BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

228 related articles for article (PubMed ID: 11448041)

  • 1. Highly comprehensive karyotype analysis by a combination of spectral karyotyping (SKY), microdissection, and reverse painting (SKY-MD).
    Weimer J; Koehler MR; Wiedemann U; Attermeyer P; Jacobsen A; Karow D; Kiechl M; Jonat W; Arnold N
    Chromosome Res; 2001; 9(5):395-402. PubMed ID: 11448041
    [TBL] [Abstract][Full Text] [Related]  

  • 2. FISH-microdissection (FISH-MD) analysis of complex chromosome rearrangements.
    Weimer J; Kiechle M; Arnold N
    Cytogenet Cell Genet; 2000; 88(1-2):114-8. PubMed ID: 10773683
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Advances in the detection of chromosomal aberrations using spectral karyotyping.
    Bayani J; Squire JA
    Clin Genet; 2001 Feb; 59(2):65-73. PubMed ID: 11260203
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overrepresentation of 21q, 11q, and 22q.
    Mrózek K; Heinonen K; Theil KS; Bloomfield CD
    Genes Chromosomes Cancer; 2002 Jun; 34(2):137-53. PubMed ID: 11979548
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Spectral karyotyping analysis of head and neck squamous cell carcinoma.
    Singh B; Gogineni S; Goberdhan A; Sacks P; Shaha A; Shah J; Rao P
    Laryngoscope; 2001 Sep; 111(9):1545-50. PubMed ID: 11568603
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Detection of unidentified chromosome abnormalities in human neuroblastoma by spectral karyotyping (SKY).
    Cohen N; Betts DR; Trakhtenbrot L; Niggli FK; Amariglio N; Brok-Simoni F; Rechavi G; Meitar D
    Genes Chromosomes Cancer; 2001 Jul; 31(3):201-8. PubMed ID: 11391790
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping.
    Veldman T; Vignon C; Schröck E; Rowley JD; Ried T
    Nat Genet; 1997 Apr; 15(4):406-10. PubMed ID: 9090389
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular cytogenetic analysis of the bladder carcinoma cell line BK-10 by spectral karyotyping.
    Padilla-Nash HM; Nash WG; Padilla GM; Roberson KM; Robertson CN; Macville M; Schröck E; Ried T
    Genes Chromosomes Cancer; 1999 May; 25(1):53-9. PubMed ID: 10221340
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Multicolor banding technique, spectral color banding (SCAN): new development and applications.
    Kakazu N; Abe T
    Cytogenet Genome Res; 2006; 114(3-4):250-6. PubMed ID: 16954662
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Analysis of complex chromosomal aberrations in patients with myelodysplastic syndromes using multiplex fluorescence in situ hybridization combined with whole chromosome painting].
    Chen LJ; Li JY; Xiao B; Zhu Y; Liu Q; Pan JL; Qiu HR; Fan L; Zhang SJ; Lu RN; Xu W; Xue YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):635-9. PubMed ID: 18067073
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Evaluation of 24-color multifluor-fluorescence in-situ hybridization (M-FISH) karyotyping by comparison with reverse chromosome painting of the human breast cancer cell line T-47D.
    Lu YJ; Morris JS; Edwards PA; Shipley J
    Chromosome Res; 2000; 8(2):127-32. PubMed ID: 10780701
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Multicolour spectral karyotyping for complex chromosomal rearrangements in repeated abortion or congenital anomalies.
    Tanemura M; Suzumori K; Nishikawa N; Ishihara Y
    Prenat Diagn; 2001 Dec; 21(13):1123-8. PubMed ID: 11787036
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of chromosomal aberrations in diffuse large B-cell lymphoma (DLBL) by G-banding and spectral karyotyping (SKY).
    Adam P; Steinlein C; Schmid M; Haralambieva E; Stocklein H; Leich E; Rosenwald A; Muller-Hermelink HK; Ott G
    Cytogenet Genome Res; 2006; 114(3-4):274-8. PubMed ID: 16954666
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A new chromosome banding technique, spectral color banding (SCAN), for full characterization of chromosomal abnormalities.
    Kakazu N; Bar-Am I; Hada S; Ago H; Abe T
    Genes Chromosomes Cancer; 2003 Aug; 37(4):412-6. PubMed ID: 12800153
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Spectral karyotyping to study chromosome abnormalities in humans and mice with polycystic kidney disease.
    AbouAlaiwi WA; Rodriguez I; Nauli SM
    J Vis Exp; 2012 Feb; (60):. PubMed ID: 22330078
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2.
    Hilgenfeld E; Padilla-Nash H; McNeil N; Knutsen T; Montagna C; Tchinda J; Horst J; Ludwig WD; Serve H; Büchner T; Berdel WE; Schröck E; Ried T
    Br J Haematol; 2001 May; 113(2):305-17. PubMed ID: 11380393
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities.
    Schröck E; Veldman T; Padilla-Nash H; Ning Y; Spurbeck J; Jalal S; Shaffer LG; Papenhausen P; Kozma C; Phelan MC; Kjeldsen E; Schonberg SA; O'Brien P; Biesecker L; du Manoir S; Ried T
    Hum Genet; 1997 Dec; 101(3):255-62. PubMed ID: 9439652
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular cytogenetic analysis of the monoblastic cell line U937. karyotype clarification by G-banding, whole chromosome painting, microdissection and reverse painting, and comparative genomic hybridization.
    Lee JY; Lee CH; Shim SH; Seo HK; Kyhm JH; Cho S; Cho YH
    Cancer Genet Cytogenet; 2002 Sep; 137(2):124-32. PubMed ID: 12393283
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An easy and reliable procedure of microdissection technique for the analysis of chromosomal breakpoints and marker chromosomes.
    Weimer J; Kiechle M; Senger G; Wiedemann U; Ovens-Raeder A; Schuierer S; Kautza M; Siebert R; Arnold N
    Chromosome Res; 1999; 7(5):355-62. PubMed ID: 10515210
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A complex chromosome rearrangement involving chromosome 8, 11, and 12 analyzed by conventional cytogenetic investigations, fluorescence in situ hybridisation, and spectral karyotyping.
    Kotzot D; Holland H; Köhler M; Froster UG
    Ann Genet; 2001; 44(3):135-8. PubMed ID: 11694225
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.