FN14 expression correlates with MET in NSCLC and promotes MET-driven cell invasion.
about
The TWEAK receptor Fn14 is a potential cell surface portal for targeted delivery of glioblastoma therapeuticsTranscriptomic and Functional Pathway Analysis of Human Cervical Carcinoma Cancer Cells Response to Microtubule Inhibitor.Identification of aurintricarboxylic acid as a selective inhibitor of the TWEAK-Fn14 signaling pathway in glioblastoma cellsTWEAK/Fn14 signaling in tumors.Kruppel-like factor 4 inhibits non-small cell lung cancer cell growth and aggressiveness by stimulating transforming growth factor-β1-meidated ERK/JNK/NF-κB signaling pathways.The TWEAK Receptor Fn14 Is an Src-Inducible Protein and a Positive Regulator of Src-Driven Cell Invasion.A Putative Blood-Based Biomarker for Autism Spectrum Disorder-Associated Ileocolitis.TWEAK promotes migration and invasion in MEFs through a mechanism dependent on ERKs activation and Fibulin 3 down-regulation.
P2860
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P2860
FN14 expression correlates with MET in NSCLC and promotes MET-driven cell invasion.
description
2014 nî lūn-bûn
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2014年の論文
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2014年学术文章
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name
FN14 expression correlates with MET in NSCLC and promotes MET-driven cell invasion.
@en
FN14 expression correlates with MET in NSCLC and promotes MET-driven cell invasion.
@nl
type
label
FN14 expression correlates with MET in NSCLC and promotes MET-driven cell invasion.
@en
FN14 expression correlates with MET in NSCLC and promotes MET-driven cell invasion.
@nl
prefLabel
FN14 expression correlates with MET in NSCLC and promotes MET-driven cell invasion.
@en
FN14 expression correlates with MET in NSCLC and promotes MET-driven cell invasion.
@nl
P2093
P2860
P1476
FN14 expression correlates with MET in NSCLC and promotes MET-driven cell invasion
@en
P2093
Christopher B Kingsley
Glen J Weiss
Harshil D Dhruv
Janine LoBello
Jeffrey W Allen
Kerri K Wolf
Landon J Inge
Nhan L Tran
Shannon P Fortin Ensign
Timothy G Whitsett
P2860
P2888
P304
P356
10.1007/S10585-014-9653-6
P577
2014-04-08T00:00:00Z