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Journal Abstract Search

175 related items for PubMed ID: 37210875

  • 1. Acute leukemias with complex karyotype show a similarly poor outcome independent of mixed, myeloid or lymphoblastic immunophenotype: A study from the Bone Marrow Pathology Group.
    Kirtek T, Chen W, Laczko D, Bagg A, Koduru P, Foucar K, Venable E, Nichols M, Rogers HJ, Tam W, Orazi A, Hsi ED, Hasserjian RP, Wang SA, Arber DA, Weinberg OK.
    Leuk Res; 2023 Jul; 130():107309. PubMed ID: 37210875
    [Abstract] [Full Text] [Related]

  • 2. ASXL1 mutation as a surrogate marker in acute myeloid leukemia with myelodysplasia-related changes and normal karyotype.
    Prats-Martín C, Burillo-Sanz S, Morales-Camacho RM, Pérez-López O, Suito M, Vargas MT, Caballero-Velázquez T, Carrillo-Cruz E, González J, Bernal R, Pérez-Simón JA.
    Cancer Med; 2020 Jun; 9(11):3637-3646. PubMed ID: 32216059
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  • 3. Genomic Landscape of Mixed-Phenotype Acute Leukemia.
    Hennawi M, Pakasticali N, Tashkandi H, Hussaini M.
    Int J Mol Sci; 2022 Sep 24; 23(19):. PubMed ID: 36232559
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  • 5. Diagnostic challenge in mixed phenotype acute leukemia with T/megakaryocyte or T/myeloid lineages accompanied by t(3;3).
    Jia Y, Lin D, Wang Z, Li C, Wang H, Wang J, Mi Y.
    Diagn Pathol; 2022 Oct 05; 17(1):74. PubMed ID: 36199105
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  • 6. TP53 mutation defines a unique subgroup within complex karyotype de novo and therapy-related MDS/AML.
    Weinberg OK, Siddon A, Madanat YF, Gagan J, Arber DA, Dal Cin P, Narayanan D, Ouseph MM, Kurzer JH, Hasserjian RP.
    Blood Adv; 2022 May 10; 6(9):2847-2853. PubMed ID: 35073573
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  • 7. Acute myeloid leukemia with mixed phenotype is characterized by stemness transcriptomic signatures and limited lineage plasticity.
    Galera P, Dilip D, Derkach A, Chan A, Zhang Y, Persuad S, Mishera T, Liu Y, Famulare C, Gao Q, Mata DA, Arcila M, Geyer MB, Stein E, Dogan A, Levine RL, Roshal M, Glass J, Xiao W.
    medRxiv; 2023 Nov 03. PubMed ID: 37961275
    [Abstract] [Full Text] [Related]

  • 8. Integrative genomic analysis of adult mixed phenotype acute leukemia delineates lineage associated molecular subtypes.
    Takahashi K, Wang F, Morita K, Yan Y, Hu P, Zhao P, Zhar AA, Wu CJ, Gumbs C, Little L, Tippen S, Thornton R, Coyle M, Mendoza M, Thompson E, Zhang J, DiNardo CD, Jain N, Ravandi F, Cortes JE, Garcia-Manero G, Kornblau S, Andreeff M, Jabbour E, Bueso-Ramos C, Takaori-Kondo A, Konopleva M, Patel K, Kantarjian H, Futreal PA.
    Nat Commun; 2018 Jul 10; 9(1):2670. PubMed ID: 29991687
    [Abstract] [Full Text] [Related]

  • 9. Prognosis of children with mixed phenotype acute leukemia treated on the basis of consistent immunophenotypic criteria.
    Mejstrikova E, Volejnikova J, Fronkova E, Zdrahalova K, Kalina T, Sterba J, Jabali Y, Mihal V, Blazek B, Cerna Z, Prochazkova D, Hak J, Zemanova Z, Jarosova M, Oltova A, Sedlacek P, Schwarz J, Zuna J, Trka J, Stary J, Hrusak O.
    Haematologica; 2010 Jun 10; 95(6):928-35. PubMed ID: 20145275
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  • 12. Single-cell RNA sequencing distinctly characterizes the wide heterogeneity in pediatric mixed phenotype acute leukemia.
    Mumme HL, Raikar SS, Bhasin SS, Thomas BE, Lawrence T, Weinzierl EP, Pang Y, DeRyckere D, Gawad C, Wechsler DS, Porter CC, Castellino SM, Graham DK, Bhasin M.
    Genome Med; 2023 Oct 16; 15(1):83. PubMed ID: 37845689
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  • 14. Adult mixed phenotype acute leukemia (MPAL): B/myeloid MPALisoMPO is distinct from other MPAL subtypes.
    Weinberg OK, Dennis J, Zia H, Chen P, Chu A, Koduru P, Luu HS, Fuda F, Chen W.
    Int J Lab Hematol; 2023 Apr 16; 45(2):170-178. PubMed ID: 36325594
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  • 15. Independent prognostic significance of TP53 mutations in adult acute myeloid leukaemia with complex karyotype.
    Xu N, Lai YY, Chen WM, Jiang H, Wang Y, Wang X, Zhao XS, Huang XJ, Jiang Q, Qin YZ.
    Int J Lab Hematol; 2022 Oct 16; 44(5):892-899. PubMed ID: 35505580
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  • 17. Complex or monosomal karyotype and not blast percentage is associated with poor survival in acute myeloid leukemia and myelodysplastic syndrome patients with inv(3)(q21q26.2)/t(3;3)(q21;q26.2): a Bone Marrow Pathology Group study.
    Rogers HJ, Vardiman JW, Anastasi J, Raca G, Savage NM, Cherry AM, Arber D, Moore E, Morrissette JJ, Bagg A, Liu YC, Mathew S, Orazi A, Lin P, Wang SA, Bueso-Ramos CE, Foucar K, Hasserjian RP, Tiu RV, Karafa M, Hsi ED.
    Haematologica; 2014 May 16; 99(5):821-9. PubMed ID: 24463215
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  • 18. Repeated Lineage Switches in an Elderly Case of Refractory B-Cell Acute Lymphoblastic Leukemia With MLL Gene Amplification: A Case Report and Literature Review.
    Takeda R, Yokoyama K, Fukuyama T, Kawamata T, Ito M, Yusa N, Kasajima R, Shimizu E, Ohno N, Uchimaru K, Yamaguchi R, Imoto S, Miyano S, Tojo A.
    Front Oncol; 2022 May 16; 12():799982. PubMed ID: 35402256
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  • 19. [The Genetic and Prognostic Characteristics of AML-MRC Patients].
    Chen Z, Mu QT, Wu A, Ouyang GF.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2022 Feb 16; 30(1):18-21. PubMed ID: 35123598
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  • 20. Mutational profiling of therapy-related myelodysplastic syndromes and acute myeloid leukemia by next generation sequencing, a comparison with de novo diseases.
    Ok CY, Patel KP, Garcia-Manero G, Routbort MJ, Fu B, Tang G, Goswami M, Singh R, Kanagal-Shamanna R, Pierce SA, Young KH, Kantarjian HM, Medeiros LJ, Luthra R, Wang SA.
    Leuk Res; 2015 Mar 16; 39(3):348-54. PubMed ID: 25573287
    [Abstract] [Full Text] [Related]

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