MiR-133b targets antiapoptotic genes and enhances death receptor-induced apoptosis. - Wikidata - wikimedia - TriplyDB

MiR-133b targets antiapoptotic genes and enhances death receptor-induced apoptosis.

MiR-133b targets antiapoptotic genes and enhances death receptor-induced apoptosis.

http://www.wikidata.org/entity/Q34245074

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Identification of novel AR-targeted microRNAs mediating androgen signalling through critical pathways to regulate cell viability in prostate cancer Roles of the canonical myomiRs miR-1, -133 and -206 in cell development and disease miRNAs associated with prostate cancer risk and progression Inhibition of nucleoporin member Nup214 expression by miR-133b perturbs mitotic timing and leads to cell death.Regulation of epigenetic traits of the glutathione S-transferase P1 gene: from detoxification toward cancer prevention and diagnosis MicroRNA-7-regulated TLR9 signaling-enhanced growth and metastatic potential of human lung cancer cells by altering the phosphoinositide-3-kinase, regulatory subunit 3/Akt pathway Deciphering the unique microRNA signature in human esophageal adenocarcinoma MicroRNA Regulating Glutathione S-Transferase P1 in Prostate Cancer.MicroRNA profiling of rats with ochratoxin A nephrotoxicity.DNA Methylation-Guided Prediction of Clinical Failure in High-Risk Prostate Cancer MicroRNA-mRNA regulatory networking fine-tunes the porcine muscle fiber type, muscular mitochondrial respiratory and metabolic enzyme activities.Understanding of tolerance in TRAIL-induced apoptosis and cancelation of its machinery by α-mangostin, a xanthone derivative Integrated gene and miRNA expression analysis of prostate cancer associated fibroblasts supports a prominent role for interleukin-6 in fibroblast activation Apoptosis is induced in cancer cells via the mitochondrial pathway by the novel xylocydine-derived compound JRS-15.Glutathione S-transferase class μ regulation of apoptosis signal-regulating kinase 1 protein during VCD-induced ovotoxicity in neonatal rat ovaries.Chemical tools for temporally and spatially resolved mass spectrometry-based proteomics.Targeting microRNAs to modulate TRAIL-induced apoptosis of cancer cells.Roles of microRNAs during prostatic tumorigenesis and tumor progression.Deciphering microRNA code in pain and inflammation: lessons from bladder pain syndrome.TRAIL and microRNAs in the treatment of prostate cancer: therapeutic potential and role of nanotechnology.Antisense therapeutics in oncology: current status.MicroRNA-133b stimulates ovarian estradiol synthesis by targeting Foxl2.Urinary microRNAs as potential biomarkers of pesticide exposure.Epigenetic Alterations in Human Papillomavirus-Associated Cancers.MicroRNAs in Sertoli cells: implications for spermatogenesis and fertility.Epigenetic and miRNAs Dysregulation in Prostate Cancer: The role of Nutraceuticals.Fas apoptosis inhibitory molecules: more than death-receptor antagonists in the nervous system.MiR-133b contributes to arsenic-induced apoptosis in U251 glioma cells by targeting the hERG channel.Impact of the Interaction between 3'-UTR SNPs and microRNA on the Expression of Human Xenobiotic Metabolism Enzyme and Transporter Genes.miR-133b acts as a tumor suppressor and negatively regulates FGFR1 in gastric cancer.miR-133b, a particular member of myomiRs, coming into playing its unique pathological role in human cancer DNA methylation is involved in the aberrant expression of miR-133b in colorectal cancer cells.Tumor Protein p63/microRNA Network in Epithelial Cancer Cells.Identification of hub miRNA biomarkers for bladder cancer by weighted gene coexpression network analysis.microRNAs as novel antidepressant targets: converging effects of ketamine and electroconvulsive shock therapy in the rat hippocampus.Impact of MiR-21 on the expression of FasL in the presence of TGF-β1.Rifampin modulation of xeno- and endobiotic conjugating enzyme mRNA expression and associated microRNAs in human hepatocytes.Transcriptional downregulation of miR-133b by REST promotes prostate cancer metastasis to bone via activating TGF-β signaling.

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P2860

MiR-133b targets antiapoptotic genes and enhances death receptor-induced apoptosis.

http://www.wikidata.org/entity/Q34245074

description

2012 nî lūn-bûn

@nan

2012 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2012 թվականի ապրիլին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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name

MiR-133b targets antiapoptotic genes and enhances death receptor-induced apoptosis.

@ast

MiR-133b targets antiapoptotic genes and enhances death receptor-induced apoptosis.

@en

MiR-133b targets antiapoptotic genes and enhances death receptor-induced apoptosis.

@nl

type

label

MiR-133b targets antiapoptotic genes and enhances death receptor-induced apoptosis.

@ast

MiR-133b targets antiapoptotic genes and enhances death receptor-induced apoptosis.

@en

MiR-133b targets antiapoptotic genes and enhances death receptor-induced apoptosis.

@nl

prefLabel

MiR-133b targets antiapoptotic genes and enhances death receptor-induced apoptosis.

@ast

MiR-133b targets antiapoptotic genes and enhances death receptor-induced apoptosis.

@en

MiR-133b targets antiapoptotic genes and enhances death receptor-induced apoptosis.

@nl

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MiR-133b targets antiapoptotic genes and enhances death receptor-induced apoptosis.

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Bernd Thiede

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Carsten Stephan

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Chloe Piso

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Henrik Müller

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Juan P Patron

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Jörg Schreiber

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Matthias Bild

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Ulrike Jung

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P2860

Ultra-high throughput sequencing-based small RNA discovery and discrete statistical biomarker analysis in a collection of cervical tumours and matched controls

Human glutathione S-transferase P1-1 interacts with TRAF2 and regulates TRAF2-ASK1 signals

Sequence-specific inhibition of microRNA- and siRNA-induced RNA silencing

Apoptosis: a basic biological phenomenon with wide-ranging implications in tissue kinetics

MicroRNA targeting specificity in mammals: determinants beyond seed pairing

miRiad roles for the miR-17-92 cluster in development and disease

Classification of cell death: recommendations of the Nomenclature Committee on Cell Death 2009

Most mammalian mRNAs are conserved targets of microRNAs

miRecords: an integrated resource for microRNA-target interactions

Sequence-specific inhibition of small RNA function

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