BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

154 related articles for article (PubMed ID: 6653061)

  • 1. A pyruvate kinase variant with an increased affinity for phosphoenolpyruvate in an individual with congenital non-spherocytic haemolytic anaemia.
    Smith O; Temperley IJ; Tipton K; McCann SR
    Clin Lab Haematol; 1983; 5(3):237-41. PubMed ID: 6653061
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Three pyruvate kinase variants with increased affinity for PEP.
    Elder GE; Lappin TR; Lawson BE; Bridges JM
    Br J Haematol; 1981 Mar; 47(3):371-81. PubMed ID: 7459276
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Seven pyruvate kinase variants characterized by the ICSH recommended methods.
    Miwa S; Fujii H; Takegawa S; Nakatsuji T; Yamato K; Ishida Y; Ninomiya N
    Br J Haematol; 1980 Aug; 45(4):575-83. PubMed ID: 7426438
    [TBL] [Abstract][Full Text] [Related]  

  • 4. PK Mondor: prenatal diagnosis of a frameshift mutation in the LR pyruvate kinase gene associated with severe hereditary non-spherocytic haemolytic anaemia.
    Rouger H; Girodon E; Goossens M; Galactéros F; Cohen-Solal M
    Prenat Diagn; 1996 Feb; 16(2):97-104. PubMed ID: 8650134
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A mutant of human red cell pyruvate kinase with high affinity for phosphoenolpyruvate.
    Boivin P; Galand C
    Enzyme; 1974; 18(1):37-47. PubMed ID: 4850232
    [No Abstract]   [Full Text] [Related]  

  • 6. Elevated pyruvate kinase activity in patients with hemolytic anemia due to red cell pyruvate kinase "deficiency".
    Beutler E; Forman L; Rios-Larrain E
    Am J Med; 1987 Nov; 83(5):899-904. PubMed ID: 3674096
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Human erythrocyte pyruvate kinase: characterization of the recombinant enzyme and a mutant form (R510Q) causing nonspherocytic hemolytic anemia.
    Wang C; Chiarelli LR; Bianchi P; Abraham DJ; Galizzi A; Mattevi A; Zanella A; Valentini G
    Blood; 2001 Nov; 98(10):3113-20. PubMed ID: 11698298
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Erythrocyte pyruvate kinase deficiency: relations of residual enzyme activity, altered regulation of defective enzymes and concentrations of high-energy phosphates with the severity of clinical manifestation.
    Lakomek M; Neubauer B; von der Lühe A; Hoch G; Winkler H; Schröter W
    Eur J Haematol; 1992 Aug; 49(2):82-92. PubMed ID: 1397245
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pyruvate kinase deficiency.
    Miwa S; Fujii H
    Clin Biochem; 1990 Apr; 23(2):155-7. PubMed ID: 2197027
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of an erythrocyte pyruvate kinase variant in a family from Latium with non-spherocytic congenital haemolytic anaemia.
    Papa G; De Laurenzi A; Isacchi GC; Bonifazi G; Parziale L; Salvati AM
    Acta Haematol; 1979; 61(5):288-94. PubMed ID: 111457
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Significance of kinetic abnormalities of erythrocyte pyruvate kinase in congenital deficiencies].
    Boivin P; Galand C
    Pathol Biol (Paris); 1977 Mar; 25(3):161-7. PubMed ID: 323784
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pyruvate kinase deficiency: characterization of two new genetic variants.
    Dente L; D'Urso M; Di Maio S; Brancaccio V; Luzzatto L
    Clin Chim Acta; 1982 Dec; 126(2):143-54. PubMed ID: 7151276
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital non-spherocytic haemolytic anaemia variants with primary and secondary pyruvate kinase deficiency. II. Enzymatic studies.
    Gumińska M; Wazewska-Czyzewska M
    Br J Haematol; 1979 Jan; 41(1):125-32. PubMed ID: 154343
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Biochemical characterization of four new erythrocyte pyruvate kinase variants.
    Tegos C; Anagnostoulis G
    Acta Haematol; 1994; 92(2):91-6. PubMed ID: 7817710
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical and biochemical studies on mutant red cell enzymes mainly associated with hemolytic anemia.
    Miwa S
    Jinrui Idengaku Zasshi; 1980 Jun; 25(2):83-92. PubMed ID: 7431680
    [No Abstract]   [Full Text] [Related]  

  • 16. HEREDITARY NON-SPHEROCYTIC HAEMOLYTIC ANAEMIA. A STUDY OF RED-CELL CARBOHYDRATE METABOLISM IN TWELVE CASES OF PYRUVATE-KINASE DEFICIENCY.
    GRIMES AJ; MEISLER A; DACIE JV
    Br J Haematol; 1964 Jul; 10():403-11. PubMed ID: 14179493
    [No Abstract]   [Full Text] [Related]  

  • 17. Two cases of pyruvate kinase deficiency: PK 'Kamakura' and PK 'Naniwa'.
    Takegawa S; Fujii H; Takahashi K; Morisaki T; Hirono A; Takizawa T; Kanno H; Tsujino G; Miwa S
    Nihon Ketsueki Gakkai Zasshi; 1985 Sep; 48(6):1332-6. PubMed ID: 4090923
    [No Abstract]   [Full Text] [Related]  

  • 18. Congenital non-spherocytic haemolytic anaemias.
    Zanella A; Colombo MB; Rossi F; Merati G; Sirchia G
    Haematologica; 1989; 74(4):387-96. PubMed ID: 2551797
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [From gene to disease; hereditary non-spherocytic hemolytic anemia caused by pyruvate kinase deficiency].
    de Vooght KM; van Wijk R; Nieuwenhuis HK; Ploos van Amstel JK; Rijksen G; van Solinge WW
    Ned Tijdschr Geneeskd; 2002 Sep; 146(39):1828-31. PubMed ID: 12382367
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Residual pyruvate kinase activity in PKLR-deficient erythroid precursors of a patient suffering from severe haemolytic anaemia.
    Klei TRL; Kheradmand Kia S; Veldthuis M; Beuger BM; Geissler J; Dehbozorgian J; Karimi M; van Bruggen R; van Zwieten R
    Eur J Haematol; 2017 Jun; 98(6):584-589. PubMed ID: 28295642
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.