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152. Supplementary Figures 1 - 3 from Dual Targeting of mTOR and Aurora-A Kinase for the Treatment of Uterine Leiomyosarcoma

154. Figure S8 from Mammary Precancerous Stem and Non-Stem Cells Evolve into Cancers of Distinct Subtypes

157. Supplementary Figure Legend from T Lymphocytes Redirected against the Chondroitin Sulfate Proteoglycan-4 Control the Growth of Multiple Solid Tumors both In Vitro and In Vivo

160. Supplementary Information from Exosome-Derived miR-25-3p and miR-92a-3p Stimulate Liposarcoma Progression

161. Supplementary Table 3-8 from DNA Methylation Signature Reveals Cell Ontogeny of Renal Cell Carcinomas

163. Tables S1-S6 from Engineering and Functional Characterization of Fusion Genes Identifies Novel Oncogenic Drivers of Cancer

164. Data from Engineering and Functional Characterization of Fusion Genes Identifies Novel Oncogenic Drivers of Cancer

165. Supplementary Figures S1-S4 from High IGF-IR Activity in Triple-Negative Breast Cancer Cell Lines and Tumorgrafts Correlates with Sensitivity to Anti–IGF-IR Therapy

166. Figures S1-S4 from Engineering and Functional Characterization of Fusion Genes Identifies Novel Oncogenic Drivers of Cancer

167. Data from A Wnt-Independent LGR4–EGFR Signaling Axis in Cancer Metastasis

168. Data from High IGF-IR Activity in Triple-Negative Breast Cancer Cell Lines and Tumorgrafts Correlates with Sensitivity to Anti–IGF-IR Therapy

169. Data from Osteoblast-Secreted Factors Mediate Dormancy of Metastatic Prostate Cancer in the Bone via Activation of the TGFβRIII–p38MAPK–pS249/T252RB Pathway

170. Supplementary Data from A Wnt-Independent LGR4–EGFR Signaling Axis in Cancer Metastasis

171. Supplementary Figure legends from MNX1 Is Oncogenically Upregulated in African-American Prostate Cancer

172. Data from MNX1 Is Oncogenically Upregulated in African-American Prostate Cancer

173. Supplementary Figures 1-2 from Survivin Is a Viable Target for the Treatment of Malignant Peripheral Nerve Sheath Tumors

174. Supplementary Tables 1 - 4 from Dual Targeting of mTOR and Aurora-A Kinase for the Treatment of Uterine Leiomyosarcoma

175. Supplementary Table 10-12 from DNA Methylation Signature Reveals Cell Ontogeny of Renal Cell Carcinomas

176. Supplementary Methods from Dual Targeting of mTOR and Aurora-A Kinase for the Treatment of Uterine Leiomyosarcoma

178. Supplementary Figure 5 from T Lymphocytes Redirected against the Chondroitin Sulfate Proteoglycan-4 Control the Growth of Multiple Solid Tumors both In Vitro and In Vivo

180. Supplementary Figure from Accumulation of Molecular Aberrations Distinctive to Hepatocellular Carcinoma Progression

186. Supplementary Table 9 from DNA Methylation Signature Reveals Cell Ontogeny of Renal Cell Carcinomas

187. Supplementary Table 2 from DNA Methylation Signature Reveals Cell Ontogeny of Renal Cell Carcinomas

188. Supplementary Table from Accumulation of Molecular Aberrations Distinctive to Hepatocellular Carcinoma Progression

189. Supplementary Figures 1-4 from Pten Inactivation Accelerates Oncogenic K-ras–Initiated Tumorigenesis in a Mouse Model of Lung Cancer

190. Data from FGFR1–WNT–TGF-β Signaling in Prostate Cancer Mouse Models Recapitulates Human Reactive Stroma

193. Data from Molecular Profiling Uncovers a p53-Associated Role for MicroRNA-31 in Inhibiting the Proliferation of Serous Ovarian Carcinomas and Other Cancers

194. Supplementary Tables from Integrative Radiogenomic Profiling of Squamous Cell Lung Cancer

196. Data from MiR-155 Is a Liposarcoma Oncogene That Targets Casein Kinase-1α and Enhances β-Catenin Signaling

197. Supplementary Figure 2 from Integrative Radiogenomic Profiling of Squamous Cell Lung Cancer

198. Supplemental Table 1 from Fibroblast Growth Factor Receptor Signaling Dramatically Accelerates Tumorigenesis and Enhances Oncoprotein Translation in the Mouse Mammary Tumor Virus–Wnt-1 Mouse Model of Breast Cancer

199. Supplementary Table 7 from Targets of the Tumor Suppressor miR-200 in Regulation of the Epithelial–Mesenchymal Transition in Cancer

200. Supplemental Table 3 from Fibroblast Growth Factor Receptor Signaling Dramatically Accelerates Tumorigenesis and Enhances Oncoprotein Translation in the Mouse Mammary Tumor Virus–Wnt-1 Mouse Model of Breast Cancer

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