BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

154 related articles for article (PubMed ID: 19027161)

  • 1. Array CGH analysis of chronic lymphocytic leukemia reveals frequent cryptic monoallelic and biallelic deletions of chromosome 22q11 that include the PRAME gene.
    Gunn SR; Bolla AR; Barron LL; Gorre ME; Mohammed MS; Bahler DW; Mellink CH; van Oers MH; Keating MJ; Ferrajoli A; Coombes KR; Abruzzo LV; Robetorye RS
    Leuk Res; 2009 Sep; 33(9):1276-81. PubMed ID: 19027161
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Detection of a deletion at 22q11 locus involving ZNF280A/ZNF280B/PRAME/GGTLC2 in B-cell malignancies: simply a consequence of an immunoglobulin lambda light chain rearrangement.
    Mraz M; Pospisilova S
    Br J Haematol; 2019 Aug; 186(4):e91-e94. PubMed ID: 30989644
    [No Abstract]   [Full Text] [Related]  

  • 3. The origin of deletion 22q11 in chronic lymphocytic leukemia is related to the rearrangement of immunoglobulin lambda light chain locus.
    Mraz M; Stano Kozubik K; Plevova K; Musilova K; Tichy B; Borsky M; Kuglik P; Doubek M; Brychtova Y; Mayer J; Pospisilova S
    Leuk Res; 2013 Jul; 37(7):802-8. PubMed ID: 23608880
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Monoallelic and biallelic deletions of 13q14 in a group of CLL/SLL patients investigated by CGH Haematological Cancer and SNP array (8x60K).
    Grygalewicz B; Woroniecka R; Rygier J; Borkowska K; Rzepecka I; Łukasik M; Budziłowska A; Rymkiewicz G; Błachnio K; Nowakowska B; Bartnik M; Gos M; Pieńkowska-Grela B
    Mol Cytogenet; 2016; 9():1. PubMed ID: 26740820
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Array CGH analysis reveals deletion of chromosome 22q11 in CLL with normal karyotype and no fish alterations.
    Mestichelli F; Dalsass A; Ferretti S; Camaioni E; Angelini M; Mei S; Pezzoni V; Travaglini F; Troiani E; Angelini S; Galieni P
    Br J Haematol; 2018 Oct; 183(1):152-155. PubMed ID: 28990183
    [No Abstract]   [Full Text] [Related]  

  • 6. High-resolution oligonucleotide array-CGH pinpoints genes involved in cryptic losses in chronic lymphocytic leukemia.
    Tyybakinoja A; Vilpo J; Knuutila S
    Cytogenet Genome Res; 2007; 118(1):8-12. PubMed ID: 17901694
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Monoallelic and biallelic deletions of 13q14.3 in chronic lymphocytic leukemia: FISH vs miRNA RT-qPCR detection.
    Smonskey MT; Block AW; Deeb G; Chanan-Khan AA; Bernstein ZP; Miller KC; Wallace PK; Starostik P
    Am J Clin Pathol; 2012 Apr; 137(4):641-6. PubMed ID: 22431542
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Contribution of comparative genomic hybridization and fluorescence in situ hybridization to the detection of chromosomal abnormalities in B-cell chronic lymphocytic leukemia.
    Jarosová M; Jedlicková K; Holzerová M; Urbanová R; Papajík T; Raida L; Pikalová Z; Lakomá I; Prekopová I; Kropácková J; Indrák K
    Onkologie; 2001 Feb; 24(1):60-5. PubMed ID: 11441283
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cryptic del(13q14.2) and physiological deletions of immunoglobulin genes detected by high-resolution array comparative genomic hybridization in a patient with indolent chronic lymphocytic leukemia.
    Bernheim A; Dessen P; Lazar V; Auger N; Fauvet D; Clausse B; Turhan A
    Cancer Genet Cytogenet; 2007 Jul; 176(1):89-91. PubMed ID: 17574971
    [No Abstract]   [Full Text] [Related]  

  • 10. The prognostic significance of various 13q14 deletions in chronic lymphocytic leukemia.
    Ouillette P; Collins R; Shakhan S; Li J; Li C; Shedden K; Malek SN
    Clin Cancer Res; 2011 Nov; 17(21):6778-90. PubMed ID: 21890456
    [TBL] [Abstract][Full Text] [Related]  

