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Items: 9

1.

Human adenylate kinase deficiency associated with hemolytic anemia. A single base substitution affecting solubility and catalytic activity of the cytosolic adenylate kinase.

Matsuura S, Igarashi M, Tanizawa Y, Yamada M, Kishi F, Kajii T, Fujii H, Miwa S, Sakurai M, Nakazawa A.

J Biol Chem. 1989 Jun 15;264(17):10148-55.

2.

Molecular aspects of erythroenzymopathies associated with hereditary hemolytic anemia.

Miwa S, Fujii H.

Am J Hematol. 1985 Jul;19(3):293-305. Review.

PMID:
2990202
3.
4.

[Pathophysiology and laboratory tests of hemolytic anemia: with special reference to erythroenzymopathies].

Fujii H, Miwa S.

Rinsho Byori. 1989 Dec;37(12):1331-43. Review. Japanese.

PMID:
2693773
5.
6.

Recent progress in the molecular genetic analysis of erythroenzymopathy.

Fujii H, Miwa S.

Am J Hematol. 1990 Aug;34(4):301-10. Review.

PMID:
2164322
7.

Mechanism of adenylate kinase: site-directed mutagenesis versus X-ray and NMR.

Tsai MD, Yan HG.

Biochemistry. 1991 Jul 16;30(28):6806-18. Review. No abstract available.

PMID:
2069947
8.

[Human adenylate kinases - classification, structure, physiological and pathological importance].

Wujak M, Czarnecka J, Gorczycka M, Hetmann A.

Postepy Hig Med Dosw (Online). 2015 Jan 2;69:933-45. doi: 10.5604/17322693.1165196. Review. Polish.

PMID:
26400880
9.

Thiamin triphosphate synthesis in animals.

Kawasaki T.

J Nutr Sci Vitaminol (Tokyo). 1992;Spec No:383-6. Review.

PMID:
1297771
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