Studies on human erythrocyte nucleotide metabolism. II. Nonspherocytic hemolytic anemia, high red cell ATP, and ribosephosphate pyrophosphokinase (RPK, E.C.2.7.6.1) deficiency.

No abstract is available for this paper.

• Publication year

  1972

• Venue

  Blood

• Publication date

  1972-05-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1182/BLOOD.V39.5.674.674PMID 5022715
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Studies on human erythrocyte nucleotide metabolism. I. Monisotopic methodologies.

  1972cited by this paper
• Phosphoribosylpyrophosphate in man: biochemical and clinical significance.

  1971cited by this paper
• Adenylosuccinase activity in human and rabbit erythrocyte lysates.

  1970cited by this paper
• [Excessive erythrocyte ATP level feature of a hereditary nonspherocytic hemolytic anemia in disturbed ATP utilization and a red cell metabolic anomaly without disease value].

  1970cited by this paper
• Erythrocyte glyoxalase II deficiency with coincidental hereditary elliptocytosis.

  1970cited by this paper
• [Hereditary nonspherocytic hemolytic anemia with high erythrocyte ATP].

  1969cited by this paper
• Elevated AMP pyrophosphorylase activity in congenital IMP pyrophosphorylase deficiencey (Lesch-Nyhan disease).

  1969cited by this paper
• On a regulatory system of the adenine level in the plasma connected with red cell maturation and its effect on the adenine nucleotides of the circulating erythrocyte. Lack of relation between ATP-level and life span of the erythrocyte.

  1969cited by this paper
• Sodium-potssum tmulated ATPase activity of mammalian hemolysates: clinical observations and ominance of ATPase deficiency in the potassium polymorphism of sheep.

  1968cited by this paper
• Hereditary hemolytic anemia associated with glucosephosphate isomerase (GPI) deficiency--a new enzyme defect of human erythrocytes.

  1968cited by this paper
• Adenine phosphoribosyltransferase deficiency: a previously undescribed genetic defect in man.

  1968cited by this paper
• The adenylate kinase of human plasma, erythrocytes and platelets in relation to the degradation of adenosine diphosphate in plasma.

  1967cited by this paper
• Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase.

  1967cited by this paper
• Hereditary hemolytic anemia with hexokinase deficiency. Role of hexokinase in erythrocyte aging.

  1967cited by this paper
• Studies of in‐vitro Autohaemolysis in Blood from Newborn Infants

  1966cited by this paper
• Separation of rabbit red cells by density in a bovine serum albumin gradient and correlation of red cell density with cell age after in vivo labeling with 59Fe

  1966cited by this paper
• Studies on the metabolism of adenosine and adenine in stored and fresh human erythrocytes.

  1966cited by this paper
• Studies on erythrocyte glycolysis. I. Determination of the glycolytic intermediates in human erythrocytes.

  1965cited by this paper
• HEREDITARY HEMOLYTIC ANEMIA WITH TRIOSEPHOSPHATE ISOMERASE DEFICIENCY.

  1965cited by this paper
• Hereditary high ATP content of human erythrocytes.

  1965cited by this paper
• A NEW INHERITED ABNORMALITY OF HUMAN ERYTHROCYTES: ELEVATED ERYTHROCYTIC ADENOSINE TRIPHOSPHATE.

  1965cited by this paper
• STUDIES ON CHROMATED ERYTHROCYTES. EFFECT OF SODIUM CHROMATE ON ERYTHROCYTE GLUTATHIONE REDUCTASE.

  1964cited by this paper
• [D-2,3-DIPHOSPHOGLYCERATE-2-PHOSPHOHYDROLASE DEFICIENCY AS A POSSIBLE CAUSE OF INCREASED ATP LEVELS].

  1964cited by this paper
• THE DISTRIBUTION OF BUOYANT DENSITY OF HUMAN ERYTHROCYTES IN BOVINE ALBUMIN SOLUTIONS.

