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Items: 1 to 20 of 177

1.

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.

2.

Erythrocyte pyruvate kinase (PK): the variable significance of "nucleotide specificity" in the characterization of mutant variants.

Valentine WN, Paglia DE, Nakatani M, Brockway RA.

Am J Hematol. 1987 Dec;26(4):353-6.

PMID:
3687932
3.

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.

4.

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
5.
6.

Studies with human erythrocyte pyruvate kinase (PK): effects of modification of sulfhydryl groups.

Valentine WN, Paglia DE.

Br J Haematol. 1983 Mar;53(3):385-98.

PMID:
6824584
7.

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
8.
9.

Cyclic AMP-dependent phosphorylation of erythrocyte variant pyruvate kinase.

Fujii S, Nakashima K, Yanagihara T, Shinohara K, Kaneko T.

Biochem Med. 1984 Feb;31(1):47-53.

PMID:
6331423
10.

Hereditary pyruvate kinase deficiency: role of the abnormal enzyme in red cell pathophysiology.

Zanella A, Rebulla P, Vullo C, Izzo C, Tedesco F, Sirchia G.

Br J Haematol. 1978 Dec;40(4):551-62.

PMID:
728372
12.

Four new pyruvate kinase (PK) variants and a classical PK deficiency.

Miwa S, Nakashima K, Ariyoshi K, Shinohara K, Oda E.

Br J Haematol. 1975 Jan;29(1):157-69.

PMID:
1201198
13.

Two homozygous cases of erythrocyte pyruvate kinase (PK) deficiency in Japan: PK Sendai and PK Shinshu.

Tani K, Tsutsumi H, Takahashi K, Ogura H, Kanno H, Hayasaka K, Narisawa K, Nakahata T, Akabane T, Morisaki T, et al.

Am J Hematol. 1988 Jul;28(3):186-90.

PMID:
3407638
14.
15.

An isozyme of erythrocyte pyruvate kinase (PK-Los Angeles) with impaired kinetics corrected by fructose-1, 6-diphosphate.

Paglia DE, Valentine WN, Williams KO, Konrad PN.

Am J Clin Pathol. 1977 Aug;68(2):229-34.

PMID:
18004
16.

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.

PMID:
7459276
17.

[Significance of kinetic abnormalities of erythrocyte pyruvate kinase in congenital deficiencies].

Boivin P, Galand C.

Pathol Biol (Paris). 1977 Mar;25(3):161-7. French.

PMID:
323784
18.

Heterogeneity of erythrocyte pyruvate kinase deficiency and related metabolic disorders in patients with hematological diseases.

Gherardi M, Bierme R, Corberand J, Vergnes H.

Clin Chim Acta. 1977 Aug 1;78(3):465-71.

PMID:
18306
19.
20.

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

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