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1. Full Text Abstract SY08-02: Reshaping cancer care delivery through multi-disciplinary molecular tumor boards
by Korn, W. Michael
Cancer Research, ISSN 0008-5472, 07/2018, Volume 78, Issue 13 Supplement, pp. SY08-02 - SY08-02
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2. Full Text Molecular Profiling of Appendiceal Adenocarcinoma and Comparison with Right-sided and Left-sided Colorectal Cancer
by Tokunaga, R and Xiu, J and Johnston, C and Goldberg, RM and Philip, PA and Seeber, A and Naseem, M and Lo, JH and Arai, H and Battaglin, F and Puccini, A and Berger, MD and Soni, S and Zhang, W and Hwang, JJ and Shields, AF and Marshall, JL and Baba, H and Korn, WM and Lenz, HJ
CLINICAL CANCER RESEARCH, ISSN 1078-0432, 05/2019, Volume 25, Issue 10, pp. 3096 - 3103
Purpose: The natural history and prognosis of appendiceal adenocarcinomas differ from those of adenocarcinomas arising in other large bowel sites. We aimed to... 
PAPILLARY MUCINOUS NEOPLASMS | FREQUENT GNAS MUTATIONS | ONCOLOGY | PREDICTIVE BIOMARKERS | ADENOMA | PSEUDOMYXOMA PERITONEI | LOW-GRADE | CARCINOMATOSIS | GENERATION | INHIBITOR | CHEMOTHERAPY
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3. Full Text Comprehensive molecular profiling of patients with pancreatic adenocarcinoma: A single institution’s experience
by Kamgar, Mandana and Dyson, Gregory and Diab, Maria and Tesfaye, Anteneh A and Korn, W. Michael and Shields, Anthony Frank and Philip, Philip Agop
Journal of Clinical Oncology, ISSN 0732-183X, 05/2018, Volume 36, Issue 15_suppl, pp. e16236 - e16236
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4. Full Text RARE-05. TUMOR PROFILING REVEALS EPITHELIAL-TO-MESENCHYMAL TRANSITION (EMT) AND ENHANCED IMMUNE SUPPRESSION IN GLIOSARCOMAS RELATIVE TO GLIOBLASTOMA
by Dardis, Christopher and Phuphanich, Surasak and Sanai, Nader and Xiu, Joanne and Mittal, Sandeep and Michelhaugh, Sharon and Subramaniam, Deepa and Pandey, Majari and Kesari, Santosh and Heimberger, Amy and Gatalica, Zoran and Michael Korn, W and Sumrall, Ashley
Neuro-Oncology, ISSN 1522-8517, 11/2018, Volume 20, Issue suppl_6, pp. vi237 - vi237
Abstract BACKGROUND Gliosarcoma (GS) accounts for approximately 2% of WHO grade 4 gliomas and have a worse prognosis relative to glioblastoma (GBM).... 
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5. Full Text RARE-22. FREQUENT HIGH TUMOR MUTATIONAL BURDEN (TMB) AND PD-L1 EXPRESSION IN PRIMARY CNS LYMPHOMA (PCNSL)
by Sumrall, Ashley and Phuphanich, Surasak and Spetzler, David and Gatalica, Zoran and Xiu, Joanne and Provenzano, Aaron and J. Brenner, Andrew and Subramaniam, Deepa and Pandey, Majari and Heimberger, Amy and Kesari, Santosh and Michael Korn, W and Mittal, Sandeep
Neuro-Oncology, ISSN 1522-8517, 11/2018, Volume 20, Issue suppl_6, pp. vi240 - vi241
Abstract BACKGROUND PD-1 and PD-L1 expression has not been well-described in PCNSL. In one report of 20 PCNSL tumors, PD-1 and PD-L1 expression on tumor cells... 
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6. Full Text Inhibition of the Raf/MEK/ERK pathway up-regulates expression of the coxsackievirus and adenovirus receptor in cancer cells
by Anders, Mario and Christian, Christine and McMahon, Martin and McCormick, Frank and Korn, W.Michael
Cancer Research, ISSN 0008-5472, 05/2003, Volume 63, Issue 9, pp. 2088 - 2095
Recombinant adenoviruses are presently being tested clinically as a new strategy for the treatment of cancer. An important determining factor for the... 
