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Journal Abstract Search

135 related items for PubMed ID: 12676774

  • 21. Androgen derivatives improve blood counts and elongate telomere length in adult cryptic dyskeratosis congenita.
    Kirschner M, Vieri M, Kricheldorf K, Ferreira MSV, Wlodarski MW, Schwarz M, Balabanov S, Rolles B, Isfort S, Koschmieder S, Höchsmann B, Panse J, Brümmendorf TH, Beier F.
    Br J Haematol; 2021 May; 193(3):669-673. PubMed ID: 32744739
    [Abstract] [Full Text] [Related]

  • 22. Structural Analysis Reveals the Deleterious Effects of Telomerase Mutations in Bone Marrow Failure Syndromes.
    Hoffman H, Rice C, Skordalakes E.
    J Biol Chem; 2017 Mar 17; 292(11):4593-4601. PubMed ID: 28154186
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  • 23. 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 17; 34(2):258-60. PubMed ID: 19942288
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  • 24. Human telomere disease due to disruption of the CCAAT box of the TERC promoter.
    Aalbers AM, Kajigaya S, van den Heuvel-Eibrink MM, van der Velden VH, Calado RT, Young NS.
    Blood; 2012 Mar 29; 119(13):3060-3. PubMed ID: 22323451
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  • 27. Recurrent somatic mutations are rare in patients with cryptic dyskeratosis congenita.
    Kirschner M, Maurer A, Wlodarski MW, Ventura Ferreira MS, Bouillon AS, Halfmeyer I, Blau W, Kreuter M, Rosewich M, Corbacioglu S, Beck J, Schwarz M, Bittenbring J, Radsak MP, Wilk CM, Koschmieder S, Begemann M, Kurth I, Schemionek M, Brümmendorf TH, Beier F.
    Leukemia; 2018 Aug 29; 32(8):1762-1767. PubMed ID: 29749397
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  • 28. [Clinical and laboratory characteristics in patients of myelodysplastic syndrome with PNH clones].
    Li Y, Qin T, Xu Z, Zhang Y, Wang J, Li B, Fang L, Pan L, Hu N, Zhang H, Qu S, Liu J, Wang H, Xiao Z.
    Zhonghua Xue Ye Xue Za Zhi; 2016 Apr 29; 37(4):313-7. PubMed ID: 27093995
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  • 29. [Gene mutations in bone marrow failure syndromes].
    Yoshizato T, Makishima H.
    Rinsho Ketsueki; 2016 Apr 29; 57(12):2519-2525. PubMed ID: 28090021
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  • 30. Impact of immunogenetic polymorphisms in bone marrow failure syndromes.
    Serio B, Selleri C, Maciejewski JP.
    Mini Rev Med Chem; 2011 Jun 29; 11(6):544-52. PubMed ID: 21561401
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  • 32. A spectrum of severe familial liver disorders associate with telomerase mutations.
    Calado RT, Regal JA, Kleiner DE, Schrump DS, Peterson NR, Pons V, Chanock SJ, Lansdorp PM, Young NS.
    PLoS One; 2009 Nov 20; 4(11):e7926. PubMed ID: 19936245
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  • 35. Lack of mutations of the human telomerase RNA gene (hTERC) in myelodysplastic syndrome.
    Ohyashiki K, Shay JW, Ohyashiki JH.
    Haematologica; 2005 May 20; 90(5):691. PubMed ID: 15921388
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  • 37. 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 20; 11(6):584-94. PubMed ID: 17663679
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  • 38. Idiopathic aplastic anemia vs hypocellular myelodysplastic syndrome.
    Durrani J, Maciejewski JP.
    Hematology Am Soc Hematol Educ Program; 2019 Dec 06; 2019(1):97-104. PubMed ID: 31808900
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  • 39. Telomeres and marrow failure.
    Calado RT.
    Hematology Am Soc Hematol Educ Program; 2009 Dec 06; ():338-43. PubMed ID: 20008219
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  • 40. Association between aplastic anaemia and mutations in telomerase RNA.
    Vulliamy T, Marrone A, Dokal I, Mason PJ.
    Lancet; 2002 Jun 22; 359(9324):2168-70. PubMed ID: 12090986
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