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Items: 1 to 20 of 311

1.
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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 15;98(10):3113-20.

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Erythrocyte PK deficiency: biochemical characterization of a patient with haemolytic anemia.

González R, Estrada M, Garcia M, Gutiérrez A, de la Torre E, Colombo B.

Haematologia (Budap). 1987;20(1):51-5.

PMID:
3596364
6.
7.

An inherited molecular lesion of erythrocyte pyruvate kinase. Identification of a kinetically aberrant isozyme associated with premature hemolysis.

Paglia DE, Valentine WN, Baughan MA, Miller DR, Reed CF, McIntyre OR.

J Clin Invest. 1968 Aug;47(8):1929-46.

8.

Thirteen cases of pyruvate kinase deficiency found in Japan.

Ishida Y, Miwa S, Fujii H, Fujinami N, Takegawa S, Yamato K.

Am J Hematol. 1981;10(3):239-50.

PMID:
7246534
9.

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 9;126(2):143-54.

PMID:
7151276
11.

Erythrocyte pyruvate kinase deficiency. The influence of physiologically important metabolites on the function of normal and defective enzymes.

Lakomek M, Winkler H, Pekrun A, Krüger N, Sander M, Huppke P, Schröter W.

Enzyme Protein. 1994-1995;48(3):149-63.

PMID:
8589802
12.

[Energy metabolism of erythrocytes in pyruvate kinase enzymopathies].

Jacobasch G, Grieger M, Gerth C, Bier K.

Acta Biol Med Ger. 1977;36(5-6):717-30. German.

PMID:
602578
13.

Pyruvate kinase Greensboro. A four-generation study of a high K0.5s (phosphoenolpyruvate) variant.

Valentine WN, Herring WB, Paglia DE, Steuterman MC, Brockway RA, Nakatani M.

Blood. 1988 Sep;72(3):1054-9. Erratum in: Blood 1988 Dec;72(6):2082.

14.

Pyruvate kinase deficiency.

Miwa S.

Prog Clin Biol Res. 1990;344:843-52. Review.

PMID:
2203063
16.

Point mutations in the L-type pyruvate kinase gene of two children with hemolytic anemia caused by pyruvate kinase deficiency.

Neubauer B, Lakomek M, Winkler H, Parke M, Hofferbert S, Schröter W.

Blood. 1991 May 1;77(9):1871-5.

17.

[Pyruvate kinase (PK) isozyme switching and genetic heterogeneity of PK deficiency].

Kanno H.

Nihon Rinsho. 1995 May;53(5):1213-20. Review. Japanese.

PMID:
7602781
18.

Characterization of pyruvate kinase from the liver of a patient with aberrant erythrocyte pyruvate kinase, PK Nagasaki.

Nakashima K, Miwa S, Fujii H, Shinohara K, Yamauchi K, Tsuji Y, Yanai M.

J Lab Clin Med. 1977 Dec;90(6):1012-20.

PMID:
925478
19.

Hereditary hemolytic anemia caused by diverse point mutations of pyruvate kinase gene found in Japan and Hong Kong.

Kanno H, Wei DC, Chan LC, Mizoguchi H, Ando M, Nakahata T, Narisawa K, Fujii H, Miwa S.

Blood. 1994 Nov 15;84(10):3505-9.

20.

Ten cases of pyruvate kinase (PK) deficiency found in Japan: enzymatic characterization of the patients' PK.

Morisaki T, Tani K, Takahashi K, Tsutsumi H, Horiuchi N, Ogura H, Kanno H, Fujimura K, Nakayama S, Watanabe C, et al.

Nihon Ketsueki Gakkai Zasshi. 1988 Sep;51(6):1080-5. No abstract available.

PMID:
3201900
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