MiR-24 tumor suppressor activity is regulated independent of p53 and through a target site polymorphism - Wikidata - wikimedia - TriplyDB

MiR-24 tumor suppressor activity is regulated independent of p53 and through a target site polymorphism

MiR-24 tumor suppressor activity is regulated independent of p53 and through a target site polymorphism

http://www.wikidata.org/entity/Q28472349

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Terminal differentiation of cardiac and skeletal myocytes induces permissivity to AAV transduction by relieving inhibition imposed by DNA damage response proteins Genome-wide mRNA and microRNA profiling of the NCI 60 cell-line screen and comparison of FdUMP[10] with fluorouracil, floxuridine, and topoisomerase 1 poisons Cardiac progenitors derived from reprogrammed mesenchymal stem cells contribute to angiomyogenic repair of the infarcted heart.Association between DNA methylation in the miR-328 5'-flanking region and inter-individual differences in miR-328 and BCRP expression in human placenta Preferential star strand biogenesis of pre-miR-24-2 targets PKC-alpha and suppresses cell survival in MCF-7 breast cancer cells Tumor suppressor miR-24 restrains gastric cancer progression by downregulating RegIV Sweating the small stuff: microRNAs and genetic changes define pancreatic cancer.Invasion front-specific expression and prognostic significance of microRNA in colorectal liver metastases.Genetic variation in microRNA networks: the implications for cancer research.Non-coding RNAs as clinical biomarkers for cancer diagnosis and prognosis.MicroRNAs as promising biomarkers in cancer diagnostics.Regulation of TRIB3 mRNA and protein in breast cancer.Involvement of microRNA-24 and DNA methylation in resistance of nasopharyngeal carcinoma to ionizing radiation Integrating microRNAs into a system biology approach to acute lung injury Reprogramming of skeletal myoblasts for induction of pluripotency for tumor-free cardiomyogenesis in the infarcted heart.The emerging role of microRNAs in drug responses Enrichment Analysis Identifies Functional MicroRNA-Disease Associations in Humans Plasma levels of microRNA-24, microRNA-320a, and microRNA-423-5p are potential biomarkers for colorectal carcinoma.Integrated Genomics Identifies miR-32/MCL-1 Pathway as a Critical Driver of Melanomagenesis: Implications for miR-Replacement and Combination Therapy.MiR-24 functions as a tumor suppressor in nasopharyngeal carcinoma through targeting FSCN1.Cell-Free miR-27a, a Potential Diagnostic and Prognostic Biomarker for Gastric Cancer.The miRNA-drug resistance connection: a new era of personalized medicine using noncoding RNA begins.Human liver stem cell-derived microvesicles inhibit hepatoma growth in SCID mice by delivering antitumor microRNAs.The targeting and functions of miRNA-383 are mediated by FMRP during spermatogenesis.MicroRNA expression and its association with DNA repair in preimplantation embryos.Interplay between heme oxygenase-1 and miR-378 affects non-small cell lung carcinoma growth, vascularization, and metastasis Overexpression of microRNA-24 increases the sensitivity to paclitaxel in drug-resistant breast carcinoma cell lines via targeting ABCB9.Evaluation of the mirn23a Cluster through an iTRAQ-based Quantitative Proteomic Approach.TRIM11, a direct target of miR-24-3p, promotes cell proliferation and inhibits apoptosis in colon cancer.Macro-management of microRNAs in cell cycle progression of tumor cells and its implications in anti-cancer therapy.miRNAs as biomarkers in colorectal cancer diagnosis and prognosis.Impact of miRNAs in gastrointestinal cancer diagnosis and prognosis.Beyond Thymidylate Synthase and Dihydrofolate Reductase: Impact of Non-coding microRNAs in Anticancer Chemoresistance.Implications of miRNAs in Colorectal Cancer Chemoresistance.Cholinesterase-Targeting microRNAs Identified in silico Affect Specific Biological Processes.Circulating miRNAs as biomarkers for endocrine disorders.miR clusters target cellular functional complexes by defining their degree of regulatory freedom.Tumour-suppressive microRNA-24-1 inhibits cancer cell proliferation through targeting FOXM1 in bladder cancer.Altered expression of miR-24, miR-126 and miR-365 does not affect viability of childhood TCF3-rearranged leukemia cells.MicroRNAs: Potential candidates for diagnosis and treatment of colorectal cancer.

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P2860

MiR-24 tumor suppressor activity is regulated independent of p53 and through a target site polymorphism

http://www.wikidata.org/entity/Q28472349

description

2009 nî lūn-bûn

@nan

2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

MiR-24 tumor suppressor activi ...... ugh a target site polymorphism

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MiR-24 tumor suppressor activi ...... ugh a target site polymorphism

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MiR-24 tumor suppressor activi ...... ugh a target site polymorphism

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type

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MiR-24 tumor suppressor activi ...... ugh a target site polymorphism

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MiR-24 tumor suppressor activi ...... ugh a target site polymorphism

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MiR-24 tumor suppressor activi ...... ugh a target site polymorphism

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prefLabel

MiR-24 tumor suppressor activi ...... ugh a target site polymorphism

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MiR-24 tumor suppressor activi ...... ugh a target site polymorphism

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MiR-24 tumor suppressor activi ...... ugh a target site polymorphism

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MiR-24 tumor suppressor activi ...... ugh a target site polymorphism

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Bo Song

http://www.w3.org/2001/XMLSchema#string

Debabrata Banerjee

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Glenn Merlino

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Jingfang Ju

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Joseph R Bertino

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Prasun J Mishra

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Pravin J Mishra

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Rita Humeniuk

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Yuan Wang

http://www.w3.org/2001/XMLSchema#string

P2860

p16(INK4a) translation suppressed by miR-24

Thymidylate synthase as an oncogene: a novel role for an essential DNA synthesis enzyme

The impact of microRNAs on protein output

miR-24 Inhibits cell proliferation by targeting E2F2, MYC, and other cell-cycle genes via binding to "seedless" 3'UTR microRNA recognition elements

Disrupting the pairing between let-7 and Hmga2 enhances oncogenic transformation

A miR-24 microRNA binding-site polymorphism in dihydrofolate reductase gene leads to methotrexate resistance

Antisense inhibition of human miRNAs and indications for an involvement of miRNA in cell growth and apoptosis

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

An extensive class of small RNAs in Caenorhabditis elegans

Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets

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scholarly article

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20041160

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