BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

270 related articles for article (PubMed ID: 10869141)

  • 61. Chromosome instability syndromes.
    Cohen MM; Levy HP
    Adv Hum Genet; 1989; 18():43-149, 365-71. PubMed ID: 2658496
    [No Abstract]   [Full Text] [Related]  

  • 62. Xeroderma pigmentosum group E and DDB2, a smaller subunit of damage-specific DNA binding protein: proposed classification of xeroderma pigmentosum, Cockayne syndrome, and ultraviolet-sensitive syndrome.
    Itoh T
    J Dermatol Sci; 2006 Feb; 41(2):87-96. PubMed ID: 16325378
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Nijmegen breakage syndrome: clinical manifestation of defective response to DNA double-strand breaks.
    Digweed M; Sperling K
    DNA Repair (Amst); 2004; 3(8-9):1207-17. PubMed ID: 15279809
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Coinheritance of BRCA1 and BRCA2 mutations with Fanconi anemia and Bloom syndrome mutations in Ashkenazi Jewish population: possible role in risk modification for cancer development.
    Koren-Michowitz M; Friedman E; Gershoni-Baruch R; Brok-Simoni F; Patael Y; Rechavi G; Amariglio N
    Am J Hematol; 2005 Mar; 78(3):203-6. PubMed ID: 15726604
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Genodermatoses with malignant potential.
    Holman JD; Dyer JA
    Curr Opin Pediatr; 2007 Aug; 19(4):446-54. PubMed ID: 17630610
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Inherited defects in DNA repair and susceptibility to DNA-damaging agents.
    Hansson J
    Toxicol Lett; 1992 Dec; 64-65 Spec No():141-8. PubMed ID: 1471167
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Conversion of replicative intermediates in human DNA-repair defective cells.
    Hurt MM; Moses RE
    Exp Cell Res; 1986 Apr; 163(2):396-404. PubMed ID: 3956584
    [TBL] [Abstract][Full Text] [Related]  

  • 68. DNA repair disorders.
    Woods CG
    Arch Dis Child; 1998 Feb; 78(2):178-84. PubMed ID: 9579166
    [No Abstract]   [Full Text] [Related]  

  • 69. Non-radioisotope method for diagnosing photosensitive genodermatoses and a new marker for xeroderma pigmentosum variant.
    Hashimoto S; Egawa K; Ihn H; Tateishi S
    J Dermatol; 2009 Mar; 36(3):138-43. PubMed ID: 19335687
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Heritable cancer-prone disorders featuring carcinogen hypersensitivity and DNA repair deficiency.
    Paterson MC
    IARC Sci Publ; 1982; (39):57-86. PubMed ID: 7152625
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Oxidative stress, mitochondrial abnormalities and antioxidant defense in Ataxia-telangiectasia, Bloom syndrome and Nijmegen breakage syndrome.
    Maciejczyk M; Mikoluc B; Pietrucha B; Heropolitanska-Pliszka E; Pac M; Motkowski R; Car H
    Redox Biol; 2017 Apr; 11():375-383. PubMed ID: 28063379
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Human DNA repair defects.
    Arlett CF
    J Inherit Metab Dis; 1986; 9 Suppl 1():69-84. PubMed ID: 3097418
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Dose response of gamma rays and iron nuclei for induction of chromosomal aberrations in normal and repair-deficient cell lines.
    George KA; Hada M; Jackson LJ; Elliott T; Kawata T; Pluth JM; Cucinotta FA
    Radiat Res; 2009 Jun; 171(6):752-63. PubMed ID: 19580482
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Photosensitivity and photodermatitis in childhood.
    Kahn G
    Dermatol Clin; 1986 Jan; 4(1):107-16. PubMed ID: 3521976
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Fanconi anemia presenting as acute myeloid leukemia: a case report.
    Bhatia A; Dash S; Varma N; Marwaha RK
    Indian J Pathol Microbiol; 2007 Apr; 50(2):441-3. PubMed ID: 17883104
    [TBL] [Abstract][Full Text] [Related]  

  • 76. The Fanconi anaemia/BRCA pathway.
    D'Andrea AD; Grompe M
    Nat Rev Cancer; 2003 Jan; 3(1):23-34. PubMed ID: 12509764
    [TBL] [Abstract][Full Text] [Related]  

  • 77. [Diagnosis of Fanconi's anemia by nitrogen mustard induction of chromosome breakage in fibroblasts].
    Desangles F
    Pathol Biol (Paris); 1991 Feb; 39(2):99-104. PubMed ID: 2017342
    [TBL] [Abstract][Full Text] [Related]  

  • 78. 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]  

  • 79. Comparative study of nucleotide excision repair defects between XPD-mutated fibroblasts derived from trichothiodystrophy and xeroderma pigmentosum patients.
    Nishiwaki T; Kobayashi N; Iwamoto T; Yamamoto A; Sugiura S; Liu YC; Sarasin A; Okahashi Y; Hirano M; Ueno S; Mori T
    DNA Repair (Amst); 2008 Dec; 7(12):1990-8. PubMed ID: 18817897
    [TBL] [Abstract][Full Text] [Related]  

  • 80. [Hereditary disease with hyper-sensitivity to radiation].
    Suzuki N; Kojima T; Sugita K
    Nihon Rinsho; 1993 Jan; 51 Suppl():1078-86. PubMed ID: 8459531
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.