Mutant KRAS is a druggable target for pancreatic cancer

scientific article published on 02 December 2013

Mutant KRAS is a druggable target for pancreatic cancer is …
instance of (P31):
scholarly articleQ13442814

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P819ADS bibcode2013PNAS..11020723Z
P356DOI10.1073/PNAS.1314307110
P932PMC publication ID3870687
P698PubMed publication ID24297898

P50authorEithan GalunQ47008783
P2093author name stringRami Eliakim
Talia Golan
Eylon Yavin
Hilla Giladi
Ludmila Rivkin
Rinat Abramovitch
Ayala Hubert
Yael Kopelman
Abraham J Domb
Abed Khalaileh
Eran Goldin
Adva Shemi
Yael Hants
Amotz Shemi
Elad Horwitz
Ariel Orbach
Maor Lahav
Sagit Arbel-Alon
Zivia Brunschwig
Elina Zorde Khvalevsky
Alina Simerzin
Alan Dancour
Itzhak Haim Rachmut
Racheli Gabai
P2860cites workSmall molecule inhibition of the KRAS-PDEδ interaction impairs oncogenic KRAS signallingQ24293500
Genetic and epigenetic alterations in pancreatic carcinogenesisQ24598655
Core signaling pathways in human pancreatic cancers revealed by global genomic analysesQ24606006
Pancreatic cancerQ29616288
In vitro scratch assay: a convenient and inexpensive method for analysis of cell migration in vitroQ29617927
Pancreatic cancer.Q30490247
K-ras as a target for cancer therapyQ36248002
Molecular genetics of pancreatic intraepithelial neoplasiaQ36829524
Oncogene addiction: setting the stage for molecularly targeted cancer therapyQ37031755
Drug delivery systems with modified release for systemic and biophase bioavailabilityQ38026125
Biopolymer nanoparticle production for controlled release of biopharmaceuticalsQ38072083
Tumor budding cells, cancer stem cells and epithelial-mesenchymal transition-type cells in pancreatic cancerQ38073775
Biomaterial-based drug delivery systems for the controlled release of neurotrophic factors.Q38079443
A gene expression signature associated with "K-Ras addiction" reveals regulators of EMT and tumor cell survivalQ39845869
Activated Kras, but not Hras or Nras, may initiate tumors of endodermal origin via stem cell expansionQ40014102
K-ras oncogene silencing strategy reduces tumor growth and enhances gemcitabine chemotherapy efficacy for pancreatic cancer treatmentQ40134965
Molecular consequences of silencing mutant K-ras in pancreatic cancer cells: justification for K-ras-directed therapyQ40392798
Diagnostic utility of K-ras mutations in fine-needle aspirates of pancreatic masses.Q40977239
Testing transgenic regulatory elements through live mouse imagingQ45869949
Characterization of the mutations of the K-ras, p53, p16, and SMAD4 genes in 15 human pancreatic cancer cell lines.Q52827026
Molecular biology of pancreatic cancerQ81973822
In vitro cell migration and invasion assaysQ84914731
P433issue51
P407language of work or nameEnglishQ1860
P921main subjectpancreatic cancerQ212961
P1104number of pages6
P304page(s)20723-20728
P577publication date2013-12-02
P1433published inProceedings of the National Academy of Sciences of the United States of AmericaQ1146531
P1476titleMutant KRAS is a druggable target for pancreatic cancer
P478volume110