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Journal Abstract Search

194 related items for PubMed ID: 16825992

  • 1. Low frequency of telomerase RNA mutations among children with aplastic anemia or myelodysplastic syndrome.
    Field JJ, Mason PJ, An P, Kasai Y, McLellan M, Jaeger S, Barnes YJ, King AA, Bessler M, Wilson DB.
    J Pediatr Hematol Oncol; 2006 Jul; 28(7):450-3. PubMed ID: 16825992
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  • 2. TERC mutations in children with refractory cytopenia.
    Ortmann CA, Niemeyer CM, Wawer A, Ebell W, Baumann I, Kratz CP.
    Haematologica; 2006 May; 91(5):707-8. PubMed ID: 16670076
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  • 4. 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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  • 5. Lack of mutations of the human telomerase RNA gene (hTERC) in myelodysplastic syndrome.
    Ohyashiki K, Shay JW, Ohyashiki JH.
    Haematologica; 2005 May; 90(5):691. PubMed ID: 15921388
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  • 6. Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome.
    Yamaguchi H, Baerlocher GM, Lansdorp PM, Chanock SJ, Nunez O, Sloand E, Young NS.
    Blood; 2003 Aug 01; 102(3):916-8. PubMed ID: 12676774
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  • 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 07; 352(14):1413-24. PubMed ID: 15814878
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  • 8. Mutations in telomerase catalytic protein in Japanese children with aplastic anemia.
    Liang J, Yagasaki H, Kamachi Y, Hama A, Matsumoto K, Kato K, Kudo K, Kojima S.
    Haematologica; 2006 May 07; 91(5):656-8. PubMed ID: 16627250
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  • 9. Telomerase gene mutation screening in Chinese patients with aplastic anemia.
    Han B, Liu B, Cui W, Wang X, Lin J, Zhao Y.
    Leuk Res; 2010 Feb 07; 34(2):258-60. PubMed ID: 19942288
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  • 10. Disease anticipation is associated with progressive telomere shortening in families with dyskeratosis congenita due to mutations in TERC.
    Vulliamy T, Marrone A, Szydlo R, Walne A, Mason PJ, Dokal I.
    Nat Genet; 2004 May 07; 36(5):447-9. PubMed ID: 15098033
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  • 11. 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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  • 13. Heterozygous telomerase RNA mutations found in dyskeratosis congenita and aplastic anemia reduce telomerase activity via haploinsufficiency.
    Marrone A, Stevens D, Vulliamy T, Dokal I, Mason PJ.
    Blood; 2004 Dec 15; 104(13):3936-42. PubMed ID: 15319288
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  • 14. Dyskeratosis congenita: a genetic disorder of many faces.
    Kirwan M, Dokal I.
    Clin Genet; 2008 Feb 15; 73(2):103-12. PubMed ID: 18005359
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  • 15. Functional characterization of novel telomerase RNA (TERC) mutations in patients with diverse clinical and pathological presentations.
    Marrone A, Sokhal P, Walne A, Beswick R, Kirwan M, Killick S, Williams M, Marsh J, Vulliamy T, Dokal I.
    Haematologica; 2007 Aug 15; 92(8):1013-20. PubMed ID: 17640862
    [Abstract] [Full Text] [Related]

  • 16. Dyskeratosis congenita and telomerase.
    Bessler M, Wilson DB, Mason PJ.
    Curr Opin Pediatr; 2004 Feb 15; 16(1):23-8. PubMed ID: 14758110
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  • 20. Stem cells, telomerase and dyskeratosis congenita.
    Mason PJ.
    Bioessays; 2003 Feb 15; 25(2):126-33. PubMed ID: 12539238
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