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Genes, Chromosomes & Cancer|February 8, 2007
Co-amplification of 8p12 and 11q13 in breast cancers is not the result of a single genomic eventAnna L Paterson, Jessica C M Pole, Katherine A Blood, et al.
Molecular Oncology|April 22, 2025
Detecting homologous recombination deficiency for breast cancer through integrative analysis of genomic dataRong Zhu, Katherine Eason, Suet-Feung Chin, et al.
Genetic Epidemiology|January 17, 2002
The importance of connections: joining components of the Hutterite pedigreeN H Chapman, A L Leutenegger, M D Badzioch, et al.
Oncogene|May 18, 2005
A 1 Mb minimal amplicon at 8p11-12 in breast cancer identifies new candidate oncogenesMaria J Garcia, Jessica C M Pole, Suet-Feung Chin, et al.
Genome Research|October 14, 2011
Estimation of rearrangement phylogeny for cancer genomesChris D Greenman, Erin D Pleasance, Scott Newman, et al.
Communications Biology|April 9, 2022
Rearrangement processes and structural variations show evidence of selection in oesophageal adenocarcinomasAlvin Wei Tian Ng, Gianmarco Contino, Sarah Killcoyne, et al.
Breast Cancer Research : BCR|January 8, 2021
NRG1 fusions in breast cancerKaren D Howarth, Tashfina Mirza, Susanna L Cooke, et al.
BMC Genomics|December 25, 2012
Structural analysis of the genome of breast cancer cell line ZR-75-30 identifies twelve expressed fusion genesIna Schulte, Elizabeth M Batty, Jessica C M Pole, et al.
Genes, Chromosomes & Cancer|June 12, 2003
A recurrent chromosome translocation breakpoint in breast and pancreatic cancer cell lines targets the neuregulin/NRG1 geneJosé Adélaïde, Huai-En Huang, Anne Murati, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2012
Tumor initiating but differentiated luminal-like breast cancer cells are highly invasive in the absence of basal-like activityJiyoung Kim, René Villadsen, Therese Sørlie, et al.
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