Search Results

There are 6274 results for: content related to: Consistent chromosome 10 rearrangements in four newly established human hepatocellular carcinoma cell lines

  1. You have free access to this content
    Multicolour fluorescence in situ hybridization analysis of t(14;18)-positive follicular lymphoma and correlation with gene expression data and clinical outcome

    British Journal of Haematology

    Volume 122, Issue 5, September 2003, Pages: 745–759, Valia S. Lestou, Randy D. Gascoyne, Laurie Sehn, Olga Ludkovski, Mukesh Chhanabhai, Richard J. Klasa, Hervé Husson, Arnold S. Freedman, Joseph M. Connors and Douglas E. Horsman

    Version of Record online : 21 AUG 2003, DOI: 10.1046/j.1365-2141.2003.04502.x

  2. Definitive molecular cytogenetic characterization of 15 colorectal cancer cell lines

    Genes, Chromosomes and Cancer

    Volume 49, Issue 3, March 2010, Pages: 204–223, Turid Knutsen, Hesed M. Padilla-Nash, Danny Wangsa, Linda Barenboim-Stapleton, Jordi Camps, Nicole McNeil, Michael J. Difilippantonio and Thomas Ried

    Version of Record online : 19 NOV 2009, DOI: 10.1002/gcc.20730

  3. Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overrepresentation of 21q, 11q, and 22q

    Genes, Chromosomes and Cancer

    Volume 34, Issue 2, June 2002, Pages: 137–153, Krzysztof Mrózek, Kristiina Heinonen, Karl S. Theil and Clara D. Bloomfield

    Version of Record online : 15 FEB 2002, DOI: 10.1002/gcc.10027

  4. Molecular cytogenetic analysis of head and neck squamous cell carcinoma: By comparative genomic hybridization, spectral karyotyping, and expression array analysis

    Head & Neck

    Volume 24, Issue 9, September 2002, Pages: 874–887, Jeremy A. Squire, Jane Bayani, Catherine Luk, Lianne Unwin, Jason Tokunaga, Christina MacMillan, Jonathan Irish, Dale Brown, Patrick Gullane and Suzanne Kamel-Reid

    Version of Record online : 24 JUL 2002, DOI: 10.1002/hed.10122

  5. Spectral karyotyping identifies recurrent complex rearrangements of chromosomes 8, 17, and 20 in osteosarcomas

    Genes, Chromosomes and Cancer

    Volume 36, Issue 1, January 2003, Pages: 7–16, Jane Bayani, Maria Zielenska, Ajay Pandita, Khaldoun Al-Romaih, Jana Karaskova, Karen Harrison, Julia A. Bridge, Poul Sorensen, Paul Thorner and Jeremy A. Squire

    Version of Record online : 5 SEP 2002, DOI: 10.1002/gcc.10132

  6. 5q11, 8p11, and 10q22 are recurrent chromosomal breakpoints in prostate cancer cell lines

    Genes, Chromosomes and Cancer

    Volume 30, Issue 2, February 2001, Pages: 187–195, Yi Pan, Weng-Onn Lui, Nina Nupponen, Catharina Larsson, Jorma Isola, Tapio Visakorpi, Ulf S.R. Bergerheim and Soili Kytölä

    Version of Record online : 5 DEC 2000, DOI: 10.1002/1098-2264(2000)9999:9999<::AID-GCC1075>3.0.CO;2-H

  7. Karyotypic similarity identified by multiplex-FISH relates four prostate adenocarcinoma cell lines: PC-3, PPC-1, ALVA-31, and ALVA-41

    Genes, Chromosomes and Cancer

    Volume 31, Issue 4, August 2001, Pages: 303–315, Marileila Varella-Garcia, Theresa Boomer and Gary J. Miller

    Version of Record online : 31 MAY 2001, DOI: 10.1002/gcc.1149

  8. Reassessment of childhood B-lineage lymphoblastic leukemia karyotypes using spectral analysis

    Genes, Chromosomes and Cancer

    Volume 30, Issue 4, April 2001, Pages: 383–392, Hatem Elghezal, Gaëlle Le Guyader, Isabella Radford-Weiss, Christine Perot, Jacqueline Van Den Akker, Patrice Eydoux, Michel Vekemans and Serge P. Romana

    Version of Record online : 1 MAR 2001, DOI: 10.1002/gcc.1104

  9. Genomic aberrations in 80 cases of primary glioblastoma multiforme: Pathogenetic heterogeneity and putative cytogenetic pathways

    Genes, Chromosomes and Cancer

    Volume 48, Issue 10, October 2009, Pages: 908–924, Hanne-Sofie S. Dahlback, Petter Brandal, Torstein R. Meling, Ludmila Gorunova, David Scheie and Sverre Heim

    Version of Record online : 14 JUL 2009, DOI: 10.1002/gcc.20690

  10. The conundrum of a jumping translocation (JT) in CVS from twins and review of JTs

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 11, November 2010, Pages: 2924–2936, Kavita S. Reddy

    Version of Record online : 26 OCT 2010, DOI: 10.1002/ajmg.a.33710

  11. Novel evidence of a role for chromosome 1 pericentric heterochromatin in the pathogenesis of B-cell lymphoma and multiple myeloma

