BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

73 related articles for article (PubMed ID: 26773847)

  • 41. Molecular basis and clinical significance of genetic aberrations in B-cell precursor acute lymphoblastic leukemia.
    Ghazavi F; Lammens T; Van Roy N; Poppe B; Speleman F; Benoit Y; Van Vlierberghe P; De Moerloose B
    Exp Hematol; 2015 Aug; 43(8):640-53. PubMed ID: 26101161
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Identification of cryptic aberrations and characterization of translocation breakpoints using array CGH in high hyperdiploid childhood acute lymphoblastic leukemia.
    Paulsson K; Heidenblad M; Mörse H; Borg A; Fioretos T; Johansson B
    Leukemia; 2006 Nov; 20(11):2002-7. PubMed ID: 16990785
    [TBL] [Abstract][Full Text] [Related]  

  • 43. The distinguishable DNA whole genome methylation profile of 2 cases of pediatric precursor B acute lymphoblastic leukaemia (BCP ALL) with prodromal, preleukemic phase: A case report.
    Chaber R; Gurgul A; Wróbel G; Tomoń A; Paszek S; Potocka N; Haus O; Lejman M; Łach K; Szmatoła T; Jasielczuk I; Rybka B; Ryczan-Krawczyk R; Stąpor S; Ciebiera K; Arthur CJ; Zawlik I
    Medicine (Baltimore); 2018 Oct; 97(42):e12763. PubMed ID: 30334962
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Copy Number Changes and Allele Distribution Patterns of Chromosome 21 in B Cell Precursor Acute Lymphoblastic Leukemia.
    Abbasi MR; Nebral K; Haslinger S; Inthal A; Zeitlhofer P; König M; Schinnerl D; Köhrer S; Strehl S; Panzer-Grümayer R; Mann G; Attarbaschi A; Haas OA
    Cancers (Basel); 2021 Sep; 13(18):. PubMed ID: 34572826
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Novel childhood ALL susceptibility locus BMI1-PIP4K2A is specifically associated with the hyperdiploid subtype.
    Walsh KM; de Smith AJ; Chokkalingam AP; Metayer C; Dahl GV; Hsu LI; Barcellos LF; Wiemels JL; Buffler PA
    Blood; 2013 Jun; 121(23):4808-9. PubMed ID: 23744494
    [No Abstract]   [Full Text] [Related]  

  • 46. Recurrent DNMT3B rearrangements are associated with unfavorable outcome in dicentric (9;20)-positive pediatric BCP-ALL.
    Antić Ž; van Bömmel A; Riege K; Lentes J; Schröder C; Alten J; Eckert C; Fuhrmann L; Steinemann D; Lenk L; Schewe DM; Zimmermann M; Schrappe M; Schlegelberger B; Cario G; Hoffmann S; Bergmann AK
    Leukemia; 2023 Dec; 37(12):2522-2525. PubMed ID: 37845283
    [No Abstract]   [Full Text] [Related]  

  • 47. Diagnosis of intrachromosomal amplification of chromosome 21 (iAMP21) by molecular cytogenetics in pediatric acute lymphoblastic leukemia.
    Duployez N; Boudry-Labis E; Decool G; Grzych G; Grardel N; Abou Chahla W; Preudhomme C; Roche-Lestienne C
    Clin Case Rep; 2015 Oct; 3(10):814-6. PubMed ID: 26509013
    [TBL] [Abstract][Full Text] [Related]  

  • 48. A Novel Homozygous Nucleotide Deletion in the JAK2 Gene in a Pediatric Patient with B-cell Precursor Acute Lymphoblastic Leukemia.
    Akın DF; Akkaya E; Kürekçi AE; Arslan C; Ezer U; Akar N
    Turk J Haematol; 2012 Jun; 29(2):185-7. PubMed ID: 24744653
    [No Abstract]   [Full Text] [Related]  

