MicroRNAs, cancer and ionizing radiation: Where are we? - Wikidata - wikimedia - TriplyDB

MicroRNAs, cancer and ionizing radiation: Where are we?

MicroRNAs, cancer and ionizing radiation: Where are we?

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MicroRNAs, DNA Damage Response, and Cancer Treatment Understanding the Pathophysiology and Challenges of Development of Medical Countermeasures for Radiation-Induced Vascular/Endothelial Cell Injuries: Report of a NIAID Workshop, August 20, 2015 miRNA-320a inhibits tumor proliferation and invasion by targeting c-Myc in human hepatocellular carcinoma.Radiation-inducible miR-770-5p sensitizes tumors to radiation through direct targeting of PDZ-binding kinase.miR-211 promotes lens epithelial cells apoptosis by targeting silent mating-type information regulation 2 homolog 1 in age-related cataracts.Survival of Mice with Gastrointestinal Acute Radiation Syndrome through Control of Bacterial Translocation.Alterations of MicroRNA Expression in the Liver, Heart, and Testis of Mice Upon Exposure to Repeated Low-Dose Radiation

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MicroRNAs, cancer and ionizing radiation: Where are we?

http://www.wikidata.org/entity/Q26801435

description

2015 nî lūn-bûn

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2015 թուականին հրատարակուած գիտական յօդուած

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2015 թվականին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

MicroRNAs, cancer and ionizing radiation: Where are we?

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MicroRNAs, cancer and ionizing radiation: Where are we?

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MicroRNAs, cancer and ionizing radiation: Where are we?

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MicroRNAs, cancer and ionizing radiation: Where are we?

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MicroRNAs, cancer and ionizing radiation: Where are we?

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MicroRNAs, cancer and ionizing radiation: Where are we?

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MicroRNAs, cancer and ionizing radiation: Where are we?

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MicroRNAs, cancer and ionizing radiation: Where are we?

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MicroRNAs, cancer and ionizing radiation: Where are we?

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1806-9282.61.03.275

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Revista da Associação Médica Brasileira

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MicroRNAs, cancer and ionizing radiation: Where are we?

@en

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Bernardo Garicochea

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Gustavo Nader Marta

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Juliana M Real

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P2860

The nuclear RNase III Drosha initiates microRNA processing

The role of PACT in the RNA silencing pathway

TRBP recruits the Dicer complex to Ago2 for microRNA processing and gene silencing

The Drosha-DGCR8 complex in primary microRNA processing

Frequent deletions and down-regulation of micro- RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia

microRNAs exhibit high frequency genomic alterations in human cancer

Human microRNA genes are frequently located at fragile sites and genomic regions involved in cancers

A reciprocal repression between ZEB1 and members of the miR-200 family promotes EMT and invasion in cancer cells

Suppression of non-small cell lung tumor development by the let-7 microRNA family

Abnormal microRNA-16 locus with synteny to human 13q14 linked to CLL in NZB mice

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275-81

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scholarly article

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10.1590/1806-9282.61.03.275

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3

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61

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Luiz Paulo Kowalski

André Lopes Carvalho

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2015-01-01T00:00:00Z

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280869598

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26248252

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