Signatures of mutation and selection in the cancer genome

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Items 601–700 of 709

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  10. CDK Inhibitors in Normal and Malignant Cells
    Alexander Besser, Joyce M. Slingerland · 2015 · Elsevier eBooks
  11. Impact of germline susceptibility variants in cancer genetic studies
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  14. Cancer: Chromosomal Abnormalities
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  15. C9orf72 expansion creates the unstable folate-sensitive fragile site FRA9A
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  18. Transcriptomic Analysis of Human Ovarian Cancer Cells: Changes Mediated by Luteinizing Hormone Receptor Activation
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  19. Genome-wide integrative analysis of copy number segments and corresponding gene expression profile
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  20. Bioinformatic Identification of Genomic Alterations in Breast Cancer
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  21. Desarrollo de algoritmos bioinformáticos para estudios de genómica funcional: aplicaciones en cáncer
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  29. This Provisional PDF corresponds to the article as it appeared upon acceptance. Copyedited and fully formatted PDF and full text (HTML) versions will be made available soon. Large-scale analysis of chromosomal aberrations in cancer karyotypes reveals two distinct paths to aneuploidy
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  38. Common Chromosomal Fragile Sites and Cancer
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  39. Characterization of simple and complex genomic structural variation: a study of human populations and leukaemia
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  41. Analysis of Somatic Copy Number Gains in Pancreatic Ductal Adenocarcinoma Implicates ECT2 as a Candidate Therapeutic Target
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  42. Defining the role(s) of non-classical tumour suppressor Wwox in cellular function using Drosophila melanogaster genetic modelling
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  43. EXPLORING GENOME INTEGRITY PATHWAYS IN SACCHAROMYCES CEREVISIAE
    M.K. Shanmugan · 2014 · Archivio Istituzionale della Ricerca (Universita Degli Studi Di Milano)
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  50. Unraveling the role of the endogenous complex gut microbiota in the Pirc rat model of human colon cancer
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  51. Digital karyotyping of cancer cell lines from NGS data
    Ahmed Ibrahim Samir Khalil · 2020 · DR-NTU (Nanyang Technological University)
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  55. Sequence Mutations of Genes Pertaining to Malignancy in Cancer
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  56. Computational and systems biology of cancer
    David Dingli · 2020 · Computational and Systems Oncology
  57. Enhanced Bayesian detection for copy number alterations from next-generation sequencing data
    Zhenhua Yu, Fang Du · 2021 · IEEE International Conference on Bioinformatics and Biomedicine (BIBM)
  58. Universality of distribution of tumor mutation burden - a biomarker for the tumor evolution and disease risk
    Xin Li, Sumit Sinha, Dave Thirumalai · 2022 · bioRxiv (Cold Spring Harbor Laboratory)
  59. DNA Double-Strand Breaks Coupled with PARP1 and HNRNPA2B1 Binding Sites Flank Coordinately Expressed Domains in Human Chromosomes
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  61. CDK Inhibitors in Normal and Malignant Cells
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  63. Actin Cytoskeletal Regulation and Matrix Metalloproteinase Targeting in Head and Neck Squamous Cell Carcinoma (HNSCC) Progression
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  67. Hereditary Factors in Carcinogenesis and the Key Cancer Syndromes
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  68. Additional file 3 of Replication stress generates distinctive landscapes of DNA copy number alterations and chromosome scale losses
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  69. Additional file 4 of Replication stress generates distinctive landscapes of DNA copy number alterations and chromosome scale losses
    Nadeem Shaikh, Alice Mazzagatti, De Angelis, Simone, Sarah C. Johnson, Björn Bakker, Diana C.J. Spierings, René Wardenaar, Eleni Maniati, Wang, Jun, Michael A. Boemo et al. · 2022 · Figshare
  70. Additional file 2 of Replication stress generates distinctive landscapes of DNA copy number alterations and chromosome scale losses
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  77. Cancer progression inference using a finite-state model to allow recurrences and losses of mutations
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  79. Hereditary Factors in Carcinogenesis and the Key Cancer Syndromes
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  80. RB1 gene mutations and their association with Endometrial Cancer
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  83. Additional file 1 of Replication stress generates distinctive landscapes of DNA copy number alterations and chromosome scale losses
    Nadeem Shaikh, Alice Mazzagatti, De Angelis, Simone, Sarah C. Johnson, Björn Bakker, Spierings, Diana C. J., René Wardenaar, Eleni Maniati, Wang, Jun, Michael A. Boemo et al. · 2022 · Figshare
  84. Additional file 1 of Hierarchical discovery of large-scale and focal copy number alterations in low-coverage cancer genomes
    Ahmed Ibrahim Samir Khalil, Khyriem, Costerwell, Chattopadhyay, Anupam, Sanyal, Amartya · 2020 · Figshare
  85. Additional file 3 of NRG1 fusions in breast cancer
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  86. Additional file 1 of NRG1 fusions in breast cancer
    Karen Howarth, Tashfina Mirza, Cooke, Susanna L., Chin, Suet-Feung, Jessica C. M. Pole, Ernest Turro, Matthew Eldridge, Garcia, Raquel Manzano, Oscar M. Rueda, Boursnell, Chris et al. · 2021 · Figshare
  87. Additional file 5 of Replication stress generates distinctive landscapes of DNA copy number alterations and chromosome scale losses
    Nadeem Shaikh, Alice Mazzagatti, De Angelis, Simone, Sarah C. Johnson, Björn Bakker, Spierings, Diana C. J., René Wardenaar, Eleni Maniati, Wang, Jun, Michael A. Boemo et al. · 2022 · Figshare
  88. Somatic Copy Number Alterations: Gene and Protein Expression Correlates in NF1-Associated Malignant Peripheral Nerve Sheath Tumors
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  89. Battenberg reference files for hg38
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  91. Impact de l'haploinsuffisance d'ATR/CHK1 et de la Topoisomérase 1 sur la réplication et les Sites Fragiles Communs.
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  100. Mechanisms of spontaneous loss of heterozygosity in adult stem cells
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