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Haemolytic anaemia associated with disorders of the purine and pyrimidine salvage pathways.

作者信息

Paglia D E, Valentine W N

出版信息

Clin Haematol. 1981 Feb;10(1):81-98.

PMID:6260409
Abstract
摘要

相似文献

1
Haemolytic anaemia associated with disorders of the purine and pyrimidine salvage pathways.
Clin Haematol. 1981 Feb;10(1):81-98.
2
Red cell nucleotide abnormalities.红细胞核苷酸异常。
Prog Clin Biol Res. 1984;165:213-25.
3
Erythrocyte disorders of purine and pyrimidine metabolism.
Hemoglobin. 1980;4(5-6):669-81. doi: 10.3109/03630268008997736.
4
Hemolytic anemias and erythrocyte enzymopathies.溶血性贫血和红细胞酶病
Ann Intern Med. 1985 Aug;103(2):245-57. doi: 10.7326/0003-4819-103-2-245.
5
Studies on pyruvate kinase deficiency, pyrimidine 5-'nucleotidase deficiency and adenosine deaminase overproduction.
Acta Biol Med Ger. 1981;40(4-5):543-6.
6
Haemolytic anaemia due to pyrimidine-5'-nucleotidase deficiency.
Int J Tissue React. 1984;6(4):351-4.
7
Haemolytic anaemia due to erythrocyte pyrimidine 5'-nucleotidase deficiency. Report of the first South African family.红细胞嘧啶5'-核苷酸酶缺乏所致的溶血性贫血。首例南非家族报告。
S Afr Med J. 1977 Oct 15;52(17):671-3.
8
Hereditary disorders of erythrocyte enzymes in non-glycolytic metabolic pathways.
Haematologia (Budap). 1982 Dec;15(4):381-8.
9
The effects of S-adenosylhomocysteine and S-adenosylmethionine on some purine- and pyrimidine-metabolizing systems.
Biosci Rep. 1982 Oct;2(10):769-75. doi: 10.1007/BF01114936.
10
Disorders of purine and pyrimidine metabolism.嘌呤和嘧啶代谢紊乱。
Mol Genet Metab. 2005 Sep-Oct;86(1-2):25-33. doi: 10.1016/j.ymgme.2005.07.027.

引用本文的文献

1
Expression of the human erythroid Rh glycoprotein (RhAG) enhances both NH3 and NH4+ transport in HeLa cells.人类红细胞Rh糖蛋白(RhAG)的表达增强了HeLa细胞中NH3和NH4+的转运。
Pflugers Arch. 2005 Jun;450(3):155-67. doi: 10.1007/s00424-005-1381-y. Epub 2005 Apr 26.
2
Expression of human adenosine deaminase using a transmissable murine retrovirus vector system.使用可传播的鼠逆转录病毒载体系统表达人腺苷脱氨酶。
Proc Natl Acad Sci U S A. 1985 Feb;82(3):703-7. doi: 10.1073/pnas.82.3.703.
3
Detection of pyrimidine 5'-nucleotidase deficiency using 1H- or 31P-nuclear magnetic resonance.
利用氢-1或磷-31核磁共振检测嘧啶5'-核苷酸酶缺乏症
Experientia. 1986 Jan 15;42(1):69-72. doi: 10.1007/BF01975900.