BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

250 related articles for article (PubMed ID: 10772876)

  • 1. Hematologically important mutations: red cell pyruvate kinase (Third update).
    Bianchi P; Zanella A
    Blood Cells Mol Dis; 2000 Feb; 26(1):47-53. PubMed ID: 10772876
    [No Abstract]   [Full Text] [Related]  

  • 2. Hematologically important mutations: red cell pyruvate kinase (2nd update).
    Baronciani L; Bianchi P; Zanella A
    Blood Cells Mol Dis; 1998 Sep; 24(3):273-9. PubMed ID: 10087985
    [No Abstract]   [Full Text] [Related]  

  • 3. Eight novel mutations and consequences on mRNA and protein level in pyruvate kinase-deficient patients with nonspherocytic hemolytic anemia.
    Kugler W; Willaschek C; Holtz C; Ohlenbusch A; Laspe P; Krügener R; Muirhead H; Schröter W; Lakomek M
    Hum Mutat; 2000; 15(3):261-72. PubMed ID: 10679942
    [TBL] [Abstract][Full Text] [Related]  

  • 4. G-->T transition at cDNA nt 110 (K37Q) in the PKLR (pyruvate kinase) gene is the molecular basis of a case of hereditary increase of red blood cell ATP.
    Beutler E; Westwood B; van Zwieten R; Roos D
    Hum Mutat; 1997; 9(3):282-5. PubMed ID: 9090535
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. Co-existence of hereditary spherocytosis and a new red cell pyruvate kinase variant: PK mallorca.
    Zarza R; Moscardó M; Alvarez R; García J; Morey M; Pujades A; Vives-Corrons JL
    Haematologica; 2000 Mar; 85(3):227-32. PubMed ID: 10702808
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pyruvate kinase deficiency.
    Miwa S
    Nihon Ketsueki Gakkai Zasshi; 1987 Dec; 50(8):1445-52. PubMed ID: 3328943
    [No Abstract]   [Full Text] [Related]  

  • 8. Hematologically important mutations: red cell pyruvate kinase.
    Baronciani L; Bianchi P; Zanella A
    Blood Cells Mol Dis; 1996; 22(1):85-9. PubMed ID: 8807089
    [No Abstract]   [Full Text] [Related]  

  • 9. [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]  

  • 10. 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]  

  • 11. [Electrophoretic heterogeneity of pyruvate kinase in erythrocytes in patients with enzymopathies].
    Rotrekl B
    Acta Univ Palacki Olomuc Fac Med; 1985; 111():467-73. PubMed ID: 2949531
    [No Abstract]   [Full Text] [Related]  

  • 12. Red cell pyruvate kinase deficiency: molecular and clinical aspects.
    Zanella A; Fermo E; Bianchi P; Valentini G
    Br J Haematol; 2005 Jul; 130(1):11-25. PubMed ID: 15982340
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular characterisation of pyruvate kinase deficiency--concerns about the description of mutant PKLR alleles.
    van Wijk R; Rijksen G; van Solinge WW
    Br J Haematol; 2007 Jan; 136(1):167-9; author reply 169-70. PubMed ID: 17222205
    [No Abstract]   [Full Text] [Related]  

  • 14. Red blood cell PK deficiency: An update of PK-LR gene mutation database.
    Canu G; De Bonis M; Minucci A; Capoluongo E
    Blood Cells Mol Dis; 2016 Mar; 57():100-9. PubMed ID: 26832193
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pyruvate kinase "Göttingen 1,2": congenital hemolytic anemia, evidence of double heterozygosity, and lack of enzyme cooperativity.
    Schröter W; Lakomek M; Scharnetzky M; Tillmann W; Winkler H
    Hum Genet; 1982; 60(4):381-6. PubMed ID: 7106777
    [No Abstract]   [Full Text] [Related]  

  • 16. Mining for allosteric information: natural mutations and positional sequence conservation in pyruvate kinase.
    Pendergrass DC; Williams R; Blair JB; Fenton AW
    IUBMB Life; 2006 Jan; 58(1):31-8. PubMed ID: 16540430
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Fifteen novel mutations in PKLR associated with pyruvate kinase (PK) deficiency: structural implications of amino acid substitutions in PK.
    van Wijk R; Huizinga EG; van Wesel AC; van Oirschot BA; Hadders MA; van Solinge WW
    Hum Mutat; 2009 Mar; 30(3):446-53. PubMed ID: 19085939
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Physico-chemical and kinetic properties of pyruvate kinase in erythrocytes in enzymopathic hemolytic anemia].
    Rotrekl B; Wiedermann B; Mlcochová E; Prokopová M
    Vnitr Lek; 1984 Jun; 30(6):542-9. PubMed ID: 6474860
    [No Abstract]   [Full Text] [Related]  

  • 19. Hemolytic anemia associated with a novel heterozygote mutation 1183A in the PK-LR gene (PK- Jordan).
    Karadsheh NS; Gelbart T; Naffa RG
    Int J Lab Hematol; 2014 Aug; 36(4):e66-8. PubMed ID: 24330591
    [No Abstract]   [Full Text] [Related]  

  • 20. First-trimester prenatal diagnosis of pyruvate kinase deficiency in an Indian family with the pyruvate kinase-Amish mutation.
    Kedar PS; Nampoothiri S; Sreedhar S; Ghosh K; Shimizu K; Kanno H; Colah RB
    Genet Mol Res; 2007 Jun; 6(2):470-5. PubMed ID: 17952871
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.