  • 49. The Eμ-Ret mouse is a novel model of hyperdiploid B-cell acute lymphoblastic leukemia.
    Farrokhi A; Atre T; Rever J; Fidanza M; Duey W; Salitra S; Myung J; Guo M; Jo S; Uzozie A; Baharvand F; Rolf N; Auer F; Hauer J; Grupp SA; Eydoux P; Lange PF; Seif AE; Maxwell CA; Reid GSD
    Leukemia; 2024 May; 38(5):969-980. PubMed ID: 38519798
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Hyperdiploidy: the longest known, most prevalent, and most enigmatic form of acute lymphoblastic leukemia in children.
    Haas OA; Borkhardt A
    Leukemia; 2022 Dec; 36(12):2769-2783. PubMed ID: 36266323
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Somatic Sex: On the Origin of Neoplasms With Chromosome Counts in Uneven Ploidy Ranges.
    Haas OA
    Front Cell Dev Biol; 2021; 9():631946. PubMed ID: 34422788
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Advantages and Limitations of SNP Array in the Molecular Characterization of Pediatric T-Cell Acute Lymphoblastic Leukemia.
    Lejman M; Włodarczyk M; Styka B; Pastorczak A; Zawitkowska J; Taha J; Sędek Ł; Skonieczka K; Braun M; Haus O; Szczepański T; Młynarski W; Kowalczyk JR
    Front Oncol; 2020; 10():1184. PubMed ID: 32766158
    [TBL] [Abstract][Full Text] [Related]  

  • 53. SH2B3 inactivation through CN-LOH 12q is uniquely associated with B-cell precursor ALL with iAMP21 or other chromosome 21 gain.
    Sinclair PB; Ryan S; Bashton M; Hollern S; Hanna R; Case M; Schwalbe EC; Schwab CJ; Cranston RE; Young BD; Irving JAE; Vora AJ; Moorman AV; Harrison CJ
    Leukemia; 2019 Aug; 33(8):1881-1894. PubMed ID: 30816328
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Whole-exome sequencing exploration of acquired uniparental disomies in B-cell precursor acute lymphoblastic leukemia.
    Lundin-Ström KB; Biloglav A; Lilljebjörn H; Rissler M; Fioretos T; Hansson M; Behrendtz M; Castor A; Olsson L; Johansson B
    Leukemia; 2018 Sep; 32(9):2058-2062. PubMed ID: 29967378
    [No Abstract]   [Full Text] [Related]  

  • 55. Patterns and frequencies of acquired and constitutional uniparental isodisomies in pediatric and adult B-cell precursor acute lymphoblastic leukemia.
    Lundin KB; Olsson L; Safavi S; Biloglav A; Paulsson K; Johansson B
    Genes Chromosomes Cancer; 2016 May; 55(5):472-9. PubMed ID: 26773847
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Deep sequencing and SNP array analyses of pediatric T-cell acute lymphoblastic leukemia reveal NOTCH1 mutations in minor subclones and a high incidence of uniparental isodisomies affecting CDKN2A.
    Karrman K; Castor A; Behrendtz M; Forestier E; Olsson L; Ehinger M; Biloglav A; Fioretos T; Paulsson K; Johansson B
    J Hematol Oncol; 2015 Apr; 8():42. PubMed ID: 25903014
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia.
    Paulsson K; Forestier E; Lilljebjörn H; Heldrup J; Behrendtz M; Young BD; Johansson B
    Proc Natl Acad Sci U S A; 2010 Dec; 107(50):21719-24. PubMed ID: 21098271
    [TBL] [Abstract][Full Text] [Related]  

  • 58. High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome.
    Lundin C; Hjorth L; Behrendtz M; Nordgren A; Palmqvist L; Andersen MK; Biloglav A; Forestier E; Paulsson K; Johansson B
    Genes Chromosomes Cancer; 2012 Feb; 51(2):196-206. PubMed ID: 22072402
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)-positive B-cell precursor acute lymphoblastic leukemias: a Nordic series of 24 cases and review of the literature.
    Forestier E; Gauffin F; Andersen MK; Autio K; Borgström G; Golovleva I; Gustafsson B; Heim S; Heinonen K; Heyman M; Hovland R; Johannsson JH; Kerndrup G; Rosenquist R; Schoumans J; Swolin B; Johansson B; Nordgren A; ; ;
    Genes Chromosomes Cancer; 2008 Feb; 47(2):149-58. PubMed ID: 17990329
    [TBL] [Abstract][Full Text] [Related]  

  • 60. High hyperdiploid childhood acute lymphoblastic leukemia.
    Paulsson K; Johansson B
    Genes Chromosomes Cancer; 2009 Aug; 48(8):637-60. PubMed ID: 19415723
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.