BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 9593287)

  • 21. 11q23 balanced chromosome aberrations in treatment-related myelodysplastic syndromes and acute leukemia: report from an international workshop.
    Bloomfield CD; Archer KJ; Mrózek K; Lillington DM; Kaneko Y; Head DR; Dal Cin P; Raimondi SC
    Genes Chromosomes Cancer; 2002 Apr; 33(4):362-78. PubMed ID: 11921271
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Abnormalities of chromosome band 11q23 and the MLL gene in pediatric myelomonocytic and monoblastic leukemias. Identification of the t(9;11) as an indicator of long survival.
    Martinez-Climent JA; Espinosa R; Thirman MJ; Le Beau MM; Rowley JD
    J Pediatr Hematol Oncol; 1995 Nov; 17(4):277-83. PubMed ID: 7583381
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Identification of complex genomic breakpoint junctions in the t(9;11) MLL-AF9 fusion gene in acute leukemia.
    Super HG; Strissel PL; Sobulo OM; Burian D; Reshmi SC; Roe B; Zeleznik-Le NJ; Diaz MO; Rowley JD
    Genes Chromosomes Cancer; 1997 Oct; 20(2):185-95. PubMed ID: 9331569
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Distinct sequences on 11q13.5 and 11q23-24 are frequently coamplified with MLL in complexly organized 11q amplicons in AML/MDS patients.
    Zatkova A; Ullmann R; Rouillard JM; Lamb BJ; Kuick R; Hanash SM; Schnittger S; Schoch C; Fonatsch C; Wimmer K
    Genes Chromosomes Cancer; 2004 Apr; 39(4):263-76. PubMed ID: 14978788
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Classification of deletions and identification of cryptic translocations involving 7q by fluorescence in situ hybridization (FISH).
    Tosi S; Harbott J; Haas OA; Douglas A; Hughes DM; Ross FM; Biondi A; Scherer SW; Kearney L
    Leukemia; 1996 Apr; 10(4):644-9. PubMed ID: 8618441
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical and biological implications of partial tandem duplication of the MLL gene in acute myeloid leukemia without chromosomal abnormalities at 11q23.
    Shiah HS; Kuo YY; Tang JL; Huang SY; Yao M; Tsay W; Chen YC; Wang CH; Shen MC; Lin DT; Lin KH; Tien HF
    Leukemia; 2002 Feb; 16(2):196-202. PubMed ID: 11840285
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Duplication or amplification of chromosome band 11q23, including the unrearranged MLL gene, is a recurrent abnormality in therapy-related MDS and AML, and is closely related to mutation of the TP53 gene and to previous therapy with alkylating agents.
    Andersen MK; Christiansen DH; Kirchhoff M; Pedersen-Bjergaard J
    Genes Chromosomes Cancer; 2001 May; 31(1):33-41. PubMed ID: 11284033
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Infant acute lymphoblastic leukemia - combined cytogenetic, immunophenotypical and molecular analysis of 77 cases.
    Borkhardt A; Wuchter C; Viehmann S; Pils S; Teigler-Schlegel A; Stanulla M; Zimmermann M; Ludwig WD; Janka-Schaub G; Schrappe M; Harbott J
    Leukemia; 2002 Sep; 16(9):1685-90. PubMed ID: 12200682
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Molecular rearrangement of the ALL-1 gene in acute myeloid leukemia without cytogenetic evidence of 11q23 chromosomal translocations.
    Caligiuri MA; Schichman SA; Strout MP; Mrózek K; Baer MR; Frankel SR; Barcos M; Herzig GP; Croce CM; Bloomfield CD
    Cancer Res; 1994 Jan; 54(2):370-3. PubMed ID: 8275471
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Clinical significance and frequency of the 11q23/MLL genetic molecular alteration in Chilean infants with acute leukemia].
    Cabrera ME; Campbell M; Quintana J; Undurraga MS; Ford AA; Greaves MF
    Rev Med Chil; 2001 Jun; 129(6):634-42. PubMed ID: 11510203
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Chromosome abnormalities and MLL rearrangements in acute myeloid leukemia of infants.
