199 results on '"Valentine, W. N."'
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2. Syndromes with Increased Red Cell Glutathione (GSH).
3. Erythrocyte Disorders of Purine and Pyrimidine Metabolism.
4. Erythrocyte pyruvate kinase (PK): The variable significance of 'nucleotide specificity' in the characterization of mutant variants.
5. International Committee for Standardization in Haematology: Recommended Methods for Red-Cell Enzyme Analysis.
6. Simultaneous Inheritance of Mutant Isoenzymes of Erythrocyte Pyruvate Kinase Associated with Chronic Haemolytic Anaemia.
7. The hereditary hemolytic anemias: recent concepts and developments.
8. Red Cell Enzyme Deficiencies as a Cause of Hemolytic Disorders.
9. The Leukocytes and the Leukopathies.
10. Erythrocyte Enzymatic Abnormalities in HEMPAS (Hereditary Erythroblastic Multinuclearity with a Positive Acidified-Serum Test).
11. Studies on Chromated Erythrocytes. MECHANISMS OF CHROMATE INHIBITION OF GLUTATHIONE REDUCTASE.
12. Human Leucocyte Arylsulphatase Activity.
13. Adenine ribo- and deoxyribonucleotide metabolism in human erythrocytes, B- and T-lymphocyte cell lines, and monocyte-macrophages.
14. Molecular lesion affecting the ADP-combining site in a mutant isozyme of erythrocyte pyruvate kinase.
15. Selective accumulation of cytosol CDP-choline as an isolated erythrocyte defect in chronic hemolysis.
16. Modification of erythrocyte enzyme activities by persulfides and methanethiol: possible regulatory role.
17. Identification of thymidine nucleotidase and deoxyribonucleotidase activities among normal isozymes of 5'-nucleotidase in human erythrocytes.
18. Studies on the Radiosensitivity of Bone Marrow
19. International Committee for Standardization in Haematology: Recommended Screening Test for Glucose-6-Phosphate Dehydrogenase (G-6-PD) Deficiency.
20. Lead poisoning. Further observations on erythrocyte pyrimidine-nucleotidase deficiency and intracellular accumulation of pyrimidine nucleotides.
21. Effects of low-level lead exposure on pyrimidine 5'-nucleotidase and other erythrocyte enzymes. Possible role of pyrimidine 5'-nucleotidase in the pathogenesis of lead-induced anemia.
22. Lead poisoning: association with hemolytic anemia, basophilic stippling, erythrocyte pyrimidine 5'-nucleotidase deficiency, and intraerythrocytic accumulation of pyrimidines.
23. Metabolism of human erythrocytes. Studies in health and disease
24. Heme Synthesis and Erythrocyte Life Span in the Cat.
25. Studies on Urinary Histamine in Chronic Myelocytic Leukemia.
26. Heme Synthesis and Erythrocyte Life Span in the Cat.∗.
27. Red cell metabolism, normal and abnormal implications for red cell aging.
28. Erythroenzymopathies and hemolytic anemia: the many faces of inherited variant enzymes.
29. Maxwell Myer Wintrobe: October 27, 1901-December 9, 1986.
30. Haemolytic anaemia associated with disorders of the purine and pyrimidine salvage pathways.
31. Hemolytic anemia: diagnosis and management.
32. Pyruvate kinase Greensboro. A four-generation study of a high K0.5s (phosphoenolpyruvate) variant.
33. Inhibition of adenylate kinase by P1,P5-di(adenosine 5') pentaphosphate in assays of erythrocyte enzyme activities requiring adenine nucleotides.
34. Pyruvate kinase isozyme (PK-Greenville) with defective allosteric activation by fructose-1,6-diphosphate: the role of F-1,6-P modulation in normal erythrocyte metabolism.
35. Unique phenotypic expression of glucosephosphate isomerase deficiency.
36. Hexokinase "New Hyde Park": a low activity erythrocyte isozyme in a Chinese kindred.
37. 3-Mercaptopyruvate sulfurtransferase (EC 2.8.1.2): a simple assay adapted to human blood cells.
38. Red cell CDP (dCDP)-choline and P-choline in normal subjects and in certain hemolytic syndromes.
39. Additional data from two kindreds with genetically induced deficiencies of erythrocyte pyrimidine nucleotidase.
40. The primary cause of hemolysis in enzymopathies of anaerobic glycolysis: a viewpoint.
41. Acute intravascular hemolysis in the black rhinoceros: erythrocyte enzymes and metabolic intermediates.
42. Control of red blood cell adenine nucleotide metabolism studies of adenosine deaminase.
43. Hereditary glucosephosphate isomerase deficiency. A review.
44. The Stratton Lecture. Hemolytic anemia and inborn errors of metabolism.
45. Pyrimidine nucleotidase deficiency with active dephosphorylation of dTMP: evidence for existence of thymidine nucleotidase in human erythrocytes.
46. Red cell nucleotide abnormalities.
47. Biphasic reaction kinetics in an anomalous isozyme of erythrocyte pyruvate kinase.
48. Simultaneous inheritance of mutant isoenzymes of erythrocyte pyruvate kinase associated with chronic haemolytic anaemia.
49. Biochemical characterization of three mutant isozymes of erythrocyte pyruvate kinase: PK-"Gainesville," PK-"San Juan," and PK-"Cape Canaveral".
50. An isozyme of erythrocyte pyruvate kinase (PK-Los Angeles) with impaired kinetics corrected by fructose-1, 6-diphosphate.
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