  • 11. t(11;14)-positive mantle cell lymphomas exhibit complex karyotypes and share similarities with B-cell chronic lymphocytic leukemia.
    Bentz M; Plesch A; Bullinger L; Stilgenbauer S; Ott G; Müller-Hermelink HK; Baudis M; Barth TF; Möller P; Lichter P; Döhner H
    Genes Chromosomes Cancer; 2000 Mar; 27(3):285-94. PubMed ID: 10679918
    [TBL] [Abstract][Full Text] [Related]  

  • 12. DNA copy-number analysis of the 22q11 deletion-syndrome region using array-CGH with genomic and PCR-based targets.
    Mantripragada KK; Tapia-Páez I; Blennow E; Nilsson P; Wedell A; Dumanski JP
    Int J Mol Med; 2004 Feb; 13(2):273-9. PubMed ID: 14719134
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 11q deletions identify a new subset of B-cell chronic lymphocytic leukemia characterized by extensive nodal involvement and inferior prognosis.
    Döhner H; Stilgenbauer S; James MR; Benner A; Weilguni T; Bentz M; Fischer K; Hunstein W; Lichter P
    Blood; 1997 Apr; 89(7):2516-22. PubMed ID: 9116297
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Expression of miR-15a and miR-16-1 in patients with chronic lymphocytic leukemia.
    Humplikova L; Kollinerova S; Papajik T; Pikalova Z; Holzerova M; Prochazka V; Divoka M; Modriansky M; Indrak K; Jarosova M
    Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub; 2013 Dec; 157(4):284-93. PubMed ID: 24026141
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cloning and gene mapping of the chromosome 13q14 region deleted in chronic lymphocytic leukemia.
    Kalachikov S; Migliazza A; Cayanis E; Fracchiolla NS; Bonaldo MF; Lawton L; Jelenc P; Ye X; Qu X; Chien M; Hauptschein R; Gaidano G; Vitolo U; Saglio G; Resegotti L; Brodjansky V; Yankovsky N; Zhang P; Soares MB; Russo J; Edelman IS; Efstratiadis A; Dalla-Favera R; Fischer SG
    Genomics; 1997 Jun; 42(3):369-77. PubMed ID: 9205107
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Frequent loss of the 11q14-24 region in chronic lymphocytic leukemia: a study by comparative genomic hybridization. Tampere CLL Group.
    Karhu R; Knuutila S; Kallioniemi OP; Siltonen S; Aine R; Vilpo L; Vilpo J
    Genes Chromosomes Cancer; 1997 Aug; 19(4):286-90. PubMed ID: 9258665
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole-genome scanning by array comparative genomic hybridization as a clinical tool for risk assessment in chronic lymphocytic leukemia.
    Gunn SR; Mohammed MS; Gorre ME; Cotter PD; Kim J; Bahler DW; Preobrazhensky SN; Higgins RA; Bolla AR; Ismail SH; de Jong D; Eldering E; van Oers MH; Mellink CH; Keating MJ; Schlette EJ; Abruzzo LV; Robetorye RS
    J Mol Diagn; 2008 Sep; 10(5):442-51. PubMed ID: 18687794
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel 5q11.2 deletion detected by microarray comparative genomic hybridisation in a child referred as a case of suspected 22q11 deletion syndrome.
    Prescott K; Woodfine K; Stubbs P; Super M; Kerr B; Palmer R; Carter NP; Scambler P
    Hum Genet; 2005 Jan; 116(1-2):83-90. PubMed ID: 15549396
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Integrated genomic profiling of chronic lymphocytic leukemia identifies subtypes of deletion 13q14.
    Ouillette P; Erba H; Kujawski L; Kaminski M; Shedden K; Malek SN
    Cancer Res; 2008 Feb; 68(4):1012-21. PubMed ID: 18281475
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Detection of single clone deletions using array CGH: identification of submicroscopic deletions in the 22q11.2 deletion syndrome as a model system.
    Tokuyasu TA; Cotter PD; Segraves R; Harris J; Elder ME; Gonzales M; Pinkel D; Albertson DG; Rauen KA
    Am J Med Genet A; 2007 May; 143A(9):925-32. PubMed ID: 17394204
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.