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 *

183 related articles for article (PubMed ID: 3026612)

  • 21. [The role of free oxygen radicals in the pathogenesis of Fanconi's anemia].
    Rumiantsev AG; Samochatova EV; Afanas'ev IB; Korkina LG; Suslova TB
    Ter Arkh; 1989; 61(7):32-6. PubMed ID: 2588140
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Synergism of bromodeoxyuridine and mitomycin C in the production of chromosomal aberrations in Fanconi's anemia].
    Frías S; Molina B; Carnevale A
    Rev Invest Clin; 1989; 41(1):31-5. PubMed ID: 2499026
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Sensitivity to five mutagens in Fanconi's anemia as measured by the micronucleus method.
    Heddle JA; Lue CB; Saunders EF; Benz RD
    Cancer Res; 1978 Sep; 38(9):2983-8. PubMed ID: 679206
    [No Abstract]   [Full Text] [Related]  

  • 24. Suppression of spontaneous and mitomycin C-induced chromosome aberrations in Fanconi's anemia by cell fusion with normal human fibroblasts.
    Yoshida MC
    Hum Genet; 1980; 55(2):223-6. PubMed ID: 7450765
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Fanconi's anemia: terminal leukemia and "Forme fruste" in one family.
    Schroeder TM; Pöhler E; Hufnagl HD; Stahl-Maugé C
    Clin Genet; 1979 Oct; 16(4):260-8. PubMed ID: 293233
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Genetic heterogenicity study in Fanconi's anemia by the addition of plasma].
    Frías S; Carnevale A; Molina B; del Castillo V
    Rev Invest Clin; 1986; 38(3):269-71. PubMed ID: 3097778
    [No Abstract]   [Full Text] [Related]  

  • 27. The rate of sister chromatid exchanges parallel to spontaneous chromosome breakage in Fanconi's anemia and to trenimon-induced aberrations in human lymphocytes and fibroblasts.
    Hayashi K; Schmid W
    Humangenetik; 1975 Sep; 29(3):201-6. PubMed ID: 1165100
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Analysis of heterogeneity in Fanconi's anemia patients of different ethnic origin.
    Zakrzewski S; Sperling K
    Hum Genet; 1982; 62(4):321-3. PubMed ID: 6819986
    [No Abstract]   [Full Text] [Related]  

  • 29. Antagonistic effect of cocultivation on mitomycin C-induced aberration rate in cells of a patient with Fanconi's anemia and in Chinese hamster ovary cells.
    Zakrzewski S; Sperling K
    Hum Genet; 1980; 56(1):85-8. PubMed ID: 7193643
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Effect of oxygen tension on chromosomal aberrations in Fanconi anaemia.
    Joenje H; Oostra AB
    Hum Genet; 1983; 65(2):99-101. PubMed ID: 6418637
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Fanconi's anemia: a cytogenetic study on lymphocyte and bone marrow cultures utilizing 1,2:3,4-diepoxybutane.
    Marx MP; Smith S; Heyns AD; van Tonder IZ
    Cancer Genet Cytogenet; 1983 May; 9(1):51-9. PubMed ID: 6839306
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Use of a test exposing lymphocytes to mitomycin C in the diagnosis of Fanconi's anemia].
    Frías S; Carnevale A; del Castillo V
    Rev Invest Clin; 1984; 36(3):219-24. PubMed ID: 6440252
    [No Abstract]   [Full Text] [Related]  

  • 33. [Chromosome abnormalities in bone marrow cells and peripheral lymphocytes in a patient with Fanconi's anemia].
    Margiotta G; Barbata G; Carbone P; Granata G; Caronia F
    Minerva Med; 1981 Sep; 72(35):2361-5. PubMed ID: 7279258
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Failure of diepoxybutane to enhance sister chromatid exchange levels in Fanconi's anemia patients and heterozygotes.
    Porfirio B; Dallapiccola B; Mokini V; Alimena G; Gandini E
    Hum Genet; 1983; 63(2):117-20. PubMed ID: 6840755
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mitomycin C induced chromosome damage in fetal blood cultures and prenatal diagnosis of Fanconi's anaemia.
    Shipley J; Rodeck CH; Garrett C; Galbraith J; Giannelli F
    Prenat Diagn; 1984; 4(3):217-21. PubMed ID: 6431403
    [TBL] [Abstract][Full Text] [Related]  

  • 36. G2 chromosomal radiosensitivity in Fanconi's anemia.
    Bigelow SB; Rary JM; Bender MA
    Mutat Res; 1979 Nov; 63(1):189-99. PubMed ID: 522866
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Frequency and types of induced and spontaneous chromosome aberrations in relation to cell kinetics.
    Mutchinick O; Ruz L; Gonsebatt ME; Mauleón P; Lisker R; García G
    Hum Genet; 1981; 59(2):137-40. PubMed ID: 7327573
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Position of chromosomes in the human interphase nucleus. An analysis of nonhomologous chromatid translocations in lymphocyte cultures after Trenimon treatment and from patients with Fanconi's anemia and Bloom's syndrome.
    Hager HD; Schroeder-Kurth TM; Vogel F
    Hum Genet; 1982; 61(4):342-56. PubMed ID: 7152519
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Cytogenetic analyses utilizing various clastogens in two sibs with Fanconi anemia, their relatives, and control individuals.
    Gebhart E; Kysela D; Matthee H; Nikol M
    Hum Genet; 1985; 69(4):309-15. PubMed ID: 3921453
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Distribution of chromosome breaks in measles, Fanconi's anemia and controls.
    von Koskull H; Aula P
    Hereditas; 1977; 87(1):1-10. PubMed ID: 591354
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.