87 related articles for article (PubMed ID: 8890566)
21. Red cell pyruvate kinase deficiency: 17 new mutations of the PK-LR gene.
Fermo E; Bianchi P; Chiarelli LR; Cotton F; Vercellati C; Writzl K; Baker K; Hann I; Rodwell R; Valentini G; Zanella A
Br J Haematol; 2005 Jun; 129(6):839-46. PubMed ID: 15953013
[TBL] [Abstract][Full Text] [Related]
22. Delayed onset of hemolytic anemia in CBA-Pk-1slc/Pk-1slc mice with a point mutation of the gene encoding red blood cell type pyruvate kinase.
Tsujino K; Kanno H; Hashimoto K; Fujii H; Jippo T; Morii E; Lee YM; Asai H; Miwa S; Kitamura Y
Blood; 1998 Mar; 91(6):2169-74. PubMed ID: 9490705
[TBL] [Abstract][Full Text] [Related]
23. [Identification of pyruvate kinase variants from red blood cells using trypsinization and electrophoresis].
Tzanev D; Schulz J; Jacobasch G; Richter A; Gerth C
Acta Biol Med Ger; 1980; 39(7):745-61. PubMed ID: 7211063
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Mechanical membrane properties of human red blood cells and their change due to metabolic disturbance.
Lerche D; Jacobasch G; Meier W; Megow D
Biomed Biochim Acta; 1983; 42(11-12):S112-6. PubMed ID: 6675680
[TBL] [Abstract][Full Text] [Related]
26. Characterization of erythrocytic glucose-6-phosphate dehydrogenase in a mouse strain with reduced G6PD activity.
Neifer S; Jung A; Bienzle U
Biomed Biochim Acta; 1991; 50(3):233-8. PubMed ID: 1953691
[TBL] [Abstract][Full Text] [Related]
27. [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]
28. Glycolytic inhibition by mutation of pyruvate kinase gene increases oxidative stress and causes apoptosis of a pyruvate kinase deficient cell line.
Aisaki K; Aizawa S; Fujii H; Kanno J; Kanno H
Exp Hematol; 2007 Aug; 35(8):1190-200. PubMed ID: 17662887
[TBL] [Abstract][Full Text] [Related]
29. Pyruvate kinase deficiency in mice protects against malaria.
Min-Oo G; Fortin A; Tam MF; Nantel A; Stevenson MM; Gros P
Nat Genet; 2003 Dec; 35(4):357-62. PubMed ID: 14595440
[TBL] [Abstract][Full Text] [Related]
30. Spectrum of novel mutations in the human PKLR gene in pyruvate kinase-deficient Indian patients with heterogeneous clinical phenotypes.
Kedar P; Hamada T; Warang P; Nadkarni A; Shimizu K; Fujji H; Ghosh K; Kanno H; Colah R
Clin Genet; 2009 Feb; 75(2):157-62. PubMed ID: 18759866
[TBL] [Abstract][Full Text] [Related]
31. Pyruvate kinase deficiency in France: a 3-year study reveals 27 new mutations.
Pissard S; Max-Audit I; Skopinski L; Vasson A; Vivien P; Bimet C; Goossens M; Galacteros F; Wajcman H
Br J Haematol; 2006 Jun; 133(6):683-9. PubMed ID: 16704447
[TBL] [Abstract][Full Text] [Related]
32. Red cell enzymopathies in leukemias.
Devi GS; Prasad MH; Pushpavathi K; Reddy PP; Rao DN
Indian J Exp Biol; 1996 Dec; 34(12):1224-8. PubMed ID: 9246916
[TBL] [Abstract][Full Text] [Related]
33. The mouse Char10 locus regulates severity of pyruvate kinase deficiency and susceptibility to malaria.
Laroque A; Min-Oo G; Tam M; Ponka P; Stevenson MM; Gros P
PLoS One; 2017; 12(5):e0177818. PubMed ID: 28542307
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Pyruvate kinase deficient hemolytic anemia in the Northern Irish population.
Percy MJ; van Wijk R; Haggan S; Savage GA; Boyd K; Dempsey S; Hamilton J; Kettle P; Kyle A; Shepherd CW; van Solinge WW; Lappin TR; McMullin MF
Blood Cells Mol Dis; 2007; 39(2):189-94. PubMed ID: 17574881
[TBL] [Abstract][Full Text] [Related]
36. Babesia rodhaini: the protective effect of pyruvate kinase deficiency in mice.
Oka H; Tabara A; Fujisawa K; Jinnai M; Nakajima R; Arai S; Ishihara C; Tsuji M
Exp Parasitol; 2008 Nov; 120(3):290-4. PubMed ID: 18789933
[TBL] [Abstract][Full Text] [Related]
37. The role of the spleen in a lactate dehydrogenase mutant mouse (Ldh-1c/Ldh-1c) with hemolytic anemia.
Datta T; Kremer JP; Hültner L; Dörmer P
Exp Hematol; 1988 May; 16(4):281-4. PubMed ID: 3360065
[TBL] [Abstract][Full Text] [Related]
38. Hereditary disorders of enzymes in the Embden-Meyerhof pathway of glycolysis.
Miwa S
Haematologia (Budap); 1982 Dec; 15(4):371-9. PubMed ID: 6225712
[TBL] [Abstract][Full Text] [Related]
39. Severe hypertriglyceridemia in an infant with red cell pyruvate kinase deficiency.
Rao A; Hulbert M; Wilson DB
Indian Pediatr; 2007 Apr; 44(4):303-5. PubMed ID: 17468529
[TBL] [Abstract][Full Text] [Related]
40. [Hereditary hemolytic anemia due to abnormal enzymes of the glycolytic pathway].
Omine M
Nihon Rinsho; 1996 Sep; 54(9):2460-6. PubMed ID: 8890579
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
