BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

103 related articles for article (PubMed ID: 10812174)

  • 21. Acquired monosomy 7 in donor cells in a patient treated for acute lymphoblastic leukemia with bone marrow transplantation.
    Shekhter-Levin S; Bloom EJ; Swerdlow SH; Sherer ME; Wald N; Gollin SM
    Cancer Genet Cytogenet; 1997 Jun; 95(2):190-7. PubMed ID: 9169040
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Trisomy 8 and monosomy 7 detected in bone marrow using primed in situ labeling, fluorescence in situ hybridization, and conventional cytogenetic analyses. A study of 54 cases with hematological disorders.
    Yan J; Zhang XX; Fetni R; Drouin R
    Cancer Genet Cytogenet; 2001 Feb; 125(1):30-40. PubMed ID: 11297765
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A diminutive chromosome 21 centromere in acute lymphoblastic leukemia.
    Roberts KA; Martineau M; Broadfield ZJ; Gibson BE; Harewood L; Stewart J; Harrison CJ
    Cancer Genet Cytogenet; 2006 May; 167(1):78-81. PubMed ID: 16682292
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
    Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S
    Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Detection of trisomy 8 and monosomy 7 in chronic granulocytic leukemia and myelodysplastic syndrome by cytogenetic analysis and fluorescence in situ hybridization].
    Szabó Gabriella P; Balogh E; Jakab Z; Germán P; Bodnár F; Kiss A; Telek B; Oláh E
    Orv Hetil; 2002 Dec; 143(50):2775-9. PubMed ID: 12583317
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Double target in situ hybridization applied to the study of numerical aberrations in childhood acute lymphoblastic leukemia.
    Tosi S; Ritterbach J; Maglia O; Harbott J; Riehm H; Masera G; Biondi A; Lampert F
    Cancer Genet Cytogenet; 1994 Apr; 73(2):103-8. PubMed ID: 8174084
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Fluorescence in situ hybridisation studies to characterise complete and partial monosomy 7 in myeloid disorders.
    Gibbons B; Lillington DM; Monard S; Young BD; Cheung KL; Lister TA; Kearney L
    Genes Chromosomes Cancer; 1994 Aug; 10(4):244-9. PubMed ID: 7522537
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Unraveling the chromosome 17 patterns of FISH in interphase nuclei: an in-depth analysis of the HER2 amplicon and chromosome 17 centromere by karyotyping, FISH and M-FISH in breast cancer cells.
    Rondón-Lagos M; Verdun Di Cantogno L; Rangel N; Mele T; Ramírez-Clavijo SR; Scagliotti G; Marchiò C; Sapino A
    BMC Cancer; 2014 Dec; 14():922. PubMed ID: 25481507
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Numerical aberrations of chromosomes 1 and 7 in renal cell carcinomas as detected by interphase cytogenetics.
    Beck JL; Hopman AH; Feitz WF; Schalken J; Schaafsma HE; Van de Kaa CA; Ramaekers FC; Hanselaar AG; De Wilde PC
    J Pathol; 1995 Jun; 176(2):123-35. PubMed ID: 7636622
    [TBL] [Abstract][Full Text] [Related]  

  • 30. High-density genome array is superior to fluorescence in-situ hybridization analysis of monosomy 3 in choroidal melanoma fine needle aspiration biopsy.
    Young TA; Burgess BL; Rao NP; Gorin MB; Straatsma BR
    Mol Vis; 2007 Dec; 13():2328-33. PubMed ID: 18199974
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Interphase fluorescence in situ hybridization analysis: a study using centromeric probes 7, 8, and 12.
    Zhao L; Khan Z; Hayes KJ; Glassman AB
    Ann Clin Lab Sci; 1998; 28(1):51-6. PubMed ID: 9512785
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Cryptic ins(4;11)(q21;q23q23) detected by fluorescence in situ hybridization: a variant of t(4;11)(q21;q23) in an infant with a precursor B-cell acute lymphoblastic leukemia report of a second case.
    Tirado CA; Meloni-Ehrig AM; Edwards T; Scheerle J; Burks K; Repetti C; Christacos NC; Kelly JC; Greenberg J; Murphy C; Croft CD; Heritage D; Mowrey PN
    Cancer Genet Cytogenet; 2007 Apr; 174(2):166-9. PubMed ID: 17452260
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Quantifying chromosome changes and lineage involvement in myelodysplastic syndrome (MDS) using fluorescent in situ hybridization (FISH).
    Han K; Lee W; Harris CP; Kim W; Shim S; Meisner LF
    Leukemia; 1994 Jan; 8(1):81-6. PubMed ID: 8289503
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Cytogenetic analyses of premature ovarian failure using karyotyping and interphase fluorescence in situ hybridization (FISH) in a group of 1000 patients.
    Lakhal B; Braham R; Berguigua R; Bouali N; Zaouali M; Chaieb M; Veitia RA; Saad A; Elghezal H
    Clin Genet; 2010 Aug; 78(2):181-5. PubMed ID: 20345472
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The monosomy 7 clone in interphase and metaphase cell population: a combined chromosome and primed in situ labeling study.
    Pedersen B; Koch J; Bendix Hansen K; Hindkjaer J; Lindbjerg Andersen C
    Acta Haematol; 1997; 97(4):216-21. PubMed ID: 9158664
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Interphasic in situ fluorescent hybridization (FISH) in 4 cases of myeloid neoplasias with chromosome 7 changes].
    Arranz E; Renedo M; Ramos C; Martínez B; Prieto E; Benítez J
    Sangre (Barc); 1994 Dec; 39(6):457-60. PubMed ID: 7855698
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Discrepant cytogenetic and fluorescence in situ hybridization results in a 26-year-old male with early T-cell acute lymphocytic leukemia.
    Chinnappan D; Cowan J; Rastogi A; Miller KB; Blanchard R; Wyandt HE
    Cancer Genet Cytogenet; 1998 Oct; 106(2):116-21. PubMed ID: 9797775
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Ph-positive CML in blastic phase with monosomy 7 in a Down syndrome patient. Monitoring by interphase cytogenetics and demonstration of maternal allelic loss.
    Seghezzi L; Dellavecchia C; Maserati E; Minelli A; Carrà A; Locatelli F; Argusti A; Lo Curto F; Danesino C; Pasquali F
    Cancer Genet Cytogenet; 1997 Nov; 99(1):77-80. PubMed ID: 9352800
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Use of fluorescence in-situ hybridization (fish) for the estimation of the aberrant cell clone in leukemias with trisomy-8 or monosomy-7 detected by karyotyping.
    Gebhart E; Trautmann U; Reichardt S; Liehr T
    Int J Oncol; 1993 Aug; 3(2):191-5. PubMed ID: 21573347
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.