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 *

88 related articles for article (PubMed ID: 1282789)

  • 41. Retracted papers damage work on DNA repair.
    Check E
    Nature; 2005 Jun; 435(7045):1015. PubMed ID: 15973373
    [No Abstract]   [Full Text] [Related]  

  • 42. When more is better.
    Petrini JH
    Nat Genet; 2000 Nov; 26(3):257-8. PubMed ID: 11062454
    [No Abstract]   [Full Text] [Related]  

  • 43. Primary fibroblasts of Cockayne syndrome patients are defective in cellular repair of 8-hydroxyguanine and 8-hydroxyadenine resulting from oxidative stress.
    Tuo J; Jaruga P; Rodriguez H; Bohr VA; Dizdaroglu M
    FASEB J; 2003 Apr; 17(6):668-74. PubMed ID: 12665480
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Mechanisms of transcription-coupled DNA repair.
    Svejstrup JQ
    Nat Rev Mol Cell Biol; 2002 Jan; 3(1):21-9. PubMed ID: 11823795
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Cockayne syndrome with delayed recovery of RNA synthesis after ultraviolet irradiation but normal ultraviolet survival.
    Sugita K; Suzuki N; Kojima T; Tanabe Y; Nakajima H; Hayashi A; Arima M
    Pediatr Res; 1987 Jan; 21(1):34-7. PubMed ID: 2432457
    [TBL] [Abstract][Full Text] [Related]  

  • 46. UV-induced ubiquitination of RNA polymerase II: a novel modification deficient in Cockayne syndrome cells.
    Bregman DB; Halaban R; van Gool AJ; Henning KA; Friedberg EC; Warren SL
    Proc Natl Acad Sci U S A; 1996 Oct; 93(21):11586-90. PubMed ID: 8876179
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Cockayne syndrome group A and B proteins converge on transcription-linked resolution of non-B DNA.
    Scheibye-Knudsen M; Tseng A; Borch Jensen M; Scheibye-Alsing K; Fang EF; Iyama T; Bharti SK; Marosi K; Froetscher L; Kassahun H; Eckley DM; Maul RW; Bastian P; De S; Ghosh S; Nilsen H; Goldberg IG; Mattson MP; Wilson DM; Brosh RM; Gorospe M; Bohr VA
    Proc Natl Acad Sci U S A; 2016 Nov; 113(44):12502-12507. PubMed ID: 27791127
    [TBL] [Abstract][Full Text] [Related]  

  • 48. [The metabolic and molecular bases of Cockayne syndrome].
    Flores-Alvarado LJ; Ramirez-Garcia SA; Núñez-Reveles NY
    Rev Invest Clin; 2010; 62(5):480-90. PubMed ID: 21416736
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Role of the ATPase domain of the Cockayne syndrome group B protein in UV induced apoptosis.
    Balajee AS; Proietti De Santis L; Brosh RM; Selzer R; Bohr VA
    Oncogene; 2000 Jan; 19(4):477-89. PubMed ID: 10698517
    [TBL] [Abstract][Full Text] [Related]  

  • 50. The ATPase domain but not the acidic region of Cockayne syndrome group B gene product is essential for DNA repair.
    Brosh RM; Balajee AS; Selzer RR; Sunesen M; Proietti De Santis L; Bohr VA
    Mol Biol Cell; 1999 Nov; 10(11):3583-94. PubMed ID: 10564257
    [TBL] [Abstract][Full Text] [Related]  

  • 51. DNA repair in human cells: in Cockayne syndrome cells rejoining of DNA strands is impaired.
    Schwaiger H; Hirsch-Kauffmann M; Schweiger M
    Eur J Cell Biol; 1986 Aug; 41(2):352-5. PubMed ID: 3758088
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Deletion of 5' sequences of the CSB gene provides insight into the pathophysiology of Cockayne syndrome.
    Laugel V; Dalloz C; Stary A; Cormier-Daire V; Desguerre I; Renouil M; Fourmaintraux A; Velez-Cruz R; Egly JM; Sarasin A; Dollfus H
    Eur J Hum Genet; 2008 Mar; 16(3):320-7. PubMed ID: 18183039
    [TBL] [Abstract][Full Text] [Related]  

  • 53. DNA repair in human cells: biochemistry of the hereditary diseases Fanconi's anaemia and Cockayne syndrome. Tenth Fritz-Lipmann lecture.
    Schweiger M; Auer B; Burtscher HJ; Hirsch-Kauffmann M; Klocker H; Schneider R
    Biol Chem Hoppe Seyler; 1986 Dec; 367(12):1185-95. PubMed ID: 3103644
    [No Abstract]   [Full Text] [Related]  

  • 54. Cockayne syndrome type III with high intelligence.
    Czeizel AE; Marchalkó M
    Clin Genet; 1995 Dec; 48(6):331-3. PubMed ID: 8835332
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Worldwide Studies on Cockayne Syndrome are Needed.
    Bohr VA
    Neurol India; 2021; 69(2):367-368. PubMed ID: 33904454
    [No Abstract]   [Full Text] [Related]  

  • 56. Effects of DNA-breaking agents on Cockayne syndrome cells.
    Antonelli A; Petrinelli P; Marcucci L; Billi D; Cardona F; Leuzzi V; Elli R
    Ann N Y Acad Sci; 1992 Nov; 663():418-20. PubMed ID: 1282789
    [No Abstract]   [Full Text] [Related]  

  • 57. Cockayne syndrome--a primary defect in DNA repair, transcription, both or neither?
    Friedberg EC
    Bioessays; 1996 Sep; 18(9):731-8. PubMed ID: 8831289
    [TBL] [Abstract][Full Text] [Related]  

  • 58. The current evidence for defective repair of oxidatively damaged DNA in Cockayne syndrome.
    Frosina G
    Free Radic Biol Med; 2007 Jul; 43(2):165-77. PubMed ID: 17603927
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Conceptual developments in the causes of Cockayne syndrome.
    Cleaver JE; Bezrookove V; Revet I; Huang EJ
    Mech Ageing Dev; 2013; 134(5-6):284-90. PubMed ID: 23428417
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Mutations in Cockayne Syndrome-Associated Genes (Csa and Csb) Predispose to Cisplatin-Induced Hearing Loss in Mice.
    Rainey RN; Ng SY; Llamas J; van der Horst GT; Segil N
    J Neurosci; 2016 Apr; 36(17):4758-70. PubMed ID: 27122034
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.