BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 32544910)

  • 1. Truncated RUNX1 Generated by the Fusion of RUNX1 to Antisense GRIK2 via a Cryptic Chromosome Translocation Enhances Sensitivity to Granulocyte Colony-Stimulating Factor.
    Abe A; Yamamoto Y; Katsumi A; Yamamoto H; Okamoto A; Inaguma Y; Iriyama C; Tokuda M; Okamoto M; Emi N; Tomita A
    Cytogenet Genome Res; 2020; 160(5):255-263. PubMed ID: 32544910
    [TBL] [Abstract][Full Text] [Related]  

  • 2. miR-17 deregulates a core RUNX1-miRNA mechanism of CBF acute myeloid leukemia.
    Fischer J; Rossetti S; Datta A; Eng K; Beghini A; Sacchi N
    Mol Cancer; 2015 Jan; 14():7. PubMed ID: 25612891
    [TBL] [Abstract][Full Text] [Related]  

  • 3. CSF3R Mutations are frequently associated with abnormalities of RUNX1, CBFB, CEBPA, and NPM1 genes in acute myeloid leukemia.
    Zhang Y; Wang F; Chen X; Zhang Y; Wang M; Liu H; Cao P; Ma X; Wang T; Zhang J; Zhang X; Lu P; Liu H
    Cancer; 2018 Aug; 124(16):3329-3338. PubMed ID: 29932212
    [TBL] [Abstract][Full Text] [Related]  

  • 4. LPXN, a member of the paxillin superfamily, is fused to RUNX1 in an acute myeloid leukemia patient with a t(11;21)(q12;q22) translocation.
    Dai HP; Xue YQ; Zhou JW; Li AP; Wu YF; Pan JL; Wang Y; Zhang J
    Genes Chromosomes Cancer; 2009 Dec; 48(12):1027-36. PubMed ID: 19760607
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of a Cryptic t(8;20;21)(q22;p13;q22) Resulting in RUNX1T1/RUNX1 Fusion in a Patient with Newly Diagnosed Acute Myeloid Leukemia.
    Macke EL; Meyer RG; Hoppman NL; Ketterling RP; Greipp PT; Xu X; Baughn LB; Shafer DA; He RR; Peterson JF
    Lab Med; 2022 Jul; 53(4):e87-e90. PubMed ID: 34791328
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Truncated RUNX1 protein generated by a novel t(1;21)(p32;q22) chromosomal translocation impairs the proliferation and differentiation of human hematopoietic progenitors.
    Rodriguez-Perales S; Torres-Ruiz R; Suela J; Acquadro F; Martin MC; Yebra E; Ramirez JC; Alvarez S; Cigudosa JC
    Oncogene; 2016 Jan; 35(1):125-34. PubMed ID: 25798834
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical Relevance of RUNX1 and CBFB Alterations in Acute Myeloid Leukemia and Other Hematological Disorders.
    Metzeler KH; Bloomfield CD
    Adv Exp Med Biol; 2017; 962():175-199. PubMed ID: 28299658
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of a novel fusion gene involving RUNX1 and the antisense strand of SV2B in a BCR-ABL1-positive acute leukemia.
    Giguère A; Hébert J
    Genes Chromosomes Cancer; 2013 Dec; 52(12):1114-22. PubMed ID: 24123676
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cbfb/Runx1 repression-independent blockage of differentiation and accumulation of Csf2rb-expressing cells by Cbfb-MYH11.
    Hyde RK; Kamikubo Y; Anderson S; Kirby M; Alemu L; Zhao L; Liu PP
    Blood; 2010 Feb; 115(7):1433-43. PubMed ID: 20007544
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel RUNX1-C11orf41 fusion gene in a case of acute myeloid leukemia with a t(11;21)(p14;q22).
    Abe A; Katsumi A; Kobayashi M; Okamoto A; Tokuda M; Kanie T; Yamamoto Y; Naoe T; Emi N
    Cancer Genet; 2012 Nov; 205(11):608-11. PubMed ID: 23102734
    [TBL] [Abstract][Full Text] [Related]  

