These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 2164322)

  • 1. Recent progress in the molecular genetic analysis of erythroenzymopathy.
    Fujii H; Miwa S
    Am J Hematol; 1990 Aug; 34(4):301-10. PubMed ID: 2164322
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Pathophysiology and laboratory tests of hemolytic anemia: with special reference to erythroenzymopathies].
    Fujii H; Miwa S
    Rinsho Byori; 1989 Dec; 37(12):1331-43. PubMed ID: 2693773
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular basis of red cell enzymopathies associated with hereditary nonspherocytic hemolytic anemia.
    Miwa S
    Haematologia (Budap); 1989; 22(4):215-31. PubMed ID: 2560452
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: tabulation of mutant enzymes.
    Miwa S; Fujii H
    Am J Hematol; 1996 Feb; 51(2):122-32. PubMed ID: 8579052
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular aspects of erythroenzymopathies associated with hereditary hemolytic anemia.
    Miwa S; Fujii H
    Am J Hematol; 1985 Jul; 19(3):293-305. PubMed ID: 2990202
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Red cell enzymopathies as a model of inborn errors of metabolism.
    Miwa S; Kanno H; Hirono A; Fujii H
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():112-9. PubMed ID: 8629088
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Metabolism of human erythrocytes. Studies in health and disease.
    Valentine WN
    Arch Intern Med; 1975 Oct; 135(10):1307-13. PubMed ID: 1164111
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Studies on pyruvate kinase deficiency, pyrimidine 5-'nucleotidase deficiency and adenosine deaminase overproduction.
    Miwa S
    Acta Biol Med Ger; 1981; 40(4-5):543-6. PubMed ID: 6274114
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Congenital red cell enzyme anomalies--classification and the hemolytic mechanism].
    Ishida Y; Miwa S
    Nihon Rinsho; 1979 Dec; 37(12):3923-9. PubMed ID: 537177
    [No Abstract]   [Full Text] [Related]  

  • 10. Hemolytic anemias and erythrocyte enzymopathies.
    Valentine WN; Tanaka KR; Paglia DE
    Ann Intern Med; 1985 Aug; 103(2):245-57. PubMed ID: 2990276
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deficiencies of glycolytic enzymes as a possible cause of hemolytic anemia.
    Martinov MV; Plotnikov AG; Vitvitsky VM; Ataullakhanov FI
    Biochim Biophys Acta; 2000 Mar; 1474(1):75-87. PubMed ID: 10699493
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A case of red-cell adenosine deaminase overproduction associated with hereditary hemolytic anemia found in Japan.
    Miwa S; Fujii H; Matsumoto N; Nakatsuji T; Oda S; Asano H; Asano S
    Am J Hematol; 1978; 5(2):107-15. PubMed ID: 736030
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Metabolic compensation for profound erythrocyte adenylate kinase deficiency. A hereditary enzyme defect without hemolytic anemia.
    Beutler E; Carson D; Dannawi H; Forman L; Kuhl W; West C; Westwood B
    J Clin Invest; 1983 Aug; 72(2):648-55. PubMed ID: 6308059
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Characterization of an adenosine deaminase-deficient human histiocytic lymphoma cell line (DHL-9) and selection of mutants deficient in adenosir kinase and deoxycytidine kinase.
    Kubota M; Kamatani N; Daddona PE; Carson DA
    Cancer Res; 1983 Jun; 43(6):2606-10. PubMed ID: 6303563
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Erythrocyte-specific overproduction of adenosine deaminase: molecular genetic studies.
    Chottiner EG; Gribbin TE; Ginsburg D; Mitchell BS
    Prog Clin Biol Res; 1989; 319():55-64; discussion 65-8. PubMed ID: 2622927
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Overproduction of structurally normal enzyme in man: hereditary haemolytic anaemia with increased red cell adenosine deaminase activity.
    Fujii H; Miwa S; Tani K; Fujinami N; Asano H
    Br J Haematol; 1982 Jul; 51(3):427-30. PubMed ID: 7104226
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Red cell phosphoglycerate kinase deficiency. A new cause of non-spherocytic hemolytic anemia.
    Kraus AP; Langston MF; Lynch BL
    Biochem Biophys Res Commun; 1968 Jan; 30(2):173-7. PubMed ID: 4230542
    [No Abstract]   [Full Text] [Related]  

  • 18. Hereditary overexpression of adenosine deaminase in erythrocytes: studies in erythroid cell lines and transgenic mice.
    Chen EH; Mitchell BS
    Blood; 1994 Oct; 84(7):2346-53. PubMed ID: 7919352
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Erythrocyte adenylate kinase deficiency: characterization of recombinant mutant forms and relationship with nonspherocytic hemolytic anemia.
    Abrusci P; Chiarelli LR; Galizzi A; Fermo E; Bianchi P; Zanella A; Valentini G
    Exp Hematol; 2007 Aug; 35(8):1182-9. PubMed ID: 17662886
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [FURTHER ACQUISITIONS ON THE SUBJECT OF ENZYME-DEFICIENT HEMOLYTIC ANEMIAS].
    LARIZZA P; BRUNETTI P
    Minerva Med; 1964 May; 55():SUPPL:1579-88. PubMed ID: 14162174
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.