These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

159 related articles for article (PubMed ID: 9420149)

  • 1. Further genetic heterogeneity in acatalasemia.
    Góth L
    Electrophoresis; 1997 Oct; 18(11):1942-3. PubMed ID: 9420149
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel catalase mutation detected by polymerase chain reaction-single strand conformation polymorphism, nucleotide sequencing, and western blot analyses is responsible for the type C of Hungarian acatalasemia.
    Góth L; Rass P; Madarasi I
    Electrophoresis; 2001 Jan; 22(1):49-51. PubMed ID: 11197178
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel human catalase mutation (358 T-->del) causing Japanese-type acatalasemia.
    Hirono A; Sasaya-Hamada F; Kanno H; Fujii H; Yoshida T; Miwa S
    Blood Cells Mol Dis; 1995; 21(3):232-4. PubMed ID: 8673475
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Polymorphism of 5' of the catalase gene in Hungarian acatalasemia and hypocatalasemia.
    Góth L; Vitai M
    Electrophoresis; 1997 Jun; 18(7):1105-8. PubMed ID: 9237564
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic heterogeneity in acatalasemia.
    Góth L; Páy A
    Electrophoresis; 1996 Aug; 17(8):1302-3. PubMed ID: 8874054
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Further characterization of Hungarian acatalasemia by Hinf1 polymorphism of catalase gene.
    Góth L; Alizadeh BN; Sussman HH
    Enzyme Protein; 1993; 47(3):156-9. PubMed ID: 7916241
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular analysis of human acatalasemia. Identification of a splicing mutation.
    Wen JK; Osumi T; Hashimoto T; Ogata M
    J Mol Biol; 1990 Jan; 211(2):383-93. PubMed ID: 2308162
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Anovel catalase mutation (a GA insertion) causes the Hungarian type of acatalasemia.
    Góth L; Shemirani A; Kalmár T
    Blood Cells Mol Dis; 2000 Apr; 26(2):151-4. PubMed ID: 11001624
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic heterogeneity of the 5' uncoding region of the catalase gene in Hungarian acatalasemic and hypocatalasemic subjects.
    Góth L
    Clin Chim Acta; 1998 Mar; 271(1):73-8. PubMed ID: 9564558
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection of a novel familial catalase mutation (Hungarian type D) and the possible risk of inherited catalase deficiency for diabetes mellitus.
    Góth L; Vitai M; Rass P; Sükei E; Páy A
    Electrophoresis; 2005 May; 26(9):1646-9. PubMed ID: 15800961
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Detection of a common mutation of the catalase gene in Japanese acatalasemic patients.
    Kishimoto Y; Murakami Y; Hayashi K; Takahara S; Sugimura T; Sekiya T
    Hum Genet; 1992 Mar; 88(5):487-90. PubMed ID: 1551654
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Catalase -262C>T polymorphisms in Hungarian vitiligo patients and in controls: further acatalasemia mutations in Hungary.
    Kósa Z; Fejes Z; Nagy T; Csordás M; Simics E; Remenyik E; Góth L
    Mol Biol Rep; 2012 Apr; 39(4):4787-95. PubMed ID: 21947853
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Immunotitration of the catalase in the blood of Japanese subjects and mice suffering from acatalasemia and hypocatalasemia.
    Ogata M; Fujii Y
    Physiol Chem Phys Med NMR; 1992; 24(4):261-9. PubMed ID: 1296208
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Further acatalasemia mutations in human patients from Hungary with diabetes and microcytic anemia.
    Nagy T; Paszti E; Kaplar M; Bhattoa HP; Goth L
    Mutat Res; 2015 Feb; 772():10-4. PubMed ID: 25772105
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Diminished synthesis of catalase due to the decrease in catalase mRNA in Japanese-type acatalasemia.
    Wen JK; Osumi T; Hashimoto T; Ogata M
    Physiol Chem Phys Med NMR; 1988; 20(3):171-6. PubMed ID: 3244798
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Properties of erythrocyte catalase from heterozygotes for Japanese type acatalasemia.
    Ogata M; Mizugaki J
    Acta Med Okayama; 1979 Jun; 33(3):205-11. PubMed ID: 40400
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mammalian acatalasemia: the perspectives of bioinformatics and genetic toxicology.
    Ogata M; Wang DH; Ogino K
    Acta Med Okayama; 2008 Dec; 62(6):345-61. PubMed ID: 19122680
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new type of inherited catalase deficiencies: its characterization and comparison to the Japanese and Swiss type of acatalasemia.
    Góth L
    Blood Cells Mol Dis; 2001; 27(2):512-7. PubMed ID: 11500062
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Simple PCR heteroduplex, SSCP mutation screening methods for the detection of novel catalase mutations in Hungarian patients with type 2 diabetes mellitus.
    Vitai M; Fátrai S; Rass P; Csordás M; Tarnai I
    Clin Chem Lab Med; 2005; 43(12):1346-50. PubMed ID: 16309371
    [TBL] [Abstract][Full Text] [Related]  

  • 20. cDNA cloning and expression of mutant catalase from the hypocatalasemic mouse: comparison with the acatalasemic mutant.
    Wang DH; Tsutsui K; Sano K; Masuoka N; Kira S
    Biochim Biophys Acta; 2001 Dec; 1522(3):217-20. PubMed ID: 11779637
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.