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51. Supplementary Table 4 from Whole-Genome Sequencing Reveals Breast Cancers with Mismatch Repair Deficiency

53. Supplementary Table 3 from Whole-Genome Sequencing Reveals Breast Cancers with Mismatch Repair Deficiency

54. Supplementary Table S1 from Estrogen Receptor Status Could Modulate the Genomic Pattern in Familial and Sporadic Breast Cancer

55. Supplementary Figures S1-S2 from Estrogen Receptor Status Could Modulate the Genomic Pattern in Familial and Sporadic Breast Cancer

56. Supplementary Table 1 from Whole-Genome Sequencing Reveals Breast Cancers with Mismatch Repair Deficiency

57. Supplementary Table S1 from Loss of the Mismatch Repair Protein MSH6 in Human Glioblastomas Is Associated with Tumor Progression during Temozolomide Treatment

58. Supplementary Glioma Genes from A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy

59. Supplementary Information from A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy

60. Supplementary Tables 1-5 from Novel Candidate Cancer Genes Identified by a Large-Scale Cross-Species Comparative Oncogenomics Approach

61. Data from A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy

62. Supplementary Table 7 from Novel Candidate Cancer Genes Identified by a Large-Scale Cross-Species Comparative Oncogenomics Approach

63. Supplementary Glioma Gene Mutations from A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy

64. Supplementary Methods from Novel Candidate Cancer Genes Identified by a Large-Scale Cross-Species Comparative Oncogenomics Approach

65. Data from Novel Candidate Cancer Genes Identified by a Large-Scale Cross-Species Comparative Oncogenomics Approach

66. Supplementary Table 6 from Novel Candidate Cancer Genes Identified by a Large-Scale Cross-Species Comparative Oncogenomics Approach

67. Mutational signatures associated with tobacco smoking in human cancer

69. Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation

70. Author Correction: Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors

71. Author Correction: Mapping the temporal and spatial dynamics of the human endometrium in vivo and in vitro

72. A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns

73. Combined burden and functional impact tests for cancer driver discovery using DriverPower

74. Integrative pathway enrichment analysis of multivariate omics data

75. Pathway and network analysis of more than 2500 whole cancer genomes

76. Divergent mutational processes distinguish hypoxic and normoxic tumours

77. Genomic footprints of activated telomere maintenance mechanisms in cancer

79. The mutational landscape of human somatic and germline cells

81. Transmissable Dog Cancer Genome Reveals the Origin and History of an Ancient Cell Lineage

85. Clinical and biological implications of driver mutations in myelodysplastic syndromes

86. Author Correction: Mapping the temporal and spatial dynamics of the human endometrium in vivo and in vitro

87. Functional patient-derived organoid screenings identify MCLA-158 as a therapeutic EGFR x LGR5 bispecific antibody with efficacy in epithelial tumors

88. High-throughput epitope discovery reveals frequent recognition of neo-antigens by [CD4.sup.+] T cells in human melanoma

89. Author Correction: Landscape of somatic mutations in 560 breast cancer whole-genome sequences

90. The evolution of two transmissible cancers in Tasmanian devils

93. Familial breast cancer

94. Genome sequencing of normal cells reveals developmental lineages and mutational processes

95. Landscape of somatic mutations in 560 breast cancer whole-genome sequences

97. Pharmacogenomic agreement between two cancer cell line data sets

98. The International Testicular Cancer Linkage Consortium: A clinicopathologic descriptive analysis of 461 familial malignant testicular germ cell tumor kindred

99. Whole genome DNA copy number changes identified by high density oligonucleotide arrays

100. Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cells

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