.[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 | S Mano | Cell Biochem. Biophys. | A leaf-peroxisomal protein, hydroxypyruvate reductase, is produced by light-regulated alternative splicing.[Pubmed] |
| 2000 | Knott Knott | Biochem. J. | The peroxisomal targeting sequence type 1 receptor, Pex5p, and the peroxisomal import efficiency of 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] |
| 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 | S Mano | Plant J. | Light regulates alternative splicing of hydroxypyruvate reductase in pumpkin.[Pubmed] |
| 1998 | Birdsey Birdsey | Biochem. J. | Evolution of alanine:glyoxylate aminotransferase intracellular targeting: structural and functional analysis of the guinea pig gene.[Pubmed] |
| 1997 | M Espeel | Microsc. Res. Tech. | Biogenesis of peroxisomes in fetal liver.[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 | S Mano | Plant Cell Physiol. | Hydroxypyruvate reductase with a carboxy-terminal targeting signal to microbodies is expressed in Arabidopsis.[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 | 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] |
| 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] |
| 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 | 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] |
| 1994 | Lumb Lumb | Eur. J. Biochem. | Molecular evolution of alanine/glyoxylate aminotransferase 1 intracellular targeting. Analysis of the feline gene.[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] |
| 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] |
| 1992 | A Katz | Kidney Int. | Success of kidney transplantation in oxalosis is unrelated to residual hepatic enzyme activity.[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 | 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 | S Yokota | Histochemistry | Immunocytochemical localization of serine: pyruvate aminotransferase in peroxisomes of the human liver parenchymal cells.[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] |
| 1987 | A Schutgens | Enzyme | Genetic diseases caused by peroxisomal dysfunction. New findings in clinical and biochemical studies.[Pubmed] |
| 1987 | Wise Wise | FEBS Lett. | Immunological heterogeneity of hepatic alanine:glyoxylate aminotransferase in primary hyperoxaluria type 1.[Pubmed] |
| 1985 | S Yokota | Histochemistry | Immunocytochemical demonstration of serine: pyruvate amino-transferase in peroxisomes and mitochondria of rat kidney.[Pubmed] |
| 1984 | Y Takada | Arch. Biochem. Biophys. | The effect of vitamin B6 deficiency on alanine: glyoxylate aminotransferase isoenzymes in rat liver.[Pubmed] |
| 1984 | S Yokota | Histochemistry | Fine localization of serine:pyruvate aminotransferase in rat hepatocytes revealed by a post-embedding immunocytochemical technique.[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 | J. Biol. Chem. | Peroxisomal localization of serine:pyruvate aminotransferase in human 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 | Mol. Genet. Metab. | Genetic heterogeneity in primary hyperoxaluria type 1: impact on diagnosis.[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] |