KINASE PATHWAY | REPLICATION | TRANSGENE EXPRESSION | EPITHELIAL-CELLS | ONCOLOGY | MAP KINASE | GENE-THERAPY | TUMOR-CELLS | E-CADHERIN | TIGHT JUNCTION | CARCINOMA | Green Fluorescent Proteins | Up-Regulation | Colorectal Neoplasms - virology | MAP Kinase Signaling System - physiology | Phosphorylation | Pancreatic Neoplasms - metabolism | Receptors, Virus - biosynthesis | Colorectal Neoplasms - genetics | Humans | Transcriptional Activation | Gene Expression Regulation, Neoplastic | Coxsackie and Adenovirus Receptor-Like Membrane Protein | Receptors, Virus - genetics | Luminescent Proteins - biosynthesis | Proto-Oncogene Proteins c-raf - physiology | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Cell Membrane - metabolism | Tumor Cells, Cultured | Colorectal Neoplasms - metabolism | Protein-Serine-Threonine Kinases - metabolism | Pancreatic Neoplasms - virology | Proto-Oncogene Proteins c-raf - biosynthesis | Recombinant Fusion Proteins - biosynthesis | Colorectal Neoplasms - enzymology | Proto-Oncogene Proteins c-raf - genetics | Protein-Serine-Threonine Kinases - physiology | Enzyme Inhibitors - pharmacology | Pancreatic Neoplasms - enzymology | Adenoviruses, Human - physiology | Pancreatic Neoplasms - genetics | G1 Phase - physiology | Proto-Oncogene Proteins c-raf - metabolism | Animals | MAP Kinase Signaling System - drug effects | Mitogen-Activated Protein Kinases - antagonists & inhibitors | Mitogen-Activated Protein Kinases - physiology | Dogs | Recombinant Fusion Proteins - genetics | Luminescent Proteins - genetics | Mice | Proto-Oncogene Proteins c-raf - antagonists & inhibitors | Adenoviruses, Human - metabolism | MAP Kinase Kinase Kinase 1 | Mitogen-Activated Protein Kinases - metabolism
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7. Full Text Loss of p14(ARF) in tumor cells facilitates replication of the adenovirus mutant dl1520 (ONYX-015)
by Ries, Stefan J and Brandts, Christian H and Chung, Alicia S and Biederer, Carola H and Hann, Byron C and Lipner, Ettie M and McCormick, Frank and Michael Korn, W
Nature Medicine, ISSN 1078-8956, 2000, Volume 6, Issue 10, pp. 1128 - 1133
The adenovirus mutant dl1520 (ONYX-015) does not express the E1B-55K protein that binds and inactivates p53. This virus replicates in tumor cells with mutant... 
MEDICINE, RESEARCH & EXPERIMENTAL | SUPPRESSOR | P19(ARF) | P53 STATUS | BIOCHEMISTRY & MOLECULAR BIOLOGY | DNA-DAMAGE | CELL BIOLOGY | G ARREST | MDM2 | INFECTION | ACCUMULATION | PROTEINS | EXPRESSION
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8. Full Text Abstract SY25-03: Targeting the RAS signal transduction network in cancer cells
by Korn, W. Michael
Cancer Research, ISSN 0008-5472, 04/2010, Volume 70, Issue 8 Supplement, pp. SY25-03 - SY25-03
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9. Full Text Basal subtype and MAPK/ERK kinase (MEK)-phosphoinositide 3-kinase feedback signaling determine susceptibility of breast cancer cells to MEK inhibition
by Mirzoeva, Olga K and Das, Debopriya and Heiser, Laura M and Bhattacharya, Sanchita and Siwak, Doris and Gendelman, Rina and Bayani, Nora and Wang, Nicholas J and Neve, Richard M and Guan, Yinghui and Hu, Zhi and Knight, Zachary and Feiler, Heidi S and Gascard, Philippe and Parvin, Bahram and Spellman, Paul T and Shokat, Kevan M and Wyrobek, Andrew J and Bissell, Mina J and McCormick, Frank and Kuo, Wen-Lin and Mills, Gordon B and Gray, Joe W and Korn, W. Michael
Cancer Research, ISSN 0008-5472, 01/2009, Volume 69, Issue 2, pp. 565 - 572
Specific inhibitors of mitogen-activated protein kinase/extracellular signal-regulated kinase (ERK) kinase (MEK) have been developed that efficiently inhibit... 
