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Paper Details

Recurrent WNT pathway alterations are frequent in relapsed small cell lung cancer.
Nat Commun
91
2018
ABCC1, APC, ASCL1, ASCL1-low expression subtype, CHD8, MSH2, MSH6, MYCL, RNA, SCLC, SCLC tumor, SCLC tumor samples, WNT, chemoresistant cell, human, human SCLC cell lines, patients, relapsed samples, small cell lung cancer, tumor, vitro-derived chemoresistant cell lines
Adenomatous Polyposis Coli Protein, Basic Helix-Loop-Helix Transcription Factors, Cadherins, Cell Line, Tumor, Drug Resistance, Neoplasm, Exome Sequencing, Gene Expression Regulation, Neoplastic, Gene Knockdown Techniques, Humans, Loss of Heterozygosity, Lung Neoplasms, Mutation, Neoplasm Recurrence, Local, Small Cell Lung Carcinoma, Wnt Signaling Pathway
Author NameAffiliation
Alex H WagnerMcDonnell Genome Institute, Washington University School of Medicine
Siddhartha DevarakondaWashington University School of Medicine
Siddhartha DevarakondaAlvin J Siteman Cancer Center, Washington University
Zachary L SkidmoreMcDonnell Genome Institute, Washington University School of Medicine
Kilannin KrysiakMcDonnell Genome Institute, Washington University School of Medicine
Kilannin KrysiakWashington University School of Medicine
Avinash RamuMcDonnell Genome Institute, Washington University School of Medicine
Avinash RamuMcDonnell Genome Institute, Washington University School of Medicine
Lee TraniMcDonnell Genome Institute, Washington University School of Medicine
Jason KunisakiMcDonnell Genome Institute, Washington University School of Medicine
Ashiq MasoodWashington University School of Medicine
Ashiq Masood
Ashiq MasoodAlvin J Siteman Cancer Center, Washington University
Saiama N WaqarWashington University School of Medicine
Saiama N WaqarAlvin J Siteman Cancer Center, Washington University
Nicholas C SpiesMcDonnell Genome Institute, Washington University School of Medicine
Daniel MorgenszternWashington University School of Medicine
Daniel MorgenszternAlvin J Siteman Cancer Center, Washington University
Jason E WaligorskiMcDonnell Genome Institute, Washington University School of Medicine
Jennifer PonceMcDonnell Genome Institute, Washington University School of Medicine
Robert S FultonMcDonnell Genome Institute, Washington University School of Medicine
Robert S FultonMcDonnell Genome Institute, Washington University School of Medicine
Leonard B MaggiWashington University School of Medicine
Leonard B MaggiICCE Institute, Washington University School of Medicine
Leonard B MaggiAlvin J Siteman Cancer Center, Washington University
Jason D WeberWashington University School of Medicine
Jason D WeberICCE Institute, Washington University School of Medicine
Jason D WeberAlvin J Siteman Cancer Center, Washington University
Mark A WatsonAlvin J Siteman Cancer Center, Washington University
Christopher J O'ConorWashington University School of Medicine
Jon H RitterWashington University School of Medicine
Rachelle R OlsenUniversity of Utah, Huntsman Cancer Institute
Haixia ChengUniversity of Utah, Huntsman Cancer Institute
Anandaroop MukhopadhyayUniversity of Utah, Huntsman Cancer Institute
Ismail CanUniversity of Utah, Huntsman Cancer Institute
Melissa H Cessna
Trudy G OliverUniversity of Utah, Huntsman Cancer Institute
Elaine R MardisMcDonnell Genome Institute, Washington University School of Medicine
Elaine R MardisNationwide Children's Hospital
Elaine R MardisWashington University School of Medicine
Elaine R MardisAlvin J Siteman Cancer Center, Washington University
Elaine R MardisMcDonnell Genome Institute, Washington University School of Medicine
Elaine R MardisNationwide Children's Hospital
Elaine R MardisWashington University School of Medicine
Elaine R MardisAlvin J Siteman Cancer Center, Washington University
Richard K WilsonMcDonnell Genome Institute, Washington University School of Medicine
Richard K WilsonNationwide Children's Hospital
Richard K WilsonWashington University School of Medicine
Richard K WilsonAlvin J Siteman Cancer Center, Washington University
Richard K WilsonMcDonnell Genome Institute, Washington University School of Medicine
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