BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 32300648)

  • 21. Expression of Genes Associated with Telomere Homeostasis in TP53 Mutant LoVo Cell Lines as a Model for Genomic Instability.
    Samassekou O; Bastien N; Yan J; Mai S; Drouin R
    Methods Mol Biol; 2018; 1769():253-262. PubMed ID: 29564829
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Impact of germline CTC1 alterations on telomere length in acquired bone marrow failure.
    Shen W; Kerr CM; Przychozen B; Mahfouz RZ; LaFramboise T; Nagata Y; Hanna R; Radivoyevitch T; Nazha A; Sekeres MA; Maciejewski JP
    Br J Haematol; 2019 Jun; 185(5):935-939. PubMed ID: 30891747
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Dyskeratosis congenita associated with leukoplakia of the tongue.
    Noto Z; Tomihara K; Furukawa K; Noguchi M
    Int J Oral Maxillofac Surg; 2016 Jun; 45(6):760-3. PubMed ID: 26778687
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Cooperative interactions of p53 mutation, telomere dysfunction, and chronic liver damage in hepatocellular carcinoma progression.
    Farazi PA; Glickman J; Horner J; Depinho RA
    Cancer Res; 2006 May; 66(9):4766-73. PubMed ID: 16651430
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The short and long telomere syndromes: paired paradigms for molecular medicine.
    Stanley SE; Armanios M
    Curr Opin Genet Dev; 2015 Aug; 33():1-9. PubMed ID: 26232116
    [TBL] [Abstract][Full Text] [Related]  

  • 26. DNA strand break-sensing molecule poly(ADP-Ribose) polymerase cooperates with p53 in telomere function, chromosome stability, and tumor suppression.
    Tong WM; Hande MP; Lansdorp PM; Wang ZQ
    Mol Cell Biol; 2001 Jun; 21(12):4046-54. PubMed ID: 11359911
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Dyskeratosis congenita: telomerase, telomeres and anticipation.
    Marrone A; Walne A; Dokal I
    Curr Opin Genet Dev; 2005 Jun; 15(3):249-57. PubMed ID: 15917199
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A role for Brca1 in chromosome end maintenance.
    McPherson JP; Hande MP; Poonepalli A; Lemmers B; Zablocki E; Migon E; Shehabeldin A; Porras A; Karaskova J; Vukovic B; Squire J; Hakem R
    Hum Mol Genet; 2006 Mar; 15(6):831-8. PubMed ID: 16446310
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The Shelterin TIN2 Subunit Mediates Recruitment of Telomerase to Telomeres.
    Frank AK; Tran DC; Qu RW; Stohr BA; Segal DJ; Xu L
    PLoS Genet; 2015 Jul; 11(7):e1005410. PubMed ID: 26230315
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Telomere dysfunction and hematologic disorders.
    Paiva RM; Calado RT
    Prog Mol Biol Transl Sci; 2014; 125():133-57. PubMed ID: 24993701
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Chromosome aberrations and telomere length modulation in bone marrow and spleen cells of melphalan-treated p53+/- mice.
    Sgura A; De Amicis A; Stronati L; Cinelli S; Pacchierotti F; Tanzarella C
    Environ Mol Mutagen; 2008 Jul; 49(6):467-75. PubMed ID: 18481314
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Short telomeres, even in the presence of telomerase, limit tissue renewal capacity.
    Hao LY; Armanios M; Strong MA; Karim B; Feldser DM; Huso D; Greider CW
    Cell; 2005 Dec; 123(6):1121-31. PubMed ID: 16360040
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Dyskeratosis congenita: a disorder of defective telomere maintenance?
    Walne AJ; Marrone A; Dokal I
    Int J Hematol; 2005 Oct; 82(3):184-9. PubMed ID: 16207588
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The wide-ranging clinical implications of the short telomere syndromes.
    Barbaro PM; Ziegler DS; Reddel RR
    Intern Med J; 2016 Apr; 46(4):393-403. PubMed ID: 26247919
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Dyskeratosis congenita: the diverse clinical presentation of mutations in the telomerase complex.
    Vulliamy TJ; Dokal I
    Biochimie; 2008 Jan; 90(1):122-30. PubMed ID: 17825470
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mdm4 loss in mice expressing a p53 hypomorph alters tumor spectrum without improving survival.
    Fang M; Simeonova I; Bardot B; Lejour V; Jaber S; Bouarich-Bourimi R; Morin A; Toledo F
    Oncogene; 2014 Mar; 33(10):1336-9. PubMed ID: 23474762
    [TBL] [Abstract][Full Text] [Related]  

  • 37. p53 pathway is involved in cell competition during mouse embryogenesis.
    Zhang G; Xie Y; Zhou Y; Xiang C; Chen L; Zhang C; Hou X; Chen J; Zong H; Liu G
    Proc Natl Acad Sci U S A; 2017 Jan; 114(3):498-503. PubMed ID: 28049824
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The germline p53 activation syndrome: A new patient further refines the clinical phenotype.
    Kumar RD; Tosur M; Lalani SR; Mahoney DH; Bertuch AA
    Am J Med Genet A; 2022 Jul; 188(7):2204-2208. PubMed ID: 35362179
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A novel DKC1 gene mutation c.1177 A>T (p.I393F) in a case of dyskeratosis congenita with severe telomere shortening.
    Mohanty P; Jadhav P; Shanmukhaiah C; Kumar S; Vundinti BR
    Int J Dermatol; 2019 Dec; 58(12):1468-1471. PubMed ID: 30868555
    [No Abstract]   [Full Text] [Related]  

  • 40. Telomere length and cancer risk: finding Goldilocks.
    Savage SA
    Biogerontology; 2024 Apr; 25(2):265-278. PubMed ID: 38109000
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.