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Paper Details

Synthetic vulnerabilities of mesenchymal subpopulations in pancreatic cancer.
Nature
87
2017
Cancer, Cancer cell, IRE1, Kras, Kras-independent escaper populations, MAPK, MKK4, Malignant neoplasms, Myc, Myc network, PDAC, Smarcb1, cancer, malignancy, mesenchymal sub-populations, mesenchymal subpopulations, mouse, oncogenic Kras, pancreatic cancer, pancreatic ductal adenocarcinoma, patient, patient-, tumour, unfolded protein
Author NameAffiliation
Liren LiThe University of Texas MD Anderson Cancer Center
Liren LiSun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China
Luigi NeziThe University of Texas MD Anderson Cancer Center
Sahil SethThe University of Texas MD Anderson Cancer Center
Sahil SethThe University of Texas MD Anderson Cancer Center
Lawrence N KwongThe University of Texas MD Anderson Cancer Center
Papia GhoshThe University of Texas MD Anderson Cancer Center
Jianhua ZhangInstitute for Applied Cancer Science, The University of Texas MD Anderson Cancer Center
Jianhua ZhangInstitute for Applied Cancer Science, The University of Texas MD Anderson Cancer Center
Timothy P HeffernanInstitute for Applied Cancer Science, The University of Texas MD Anderson Cancer Center
Abbas AgaimyFriedrich Alexander University Erlangen-Nuremberg, University Hospital
Anirban MaitraThe University of Texas MD Anderson Cancer Center
Anirban MaitraSheikh Ahmed Bin Zayed Al Nahyan Center for Pancreatic Cancer Research, The University of Texas MD Anderson Cancer Center
Charles W M RobertsComprehensive Cancer Center and Department of Oncology, St Jude Children's Research Hospital
Andrea VialeThe University of Texas MD Anderson Cancer Center
Lynda ChinThe University of Texas MD Anderson Cancer Center
Lynda ChinInstitute for Applied Cancer Science, The University of Texas MD Anderson Cancer Center
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