Oncology drug discovery: planning a turnaround.
暂无分享,去创建一个
Giulio Draetta | C. Toniatti | G. Draetta | Carlo Toniatti | Philip Jones | Hilary Graham | Bruno Pagliara | Philip Jones | Hilary Graham | Bruno Pagliara
[1] D. Hanahan,et al. The Hallmarks of Cancer , 2000, Cell.
[2] Colleen V. Chien,et al. Managing innovation: university-industry partnerships and the licensing of the Harvard mouse , 2004, Nature Biotechnology.
[3] S. Liou,et al. Randomized phase II study of multiple dose levels of CCI-779, a novel mammalian target of rapamycin kinase inhibitor, in patients with advanced refractory renal cell carcinoma. , 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[4] D. Haber,et al. Molecular targeted therapy of lung cancer: EGFR mutations and response to EGFR inhibitors. , 2005, Cold Spring Harbor symposia on quantitative biology.
[5] G. Schwartz,et al. Targeting Checkpoint Kinase 1 in Cancer Therapeutics , 2007, Clinical Cancer Research.
[6] Alexander Kamb,et al. Why is cancer drug discovery so difficult? , 2007, Nature Reviews Drug Discovery.
[7] Lee Harland,et al. Lowering industry firewalls: pre-competitive informatics initiatives in drug discovery , 2009, Nature Reviews Drug Discovery.
[8] Ben S. Wittner,et al. Systematic RNA interference reveals that oncogenic KRAS-driven cancers require TBK1 , 2009, Nature.
[9] C. Kenific,et al. Down‐regulation of the Notch pathway mediated by a γ‐secretase inhibitor induces anti‐tumour effects in mouse models of T‐cell leukaemia , 2009, British journal of pharmacology.
[10] F. D. de Sauvage,et al. Mechanisms of Hedgehog pathway activation in cancer and implications for therapy. , 2009, Trends in pharmacological sciences.
[11] Sridhar Ramaswamy,et al. Synthetic Lethal Interaction between Oncogenic KRAS Dependency and STK33 Suppression in Human Cancer Cells , 2009, Cell.
[12] C. Tralau-Stewart,et al. Drug discovery: new models for industry-academic partnerships. , 2009, Drug discovery today.
[13] Paul Workman,et al. Drugging the PI3 kinome: from chemical tools to drugs in the clinic. , 2010, Cancer research.
[14] Ian Collins,et al. Probing the Probes: Fitness Factors For Small Molecule Tools , 2010, Chemistry & biology.
[15] L. Chin,et al. Non-germline genetically engineered mouse models for translational cancer research , 2010, Nature Reviews Cancer.
[16] John E. Harlan,et al. Iniparib Nonselectively Modifies Cysteine-Containing Proteins in Tumor Cells and Is Not a Bona Fide PARP Inhibitor , 2011, Clinical Cancer Research.
[17] René Bernards,et al. Taming the dragon: genomic biomarkers to individualize the treatment of cancer , 2011, Nature Medicine.
[18] J. McCarter,et al. STK33 kinase activity is nonessential in KRAS-dependent cancer cells. , 2011, Cancer research.
[19] D. Hanahan,et al. Hallmarks of Cancer: The Next Generation , 2011, Cell.
[20] W. Pao,et al. How genetically engineered mouse tumor models provide insights into human cancers. , 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[21] J. Licinio,et al. Improving the efficacy of translational medicine by optimally integrating health care, academia and industry , 2011, Nature Medicine.
[22] Scott H. Kaufmann,et al. Failure of Iniparib to Inhibit Poly(ADP-Ribose) Polymerase In Vitro , 2012, Clinical Cancer Research.
[23] G. Dranoff,et al. Experimental mouse tumour models: what can be learnt about human cancer immunology? , 2011, Nature Reviews Immunology.
[24] Mallika Singh,et al. Modeling and predicting clinical efficacy for drugs targeting the tumor milieu , 2012, Nature Biotechnology.
[25] Nathan T. Ross,et al. STK33 kinase inhibitor BRD-8899 has no effect on KRAS-dependent cancer cell viability , 2012, Proceedings of the National Academy of Sciences.