  1964cited by this paper
• Hereditary Heinz‐Body Anaemia

  1964cited by this paper
• STARCH-GEL ELECTROPHORESIS OF K-CASEIN.

  1964cited by this paper
• Improved method for the determination of blood glutathione.

  1963cited by this paper
• Enzymatic deficiencies of purine nucleotide synthesis in the human erythrocyte.

  1962cited by this paper
• Pyruvate kinase (PK) deficiency hereditary nonspherocytic hemolytic anemia.

  1962cited by this paper
• Transport of adenine-8-C14 among mouse tissues by blood cells.

  1959cited by this paper
• Erythrocyte metabolism. I. Purine nucleoside phosphorylase.

  1956cited by this paper
• Enzymatic synthesis of purine nucleotides.

  1955cited by this paper
• Autohemolysis and other changes resulting from the incubation in vitro of red cells from patients with congenital hemolytic anemia.

  1954cited by this paper
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  1951cited by this paper

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• The functional logic of cytosolic 5'-nucleotidases.

  2013cites this paper
• deficiency nucleotidase ' Genetic basis of hemolytic anemia caused by pyrimidine 5

  2013cites this paper
• AMPD3‐deficient mice exhibit increased erythrocyte ATP levels but anemia not improved due to PK deficiency

  2012influential citation
• Elevated levels of redox regulators, membrane‐bound globin chains, and cytoskeletal protein fragments in hereditary spherocytosis erythrocyte proteome

  2011cites this paper
• with pyrimidine nucleotidase deficiency Identification of cytidine diphosphodiesters in erythrocytes from a patient

  2011cites this paper
• Cytosolic 5′-nucleotidase III (NT5C3): gene sequence variation and functional genomics

  2009cites this paper
• Hereditary pyrimidine 5′‐nucleotidase deficiency: from genetics to clinical manifestations

  2006cites this paper
• Hereditary erythrocyte pyrimidine 5′-nucleotidase deficiency: A biochemical, genetic and clinical overview

  2006cites this paper
• A Family With Red Cell Pyrimidine Deficiency

  2005cites this paper
• Evidence for essential catalytic determinants for human erythrocyte pyrimidine 5′-nucleotidase

  2005cites this paper
• Pyrimidine 5'‐nucleotidase activities detected in real samples by means of micellar electrokinetic chromatography

  2004cites this paper
• Advances in hereditary red cell enzyme anomalies

  2004cites this paper
• Pyrimidine 5′ Nucleotidase Deficiency

  2003cites this paper
• Human erythrocyte pyrimidine 5'-nucleotidase, PN-I.

  2002cites this paper
• Genetic basis of hemolytic anemia caused by pyrimidine 5' nucleotidase deficiency.

  2001cites this paper
• Genetic basis of hemolytic anemia caused by pyrimidine 5 9 nucleotidase deficiency

  2001cites this paper
• Chronic non-spherocytic haemolytic anaemia due to congenital pyrimidine 5' nucleotidase deficiency: 25 years later.

  2000cites this paper
• Chronic non-spherocytic haemolytic anaemia due to congenital pyrimidine 5' nucleotidase deficiency: 25 years later.

  2000cites this paper
• Enhanced Activity of Pyrimidine 5′-Nucleotidase in Rat Red Blood Cells during Erythropoiesis

  1998cites this paper
• Guanine uptake by human erythrocytes.

  1991cites this paper
• Störungen des Pyrimidinstoffwechsels

  1990cites this paper
• Localization of human phosphoribosylpyrophosphate synthetase subunit I and II genes (PRPS1 and PRPS2) to different regions of the X chromosome and assignment of two PRPS1-related genes to autosomes

  1989cites this paper
• Pyrimidine nucleotides impair phosphoribosylpyrophosphate (PRPP) synthetase subunit aggregation by sequestering magnesium. A mechanism for the decreased PRPP synthetase activity in hereditary erythrocyte pyrimidine 5'-nucleotidase deficiency.

  1989cites this paper
• Erythrocyte pyrimidine 5'-nucleotidase and deoxynucleotidase isozymes: metallosensitivity and kinetics.

