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Delivery of gene silencing agents for breast cancer therapyFolate Receptor Targeted Delivery of siRNA and Paclitaxel to Ovarian Cancer Cells via Folate Conjugated Triblock Copolymer to Overcome TLR4 Driven Chemotherapy Resistance.Comparison of expression profiles in ovarian epithelium in vivo and ovarian cancer identifies novel candidate genes involved in disease pathogenesis.Use of Nanotechnology to Develop Multi-Drug Inhibitors For Cancer TherapyLack of ephrin receptor A1 is a favorable independent prognostic factor in clear cell renal cell carcinoma.Eph receptors and ephrins in cancer: bidirectional signalling and beyond.Prognostic biomarkers in ovarian cancer.Emerging strategies for EphA2 receptor targeting for cancer therapeutics.Ephrin (Eph) receptor A1, A4, A5 and A7 expression in human non-small cell lung carcinoma: associations with clinicopathological parameters, tumor proliferative capacity and patients' survivalTargeted delivery of small interfering RNA using reconstituted high-density lipoprotein nanoparticles.Functional roles of Src and Fgr in ovarian carcinoma.Src family kinases and paclitaxel sensitivity.Eph receptors and ephrins as targets for cancer therapy.Therapeutic advances in women's cancersTherapeutic silencing of KRAS using systemically delivered siRNAs.Paraneoplastic thrombocytosis in ovarian cancer.Biological significance of HORMA domain containing protein 1 (HORMAD1) in epithelial ovarian carcinomaRegulation of apoptosis in HL-1 cardiomyocytes by phosphorylation of the receptor tyrosine kinase EphA2 and protection by lithocholic acid.Toward personalized cancer nanomedicine - past, present, and future.Indium-Labeling of siRNA for Small Animal SPECT Imaging.Moving beyond VEGF for anti-angiogenesis strategies in gynecologic cancerTherapeutic synergy between microRNA and siRNA in ovarian cancer treatment.Platelet-derived growth factor receptor alpha (PDGFRα) targeting and relevant biomarkers in ovarian carcinoma.RNA interference in the clinic: challenges and future directions.Strategies for tumor-directed delivery of siRNA.Leveraging therapeutic potential of multi-targeted siRNA inhibitors.Challenging the future of siRNA therapeutics against cancer: the crucial role of nanotechnology.Eph receptors and ephrins: therapeutic opportunities.Recent advances in siRNA delivery.Inhibition of the integrin/FAK signaling axis and c-Myc synergistically disrupts ovarian cancer malignancy.Administration of PLGA nanoparticles carrying shRNA against focal adhesion kinase and CD44 results in enhanced antitumor effects against ovarian cancer.Selection of optimal combinations of target genes for therapeutic multi-gene silencing based on miRNA co-regulation.Ephrin receptor (Eph) -A1, -A2, -A4 and -A7 expression in mobile tongue squamous cell carcinoma: associations with clinicopathological parameters and patients survival.
P2860
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P2860
description
article científic
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article scientifique
@fr
articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 24 June 2009
@en
vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Dual targeting of EphA2 and FAK in ovarian carcinoma.
@en
Dual targeting of EphA2 and FAK in ovarian carcinoma.
@nl
type
label
Dual targeting of EphA2 and FAK in ovarian carcinoma.
@en
Dual targeting of EphA2 and FAK in ovarian carcinoma.
@nl
prefLabel
Dual targeting of EphA2 and FAK in ovarian carcinoma.
@en
Dual targeting of EphA2 and FAK in ovarian carcinoma.
@nl
P2093
P2860
P356
P1476
Dual targeting of EphA2 and FAK in ovarian carcinoma.
@en
P2093
Alpa M Nick
Anil K Sood
Charles N Landen
Christopher G Danes
Chunhua Lu
Gabriel Lopez-Berestein
Hye-Sun Kim
Jeong-Won Lee
Jyotsnabaran Halder
Keith A Baggerly
P2860
P304
P356
10.4161/CBT.8.11.8523
P577
2009-06-24T00:00:00Z