BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

352 related articles for article (PubMed ID: 25678190)

  • 21. Clinical laboratory implementation of cytogenomic microarrays.
    South ST; Brothman AR
    Cytogenet Genome Res; 2011; 135(3-4):203-11. PubMed ID: 21934287
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genes commonly deleted in childhood B-cell precursor acute lymphoblastic leukemia: association with cytogenetics and clinical features.
    Schwab CJ; Chilton L; Morrison H; Jones L; Al-Shehhi H; Erhorn A; Russell LJ; Moorman AV; Harrison CJ
    Haematologica; 2013 Jul; 98(7):1081-8. PubMed ID: 23508010
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Integrated analysis of gene copy number, copy neutral LOH, and microRNA profiles in adult acute lymphoblastic leukemia.
    Ninomiya S; Tyybäkinoja A; Borze I; Räty R; Saarinen-Pihkala UM; Usvasalo A; Elonen E; Knuutila S
    Cytogenet Genome Res; 2012; 136(4):246-55. PubMed ID: 22456238
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Chromosomal aberrations in childhood acute lymphoblastic leukemia: 15-year single center experience.
    Jarosova M; Volejnikova J; Porizkova I; Holzerova M; Pospisilova D; Novak Z; Vrbkova J; Mihal V
    Cancer Genet; 2016; 209(7-8):340-7. PubMed ID: 27341996
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Array-based karyotyping for prognostic assessment in chronic lymphocytic leukemia: performance comparison of Affymetrix 10K2.0, 250K Nsp, and SNP6.0 arrays.
    Hagenkord JM; Monzon FA; Kash SF; Lilleberg S; Xie Q; Kant JA
    J Mol Diagn; 2010 Mar; 12(2):184-96. PubMed ID: 20075210
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Detailed gene dose analysis reveals recurrent focal gene deletions in pediatric B-cell precursor acute lymphoblastic leukemia.
    Ivanov Öfverholm I; Tran AN; Olsson L; Zachariadis V; Heyman M; Rudd E; Syk Lundberg E; Nordenskjöld M; Johansson B; Nordgren A; Barbany G
    Leuk Lymphoma; 2016 Sep; 57(9):2161-70. PubMed ID: 27090575
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The advantage of using SNP array in clinical testing for hematological malignancies--a comparative study of three genetic testing methods.
    Xu X; Johnson EB; Leverton L; Arthur A; Watson Q; Chang FL; Raca G; Laffin JJ
    Cancer Genet; 2013; 206(9-10):317-26. PubMed ID: 24269304
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The Utilization of Chromosomal Microarray Technologies for Hematologic Neoplasms: An ACLPS Critical Review.
    Peterson JF; Van Dyke DL; Hoppman NL; Kearney HM; Sukov WR; Greipp PT; Ketterling RP; Baughn LB
    Am J Clin Pathol; 2018 Oct; 150(5):375-384. PubMed ID: 30052716
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia--a comparative study of four differently designed, high resolution microarray platforms.
    Gunnarsson R; Staaf J; Jansson M; Ottesen AM; Göransson H; Liljedahl U; Ralfkiaer U; Mansouri M; Buhl AM; Smedby KE; Hjalgrim H; Syvänen AC; Borg A; Isaksson A; Jurlander J; Juliusson G; Rosenquist R
    Genes Chromosomes Cancer; 2008 Aug; 47(8):697-711. PubMed ID: 18484635
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Density matters: comparison of array platforms for detection of copy-number variation and copy-neutral abnormalities.
    Mason-Suares H; Kim W; Grimmett L; Williams ES; Horner VL; Kunig D; Goldlust IS; Wu BL; Shen Y; Miller DT; Martin CL; Rudd MK
    Genet Med; 2013 Sep; 15(9):706-12. PubMed ID: 23558256
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Digital Multiplex Ligation-Dependent Probe Amplification for Detection of Key Copy Number Alterations in T- and B-Cell Lymphoblastic Leukemia.
    Benard-Slagter A; Zondervan I; de Groot K; Ghazavi F; Sarhadi V; Van Vlierberghe P; De Moerloose B; Schwab C; Vettenranta K; Harrison CJ; Knuutila S; Schouten J; Lammens T; Savola S
    J Mol Diagn; 2017 Sep; 19(5):659-672. PubMed ID: 28736295
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Prognostic significance of acquired copy-neutral loss of heterozygosity in acute myeloid leukemia.
    Gronseth CM; McElhone SE; Storer BE; Kroeger KA; Sandhu V; Fero ML; Appelbaum FR; Estey EH; Fang M
    Cancer; 2015 Sep; 121(17):2900-8. PubMed ID: 26033747
    [TBL] [Abstract][Full Text] [Related]  