STEM-CELLS | PTEN LOSS | PIK3CA MUTATIONS | GENE | ONCOLOGY | PI3K PATHWAY | OVARIAN | EXPRESSION | CARCINOMA | ESTROGEN-RECEPTOR | LINES | Cyclin D1 - metabolism | Humans | Mitogen-Activated Protein Kinase Kinases - antagonists & inhibitors | Phosphatidylinositol 3-Kinases - metabolism | G1 Phase - drug effects | Phosphatidylinositol 3-Kinases - antagonists & inhibitors | Breast Neoplasms - drug therapy | Drug Synergism | Mitogen-Activated Protein Kinase Kinases - metabolism | Breast Neoplasms - enzymology | Cyclin D1 - antagonists & inhibitors | Feedback, Physiological | Receptor, Epidermal Growth Factor - metabolism | MAP Kinase Signaling System - drug effects | Breast Neoplasms - pathology | Cell Line, Tumor | Protein Kinase Inhibitors - pharmacology | Camptothecin - pharmacology | Index Medicus
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10. Full Text Bayesian network inference modeling identifies TRIB1 as a novel regulator of cell-cycle progression and survival in cancer cells
by Gendelman, Rina and Xing, Heming and Mirzoeva, Olga K and Sarde, Preeti and Curtis, Christina and Feiler, Heidi S and McDonagh, Paul and Gray, Joe W and Khalil, Iya and Korn, W. Michael
Cancer Research, ISSN 0008-5472, 2017, Volume 77, Issue 7, pp. 1575 - 1585
Molecular networks governing responses to targeted therapies in cancer cells are complex dynamic systems that demonstrate nonintuitive behaviors. We applied a... 
BREAST-CANCER | KAPPA-B ACTIVATION | SIGNALING PATHWAYS | PROTEIN | MEK INHIBITION | ONCOLOGY | KINASE | GENE-EXPRESSION | PROLIFERATION | TRIBBLES | Promoter Regions, Genetic | Cell Survival | Protein-Serine-Threonine Kinases - physiology | Humans | Mitogen-Activated Protein Kinase Kinases - antagonists & inhibitors | Protein-Serine-Threonine Kinases - genetics | Proto-Oncogene Proteins c-akt - physiology | Breast Neoplasms - drug therapy | Breast Neoplasms - genetics | Cell Cycle | Cyclin D1 - genetics | Breast Neoplasms - pathology | Bayes Theorem | NF-kappa B - physiology | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Cell Line, Tumor | Phosphatidylinositol 3-Kinases - physiology | Female | Signal Transduction - physiology | Intracellular Signaling Peptides and Proteins - physiology | Intracellular Signaling Peptides and Proteins - genetics | Cell culture | Regulators | Transcription factors | Copy number | Genes | Cyclin D1 | Machinery | Signal transduction | Interrogation | Cell cycle | Mathematical models | Inhibition | Interleukin 8 | Multidimensional data | Cell survival | Computer simulation | Breast cancer | Gene expression | Survival | Signaling | Computer applications | Predictions | Transduction | Bayesian analysis | Cancer | Apoptosis | apoptosis | MEK | Molecular network biology | NFκB | cell cycle regulation | TRIB1
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11. Full Text Autophagy suppression promotes apoptotic cell death in response to inhibition of the PI3K—mTOR pathway in pancreatic adenocarcinoma
by Mirzoeva, Olga K and Hann, Byron and Hom, Yun K and Debnath, Jayanta and Aftab, Dana and Shokat, Kevan and Korn, W Michael
Journal of Molecular Medicine, ISSN 0946-2716, 9/2011, Volume 89, Issue 9, pp. 877 - 889
Targeting of pathways downstream of RAS represents a promising therapeutic strategy for pancreatic cancer, the fourth leading cause of cancer-related death in... 
