MicroRNAs as putative mediators of treatment response in prostate cancer. - Wikidata - wikimedia - TriplyDB

MicroRNAs as putative mediators of treatment response in prostate cancer.

MicroRNAs as putative mediators of treatment response in prostate cancer.

http://www.wikidata.org/entity/Q38011943

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When Prostate Cancer Circulates in the Bloodstream MiR-23a sensitizes nasopharyngeal carcinoma to irradiation by targeting IL-8/Stat3 pathway.Involvement of miR-20a in promoting gastric cancer progression by targeting early growth response 2 (EGR2)Downregulation of miR-130b~301b cluster is mediated by aberrant promoter methylation and impairs cellular senescence in prostate cancer.The genomic landscape of prostate cancer Aberrant expression of microRNAs in bladder cancer.Radiation-induced microRNA: discovery, functional analysis, and cancer radiotherapy.Role of microRNA in response to ionizing radiations: evidences and potential impact on clinical practice for radiotherapy.Molecular markers to guide primary radical treatment selection in localized prostate cancer.MiR-1247-5p is overexpressed in castration resistant prostate cancer and targets MYCBP2.miRNA in Prostate Cancer: New Prospects for Old Challenges A prognostic model for lung adenocarcinoma patient survival with a focus on four miRNAs.Gene suppression approaches to neurodegeneration.MicroRNAs Associated with Von Hippel-Lindau Pathway in Renal Cell Carcinoma: A Comprehensive Review.Profiling of a panel of radioresistant prostate cancer cells identifies deregulation of key miRNAs.

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MicroRNAs as putative mediators of treatment response in prostate cancer.

http://www.wikidata.org/entity/Q38011943

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article científic

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article scientifique

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artigo científico

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artikel ilmiah

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artículo científico

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name

MicroRNAs as putative mediators of treatment response in prostate cancer.

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type

label

MicroRNAs as putative mediators of treatment response in prostate cancer.

@en

prefLabel

MicroRNAs as putative mediators of treatment response in prostate cancer.

@en

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NRUROL.2012.104

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Nature Reviews Urology

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MicroRNAs as putative mediators of treatment response in prostate cancer.

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Armelle Meunier

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Donal Hollywood

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Fardod O'Kelly

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Laure Marignol

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Thomas H Lynch

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P2860

miR-143 interferes with ERK5 signaling, and abrogates prostate cancer progression in mice

An integrated network of androgen receptor, polycomb, and TMPRSS2-ERG gene fusions in prostate cancer progression

Fast and effective prediction of microRNA/target duplexes

A microRNA expression signature of human solid tumors defines cancer gene targets

Ectopic expression of miR-126*, an intronic product of the vascular endothelial EGF-like 7 gene, regulates prostein translation and invasiveness of prostate cancer LNCaP cells

Circulating microRNAs as stable blood-based markers for cancer detection.

The role of microRNA-221 and microRNA-222 in androgen-independent prostate cancer cell lines

Comparative analysis of prostate-specific antigen free survival outcomes for patients with low, intermediate and high risk prostate cancer treatment by radical therapy. Results from the Prostate Cancer Results Study Group

The miR-200 family and miR-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1

MicroRNA expression profiles classify human cancers

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nrurol.2012.104

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397-407

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scholarly article

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10.1038/NRUROL.2012.104

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7

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9

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Antoinette S. Perry

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2012-05-22T00:00:00Z

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225053143

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