BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 5127632)

  • 1. Actalasemia and hypocatalasemia in the Orient.
    Takahara S
    Semin Hematol; 1971 Oct; 8(4):397-416. PubMed ID: 5127632
    [No Abstract]   [Full Text] [Related]  

  • 2. Acatalasemia.
    Aebi H; Suter H
    Adv Hum Genet; 1971; 2():143-99. PubMed ID: 4950475
    [No Abstract]   [Full Text] [Related]  

  • 3. [Effects of enzyme deficiencies on the erythrocyte metabolism (illustrated by the example of catalase deficiency)].
    Aebi H
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1969; 91(1):5-21. PubMed ID: 4180963
    [No Abstract]   [Full Text] [Related]  

  • 4. Estimation of the frequency of the recessive gene of acatalasemia in Japan.
    Ogata M; Hayashi S; Takahara S
    Acta Med Okayama (1952); 1971 Jun; 25(3):193-8. PubMed ID: 4263520
    [No Abstract]   [Full Text] [Related]  

  • 5. Studies of acatalasemia.
    Feinstein RN
    Birth Defects Orig Artic Ser; 1973 Mar; 9(2):55-61. PubMed ID: 4611537
    [No Abstract]   [Full Text] [Related]  

  • 6. [Characterization of erythrocyte catalase in a patient with symptoms of Takahara disease].
    Gross J; Scherz B; Wyss S; Künzel W; Maiwald HJ; Hartwig A; Polster H
    Kinderarztl Prax; 1977 Apr; 45(4):168-75. PubMed ID: 556484
    [No Abstract]   [Full Text] [Related]  

  • 7. Pyruvate kinase deficiency.
    Tanaka KR; Paglia DE
    Semin Hematol; 1971 Oct; 8(4):367-96. PubMed ID: 4942588
    [No Abstract]   [Full Text] [Related]  

  • 8. [Heterozygous NADH-methemoglobin reductase defect with methemoglobinemia in an infant (author's transl)].
    Witt I; Gunkel J; Seibert G; Wehinger H; Schuchmann L; Künzer W
    Z Kinderheilkd; 1973 Nov; 115(4):273-81. PubMed ID: 4149782
    [No Abstract]   [Full Text] [Related]  

  • 9. Role of erythrocyte catalase in the protection of haemoglobin against hydrogen peroxide.
    Paniker NV; Iyer GY
    Indian J Biochem Biophys; 1972 Jun; 9(2):176-8. PubMed ID: 4676877
    [No Abstract]   [Full Text] [Related]  

  • 10. [Familial NADH diaphorase deficiency].
    Vergnes H; Gherardi M; Bernadet P; Biermé R
    Nouv Rev Fr Hematol; 1972; 12(4):560-3. PubMed ID: 4344374
    [No Abstract]   [Full Text] [Related]  

  • 11. Uridine diphosphate galactose 4-epimerase deficiency. II. Clinical follow-up, biochemical studies and family investigation.
    Gitzelmann R; Steinmann B
    Helv Paediatr Acta; 1973 Dec; 28(6):497-510. PubMed ID: 4785150
    [No Abstract]   [Full Text] [Related]  

  • 12. [Ultracentrifugal analysis of the fluid extract from the cases with hypocatalasemia and acatalasemia].
    Ogata M; Hasegawa N; Takahara S
    Igaku To Seibutsugaku; 1967 Feb; 74(2):64-7. PubMed ID: 5624329
    [No Abstract]   [Full Text] [Related]  

  • 13. The field investigation for acatalasemic gene carriers.
    Wakisaka G; Yamamoto T; Yamamoto Y; Sakamoto K; Sawada M
    Naika Hokan; 1967 May; 14(5):151-7. PubMed ID: 5624288
    [No Abstract]   [Full Text] [Related]  

  • 14. [What is pharmacogenetics?].
    Jörgensen G
    Ther Ggw; 1979 May; 118(5):699-42. PubMed ID: 473098
    [No Abstract]   [Full Text] [Related]  

  • 15. Hereditary orotic aciduria. I. A new case with family studies.
    Rogers LE; Warford LR; Patterson RB; Porter FS
    Pediatrics; 1968 Sep; 42(3):415-22. PubMed ID: 5677482
    [No Abstract]   [Full Text] [Related]  

  • 16. [REPORT OF FIELD SURVEY ON ACATALASEMIA AND HYPOCATALASEMIA DURING 1959-1962].
    TAKAHARA S; OGURA Y; ORITA Y; NAKAGAWA Y; KONISHI S; MORIA K
    Nihon Jibiinkoka Gakkai Kaiho; 1964 Oct; 67():1421-6. PubMed ID: 14219713
    [No Abstract]   [Full Text] [Related]  

  • 17. Activities of catalase in leucocytes and glucose-6-phosphate dehydrogenase in erythrocytes of hypocatalasemia and acatalasemia.
    Ogata M; Mizugaki J; Taketa K; Takahara S
    Tohoku J Exp Med; 1977 May; 122(1):93-7. PubMed ID: 918959
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Serum carnosinase deficiency concomitant with mental retardation.
    Murphey WH; Lindmark DG; Patchen LI; Housler ME; Harrod EK; Mosovich L
    Pediatr Res; 1973 Jul; 7(7):601-6. PubMed ID: 4718759
    [No Abstract]   [Full Text] [Related]  

  • 19. [On the cellular distribution of catalase in the blood of homozygous and heterozygous defect-carriers (acatalasia)].
    Aebi H; Cantz M
    Humangenetik; 1966; 3(1):50-63. PubMed ID: 5986055
    [No Abstract]   [Full Text] [Related]  

  • 20. Catalase activity of immature and mature red cells from acatalasemic mouse mutant.
    Ogata M; Inoue T; Tomokuni K; Takahara S
    Acta Haematol; 1970; 44(1):11-20. PubMed ID: 4991322
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.