Human Genetics | EGFR pathway | Biomedicine | Cancer signal transduction | PI3K | Chloroquine | mTOR | Pancreatic adenocarcinoma | Internal Medicine | Molecular Medicine | Autophagy | Apoptosis | MAMMALIAN TARGET | TRANSCRIPTION FACTORS | RAPAMYCIN | MEDICINE, RESEARCH & EXPERIMENTAL | SIGNALING PATHWAYS | ACTIVATION | PHOSPHORYLATION | INDUCTION | BREAST-CANCER CELLS | GENETICS & HEREDITY | NF-KAPPA-B | EXPRESSION | Pancreatic Neoplasms - metabolism | TOR Serine-Threonine Kinases - metabolism | Apoptosis - drug effects | Humans | Apoptosis - genetics | Antineoplastic Agents - therapeutic use | Phosphatidylinositol 3-Kinases - metabolism | Phosphatidylinositol 3-Kinases - antagonists & inhibitors | Autophagy - drug effects | Pancreatic Neoplasms - drug therapy | TOR Serine-Threonine Kinases - antagonists & inhibitors | Adenocarcinoma - metabolism | Cell Death - genetics | Female | Adenocarcinoma - genetics | Autophagy - genetics | Cell Death - drug effects | Pancreatic Neoplasms - genetics | Signal Transduction - genetics | Adenocarcinoma - drug therapy | Xenograft Model Antitumor Assays | Animals | Signal Transduction - drug effects | Mice, Nude | Protein Kinase Inhibitors - therapeutic use | Cell Line, Tumor | Cell Proliferation - drug effects | Mice | Autophagy (Cytology) | Care and treatment | Enzyme inhibitors | Pancreatic cancer | Cellular signal transduction | Research | Health aspects
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12. Full Text Genomic landscape of cell-free DNA in patients with colorectal cancer
by Strickler, John H and Loree, Jonathan M and Ahronian, Leanne G and Parikh, Aparna R and Niedzwiecki, Donna and Pereira, Allan Andresson Lima and McKinney, Matthew and Michael Korn, W and Atreya, Chloe E and Banks, Kimberly C and Nagy, Rebecca J and Meric-Bernstam, Funda and Lanman, Richard B and Talasaz, AmirAli and Tsigelny, Igor F and Corcoran, Ryan B and Kopetz, Scott
Cancer Discovery, ISSN 2159-8274, 02/2018, Volume 8, Issue 2, pp. 164 - 173
"Liquid biopsy" approaches analyzing cell-free DNA (cfDNA) from the blood of patients with cancer are increasingly utilized in clinical practice. However, it... 
TARGETED THERAPY | KRAS MUTATIONS | HETEROGENEITY | EGFR MONOCLONAL-ANTIBODIES | EVOLUTION | ONCOLOGY | CLONAL HEMATOPOIESIS | ACQUIRED-RESISTANCE | EXTRACELLULAR DOMAIN | BLOCKADE | CETUXIMAB RESISTANCE | Cell-free DNA | colorectal cancer | circulating tumor DNA
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13. Esophageal and esophagogastric junction cancers, Version 1.2015
by Ajani, Jaffer A and D'Amico, Thomas A and Almhanna, Khaldoun and Bentrem, David J and Besh, Stephen and Chao, Joseph and Das, Prajnan and Denlinger, Crystal and Fanta, Paul and Fuchs, Charles S and Gerdes, Hans and Glasgow, Robert E and Hayman, James A and Hochwald, Steven and Hofstetter, Wayne L and Ilson, David H and Jaroszewski, Dawn and Jasperson, Kory and Keswani, Rajesh N and Kleinberg, Lawrence R and Korn, W. Michael and Leong, Stephen and Lockhart, A. Craig and Mulcahy, Mary F and Orringer, Mark B and Posey, James A and Poultsides, George A and Sasson, Aaron R and Scott, Walter J and Strong, Vivian E and Varghese, Thomas K and Washington, Mary Kay and Willett, Christopher G and Wright, Cameron D and Zelman, Debra and McMillian, Nicole and Sundar, Hema and National comprehensive cancer network
JNCCN Journal of the National Comprehensive Cancer Network, ISSN 1540-1405, 02/2015, Volume 13, Issue 2, pp. 194 - 227
Esophageal cancer is the sixth most common cause of cancer deaths worldwide. Adenocarcinoma is more common in North America and Western European countries,... 