  • 33. IKZF1 deletions predict relapse in uniformly treated pediatric precursor B-ALL.
    Kuiper RP; Waanders E; van der Velden VH; van Reijmersdal SV; Venkatachalam R; Scheijen B; Sonneveld E; van Dongen JJ; Veerman AJ; van Leeuwen FN; van Kessel AG; Hoogerbrugge PM
    Leukemia; 2010 Jul; 24(7):1258-64. PubMed ID: 20445578
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Frequency of copy number abnormalities in common genes associated with B-cell precursor acute lymphoblastic leukemia cytogenetic subtypes in Brazilian children.
    Barbosa TC; Terra-Granado E; Quezado Magalhães IM; Neves GR; Gadelha A; Guedes Filho GE; Souza MS; Melaragno R; Emerenciano M; Pombo-de-Oliveira MS
    Cancer Genet; 2015 Oct; 208(10):492-501. PubMed ID: 26277549
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Performance comparison of Affymetrix SNP6.0 and cytogenetic 2.7M whole-genome microarrays in complex cancer samples.
    Bødker JS; Gyrup C; Johansen P; Schmitz A; Madsen J; Johnsen HE; Bøgsted M; Dybkær K; Nyegaard M
    Cytogenet Genome Res; 2013; 139(2):80-7. PubMed ID: 23182917
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Copy number neutral loss of heterozygosity at 17p and homozygous mutations of TP53 are associated with complex chromosomal aberrations in patients newly diagnosed with myelodysplastic syndromes.
    Svobodova K; Zemanova Z; Lhotska H; Novakova M; Podskalska L; Belickova M; Brezinova J; Sarova I; Izakova S; Lizcova L; Berkova A; Siskova M; Jonasova A; Cermak J; Michalova K
    Leuk Res; 2016 Mar; 42():7-12. PubMed ID: 26851439
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.
    Kloth JN; Oosting J; van Wezel T; Szuhai K; Knijnenburg J; Gorter A; Kenter GG; Fleuren GJ; Jordanova ES
    BMC Genomics; 2007 Feb; 8():53. PubMed ID: 17311676
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Gene copy number alteration profile and its clinical correlation in B-cell acute lymphoblastic leukemia.
    Gupta SK; Bakhshi S; Kumar L; Kamal VK; Kumar R
    Leuk Lymphoma; 2017 Feb; 58(2):333-342. PubMed ID: 27339065
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Detection of novel genomic aberrations in anaplastic astrocytomas by GTG-banding, SKY, locus-specific FISH, and high density SNP-array.
    Holland H; Ahnert P; Koschny R; Kirsten H; Bauer M; Schober R; Meixensberger J; Fritzsch D; Krupp W
    Pathol Res Pract; 2012 Jun; 208(6):325-30. PubMed ID: 22575435
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Genomic abnormalities in children with mental retardation and autism: the use of comparative genomic hybridization in situ (HRCGH) and molecular karyotyping with DNA-microchips (array CGH)].
    Vorsanova SG; Iurov IIu; Kurinnaia OS; Voinova VIu; Iurov IuB
    Zh Nevrol Psikhiatr Im S S Korsakova; 2013; 113(8):46-9. PubMed ID: 24077551
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.