BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

329 related articles for article (PubMed ID: 20124335)

  • 1. Acute myeloid leukemia with del(X)(p21) and cryptic RUNX1/RUNX1T1 from ins(8;21)(q22;q22q22) revealed by atypical FISH signals.
    Jang JH; Yoo EH; Kim HJ; Kim DH; Jung CW; Kim SH
    Ann Clin Lab Sci; 2010; 40(1):80-4. PubMed ID: 20124335
    [TBL] [Abstract][Full Text] [Related]  

  • 2. t(8;21)(q22;q22) Translocation involving AML1 and ETO in B lymphoblastic leukemia [corrected].
    Wang HY; Tirado CA
    Hum Pathol; 2010 Feb; 41(2):286-92. PubMed ID: 19896694
    [TBL] [Abstract][Full Text] [Related]  

  • 3. PRDX4, a member of the peroxiredoxin family, is fused to AML1 (RUNX1) in an acute myeloid leukemia patient with a t(X;21)(p22;q22).
    Zhang Y; Emmanuel N; Kamboj G; Chen J; Shurafa M; Van Dyke DL; Wiktor A; Rowley JD
    Genes Chromosomes Cancer; 2004 Aug; 40(4):365-70. PubMed ID: 15188461
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular cytogenetic investigations in a novel complex variant of t(8;21)(q22;q22) with ins(15;21)(q15;q22.2q22.3) in a patient with AML-M2 subtype.
    Kokate P; Ahmad F; Dalvi R; Das BR; Mandava S
    Cancer Genet Cytogenet; 2008 Jul; 184(1):52-6. PubMed ID: 18558290
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel four-way t(6;16;21;8)(p21.3;p11.2;q22;q22) in acute myeloid leukemia with RUNX1/RUNX1T1 rearrangement.
    Park KJ; Park HD; Kim HJ; Yoo KH; Koo HH; Kim SH
    Cancer Genet Cytogenet; 2009 Jul; 192(2):90-2. PubMed ID: 19596262
    [No Abstract]   [Full Text] [Related]  

  • 6. [Fluorescence in situ hybridization studies on a myeloid leukemia patient with ins(8;21)(q22;q22.1q22.3)].
    Wu YF; Xue YQ; Bai SX; Zhang J; Yao L; Wang Y; Qiu HY; Shen J; Pan JL; Ma QF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):203-6. PubMed ID: 19350517
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Marker chromosomes are a significant mechanism of high-level RUNX1 gene amplification in hematologic malignancies.
    Moosavi SA; Sanchez J; Adeyinka A
    Cancer Genet Cytogenet; 2009 Feb; 189(1):24-8. PubMed ID: 19167608
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular characterisation of a recurrent, semi-cryptic RUNX1 translocation t(7;21) in myelodysplastic syndrome and acute myeloid leukaemia.
    Foster N; Paulsson K; Sales M; Cunningham J; Groves M; O'Connor N; Begum S; Stubbs T; McMullan DJ; Griffiths M; Pratt N; Tauro S
    Br J Haematol; 2010 Mar; 148(6):938-43. PubMed ID: 20064152
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Acute myeloid leukemia (M2) with a cryptic RUNX1/RUNX1T1 t(1;21;8)(p36;q22;q22) variant.
    Tirado CA; Chen W; Valdez FJ; Henderson S; Doolittle J; Garcia R; Patel S; Holdridge S; Chastain C; Collins RH
    Cancer Genet Cytogenet; 2009 Aug; 193(1):67-9. PubMed ID: 19602466
    [No Abstract]   [Full Text] [Related]  

  • 10. Molecular characterization of AML with ins(21;8)(q22;q22q22) reveals similarity to t(8;21) AML.
    Rücker FG; Bullinger L; Gribov A; Sill M; Schlenk RF; Lichter P; Döhner H; Döhner K
    Genes Chromosomes Cancer; 2011 Jan; 50(1):51-8. PubMed ID: 20967878
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Poor outcome in a pediatric patient with acute myeloid leukemia associated with a variant t(8;21) and trisomy 6.
    Kelly MJ; Meloni-Ehrig AM; Manley PE; Altura RA
    Cancer Genet Cytogenet; 2009 Feb; 189(1):48-52. PubMed ID: 19167612
    [TBL] [Abstract][Full Text] [Related]  

  • 12. RUNX1-MTG16 fusion gene in acute myeloblastic leukemia with t(16;21)(q24;q22): case report and review of the literature.
    De Braekeleer E; Douet-Guilbert N; Le Bris MJ; Morel F; Férec C; De Braekeleer M
    Cancer Genet Cytogenet; 2008 Aug; 185(1):47-50. PubMed ID: 18656694
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cryptic chromosomal aberrations leading to an AML1/ETO rearrangement are frequently caused by small insertions.
    Gamerdinger U; Teigler-Schlegel A; Pils S; Bruch J; Viehmann S; Keller M; Jauch A; Harbott J
    Genes Chromosomes Cancer; 2003 Mar; 36(3):261-72. PubMed ID: 12557226
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular cytogenetic findings in a three-way novel variant of t(1;8;21)(p35;q22;q22): a unique relocation of the AML1/ETO fusion gene 1p35 in AML-M2.
    Ahmad F; Kokate P; Chheda P; Dalvi R; Das BR; Mandava S
    Cancer Genet Cytogenet; 2008 Jan; 180(2):153-7. PubMed ID: 18206543
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Acute myeloid leukemia with a RUNX1-RUNX1T1 t(1;21;8)(q21;q22;q22) novel variant: a case report and review of the literature.
    Kim H; Moon HW; Hur M; Yun YM; Lee MH
    Acta Haematol; 2011; 125(4):237-41. PubMed ID: 21325813
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Complex t(8;13;21)(q22;q14;q22)--a novel variant of t(8;21) in a patient with acute myeloid leukemia (AML-M2).
    Udayakumar AM; Alkindi S; Pathare AV; Raeburn JA
    Arch Med Res; 2008 Feb; 39(2):252-6. PubMed ID: 18164974
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Acute myeloid leukemia with t(16;21)(q24;q22) and eosinophilia: case report and review of the literature.
    Park IJ; Park JE; Kim HJ; Jung HJ; Lee WG; Cho SR
    Cancer Genet Cytogenet; 2010 Jan; 196(1):105-8. PubMed ID: 19963144
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Acute myeloid leukemia (AML-M2) associated with variant t(8;21): report of three cases.
    Bae SY; Kim JS; Ryeu BJ; Lee KN; Lee CK; Kim YK; Lim CS; Cho Y; Choi CW; Ryu SW; Yoon SY
    Cancer Genet Cytogenet; 2010 May; 199(1):31-7. PubMed ID: 20417866
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Persistent altered fusion transcript splicing identifies RUNX1-RUNX1T1+ AML patients likely to relapse.
    Ommen HB; Ostergaard M; Yan M; Braendstrup K; Zhang DE; Hokland P
    Eur J Haematol; 2010 Feb; 84(2):128-32. PubMed ID: 19891700
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Insertions generating the 5'RUNX1/3'CBFA2T1 gene in acute myeloid leukemia cases show variable breakpoints.
    Specchia G; Albano F; Anelli L; Zagaria A; Liso A; La Starza R; Mancini M; Sebastio L; Giugliano E; Saglio G; Liso V; Rocchi M
    Genes Chromosomes Cancer; 2004 Sep; 41(1):86-91. PubMed ID: 15236320
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.