BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 8383888)

  • 21. Human genetic instability syndromes: single gene defects with increased risk of cancer.
    Digweed M
    Toxicol Lett; 1993 Apr; 67(1-3):259-81. PubMed ID: 8451764
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Topo IIIalpha and BLM act within the Fanconi anemia pathway in response to DNA-crosslinking agents.
    Hemphill AW; Akkari Y; Newell AH; Schultz RA; Grompe M; North PS; Hickson ID; Jakobs PM; Rennie S; Pauw D; Hejna J; Olson SB; Moses RE
    Cytogenet Genome Res; 2009; 125(3):165-75. PubMed ID: 19738377
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Retinoblastoma in association with the chromosome breakage syndromes Fanconi's anaemia and Bloom's syndrome: clinical and cytogenetic findings.
    Gibbons B; Scott D; Hungerford JL; Cheung KL; Harrison C; Attard-Montalto S; Evans M; Birch JM; Kingston JE
    Clin Genet; 1995 Jun; 47(6):311-7. PubMed ID: 7554365
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Study of molecular markers of resistance to m-AMSA in a human breast cancer cell line. Decrease of topoisomerase II and increase of both topoisomerase I and acidic glutathione S transferase.
    Lefevre D; Riou JF; Ahomadegbe JC; Zhou DY; Benard J; Riou G
    Biochem Pharmacol; 1991 Jun; 41(12):1967-79. PubMed ID: 1645555
    [TBL] [Abstract][Full Text] [Related]  

  • 25. BLM promotes the activation of Fanconi Anemia signaling pathway.
    Panneerselvam J; Wang H; Zhang J; Che R; Yu H; Fei P
    Oncotarget; 2016 May; 7(22):32351-61. PubMed ID: 27083049
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Fanconi anemia cells have a normal gene structure for topoisomerase I.
    Saito H; Grompe M; Neeley TL; Jakobs PM; Moses RE
    Hum Genet; 1994 May; 93(5):583-6. PubMed ID: 8168839
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Delayed DNA maturation, a possible cause of the elevated sister-chromatid exchange in Bloom's syndrome.
    Ockey CH; Saffhill R
    Carcinogenesis; 1986 Jan; 7(1):53-7. PubMed ID: 3943145
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A high incidence of mitotic chiasmata in endoreduplicated Bloom's syndrome cells.
    Kuhn EM
    Hum Genet; 1981; 58(4):417-21. PubMed ID: 7327564
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Diagnosis of Fanconi Anaemia by ionising radiation- or mitomycin C-induced micronuclei.
    Francies FZ; Wainwright R; Poole J; De Leeneer K; Coene I; Wieme G; Poirel HA; Brichard B; Vermeulen S; Vral A; Slabbert J; Claes K; Baeyens A
    DNA Repair (Amst); 2018 Jan; 61():17-24. PubMed ID: 29154021
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Detection of free radical-induced DNA damage with bromodeoxyuridine/Hoechst flow cytometry: implications for Bloom's syndrome.
    Poot M; Rüdiger HW; Hoehn H
    Mutat Res; 1990 May; 238(3):203-7. PubMed ID: 1692968
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Relationship of DNA strand breakage produced by bromodeoxyuridine to topoisomerase II activity in Bloom-syndrome fibroblasts.
    Pommier Y; Rünger TM; Kerrigan D; Kraemer KH
    Mutat Res; 1991 Mar; 254(2):185-90. PubMed ID: 1848352
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Cytogenetic effects of inhibition of topoisomerase I or II activities in the CHO mutant EM9 and its parental line AA8.
    Cortés F; Piñero J; Palitti F
    Mutat Res; 1993 Aug; 288(2):281-9. PubMed ID: 7688089
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Evidence for BLM and Topoisomerase IIIalpha interaction in genomic stability.
    Hu P; Beresten SF; van Brabant AJ; Ye TZ; Pandolfi PP; Johnson FB; Guarente L; Ellis NA
    Hum Mol Genet; 2001 Jun; 10(12):1287-98. PubMed ID: 11406610
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Chromosomal instability in B-lymphoblasotoid cell lines from Werner and Bloom syndrome patients.
    Honma M; Tadokoro S; Sakamoto H; Tanabe H; Sugimoto M; Furuichi Y; Satoh T; Sofuni T; Goto M; Hayashi M
    Mutat Res; 2002 Sep; 520(1-2):15-24. PubMed ID: 12297140
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Fanconi anaemia proteins are associated with sister chromatid bridging in mitosis.
    Ying S; Hickson ID
    Int J Hematol; 2011 Apr; 93(4):440-445. PubMed ID: 21472397
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Characterization of a new BLM mutation associated with a topoisomerase II alpha defect in a patient with Bloom's syndrome.
    Foucault F; Vaury C; Barakat A; Thibout D; Planchon P; Jaulin C; Praz F; Amor-Guéret M
    Hum Mol Genet; 1997 Sep; 6(9):1427-34. PubMed ID: 9285778
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Hydrogen peroxide: effects on DNA, chromosomes, cell cycle and apoptosis induction in Fanconi's anemia cell lines.
    Zunino A; Degan P; Vigo T; Abbondandolo A
    Mutagenesis; 2001 May; 16(3):283-8. PubMed ID: 11320156
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Induction of sister chromatid exchanges by inhibitors of topoisomerases.
    Lim M; Liu LF; Jacobson-Kram D; Williams JR
    Cell Biol Toxicol; 1986 Dec; 2(4):485-94. PubMed ID: 2855799
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Elevated superoxide dismutase in Bloom's syndrome: a genetic condition of oxidative stress.
    Nicotera TM; Notaro J; Notaro S; Schumer J; Sandberg AA
    Cancer Res; 1989 Oct; 49(19):5239-43. PubMed ID: 2766291
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.