BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 32054878)

  • 1. Refined detection and phasing of structural aberrations in pediatric acute lymphoblastic leukemia by linked-read whole-genome sequencing.
    Nordlund J; Marincevic-Zuniga Y; Cavelier L; Raine A; Martin T; Lundmark A; Abrahamsson J; Norén-Nyström U; Lönnerholm G; Syvänen AC
    Sci Rep; 2020 Feb; 10(1):2512. PubMed ID: 32054878
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Spectral karyotyping and interphase FISH reveal abnormalities not detected by conventional G-banding. Implications for treatment stratification of childhood acute lymphoblastic leukaemia: detailed analysis of 70 cases.
    Nordgren A; Heyman M; Sahlén S; Schoumans J; Söderhäll S; Nordenskjöld M; Blennow E
    Eur J Haematol; 2002 Jan; 68(1):31-41. PubMed ID: 11952819
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Oligo-based aCGH analysis reveals cryptic unbalanced der(6)t(X;6) in pediatric t(12;21)-positive acute lymphoblastic leukemia.
    Kjeldsen E
    Exp Mol Pathol; 2016 Aug; 101(1):38-43. PubMed ID: 27215399
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. [Cytogenetic and FISH findings are complementary in childhood ALL].
    Haltrich I; Csóka M; Kovács G; Fekete G
    Magy Onkol; 2008 Sep; 52(3):283-91. PubMed ID: 18845499
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Classical and molecular cytogenetic abnormalities in 124 pediatric patients with acute lymphoblastic leukemia].
    Chai YH; Lü H; Li JQ; Lu J; Xiao PF; He YX; Shao XJ
    Zhonghua Er Ke Za Zhi; 2007 Sep; 45(9):684-6. PubMed ID: 18021563
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Importance of FISH combined with Morphology, Immunophenotype and Cytogenetic Analysis of Childhood/ Adult Acute Lymphoblastic Leukemia in Omani Patients.
    Goud TM; Al Salmani KK; Al Harasi SM; Al Musalhi M; Wasifuddin SM; Rajab A
    Asian Pac J Cancer Prev; 2015; 16(16):7343-50. PubMed ID: 26514535
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A survey of undetected, clinically relevant chromosome abnormalities when replacing postnatal karyotyping by Whole Genome Sequencing.
    Hochstenbach R; van Binsbergen E; Schuring-Blom H; Buijs A; Ploos van Amstel HK
    Eur J Med Genet; 2019 Sep; 62(9):103543. PubMed ID: 30248410
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Transcriptome sequencing in pediatric acute lymphoblastic leukemia identifies fusion genes associated with distinct DNA methylation profiles.
    Marincevic-Zuniga Y; Dahlberg J; Nilsson S; Raine A; Nystedt S; Lindqvist CM; Berglund EC; Abrahamsson J; Cavelier L; Forestier E; Heyman M; Lönnerholm G; Nordlund J; Syvänen AC
    J Hematol Oncol; 2017 Aug; 10(1):148. PubMed ID: 28806978
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Interphase fluorescence in situ hybridization and spectral karyotyping reveals hidden genetic aberrations in children with acute lymphoblastic leukaemia and a normal banded karyotype.
    Nordgren A; Schoumans J; Söderhäll S; Nordenskjöld M; Blennow E
    Br J Haematol; 2001 Sep; 114(4):786-93. PubMed ID: 11564064
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical cytogenetics in pediatric acute leukemia: an update.
    Braoudaki M; Tzortzatou-Stathopoulou F
    Clin Lymphoma Myeloma Leuk; 2012 Aug; 12(4):230-7. PubMed ID: 22609262
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel cryptic chromosomal rearrangements detected in acute lymphoblastic leukemia detected by application of new multicolor fluorescent in situ hybridization approaches.
    Karst C; Gross M; Haase D; Wedding U; Höffken K; Liehr T; Mkrtchyan H
    Int J Oncol; 2006 Apr; 28(4):891-7. PubMed ID: 16525638
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Structural rearrangements of chromosome 13 as additional abnormalities in Burkitt lymphoma and type 3 acute lymphoblastic leukemia.
    Barin C; Valtat C; Briault S; Bremond JL; Petit A; Lejars O; Linassier C; Gaschard P; Moraine C
    Cancer Genet Cytogenet; 1992 Jun; 60(2):206-9. PubMed ID: 1606568
    [TBL] [Abstract][Full Text] [Related]  

  • 14. High-resolution comparative genomic hybridisation yields a high detection rate of chromosomal aberrations in childhood acute lymphoblastic leukaemia.
    Kristensen TD; Wesenberg F; Jonsson OG; Carlsen NT; Forestier E; Kirchhoff M; Lundsteen C; Schmiegelow K
    Eur J Haematol; 2003 Jun; 70(6):363-72. PubMed ID: 12756018
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Interphase-FISH screening for eight common rearrangements in pediatric B-cell precursor acute lymphoblastic leukemia.
    Hutspardol S; Pakakasama S; Kanta K; Nuntakarn L; Anurathapan U; Sirachainan N; Songdej D; Sawangpanich R; Tiyasirichokchai R; Rerkamnuaychoke B; Hongeng S
    Int J Lab Hematol; 2013 Aug; 35(4):406-15. PubMed ID: 23190578
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Biological and clinical significance of cytogenetic study on 100 acute lymphoblastic leukemia and 219 acute non-lymphoblastic leukemia.
    Ye J; Cao Q; Su X; Huang Q; Ma Z; Wang Z; Huang W; Chen Z; Chen S
    Chin Med J (Engl); 1997 Feb; 110(2):90-5. PubMed ID: 9594276
    [TBL] [Abstract][Full Text] [Related]  

  • 17. High-resolution detection of chromosomal rearrangements in leukemias through mate pair whole genome sequencing.
    Tran AN; Taylan F; Zachariadis V; Ivanov Öfverholm I; Lindstrand A; Vezzi F; Lötstedt B; Nordenskjöld M; Nordgren A; Nilsson D; Barbany G
    PLoS One; 2018; 13(3):e0193928. PubMed ID: 29529047
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel cryptic chromosomal rearrangements in childhood acute lymphoblastic leukemia detected by multiple color fluorescent in situ hybridization.
    Poppe B; Cauwelier B; Van Limbergen H; Yigit N; Philippé J; Verhasselt B; De Paepe A; Benoit Y; Speleman F
    Haematologica; 2005 Sep; 90(9):1179-85. PubMed ID: 16154840
    [TBL] [Abstract][Full Text] [Related]  

  • 19. From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability.
    Lindstrand A; Eisfeldt J; Pettersson M; Carvalho CMB; Kvarnung M; Grigelioniene G; Anderlid BM; Bjerin O; Gustavsson P; Hammarsjö A; Georgii-Hemming P; Iwarsson E; Johansson-Soller M; Lagerstedt-Robinson K; Lieden A; Magnusson M; Martin M; Malmgren H; Nordenskjöld M; Norling A; Sahlin E; Stranneheim H; Tham E; Wincent J; Ygberg S; Wedell A; Wirta V; Nordgren A; Lundin J; Nilsson D
    Genome Med; 2019 Nov; 11(1):68. PubMed ID: 31694722
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Twenty-three cases of acute lymphoblastic leukemia with translocation t(4;11)(q21;q23): the implication of additional chromosomal aberrations.
    Schoch C; Rieder H; Freund M; Hoelzer D; Riehm H; Fonatsch C
    Ann Hematol; 1995 Apr; 70(4):195-201. PubMed ID: 7748964
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.