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Paper Details

Spatially restricted drivers and transitional cell populations cooperate with the microenvironment in untreated and chemo-resistant pancreatic cancer.
Nat Genet
63
2022
Chemo-, KRAS, Nectin, Pancreatic ductal adenocarcinoma, TIGIT, acinar-to-ductal metaplasia, cancer, chemo-resistant, inflammatory cancer-associated fibroblasts, metallothioneins, pancreatic cancer, pancreatic ductal adenocarcinoma tumors, pancreatic intraepithelial neoplasia, patients, regulatory T cells, transitional cell populations, transitional cells, transitional subpopulations, tumor, tumor cells, tumor populations
Author NameAffiliation
Reyka G JayasingheWashington University in St Louis
Reyka G JayasingheMcDonnell Genome Institute, Washington University in St Louis
Reyka G JayasingheWashington University in St Louis
Reyka G JayasingheMcDonnell Genome Institute, Washington University in St Louis
Michael C WendlMcDonnell Genome Institute, Washington University in St Louis
Michael C WendlWashington University in St Louis
Michael C WendlWashington University in St Louis
Michael C WendlMcDonnell Genome Institute, Washington University in St Louis
Michael C WendlWashington University in St Louis
Michael C WendlWashington University in St Louis
Wagma CaravanWashington University in St Louis
Wagma CaravanMcDonnell Genome Institute, Washington University in St Louis
Kazuhito SatoWashington University in St Louis
Kazuhito SatoMcDonnell Genome Institute, Washington University in St Louis
Chia-Kuei MoWashington University in St Louis
Chia-Kuei MoMcDonnell Genome Institute, Washington University in St Louis
Nataly Naser Al DeenWashington University in St Louis
Nataly Naser Al DeenMcDonnell Genome Institute, Washington University in St Louis
Robert S FultonMcDonnell Genome Institute, Washington University in St Louis
Robert S FultonMcDonnell Genome Institute, Washington University in St Louis
Matthew A WyczalkowskiWashington University in St Louis
Matthew A WyczalkowskiMcDonnell Genome Institute, Washington University in St Louis
Matthew A WyczalkowskiWashington University in St Louis
Matthew A WyczalkowskiMcDonnell Genome Institute, Washington University in St Louis
Ruiyang LiuWashington University in St Louis
Ruiyang LiuMcDonnell Genome Institute, Washington University in St Louis
Catrina FronickMcDonnell Genome Institute, Washington University in St Louis
Lucinda FultonMcDonnell Genome Institute, Washington University in St Louis
Houxiang ZhuWashington University in St Louis
Houxiang ZhuMcDonnell Genome Institute, Washington University in St Louis
Liang-Bo WangWashington University in St Louis
Liang-Bo WangMcDonnell Genome Institute, Washington University in St Louis
Liang-Bo WangWashington University in St Louis
Liang-Bo WangMcDonnell Genome Institute, Washington University in St Louis
Yize LiWashington University in St Louis
Yize LiMcDonnell Genome Institute, Washington University in St Louis
Joshua F McMichaelWashington University in St Louis
Joshua F McMichaelMcDonnell Genome Institute, Washington University in St Louis
Joshua F McMichaelWashington University in St Louis
Joshua F McMichaelMcDonnell Genome Institute, Washington University in St Louis
Sherri R DaviesWashington University in St Louis
Clara OhWashington University in St Louis
Clara OhMcDonnell Genome Institute, Washington University in St Louis
Mamatha SerasanambatiWashington University in St Louis
Mamatha SerasanambatiMcDonnell Genome Institute, Washington University in St Louis
Robert J MashlWashington University in St Louis
Robert J MashlMcDonnell Genome Institute, Washington University in St Louis
Robert J MashlWashington University in St Louis
Robert J MashlMcDonnell Genome Institute, Washington University in St Louis
Jennifer PonceMcDonnell Genome Institute, Washington University in St Louis
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