    Genes, Chromosomes and Cancer

    Volume 32, Issue 3, November 2001, Pages: 250–264, Patricia Le Baccon, Dominique Leroux, Christina Dascalescu, Samuel Duley, Danielle Marais, Eliane Esmenjaud, Jean Jacques Sotto and Mary Callanan

    Version of Record online : 25 SEP 2001, DOI: 10.1002/gcc.1189

  12. Characterization of chromosome 11 breakpoints and the areas of deletion and amplification in patients with newly diagnosed acute myeloid leukemia

    Genes, Chromosomes and Cancer

    Volume 52, Issue 7, July 2013, Pages: 619–635, Iveta Sarova, Jana Brezinova, Zuzana Zemanova, Dagmar Bystricka, Zdenek Krejcik, Petr Soukup, Jan Vydra, Jaroslav Cermak, Anna Jonasova and Kyra Michalova

    Version of Record online : 12 APR 2013, DOI: 10.1002/gcc.22058

  13. Reverse painting of microdissected chromosome 19 markers in ovarian carcinoma identifies a complex rearrangement map

    Genes, Chromosomes and Cancer

    Volume 48, Issue 2, February 2009, Pages: 184–193, Francesca Micci, Jörg Weimer, Lisbeth Haugom, Rolf I. Skotheim, Regina Grunewald, Vera M. Abeler, Ilvar Silins, Ragnhild A. Lothe, Claes G. Trope, Norbert Arnold and Sverre Heim

    Version of Record online : 30 OCT 2008, DOI: 10.1002/gcc.20628

  14. Analysis of myelodysplastic syndromes with complex karyotypes by high-resolution comparative genomic hybridization and subtelomeric CGH array

    Genes, Chromosomes and Cancer

    Volume 42, Issue 3, March 2005, Pages: 287–298, Angel Martínez-Ramírez, Miguel Urioste, Lorenzo Melchor, David Blesa, Laura Valle, Sara Alvarez de Andrés, Klaas Kok, Maria José Calasanz, Juan Cruz Cigudosa and Javier Benítez

    Version of Record online : 20 DEC 2004, DOI: 10.1002/gcc.20154

  15. Omphalocele in trisomy 3q: further delineation of phenotype

    Clinical Genetics

    Volume 64, Issue 5, November 2003, Pages: 404–413, SA Yatsenko, R Mendoza-Londono, JW Belmont and LG Shaffer

    Version of Record online : 21 OCT 2003, DOI: 10.1034/j.1399-0004.2003.00159.x

  16. Genome-wide analysis of sixteen chordomas by comparative genomic hybridization and cytogenetics of the first human chordoma cell line, U-CH1

    Genes, Chromosomes and Cancer

    Volume 32, Issue 3, November 2001, Pages: 203–211, Stefanie Scheil, Silke Brüderlein, Thomas Liehr, Heike Starke, Jochen Herms, Michael Schulte and Peter Möller

    Version of Record online : 28 AUG 2001, DOI: 10.1002/gcc.1184

  17. Genomic imbalances in CML blast crisis: 8q24.12–q24.13 Segment identified as a common region of over-representation

    Genes, Chromosomes and Cancer

    Volume 37, Issue 4, August 2003, Pages: 346–358, Susan M. Gribble, Alistair G. Reid, Ian Roberts, Colin Grace, Anthony R. Green and Elizabeth P. Nacheva

    Version of Record online : 22 APR 2003, DOI: 10.1002/gcc.10173

  18. Multiple recurrent chromosomal breakpoints in mantle cell lymphoma revealed by a combination of molecular cytogenetic techniques

    Genes, Chromosomes and Cancer

    Volume 47, Issue 12, December 2008, Pages: 1086–1097, Itziar Salaverria, Blanca Espinet, Ana Carrió, Dolors Costa, Laura Astier, Julia Slotta-Huspenina, Leticia Quintanilla-Martinez, Falko Fend, Francesc Solé, Dolors Colomer, Sergio Serrano, Rosa Miró, Sílvia Beà and Elías Campo

    Version of Record online : 15 AUG 2008, DOI: 10.1002/gcc.20609

  19. GAB2 is a novel target of 11q amplification in AML/MDS

    Genes, Chromosomes and Cancer

    Volume 45, Issue 9, September 2006, Pages: 798–807, Andrea Zatkova, Claudia Schoch, Frank Speleman, Bruce Poppe, Christine Mannhalter, Christa Fonatsch and Katharina Wimmer

    Version of Record online : 30 MAY 2006, DOI: 10.1002/gcc.20344

  20. Detection of unidentified chromosome abnormalities in human neuroblastoma by spectral karyotyping (SKY)

    Genes, Chromosomes and Cancer

    Volume 31, Issue 3, July 2001, Pages: 201–208, Ninette Cohen, David R. Betts, Luba Trakhtenbrot, Felix K. Niggli, Ninette Amariglio, Frida Brok-Simoni, Gideon Rechavi and Dafna Meitar

    Version of Record online : 26 APR 2001, DOI: 10.1002/gcc.1136