    Satake N; Maseki N; Nishiyama M; Kobayashi H; Sakurai M; Inaba H; Katano N; Horikoshi Y; Eguchi H; Miyake M; Seto M; Kaneko Y
    Leukemia; 1999 Jul; 13(7):1013-7. PubMed ID: 10400416
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Cellular drug sensitivity in MLL-rearranged childhood acute leukaemia is correlated to partner genes and cell lineage.
    Palle J; Frost BM; Forestier E; Gustafsson G; Nygren P; Hellebostad M; Jonsson OG; Kanerva J; Schmiegelow K; Larsson R; Lönnerholm G;
    Br J Haematol; 2005 Apr; 129(2):189-98. PubMed ID: 15813846
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Polysomy 8 defines a clinico-cytogenetic entity representing a subset of myeloid hematologic malignancies associated with a poor prognosis: report on a cohort of 12 patients and review of 105 published cases.
    Beyer V; Mühlematter D; Parlier V; Cabrol C; Bougeon-Mamin S; Solenthaler M; Tobler A; Pugin P; Gregor M; Hitz F; Hess U; Chapuis B; Laurencet F; Schanz U; Schmidt PM; van Melle G; Jotterand M
    Cancer Genet Cytogenet; 2005 Jul; 160(2):97-119. PubMed ID: 15993266
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Chromosomal abnormalities in secondary MDS and AML. Relationship to drugs and radiation with specific emphasis on the balanced rearrangements.
    Andersen MK; Johansson B; Larsen SO; Pedersen-Bjergaard J
    Haematologica; 1998 Jun; 83(6):483-8. PubMed ID: 9676019
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Cryptic insertion and translocation or nondividing leukemic cells disclosed by FISH analysis in infant acute leukemia with discrepant molecular and cytogenetic findings.
    Watanabe N; Kobayashi H; Ichiji O; Yoshida MA; Kikuta A; Komada Y; Sekine I; Ishida Y; Horiukoshi Y; Tsunematsu Y; Yano M; Nakadate H; Kaneko Y
    Leukemia; 2003 May; 17(5):876-82. PubMed ID: 12750700
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Do terminal deletions of 11q23 exist? Identification of undetected translocations with fluorescence in situ hybridization.
    Kobayashi H; Espinosa R; Thirman MJ; Fernald AA; Shannon K; Diaz MO; Le Beau MM; Rowley JD
    Genes Chromosomes Cancer; 1993 Aug; 7(4):204-8. PubMed ID: 7692945
    [TBL] [Abstract][Full Text] [Related]  

  • 37. MDS/AML del(11)(q14) Share Common Morphological Features Despite Different Chromosomal Breakpoints.
    Dambruoso I; Invernizzi R; Boni M; Zappatore R; Giardini I; Cavigliano MP; Rocca B; Calvello C; Bastia R; Caresana M; Pasi F; Nano R; Bernasconi P
    Anticancer Res; 2017 Feb; 37(2):645-649. PubMed ID: 28179312
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Pediatric T-cell acute lymphoblastic leukemia with aberrations of both MLL loci.
    Quigley DI; Wolff DJ
    Cancer Genet Cytogenet; 2006 Jul; 168(1):77-9. PubMed ID: 16772125
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Myelodysplastic syndromes and acute myeloid leukemia with 17p deletion. An entity characterized by specific dysgranulopoïesis and a high incidence of P53 mutations.
    Lai JL; Preudhomme C; Zandecki M; Flactif M; Vanrumbeke M; Lepelley P; Wattel E; Fenaux P
    Leukemia; 1995 Mar; 9(3):370-81. PubMed ID: 7885035
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Molecular rearrangements of the MLL gene are present in most cases of infant acute myeloid leukemia and are strongly correlated with monocytic or myelomonocytic phenotypes.
    Sorensen PH; Chen CS; Smith FO; Arthur DC; Domer PH; Bernstein ID; Korsmeyer SJ; Hammond GD; Kersey JH
    J Clin Invest; 1994 Jan; 93(1):429-37. PubMed ID: 8282816
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.