MiR-195, miR-196b, miR-181c, miR-21 expression levels and O-6-methylguanine-DNA methyltransferase methylation status are associated with clinical outcome in glioblastoma patients. - Wikidata - awgldk - TriplyDB

MiR-195, miR-196b, miR-181c, miR-21 expression levels and O-6-methylguanine-DNA methyltransferase methylation status are associated with clinical outcome in glioblastoma patients.

MiR-195, miR-196b, miR-181c, miR-21 expression levels and O-6-methylguanine-DNA methyltransferase methylation status are associated with clinical outcome in glioblastoma patients.

http://www.wikidata.org/entity/Q44273844

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A systematic review of microRNA in glioblastoma multiforme: micro-modulators in the mesenchymal mode of migration and invasion MicroRNAs in glioblastoma multiforme pathogenesis and therapeutics NF-κB and STAT3 in glioblastoma: therapeutic targets coming of age Significance of miR-196b in tumor-related epilepsy of patients with gliomas.Differential expression of miR200a-3p and miR21 in grade II-III and grade IV gliomas: evidence that miR200a-3p is regulated by O⁶-methylguanine methyltransferase and promotes temozolomide responsiveness.Upregulation of miR-196b confers a poor prognosis in glioblastoma patients via inducing a proliferative phenotype.MicroRNA expression signatures determine prognosis and survival in glioblastoma multiforme--a systematic overview.Smoking status impacts microRNA mediated prognosis and lung adenocarcinoma biology MiR-328 expression is decreased in high-grade gliomas and is associated with worse survival in primary glioblastoma.Regulation of expression of O6-methylguanine-DNA methyltransferase and the treatment of glioblastoma (Review).MicroRNA-196b regulates the homeobox B7-vascular endothelial growth factor axis in cervical cancer.MicroRNA-27a distinguishes glioblastoma multiforme from diffuse and anaplastic astrocytomas and has prognostic value Comparative methylome analysis identifies new tumour subtypes and biomarkers for transformation of nephrogenic rests into Wilms tumour Prognostic microRNAs in high-grade glioma reveal a link to oligodendrocyte precursor differentiation.MicroRNA-503 acts as a tumor suppressor in glioblastoma for multiple antitumor effects by targeting IGF-1R Specific microRNAs as novel biomarkers for combination chemotherapy resistance detection of colon adenocarcinoma.Epigenetic silencing of miR-181c by DNA methylation in glioblastoma cell lines.High level of miR-221/222 confers increased cell invasion and poor prognosis in glioma.Novel classes of non-coding RNAs and cancer MicroRNA expression profile associated with response to neoadjuvant chemoradiotherapy in locally advanced rectal cancer patients.Functional microRNAs in Alzheimer's disease and cancer: differential regulation of common mechanisms and pathways.Interactions of miR-323/miR-326/miR-329 and miR-130a/miR-155/miR-210 as prognostic indicators for clinical outcome of glioblastoma patients Role of MicroRNAs in Malignant Glioma Inhibition of miR-21 in glioma cells using catalytic nucleic acids Epigenetic regulation of miRNA-211 by MMP-9 governs glioma cell apoptosis, chemosensitivity and radiosensitivity.Emerging biomarkers in glioblastoma The prognostic value of a seven-microRNA classifier as a novel biomarker for the prediction and detection of recurrence in glioma patients.MiR-196a exerts its oncogenic effect in glioblastoma multiforme by inhibition of IκBα both in vitro and in vivo.High expression of miR-181c as a predictive marker of recurrence in stage II colorectal cancer.Role of microRNAs in gliomagenesis: targeting miRNAs in glioblastoma multiforme therapy.Current Progress on Understanding MicroRNAs in Glioblastoma Multiforme.MicroRNAs in cancer diagnosis and therapy: from bench to bedside.MicroRNAs involved in chemo- and radioresistance of high-grade gliomas.Current progress for the use of miRNAs in glioblastoma treatment.MicroRNA biomarkers in glioblastoma.The role of miRNAs in cancer: from pathogenesis to therapeutic implications.Molecular prognostic factors in glioblastoma: state of the art and future challenges.Warburg meets non-coding RNAs: the emerging role of ncRNA in regulating the glucose metabolism of cancer cells.Prognostic Role of microRNA-21 Expression in Brain Tumors: a Meta-analysis.microRNA therapies in cancer.

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MiR-195, miR-196b, miR-181c, miR-21 expression levels and O-6-methylguanine-DNA methyltransferase methylation status are associated with clinical outcome in glioblastoma patients.

http://www.wikidata.org/entity/Q44273844

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name

MiR-195, miR-196b, miR-181c, m ...... come in glioblastoma patients.

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MiR-195, miR-196b, miR-181c, m ...... come in glioblastoma patients.

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type

label

MiR-195, miR-196b, miR-181c, m ...... come in glioblastoma patients.

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MiR-195, miR-196b, miR-181c, m ...... come in glioblastoma patients.

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prefLabel

MiR-195, miR-196b, miR-181c, m ...... come in glioblastoma patients.

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MiR-195, miR-196b, miR-181c, m ...... come in glioblastoma patients.

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MiR-195, miR-196b, miR-181c, m ...... come in glioblastoma patients.

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Eva Lzicarova

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Hana Dolezelova

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Jaroslav Michalek

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Jiri Sana

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Leos Kren

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Marek Svoboda

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Marian Hajduch

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Martin Smrcka

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Ondrej Slaby

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Pavel Fadrus

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P2860

Methylation-sensitive high resolution melting (MS-HRM): a new approach for sensitive and high-throughput assessment of methylation

MGMT gene silencing and benefit from temozolomide in glioblastoma.

Oncomirs - microRNAs with a role in cancer

Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma

MicroRNA-21 is an antiapoptotic factor in human glioblastoma cells

Extensive modulation of a set of microRNAs in primary glioblastoma

MiRNA-196 is upregulated in glioblastoma but not in anaplastic astrocytoma and has prognostic significance

Effects of radiotherapy with concomitant and adjuvant temozolomide versus radiotherapy alone on survival in glioblastoma in a randomised phase III study: 5-year analysis of the EORTC-NCIC trial

A ten-microRNA expression signature predicts survival in glioblastoma

miR-195, miR-455-3p and miR-10a( *) are implicated in acquired temozolomide resistance in glioblastoma multiforme cells.

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