BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 8242591)

  • 21. [Comparison of detection of trisomy 8 with fluorescence in situ hybridization and conventional karyotype analysis in myelodysplastic syndrome].
    Zhang ZB; Liu SH; Li J; Bo LJ; Cui HY; Liu XP; Nie YX; Qin S
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2002 Apr; 10(2):115-8. PubMed ID: 12513811
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Multiplex fluorescence in situ hybridization in identifying chromosome involvement of complex karyotypes in de novo myelodysplastic syndromes and acute myeloid leukemia.
    Xu W; Li JY; Liu Q; Zhu Y; Pan JL; Qiu HR; Xue YQ
    Int J Lab Hematol; 2010 Feb; 32(1 Pt 1):e86-95. PubMed ID: 20089000
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Trisomy of the long arm of chromosome 1 resulting in a dicentric derivative (6)t(1;6) chromosome in a child with myelodysplastic syndrome following treatment for a primitive neuroectodermal tumor.
    Mathew S; Head D; Rodriguez-Galindo C; Raimondi SC
    Leuk Lymphoma; 2000 Mar; 37(1-2):213-8. PubMed ID: 10721789
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular cytogenetics and the myelodysplastic syndromes.
    Anastasi J
    Leuk Res; 1996 Jul; 20(7):559-62. PubMed ID: 8795689
    [No Abstract]   [Full Text] [Related]  

  • 25. Association between trisomy 8 and the immunophenotype of blast cells from acute leukemias secondary to a myelodysplastic syndrome or chronic myeloproliferative disorders.
    Garcia-Isidoro M; Tabernero MD; Najera ML; Lopez-Berges MC; Martinez A; Durán A; Garcia JL; Hernandez JM; Garcia Marcos MA; San Miguel JF; Orfao A
    Ann Hematol; 1997 May; 74(5):209-14. PubMed ID: 9200992
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clonal analysis of myelodysplastic syndrome: monosomy 7 is expressed in the myeloid lineage, but not in the lymphoid lineage as detected by fluorescent in situ hybridization.
    Gerritsen WR; Donohue J; Bauman J; Jhanwar SC; Kernan NA; Castro-Malaspina H; O'Reilly RJ; Bourhis JH
    Blood; 1992 Jul; 80(1):217-24. PubMed ID: 1611087
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Recurrent Abnormal Clones in Myelodysplastic Syndrome Marrow Originate from Cells at a Pluripotent Stem Level and Maintain Their Early Differentiation Potency.
    Qi H; Qingxia Z; Xiao L; Lingyun W; Feng X; Zheng Z; Chunkang C
    Cancer Invest; 2015; 33(8):369-77. PubMed ID: 26135215
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Routine fluorescence in situ hybridization with the MLL probe does not reliably detect two separate signals on one chromosome 11 in patients with trisomy 11.
    Smith A; Robson L; Heaps LS; Sharma P; Dunlop L; Bhave A; Bradstock K
    Cancer Genet Cytogenet; 2001 Sep; 129(2):173-6. PubMed ID: 11566351
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Dual-color FISH study on myelodysplastic syndrome with 1;7 translocation].
    Shen Y; Xue Y; Li J; Pan J; Wu Y; Guo Y; Lu D
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Aug; 19(4):313-6. PubMed ID: 12170469
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Systematic screening at diagnosis of -5/del(5)(q31), -7, or chromosome 8 aneuploidy by interphase fluorescence in situ hybridization in 110 acute myelocytic leukemia and high-risk myelodysplastic syndrome patients: concordances and discrepancies with conventional cytogenetics.
    Beyer V; Castagné C; Mühlematter D; Parlier V; Gmür J; Hess U; Kovacsovics T; Meyer-Monard S; Tichelli A; Tobler A; Jacky E; Schanz U; Bargetzi M; Hagemeijer A; de Witte T; van Melle G; Jotterand M
    Cancer Genet Cytogenet; 2004 Jul; 152(1):29-41. PubMed ID: 15193439
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Fluorescence in situ hybridization to assess aneuploidy for chromosomes 7 and 8 in hematologic disorders.
    Wyandt HE; Chinnappan D; Ioannidou S; Salama M; O'Hara C
    Cancer Genet Cytogenet; 1998 Apr; 102(2):114-24. PubMed ID: 9546063
    [TBL] [Abstract][Full Text] [Related]  

  • 32. High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration.
    Paulsson K; Heidenblad M; Strömbeck B; Staaf J; Jönsson G; Borg A; Fioretos T; Johansson B
    Leukemia; 2006 May; 20(5):840-6. PubMed ID: 16498392
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Interphase cytogenetics by fluorescent in situ hybridization (FISH) for characterization of monosomy-7-associated myeloid disorders.
    Baurmann H; Cherif D; Berger R
    Leukemia; 1993 Mar; 7(3):384-91. PubMed ID: 8445944
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Cell lineage involvement of recurrent chromosomal abnormalities in hematologic neoplasms.
    Knuutila S; Teerenhovi L; Larramendy ML; Elonen E; Franssila KO; Nylund SJ; Timonen T; Heinonen K; Mahlamäki E; Winqvist R
    Genes Chromosomes Cancer; 1994 Jun; 10(2):95-102. PubMed ID: 7520272
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Trisomy 8 detection in granulomonocytic, erythrocytic and megakaryocytic lineages by chromosomal in situ suppression hybridization in a case of refractory anaemia with ringed sideroblasts complicating the course of paroxysmal nocturnal haemoglobinuria.
    Parlier V; Tiainen M; Beris P; Miescher PA; Knuutila S; Jotterand Bellomo M
    Br J Haematol; 1992 Jun; 81(2):296-304. PubMed ID: 1643028
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Trisomy 8, a Cytogenetic Abnormality in Myelodysplastic Syndromes, Is Constitutional or Not?
    Saumell S; Solé F; Arenillas L; Montoro J; Valcárcel D; Pedro C; Sanzo C; Luño E; Giménez T; Arnan M; Pomares H; De Paz R; Arrizabalaga B; Jerez A; Martínez AB; Sánchez-Castro J; Rodríguez-Gambarte JD; Raya JM; Ríos E; Rodríguez-Rivera M; Espinet B; Florensa L
    PLoS One; 2015; 10(6):e0129375. PubMed ID: 26066831
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Determination of the breakpoints of 1;7 translocations in myelodysplastic syndrome by in situ hybridization using chromosome-specific alpha satellite DNA from human chromosomes 1 and 7.
    Alitalo T; Willard HF; de la Chapelle A
    Cytogenet Cell Genet; 1989; 50(1):49-53. PubMed ID: 2743817
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes.
    Paulsson K; Johansson B
    Pathol Biol (Paris); 2007 Feb; 55(1):37-48. PubMed ID: 16697122
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a multicolor and locus-specific fluorescence in situ hybridization study.
    Paulsson K; Fioretos T; Strömbeck B; Mauritzson N; Tanke HJ; Johansson B
    Cancer Genet Cytogenet; 2003 Jan; 140(1):66-9. PubMed ID: 12550762
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Detection of common chromosome abnormalities in myelodysplastic syndrome with a panel fluorescence in situ hybridization].
    Shen Y; Xue Y; Li J; Pan J; Wu Y; Chen S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Apr; 20(2):160-3. PubMed ID: 12673589
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.