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Journal Abstract Search

182 related items for PubMed ID: 32150348

  • 1. TERT and TERC mutations detected in cryptic dyskeratosis congenita suppress telomerase activity.
    Terada K, Miyake K, Yamaguchi H, Miyake N, Yamanaka K, Kojima S, Ito E, Inokuchi K, Okada T.
    Int J Lab Hematol; 2020 Jun; 42(3):316-321. PubMed ID: 32150348
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  • 2. TERC and TERT gene mutations in patients with bone marrow failure and the significance of telomere length measurements.
    Du HY, Pumbo E, Ivanovich J, An P, Maziarz RT, Reiss UM, Chirnomas D, Shimamura A, Vlachos A, Lipton JM, Goyal RK, Goldman F, Wilson DB, Mason PJ, Bessler M.
    Blood; 2009 Jan 08; 113(2):309-16. PubMed ID: 18931339
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  • 4. Proliferative defects in dyskeratosis congenita skin keratinocytes are corrected by expression of the telomerase reverse transcriptase, TERT, or by activation of endogenous telomerase through expression of papillomavirus E6/E7 or the telomerase RNA component, TERC.
    Gourronc FA, Robertson mM, Herrig AK, Lansdorp PM, Goldman FD, Klingelhutz AJ.
    Exp Dermatol; 2010 Mar 08; 19(3):279-88. PubMed ID: 19558498
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  • 5. 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 08; 193(3):669-673. PubMed ID: 32744739
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  • 8. HuR regulates telomerase activity through TERC methylation.
    Tang H, Wang H, Cheng X, Fan X, Yang F, Zhang M, Chen Y, Tian Y, Liu C, Shao D, Jiang B, Dou Y, Cong Y, Xing J, Zhang X, Yi X, Songyang Z, Ma W, Zhao Y, Wang X, Ma J, Gorospe M, Ju Z, Wang W.
    Nat Commun; 2018 Jun 07; 9(1):2213. PubMed ID: 29880812
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  • 9. Dyskeratosis congenita: the diverse clinical presentation of mutations in the telomerase complex.
    Vulliamy TJ, Dokal I.
    Biochimie; 2008 Jan 07; 90(1):122-30. PubMed ID: 17825470
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  • 11. Telomere shortening and loss of self-renewal in dyskeratosis congenita induced pluripotent stem cells.
    Batista LF, Pech MF, Zhong FL, Nguyen HN, Xie KT, Zaug AJ, Crary SM, Choi J, Sebastiano V, Cherry A, Giri N, Wernig M, Alter BP, Cech TR, Savage SA, Reijo Pera RA, Artandi SE.
    Nature; 2011 May 22; 474(7351):399-402. PubMed ID: 21602826
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  • 12. 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 10; 105(23):8073-8. PubMed ID: 18523010
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  • 13. Telomere restoration and extension of proliferative lifespan in dyskeratosis congenita fibroblasts.
    Westin ER, Chavez E, Lee KM, Gourronc FA, Riley S, Lansdorp PM, Goldman FD, Klingelhutz AJ.
    Aging Cell; 2007 Jun 10; 6(3):383-94. PubMed ID: 17381549
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  • 14. Dyskeratosis congenita: telomerase, telomeres and anticipation.
    Marrone A, Walne A, Dokal I.
    Curr Opin Genet Dev; 2005 Jun 10; 15(3):249-57. PubMed ID: 15917199
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  • 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 10; 144(5):771-81. PubMed ID: 19036115
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  • 20. 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 01; 286(26):23022-30. PubMed ID: 21536674
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