Published in Plant Physiol on November 01, 1982
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In vivo metabolism of 5'-methylthioadenosine in lemna. Plant Physiol (1983) 1.24
Threonine Synthase of Lemna paucicostata Hegelm. 6746. Plant Physiol (1984) 1.20
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Lemna paucicostata Hegelm. 6746: DEVELOPMENT OF STANDARDIZED GROWTH CONDITIONS SUITABLE FOR BIOCHEMICAL EXPERIMENTATION. Plant Physiol (1980) 2.76
Sulfur-containing Compounds in Lemna perpusilla 6746 Grown at a Range of Sulfate Concentrations. Plant Physiol (1978) 2.35
Methionine biosynthesis in lemna: inhibitor studies. Plant Physiol (1982) 2.22
Methionine Biosynthesis in Lemna: STUDIES ON THE REGULATION OF CYSTATHIONINE gamma-SYNTHASE, O-PHOSPHOHOMOSERINE SULFHYDRYLASE, AND O-ACETYLSERINE SULFHYDRYLASE. Plant Physiol (1982) 2.06
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Homocysteine biosynthesis in green plants. Physiological importance of the transsulfuration pathway in Chlorella sorokiniana growing under steady state conditions with limiting sulfate. J Biol Chem (1978) 2.42
Sulfur-containing Compounds in Lemna perpusilla 6746 Grown at a Range of Sulfate Concentrations. Plant Physiol (1978) 2.35
Methionine biosynthesis in lemna: inhibitor studies. Plant Physiol (1982) 2.22
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Homocysteine biosynthesis in green plants. O-Phosphorylhomoserine as the physiological substrate for cystathionine gamma-synthase. J Biol Chem (1974) 1.85
Folate-responsive homocystinuria and "schizophrenia". A defect in methylation due to deficient 5,10-methylenetetrahydrofolate reductase activity. N Engl J Med (1975) 1.83
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Homocystinuria associated with decreased methylenetetrahydrofolate reductase activity. Biochem Biophys Res Commun (1972) 1.79
Enzymes of phosphatidylcholine synthesis in lemna, soybean, and carrot. Plant Physiol (1988) 1.73
Responses of Sulfur-Containing Compounds in Lemna paucicostata Hegelm. 6746 to Changes in Availability of Sulfur Sources. Plant Physiol (1984) 1.69
Consensus nomenclature for the mammalian methionine adenosyltransferase genes and gene products. Trends Genet (1997) 1.67
Homocysteine biosynthesis in green plants: studies of the homocysteine-forming sulfhydrylase. J Biol Chem (1977) 1.64
Methionine methyl group metabolism in lemna. Plant Physiol (1986) 1.64
Uptake of Amino Acids and Other Organic Compounds by Lemna paucicostata Hegelm. 6746. Plant Physiol (1985) 1.62
Phosphoethanolamine bases as intermediates in phosphatidylcholine synthesis by lemna. Plant Physiol (1986) 1.62
The S-Methylmethionine Cycle in Lemna paucicostata. Plant Physiol (1990) 1.57
A study of cardiovascular risk in heterozygotes for homocystinuria. Am J Hum Genet (1981) 1.54
Sulfate Uptake and Its Regulation in Lemna paucicostata Hegelm. 6746. Plant Physiol (1984) 1.53
Trans-sulfuration in mammals. The methionine-sparing effect of cystine. J Biol Chem (1967) 1.52
Phosphatidylcholine synthesis: differing patterns in soybean and carrot. Plant Physiol (1988) 1.50
Recycling of methionine sulfur in a higher plant by two pathways characterized by either loss or retention of the 4-carbon moiety. Biochem Biophys Res Commun (1981) 1.47
In vivo regulation of de novo methionine biosynthesis in a higher plant (lemna). Plant Physiol (1985) 1.45
Regulatory Structure of the Biosynthetic Pathway for the Aspartate Family of Amino Acids in Lemna paucicostata Hegelm. 6746, with Special Reference to the Role of Aspartokinase. Plant Physiol (1989) 1.44
Glycine N -methyltransferase deficiency: a new patient with a novel mutation. J Inherit Metab Dis (2003) 1.44
Homocystinuria due to cystathionine synthase deficiency: the effect of pyridoxine. J Clin Invest (1970) 1.43
Synthesis of methylated ethanolamine moieties: regulation by choline in lemna. Plant Physiol (1989) 1.40
Homocystinuria: studies in tissue culture. Pediatr Res (1973) 1.39
Synthesis of methylated ethanolamine moieties: regulation by choline in soybean and carrot. Plant Physiol (1989) 1.38
Lemna paucicostata Hegelm. 6746: LIFE CYCLE AND CHARACTERIZATION OF THE COLONY TYPES IN A POPULATION. Plant Physiol (1980) 1.36
Homoserine esterification in green plants. Plant Physiol (1974) 1.35
Labile methyl group balances in the human: the role of sarcosine. Metabolism (1980) 1.34
