BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

474 related articles for article (PubMed ID: 18239083)

  • 1. Telomere maintenance and human bone marrow failure.
    Calado RT; Young NS
    Blood; 2008 May; 111(9):4446-55. PubMed ID: 18239083
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Differences in disease severity but similar telomere lengths in genetic subgroups of patients with telomerase and shelterin mutations.
    Vulliamy TJ; Kirwan MJ; Beswick R; Hossain U; Baqai C; Ratcliffe A; Marsh J; Walne A; Dokal I
    PLoS One; 2011; 6(9):e24383. PubMed ID: 21931702
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Telomeres and marrow failure.
    Calado RT
    Hematology Am Soc Hematol Educ Program; 2009; ():338-43. PubMed ID: 20008219
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Short telomeres in pulmonary fibrosis: from genetics to clinical significance.
    Trăilă D; Mlădinescu OF; Oancea C; Tudorache V
    Pneumologia; 2015; 64(1):8, 11-3. PubMed ID: 26016050
    [TBL] [Abstract][Full Text] [Related]  

  • 5. TINF2 mutations result in very short telomeres: analysis of a large cohort of patients with dyskeratosis congenita and related bone marrow failure syndromes.
    Walne AJ; Vulliamy T; Beswick R; Kirwan M; Dokal I
    Blood; 2008 Nov; 112(9):3594-600. PubMed ID: 18669893
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in the reverse transcriptase component of telomerase (TERT) in patients with bone marrow failure.
    Vulliamy TJ; Walne A; Baskaradas A; Mason PJ; Marrone A; Dokal I
    Blood Cells Mol Dis; 2005; 34(3):257-63. PubMed ID: 15885610
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia.
    Yamaguchi H; Calado RT; Ly H; Kajigaya S; Baerlocher GM; Chanock SJ; Lansdorp PM; Young NS
    N Engl J Med; 2005 Apr; 352(14):1413-24. PubMed ID: 15814878
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Short telomeres: from dyskeratosis congenita to sporadic aplastic anemia and malignancy.
    Gramatges MM; Bertuch AA
    Transl Res; 2013 Dec; 162(6):353-63. PubMed ID: 23732052
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Telomere dynamics and hematopoietic differentiation of human DKC1-mutant induced pluripotent stem cells.
    Donaires FS; Alves-Paiva RM; Gutierrez-Rodrigues F; da Silva FB; Tellechea MF; Moreira LF; Santana BA; Traina F; Dunbar CE; Winkler T; Calado RT
    Stem Cell Res; 2019 Oct; 40():101540. PubMed ID: 31479877
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Abnormality of telomere maintenance linked to bone marrow failures].
    Yamaguchi H
    Nihon Rinsho; 2008 Mar; 66(3):483-9. PubMed ID: 18326318
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dyskeratosis congenita, stem cells and telomeres.
    Kirwan M; Dokal I
    Biochim Biophys Acta; 2009 Apr; 1792(4):371-9. PubMed ID: 19419704
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Erosion of telomeric single-stranded overhang in patients with aplastic anaemia carrying telomerase complex mutations.
    Calado RT; Regal JA; Kajigaya S; Young NS
    Eur J Clin Invest; 2009 Nov; 39(11):1025-32. PubMed ID: 19674077
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Bone marrow failure and the new telomere diseases: practice and research.
    Young NS
    Hematology; 2012 Apr; 17 Suppl 1():S18-21. PubMed ID: 22507770
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Editing TINF2 as a potential therapeutic approach to restore telomere length in dyskeratosis congenita.
    Choo S; Lorbeer FK; Regalado SG; Short SB; Wu S; Rieser G; Bertuch AA; Hockemeyer D
    Blood; 2022 Aug; 140(6):608-618. PubMed ID: 35421215
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Exogenous TERC alone can enhance proliferative potential, telomerase activity and telomere length in lymphocytes from dyskeratosis congenita patients.
    Kirwan M; Beswick R; Vulliamy T; Nathwani AC; Walne AJ; Casimir C; Dokal I
    Br J Haematol; 2009 Mar; 144(5):771-81. PubMed ID: 19036115
    [TBL] [Abstract][Full Text] [Related]  

  • 16. TIN2 protein dyskeratosis congenita missense mutants are defective in association with telomerase.
    Yang D; He Q; Kim H; Ma W; Songyang Z
    J Biol Chem; 2011 Jul; 286(26):23022-30. PubMed ID: 21536674
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Advances in the understanding of dyskeratosis congenita.
    Walne AJ; Dokal I
    Br J Haematol; 2009 Apr; 145(2):164-72. PubMed ID: 19208095
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Telomerase gene therapy rescues telomere length, bone marrow aplasia, and survival in mice with aplastic anemia.
    Bär C; Povedano JM; Serrano R; Benitez-Buelga C; Popkes M; Formentini I; Bobadilla M; Bosch F; Blasco MA
    Blood; 2016 Apr; 127(14):1770-9. PubMed ID: 26903545
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita.
    Vulliamy T; Beswick R; Kirwan M; Marrone A; Digweed M; Walne A; Dokal I
    Proc Natl Acad Sci U S A; 2008 Jun; 105(23):8073-8. PubMed ID: 18523010
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 24.