PHASE-II TRIAL | POSITRON-EMISSION-TOMOGRAPHY | COMBINED-MODALITY THERAPY | GASTROESOPHAGEAL JUNCTION | ONCOLOGY | DOCETAXEL PLUS CISPLATIN | GASTRIC-CANCER | SQUAMOUS-CELL CARCINOMA | RANDOMIZED-TRIAL | PREOPERATIVE CHEMORADIOTHERAPY | METASTATIC ADENOCARCINOMA | Esophagogastric Junction - pathology | Esophageal Neoplasms - diagnosis | Stomach Neoplasms - diagnosis | Esophageal Neoplasms - therapy | Humans | Stomach Neoplasms - therapy
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14. Full Text Targeted next-generation sequencing of pediatric neuro-oncology patients improves diagnosis, identifies pathogenic germline mutations, and directs targeted therapy
by Kline, Cassie N and Joseph, Nancy M and Grenert, James P and Van Ziffle, Jessica and Talevich, Eric and Onodera, Courtney and Aboian, Mariam and Cha, Soonmee and Raleigh, David R and Braunstein, Steve and Torkildson, Joseph and Samuel, David and Bloomer, Michelle and De Alba Campomanes, Alejandra G and Banerjee, Anuradha and Butowski, Nicholas and Raffel, Corey and Tihan, Tarik and Bollen, Andrew W and Phillips, Joanna J and Michael Korn, W and Yeh, Iwei and Bastian, Boris C and Gupta, Nalin and Mueller, Sabine and Perry, Arie and Nicolaides, Theodore and Solomon, David A
Neuro-Oncology, ISSN 1522-8517, 05/2017, Volume 19, Issue 5, pp. 699 - 709
Molecular profiling is revolutionizing cancer diagnostics and leading to personalized therapeutic approaches. Herein we describe our clinical experience... 
Targeted therapeutics | Next-generation sequencing | Personalized therapy | Pediatric brain tumors | Molecular profling | MISMATCH-REPAIR DEFICIENCY | ASTROCYTOMA | MAP2K1 | next-generation sequencing | LANDSCAPE | pediatric brain tumors | CANCER | SOMATIC MUTATIONS | CLINICAL NEUROLOGY | BRAIN-TUMORS | ONCOLOGY | targeted therapeutics | molecular profiling | personalized therapy | FGFR1 | Prognosis | Brain Neoplasms - diagnosis | Humans | Brain Neoplasms - genetics | Child, Preschool | Infant | Male | Antineoplastic Agents - therapeutic use | Brain Neoplasms - drug therapy | Molecular Targeted Therapy | Young Adult | Brain Neoplasms - classification | Adolescent | Germ-Line Mutation | Adult | Female | Biomarkers, Tumor - genetics | High-Throughput Nucleotide Sequencing - methods | Child | Pediatric Neuro-Oncology
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15. Full Text Landscape of tumor mutation load, mismatch repair deficiency, and PD-L1 expression in a large patient cohort of gastrointestinal cancers
by Salem, Mohamed E and Puccini, Alberto and Grothey, Axel and Raghavan, Derek and Goldberg, Richard M and Xiu, Joanne and Michael Korn, W and Weinberg, Benjamin A and Hwang, Jimmy J and Shields, Anthony F and Marshall, John L and Philip, Philip A and Lenz, Heinz-Josef
Molecular Cancer Research, ISSN 1541-7786, 05/2018, Volume 16, Issue 5, pp. 805 - 812
The efficacy of immunotherapy varies widely among different gastrointestinal cancers. Response to immune checkpoint inhibitors is shown to correlate with tumor... 
