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Journal Abstract Search

311 related items for PubMed ID: 17663679

  • 1. Dyskeratosis congenita: advances in the understanding of the telomerase defect and the role of stem cell transplantation.
    de la Fuente J, Dokal I.
    Pediatr Transplant; 2007 Sep; 11(6):584-94. PubMed ID: 17663679
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  • 2. Dyskeratosis congenita: a genetic disorder of many faces.
    Kirwan M, Dokal I.
    Clin Genet; 2008 Feb; 73(2):103-12. PubMed ID: 18005359
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  • 3. Dyskeratosis congenita: molecular insights into telomerase function, ageing and cancer.
    Marrone A, Dokal I.
    Expert Rev Mol Med; 2004 Dec 20; 6(26):1-23. PubMed ID: 15613268
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  • 4. Very short telomeres in the peripheral blood of patients with X-linked and autosomal dyskeratosis congenita.
    Vulliamy TJ, Knight SW, Mason PJ, Dokal I.
    Blood Cells Mol Dis; 2001 Dec 20; 27(2):353-7. PubMed ID: 11259155
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  • 5. Dyskeratosis congenita: its link to telomerase and aplastic anaemia.
    Dokal I, Vulliamy T.
    Blood Rev; 2003 Dec 20; 17(4):217-25. PubMed ID: 14556776
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  • 6. Stem cells, telomerase and dyskeratosis congenita.
    Mason PJ.
    Bioessays; 2003 Feb 20; 25(2):126-33. PubMed ID: 12539238
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  • 8. Dyskeratosis congenita.
    Handley TP, McCaul JA, Ogden GR.
    Oral Oncol; 2006 Apr 20; 42(4):331-6. PubMed ID: 16140563
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  • 10. 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 Apr 20; 34(3):257-63. PubMed ID: 15885610
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  • 11. Dyskeratosis congenita: a disorder of defective telomere maintenance?
    Walne AJ, Marrone A, Dokal I.
    Int J Hematol; 2005 Oct 20; 82(3):184-9. PubMed ID: 16207588
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  • 12. Identification of DKC1 gene mutations in Japanese patients with X-linked dyskeratosis congenita.
    Kanegane H, Kasahara Y, Okamura J, Hongo T, Tanaka R, Nomura K, Kojima S, Miyawaki T.
    Br J Haematol; 2005 May 20; 129(3):432-4. PubMed ID: 15842668
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  • 13. Gene structure and expression of the mouse dyskeratosis congenita gene, dkc1.
    Heiss NS, Bächner D, Salowsky R, Kolb A, Kioschis P, Poustka A.
    Genomics; 2000 Jul 15; 67(2):153-63. PubMed ID: 10903840
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  • 17. Dyskeratosis congenita: the diverse clinical presentation of mutations in the telomerase complex.
    Vulliamy TJ, Dokal I.
    Biochimie; 2008 Jan 15; 90(1):122-30. PubMed ID: 17825470
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  • 18. Dyskeratosis congenita and cancer in mice deficient in ribosomal RNA modification.
    Ruggero D, Grisendi S, Piazza F, Rego E, Mari F, Rao PH, Cordon-Cardo C, Pandolfi PP.
    Science; 2003 Jan 10; 299(5604):259-62. PubMed ID: 12522253
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  • 19. TERC mutations in children with refractory cytopenia.
    Ortmann CA, Niemeyer CM, Wawer A, Ebell W, Baumann I, Kratz CP.
    Haematologica; 2006 May 10; 91(5):707-8. PubMed ID: 16670076
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  • 20. Telomerase reverse-transcriptase homozygous mutations in autosomal recessive dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome.
    Marrone A, Walne A, Tamary H, Masunari Y, Kirwan M, Beswick R, Vulliamy T, Dokal I.
    Blood; 2007 Dec 15; 110(13):4198-205. PubMed ID: 17785587
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