Literature DB >> 5388241

Functionally abnormal pyruvate kinase in congenital hemolytic anemia.

H Oyama, T Kumatori, T Nishina, S Miwa.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1969        PMID： 5388241

Source DB:  PubMed          Journal:  Nihon Ketsueki Gakkai Zasshi        ISSN： 0001-5806


× No keyword cloud information.
  3 in total

1.  Hereditary erythrocyte pyruvate-kinase (PK) deficiency and chronic hemolytic anemia: clinical, genetic and molecular studies in six new Spanish patients.

Authors:  J L Vives-Corrons; J Marie; M A Pujades; A Kahn
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

2.  cDNA cloning of human R-type pyruvate kinase and identification of a single amino acid substitution (Thr384----Met) affecting enzymatic stability in a pyruvate kinase variant (PK Tokyo) associated with hereditary hemolytic anemia.

Authors:  H Kanno; H Fujii; A Hirono; S Miwa
Journal:  Proc Natl Acad Sci U S A       Date:  1991-09-15       Impact factor: 11.205

Review 3.  [Enzyme deficiencies in glycolysis and nucleotide metabolism of red blood cells in nonspherocytic hemolytic anemia (author's transl)].

Authors:  H D Waller; H C Benöhr
Journal:  Klin Wochenschr       Date:  1976-09-01
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.