Gastrointestinal Neoplasms - genetics | Colorectal Neoplasms - genetics | Humans | Brain Neoplasms - genetics | Male | Neoplastic Syndromes, Hereditary - metabolism | B7-H1 Antigen - genetics | Brain Neoplasms - metabolism | Gastrointestinal Neoplasms - pathology | B7-H1 Antigen - biosynthesis | Neoplastic Syndromes, Hereditary - genetics | Mutation | Colorectal Neoplasms - metabolism | Cohort Studies | Gastrointestinal Neoplasms - metabolism | Clinical trials | Microsatellite instability | Paraffin | Gene sequencing | Missense mutation | Intestine | Immunotherapy | Mismatch repair | Colon | Pancreas | Repair | Movement disorders | Deoxyribonucleic acid--DNA | Medical research | Microsatellites | Stability | Stability analysis | Gene expression | Immune checkpoint | Cell death | PD-L1 protein | DNA sequencing | Cancer | Neuroendocrine tumors | Tumors | Apoptosis
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16. Prolonged response to HER2-directed therapy in a patient With HER2-amplified, rapidly progressive metastatic colorectal cancer
by Parikh, Aparna and Atreya, Chloe and Korn, W. Michael and Venook, Alan P
JNCCN Journal of the National Comprehensive Cancer Network, ISSN 1540-1405, 01/2017, Volume 15, Issue 1, pp. 3 - 8
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17. Full Text A phase 1 study of MM-121 (a fully human monoclonal antibody targeting the epidermal growth factor receptor family member ErbB3) in combination with cetuximab and irinotecan in patients with advanced cancers
by Cleary, James M and McRee, Autumn Jackson and O'Neil, Bert H and Sharma, Sunil and Pearlberg, Joseph and Manoli, Sara and Kubasek, William Lloyd and Korn, W. Michael
Journal of Clinical Oncology, ISSN 0732-183X, 05/2014, Volume 32, Issue 15_suppl, pp. 3076 - 3076
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18. Full Text A multicenter, open-label phase II clinical trial of combined MEK plus EGFR inhibition for chemotherapy-refractory advanced pancreatic adenocarcinoma
by Ko, Andrew H and Bekaii-Saab, Tanios and Van Ziffle, Jessica and Mirzoeva, Olga M and Joseph, Nancy M and Talasaz, Amir Ali and Kuhn, Peter and Tempero, Margaret A and Collisson, Eric A and Kelley, R. Kate and Venook, Alan P and Dito, Elizabeth and Ong, Anna and Ziyeh, Sharvina and Courtin, Ryan and Linetskaya, Regina and Tahiri, Sanaa and Korn, W. Michael
Clinical Cancer Research, ISSN 1078-0432, 01/2016, Volume 22, Issue 1, pp. 61 - 68
Purpose: On the basis of preclinical evidence of synergistic activity between MEK and EGFR inhibitors in pancreatic ductal adenocarcinoma (PDAC), we evaluated... 
PATHWAYS | ONCOLOGY | TRAMETINIB | E-CADHERIN EXPRESSION | KINASE | GROWTH | RECEPTOR | CANCER | GEMCITABINE | ERLOTINIB | FEEDBACK | Adenocarcinoma - pathology | Humans | Middle Aged | Antineoplastic Combined Chemotherapy Protocols - adverse effects | Drug Resistance, Neoplasm | Male | Molecular Targeted Therapy | Pancreatic Neoplasms - drug therapy | Benzimidazoles - administration & dosage | DNA, Neoplasm - blood | Aged, 80 and over | Adult | Female | Pancreatic Neoplasms - mortality | Pancreatic Neoplasms - pathology | Erlotinib Hydrochloride - administration & dosage | Kaplan-Meier Estimate | Adenocarcinoma - drug therapy | Retreatment | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Neoplastic Cells, Circulating | Biomarkers | Aged | Neoplasm Staging | Adenocarcinoma - mortality | clinical trial | pancreatic cancer | MEK | EGFR | molecular subtype
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19. Full Text Fluid biopsy in patients with metastatic prostate, pancreatic and breast cancers
by Marrinucci, Dena and Bethel, Kelly and Kolatkar, Anand and Luttgen, Madelyn S and Malchiodi, Michael and Baehring, Franziska and Voigt, Katharina and Lazar, Daniel and Nieva, Jorge and Bazhenova, Lyudmila and Ko, Andrew H and Korn, W Michael and Schram, Ethan and Coward, Michael and Yang, Xing and Metzner, Thomas and Lamy, Rachelle and Honnatti, Meghana and Yoshioka, Craig and Kunken, Joshua and Petrova, Yelena and Sok, Devin and Nelson, David and Kuhn, Peter
Physical Biology, ISSN 1478-3967, 02/2012, Volume 9, Issue 1, pp. 016003 - 016003
Hematologic spread of carcinoma results in incurable metastasis; yet, the basic characteristics and travel mechanisms of cancer cells in the bloodstream are... 
SURVIVAL | CIRCULATING-TUMOR-CELLS | BIOPHYSICS | BIOCHEMISTRY & MOLECULAR BIOLOGY | Biopsy - methods | Prostatic Neoplasms - pathology | Neoplastic Cells, Circulating - pathology | Humans | Middle Aged | Pancreatic Neoplasms - pathology | Image Interpretation, Computer-Assisted | Male | Young Adult | Keratins - metabolism | Breast Neoplasms - pathology | Sensitivity and Specificity | Adult | Female | breast cancer | pancreatic cancer | prostate cancer | circulating tumor cells | fluid biopsy | microtumor emboli
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