BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

317 related articles for article (PubMed ID: 26940275)

  • 41. Array CGH in human leukemia: from somatics to genetics.
    van der Veken LT; Buijs A
    Cytogenet Genome Res; 2011; 135(3-4):260-70. PubMed ID: 21893961
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Monozygotic twins with shared de novo GATA2 mutation but dissimilar phenotypes due to differential promoter methylation.
    Kim N; Choi S; Kim SM; Lee AC; Im K; Park HS; Kim JA; Kim K; Kim I; Chang YH; Lee DS
    Leuk Lymphoma; 2019 Apr; 60(4):1053-1061. PubMed ID: 30714451
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Integrating germline variant assessment into routine clinical practice for myelodysplastic syndrome and acute myeloid leukaemia: current strategies and challenges.
    Tawana K; Brown AL; Churpek JE
    Br J Haematol; 2022 Mar; 196(6):1293-1310. PubMed ID: 34658019
    [TBL] [Abstract][Full Text] [Related]  

  • 44. The New Clinicopathologic and Molecular Findings in Myeloid Neoplasms With inv(3)(q21q26)/t(3;3)(q21;q26.2).
    Wang HY; Rashidi HH
    Arch Pathol Lab Med; 2016 Dec; 140(12):1404-1410. PubMed ID: 27628325
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Genetic predisposition in acute leukaemia.
    Wiggins M; Stevenson W
    Int J Lab Hematol; 2020 Jun; 42 Suppl 1():75-81. PubMed ID: 32115888
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Inherited predisposition to acute myeloid leukemia.
    Godley LA
    Semin Hematol; 2014 Oct; 51(4):306-21. PubMed ID: 25311743
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Phenotypic heterogeneity associated with germline
    Haddox CL; Carr RM; Abraham RS; Perez Botero J; Rodriguez V; Pardanani A; Patnaik MM
    Leuk Lymphoma; 2019 Dec; 60(13):3282-3286. PubMed ID: 31246134
    [No Abstract]   [Full Text] [Related]  

  • 48. Assessment of Factors Associated With the Evaluation of Children for Leukemia Predisposition Syndromes: A Retrospective Single-center Study.
    D'Aquila KR; Kessler E; Cooper KL; Durst A; Meade J
    J Pediatr Hematol Oncol; 2023 Jul; 45(5):e597-e602. PubMed ID: 37027191
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Hereditary Predisposition to Hematopoietic Neoplasms: When Bloodline Matters for Blood Cancers.
    Mangaonkar AA; Patnaik MM
    Mayo Clin Proc; 2020 Jul; 95(7):1482-1498. PubMed ID: 32571604
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Clinical and functional characterization of telomerase variants in patients with pediatric acute myeloid leukemia/myelodysplastic syndrome.
    Tomlinson CG; Sasa G; Aubert G; Martin-Giacalone B; Plon SE; Bryan TM; Bertuch AA; Gramatges MM
    Leukemia; 2021 Jan; 35(1):269-273. PubMed ID: 32313107
    [No Abstract]   [Full Text] [Related]  

  • 51. NPM1 mutations may reveal acute myeloid leukemia in cases otherwise morphologically diagnosed as myelodysplastic syndromes or myelodysplastic/myeloproliferative neoplasms.
    Forghieri F; Paolini A; Morselli M; Bigliardi S; Bonacorsi G; Leonardi G; Coluccio V; Maccaferri M; Fantuzzi V; Faglioni L; Colaci E; Soci F; Nasillo V; Messerotti A; Arletti L; Pioli V; Zucchini P; Quadrelli C; Corradini G; Giacobbi F; Vallerini D; Riva G; Barozzi P; Lagreca I; Marasca R; Narni F; Mecucci C; Ottaviani E; Martinelli G; Falini B; Luppi M; Potenza L
    Leuk Lymphoma; 2015; 56(11):3222-6. PubMed ID: 25813079
    [No Abstract]   [Full Text] [Related]  

  • 52. Targeted Next-Generation Sequencing in Myelodysplastic Syndrome and Chronic Myelomonocytic Leukemia Aids Diagnosis in Challenging Cases and Identifies Frequent Spliceosome Mutations in Transformed Acute Myeloid Leukemia.
    Reinig E; Yang F; Traer E; Arora R; Brown S; Rattray R; Braziel R; Fan G; Press R; Dunlap J
    Am J Clin Pathol; 2016 Apr; 145(4):497-506. PubMed ID: 27124934
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Aplastic anemia and clonal evolution: germ line and somatic genetics.
    Shimamura A
    Hematology Am Soc Hematol Educ Program; 2016 Dec; 2016(1):74-82. PubMed ID: 27913465
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Practical considerations for diagnosis and management of patients and carriers.
    Niemeyer CM; Mecucci C
    Semin Hematol; 2017 Apr; 54(2):69-74. PubMed ID: 28637619
    [TBL] [Abstract][Full Text] [Related]  

  • 55. The role of p53 in myelodysplastic syndromes and acute myeloid leukemia: molecular aspects and clinical implications.
    Zhang L; McGraw KL; Sallman DA; List AF
    Leuk Lymphoma; 2017 Aug; 58(8):1777-1790. PubMed ID: 27967292
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Transcription factor mutations as a cause of familial myeloid neoplasms.
    Churpek JE; Bresnick EH
    J Clin Invest; 2019 Feb; 129(2):476-488. PubMed ID: 30707109
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Connections between constitutional mismatch repair deficiency syndrome and neurofibromatosis type 1.
    Wimmer K; Rosenbaum T; Messiaen L
    Clin Genet; 2017 Apr; 91(4):507-519. PubMed ID: 27779754
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Fifth Edition of the World Health Classification of Tumors of the Hematopoietic and Lymphoid Tissue: Myeloid Neoplasms.
    Loghavi S; Kanagal-Shamanna R; Khoury JD; Medeiros LJ; Naresh KN; Nejati R; Patnaik MM;
    Mod Pathol; 2024 Feb; 37(2):100397. PubMed ID: 38043791
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Germline Predisposition to Myelodysplastic Syndromes.
    Gener-Ricos G; Gerstein YS; Hammond D; DiNardo CD
    Cancer J; 2023 May-Jun 01; 29(3):143-151. PubMed ID: 37195770
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Critical evaluation of the World Health Organization classification of myelodysplasia and acute myeloid leukemia.
    Heaney ML; Golde DW;
    Curr Oncol Rep; 2000 Mar; 2(2):140-3. PubMed ID: 11122835
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.