  • 11. RUNX1 truncation resulting from a cryptic and novel t(6;21)(q25;q22) chromosome translocation in acute myeloid leukemia: A case report.
    Panagopoulos I; Torkildsen S; Gorunova L; Ulvmoen A; Tierens A; Zeller B; Heim S
    Oncol Rep; 2016 Nov; 36(5):2481-2488. PubMed ID: 27667292
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Novel and Cytogenetically Cryptic t(7;21)(q36.1;q22) Disrupting RUNX1 in Acute Myeloid Leukemia.
    Zámečníkova A; Al Bahar S
    Cytogenet Genome Res; 2018; 156(3):140-143. PubMed ID: 30439701
    [TBL] [Abstract][Full Text] [Related]  

  • 13. RUNX1 and CBFβ-SMMHC transactivate target genes together in abnormal myeloid progenitors for leukemia development.
    Zhen T; Cao Y; Ren G; Zhao L; Hyde RK; Lopez G; Feng D; Alemu L; Zhao K; Liu PP
    Blood; 2020 Nov; 136(21):2373-2385. PubMed ID: 32929473
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rare CBFB-MYH11 fusion transcripts in AML with inv(16)/t(16;16) are associated with therapy-related AML M4eo, atypical cytomorphology, atypical immunophenotype, atypical additional chromosomal rearrangements and low white blood cell count: a study on 162 patients.
    Schnittger S; Bacher U; Haferlach C; Kern W; Haferlach T
    Leukemia; 2007 Apr; 21(4):725-31. PubMed ID: 17287858
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Myeloid neoplasms with t(16;21)(q24;q22)/RUNX1-RUNX1T3 mimics acute myeloid leukemia with RUNX1-RUNX1T1.
    Liu H; Wang SA; Schlette EJ; Xu J; Jorgensen JL; Cameron Yin C; Li S; Jeffrey Medeiros L; Tang G
    Ann Hematol; 2018 Oct; 97(10):1775-1783. PubMed ID: 29872884
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Acute myeloid leukemia with t(7;21)(q11.2;q22) expresses a novel, reversed-sequence RUNX1-DTX2 chimera.
    Maki K; Sasaki K; Sugita F; Nakamura Y; Mitani K
    Int J Hematol; 2012 Aug; 96(2):268-73. PubMed ID: 22661044
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CLCA2, a novel RUNX1 partner gene in a therapy-related leukemia with t(1;21)(p22;q22).
    Giguère A; Hébert J
    Cancer Genet Cytogenet; 2010 Oct; 202(2):94-100. PubMed ID: 20875871
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Transcriptome sequencing reveals CHD1 as a novel fusion partner of RUNX1 in acute myeloid leukemia with t(5;21)(q21;q22).
    Yao H; Pan J; Wu C; Shen H; Xie J; Wang Q; Wen L; Wang Q; Ma L; Wu L; Ping N; Zhao Y; Sun A; Chen S
    Mol Cancer; 2015 Apr; 14():81. PubMed ID: 25879624
    [TBL] [Abstract][Full Text] [Related]  

  • 19. RUNX1 haploinsufficiency results in granulocyte colony-stimulating factor hypersensitivity.
    Chin DW; Sakurai M; Nah GS; Du L; Jacob B; Yokomizo T; Matsumura T; Suda T; Huang G; Fu XY; Ito Y; Nakajima H; Osato M
    Blood Cancer J; 2016 Jan; 6(1):e379. PubMed ID: 26745853
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Myeloid leukemia with t(7;21)(p22;q22) and 5q deletion.
    Panagopoulos I; Gorunova L; Brandal P; Garnes M; Tierens A; Heim S
    Oncol Rep; 2013 Oct; 30(4):1549-52. PubMed ID: 23877199
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.