A derangement in B12 metabolism associated with homocystinemia, cystathioninemia, hypomethioninemia and methylmalonic aciduria. Am J Med (1970) 1.28
Defective metabolism of vitamin B 12 in fibroblasts from children with methylmalonicaciduria. Biochem Biophys Res Commun (1971) 1.28
Pyridoxine-responsive genetic disease. Fed Proc (1971) 1.28
In vivo metabolism of 5'-methylthioadenosine in lemna. Plant Physiol (1983) 1.24
Homocysteine Biosynthesis in Green Plants: Physiological Importance of the Transsulfuration Pathway in Lemna paucicostata. Plant Physiol (1981) 1.24
Sulfite oxidase deficiency in man: demonstration of the enzymatic defect. Science (1967) 1.23
Synthesis of homocysteine and cysteine by enzyme extracts of spinach. Biochem Biophys Res Commun (1967) 1.23
Phytostat for the growth of lemna in semicontinuous culture with low sulfate. Plant Physiol (1978) 1.20
Threonine Synthase of Lemna paucicostata Hegelm. 6746. Plant Physiol (1984) 1.20
Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency. J Clin Invest (1996) 1.18
Uptake of Choline and Ethanolamine by Lemna paucicostata Hegelm. 6746. Plant Physiol (1986) 1.17
Deranged B 12 metabolism: studies of fibroblasts grown in tissue culture. Biochem Med (1970) 1.17
Homocystinuria due to cystathionine synthase deficiency. Studies of nitrogen balance and sulfur excretion. J Clin Invest (1975) 1.15
Enzymatic synthesis of cystathionine by extracts of spinach, requiring O-acetylhomoserine or O-succinylhomoserine. Biochem Biophys Res Commun (1966) 1.15
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Sulfuration of O-acetylhomoserine and O-acetylserine by two enzyme fractions from spinach. Biochem Biophys Res Commun (1968) 1.14
In Vivo Regulation of Threonine and Isoleucine Biosynthesis in Lemna paucicostata Hegelm. 6746. Plant Physiol (1988) 1.12
Homocystinuria with methylmalonic aciduria: two cases in a sibship. Biochem Med (1970) 1.11
Transsulfuration in an adult with hepatic methionine adenosyltransferase deficiency. J Clin Invest (1988) 1.11
Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene. Am J Hum Genet (1997) 1.10
Synthesis of Ethanolamine and Its Regulation in Lemna paucicostata. Plant Physiol (1989) 1.10
Molecular mechanisms of an inborn error of methionine pathway. Methionine adenosyltransferase deficiency. J Clin Invest (1995) 1.05
Effects of Orthophosphate and Adenosine 5'-Phosphate on Threonine Synthase and Cystathionine gamma-Synthate of Lemna paucicostata Hegelm. 6746. Plant Physiol (1986) 1.04
S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapy. J Inherit Metab Dis (2005) 1.03
S-adenosylhomocysteine hydrolase deficiency in a 26-year-old man. J Inherit Metab Dis (2006) 1.03
Biochemical basis for the dominant inheritance of hypermethioninemia associated with the R264H mutation of the MAT1A gene. A monomeric methionine adenosyltransferase with tripolyphosphatase activity. J Biol Chem (2001) 1.00
Deranged B 12 metabolism: effects on sulfur amino acid metabolism. Biochem Med (1970) 1.00
Vascular disease and homocysteine metabolism. N Engl J Med (1985) 0.97
Hypermethioninaemia due to methionine adenosyltransferase I/III (MAT I/III) deficiency: diagnosis in an expanded neonatal screening programme. J Inherit Metab Dis (2008) 0.96
Mental retardation, megaloblastic anaemia, methylmalonic aciduria and abnormal homocysteine metabolism due to an error in vitamin B12 metabolism. Clin Sci Mol Med (1974) 0.96
Deficiencies of cystathionase and homoserine dehydratase activities in cystathioninuria. Proc Natl Acad Sci U S A (1966) 0.95
Adaptation of Lemna paucicostata to Sublethal Methionine Deprivation. Plant Physiol (1983) 0.94
Cobalamins in fibroblasts cultured from normal control subjects and patients with methylmalonic aciduria. Pediatr Res (1976) 0.93
Hepatic methionine adenosyltransferase deficiency in a 31-year-old man. Am J Hum Genet (1987) 0.93
Aspartokinase of Lemna paucicostata Hegelm. 6746. Plant Physiol (1989) 0.90
Persistent hypermethioninaemia with dominant inheritance. J Inherit Metab Dis (1992) 0.87
Plasma homocyst(e)ine or homocysteine? N Engl J Med (1995) 0.86
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Methionine transamination in patients with homocystinuria due to cystathionine beta-synthase deficiency. Metabolism (2000) 0.85
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