Inhibition of hexose monophosphate shunt in young erythrocytes by pyrimidine nucleotides in hereditary pyrimidine 5‘ nucleotidase deficiency
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1991.tb00560.x/fullpdf
Reference18 articles.
1. Age-related red cell enzymes in children with transient erythroblastopenia of chilhood and with hemolityc anemia;Beutler;Ped Res,1985
2. Hereditary hemolitic anemia with human erythrocyte pyrimidine 5′-nucleotidase deficiency;Valentine;J Clin Invest,1974
3. Erythrocyte disorders of purine and pyrimidine metabolism;Valentine;Hemoglobin,1980
4. Hemolytic anemia due to pyrimidine 5′-nucleotidase deficiency: report of eight cases in six families;Beutler;Blood,1980
5. Erythrocyte pyrimidine 5′-nucleotidase deficiency;Hansen;Scand J Haematol,1983
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1. A rare mutation (p.F149del) of the NT5C3A gene is associated with pyrimidine 5′-nucleotidase deficiency;Cellular & Molecular Biology Letters;2022-11-24
2. Proteomics reveals reduced expression of transketolase in pyrimidine 5′-nucleotidase deficient patients;PROTEOMICS - Clinical Applications;2016-08
3. Hereditary pyrimidine 5'-nucleotidase deficiency: from genetics to clinical manifestations;British Journal of Haematology;2006-04
4. Hereditary erythrocyte pyrimidine 5′-nucleotidase deficiency: A biochemical, genetic and clinical overview;Hematology;2006-02
5. Chronic non-spherocytic haemolytic anaemia due to congenital pyrimidine 5′ nucleotidase deficiency: 25 years later;Best Practice & Research Clinical Haematology;2000-03
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