  1988cites this paper
• Identification of cytidine diphosphodiesters in erythrocytes from a patient with pyrimidine nucleotidase deficiency.

  1984cites this paper
• Erythrocyte nucleotide pattern in two children in a Norwegian family with pyrimidine 5'-nucleotidase deficiency.

  1983cites this paper
• Hereditary haemolytic anaemia due to red cell pyrimidine 5'-nucleotidase deficiency in two Irish families with a note on the benefit of splenectomy.

  1981cites this paper
• A case of hemolytic anemia due to erythrocyte pyrimidine 5'-nucleotidase deficiency.

  1981cites this paper
• Hereditary high-adenosine triphosphate syndrome: Study of a new variant

  1981cites this paper
• Hexokinase “New Hyde Park”: A low activity erythrocyte isozyme in a chinese kindred

  1981cites this paper
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  1981cites this paper
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  1980cites this paper
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  1980cites this paper
• Synthesis of phosphoribosylpyrophosphate in mammalian cells.

  1979cites this paper
• Pyrimidine metabolism in hereditary erythrocyte pyrimidine 5' nucleotidase deficiency.

  1978cites this paper
• Disorders of Purine and Pyrimidine Metabolism

  1978cites this paper
• Abnormalities of PRPP Metabolism Leading to an Overproduction of Uric Acid

  1978cites this paper
• Glycolytic intermediates and glutathione levels of erythrocyte: Comparisons between erythrocytes of humans and thoroughbred horses

  1977cites this paper
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  1977cites this paper
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  1977cites this paper
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  1977cites this paper
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  1977cites this paper
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  1976cites this paper
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  1976cites this paper
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  1976cites this paper
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  1975cites this paper
• Red cell enzymes.

  1975cites this paper
• Characteristics of a pyrimidine-specific 5'-nucleotidase in human erythrocytes.

  1975cites this paper
• Human phosphoribosylpyrophosphate synthetase. Comparison of purified normal and mutant enzymes.

  1975cites this paper
• [A modified method for phosphoribosyl pyrophosphate synthesis].

  1975cites this paper
• Metabolism in haemolytic states.

  1975cites this paper
• Chapter 29 – New Knowledge of Red Cell Purine and Pyrimidine Metabolism Coming from the Study of Human Disease

  1975cites this paper
• Evaluation of the role of 5-phosphoribosyl-alpha-1-pyrophosphate synthetase in congenital hyperuricemia and gout: a simple isotopic assay and an activity stain for the enzyme.

  1974cites this paper
• Hypouricemic, mentally retarded infant with a defect of 5-phosphoribosyl-1-pyrophosphate synthetase of erythrocytes.

  1974cites this paper
• Hemolysis in the newborn infant resulting from deficiencies of red blood cell enzymes: diagnosis and management.

  1974cites this paper
• Hereditary hemolytic anemia with human erythrocyte pyrimidine 5'-nucleotidase deficiency.

  1974influential citation
• Chapter 9 – General Red Cell Metabolism

  1974cites this paper
• Observations of altered intracellular phosphoribosylpyrophosphate (PP-ribose-P) in human disease.

  1974cites this paper
• Enzymology of gout.

  1974cites this paper
• Maternal medication and its effect on the fetus.

  1973cites this paper
• Decreased gamma-glutamylcysteine synthetase: the probable cause of glutathione deficiency in sheep erythrocytes.

  1973cites this paper
• Congenital hemolytic anemias and red cell enzyme deficiencies.

  1973cites this paper
• Nonspherocytic Haemolytic Anaemia with Increased Red Cell Adenine Nucleotides, Glutathione and Basophilic Stippling and Ribosephosphate Pyrophosphokinase (RPK) Deficiency: Studies on Two New Kindreds

  1973cites this paper
• Studies on human erythrocyte nucleotide metabolism. I. Monisotopic methodologies.

  1972cites this paper
• Disorders due to enzyme defects in the red blood cell.

  1972cites this paper