[26] Nathan T. Ross,et al. A Potent and Selective Quinoxalinone-Based STK33 Inhibitor Does Not Show Synthetic Lethality in KRAS-Dependent Cells , 2012, ACS medicinal chemistry letters.
[27] Daniel Q. Bach,et al. Trends in Personalized Therapies in Oncology: The (Venture) Capitalist’s Perspective , 2012, Journal of personalized medicine.
[28] Andrew L. Kung,et al. A murine lung cancer co-clinical trial identifies genetic modifiers of therapeutic response , 2012, Nature.
[29] I. Khanna,et al. Drug discovery in pharmaceutical industry: productivity challenges and trends. , 2012, Drug discovery today.
[30] J. Settleman,et al. Mechanisms of acquired resistance to targeted cancer therapies. , 2012, Future oncology.
[31] D. Berry. Adaptive clinical trials in oncology , 2012, Nature Reviews Clinical Oncology.
[32] Aik Choon Tan,et al. Patient-derived tumour xenografts as models for oncology drug development , 2012, Nature Reviews Clinical Oncology.
[33] S. Fesik,et al. Abstract 1813: Evaluation of TBK1 as a novel cancer target in the K-Ras pathway , 2012 .
[34] C. Swanton. Intratumor heterogeneity: evolution through space and time. , 2012, Cancer research.
[35] E. Richard Gold,et al. Recalibrating Intellectual Property Rights to Enhance Translational Research Collaborations , 2012, Science Translational Medicine.
[36] A. Fojo,et al. Inhibitors Targeting Mitosis: Tales of How Great Drugs against a Promising Target Were Brought Down by a Flawed Rationale , 2012, Clinical Cancer Research.
[37] Funda Meric-Bernstam,et al. Overcoming implementation challenges of personalized cancer therapy , 2012, Nature Reviews Clinical Oncology.
[38] C. Sigman,et al. Cancer biomarkers: selecting the right drug for the right patient , 2012, Nature Reviews Drug Discovery.
[39] Promoting drug discovery by collaborative innovation: a novel risk- and reward-sharing partnership between the German Cancer Research Center and Bayer HealthCare. , 2012, Drug discovery today.
[40] David R Parkinson,et al. Making Personalized Cancer Medicine a Reality: Challenges and Opportunities in the Development of Biomarkers and Companion Diagnostics , 2012, Clinical Cancer Research.
[41] Hakim Djaballah. Editorial. Random RNAi screening data analysis: a call for standardization. , 2012, Combinatorial chemistry & high throughput screening.
[42] W. Kaelin,et al. Use and Abuse of RNAi to Study Mammalian Gene Function , 2012, Science.
[43] Razelle Kurzrock,et al. Personalized Medicine in a Phase I Clinical Trials Program: The MD Anderson Cancer Center Initiative , 2012, Clinical Cancer Research.
[44] Ryohei Katayama,et al. Cytotoxic activity of tivantinib (ARQ 197) is not due solely to c-MET inhibition. , 2013, Cancer research.
[45] Laura E. MacConaill,et al. Existing and emerging technologies for tumor genomic profiling. , 2013, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[46] K. Kinzler,et al. Cancer Genome Landscapes , 2013, Science.
[47] J. Mendelsohn. Personalizing oncology: perspectives and prospects. , 2013, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[48] E. Lander,et al. Lessons from the Cancer Genome , 2013, Cell.
[49] Levi A Garraway,et al. Genomics-driven oncology: framework for an emerging paradigm. , 2013, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[50] A. Bardelli,et al. Tivantinib (ARQ197) Displays Cytotoxic Activity That Is Independent of Its Ability to Bind MET , 2013, Clinical Cancer Research.
[51] R. Sullivan,et al. Resistance to BRAF-targeted therapy in melanoma. , 2013, European journal of cancer.
[52] T. Yap,et al. Development of therapeutic combinations targeting major cancer signaling pathways. , 2013, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[53] Richard Simon,et al. Implementing personalized cancer genomics in clinical trials , 2013, Nature Reviews Drug Discovery.
[54] M. Loda,et al. A co-clinical approach identifies mechanisms and potential therapies for androgen deprivation resistance in prostate cancer , 2013, Nature Genetics.