MiR-17-92 cluster is associated with 13q gain and c-myc expression during colorectal adenoma to adenocarcinoma progression - Test2 - elhamkhani - TriplyDB

MiR-17-92 cluster is associated with 13q gain and c-myc expression during colorectal adenoma to adenocarcinoma progression

MiR-17-92 cluster is associated with 13q gain and c-myc expression during colorectal adenoma to adenocarcinoma progression

http://www.wikidata.org/entity/Q24643470

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miRNA expression in colon polyps provides evidence for a multihit model of colon cancer An in silico analysis of dynamic changes in microRNA expression profiles in stepwise development of nasopharyngeal carcinoma Estrogen receptor {beta}1 expression is regulated by miR-92 in breast cancer Tumorigenicity of the miR-17-92 cluster distilled MicroRNAs: Novel immunotherapeutic targets in colorectal carcinoma MicroRNAs as non-invasive screening biomarkers of colorectal cancer Appraising MicroRNA-155 as a Noninvasive Diagnostic Biomarker for Cancer Detection: A Meta-Analysis MicroRNAs as growth regulators, their function and biomarker status in colorectal cancer Post-transcriptional regulation of MTA family by microRNAs in the context of cancer The miR-17/92 cluster: a comprehensive update on its genomics, genetics, functions and increasingly important and numerous roles in health and disease An update on microRNAs as colorectal cancer biomarkers: where are we and what's next?Regulating miRNA by natural agents as a new strategy for cancer treatment The Role of Bioactive Dietary Components in Modulating miRNA Expression in Colorectal Cancer Detection of miRNA as non-invasive biomarkers of colorectal cancer The myc-miR-17~92 axis blunts TGF{beta} signaling and production of multiple TGF{beta}-dependent antiangiogenic factors Heterogeneity of microRNAs expression in cervical cancer cells: over-expression of miR-196a.Vitamin D, intermediary metabolism and prostate cancer tumor progression.miR-18a downregulates DICER1 and promotes proliferation and metastasis of nasopharyngeal carcinoma Genome and transcriptome profiles of CD133-positive colorectal cancer cells.Implication of microRNAs in drug resistance for designing novel cancer therapy Targeting microRNAs in cancer: rationale, strategies and challenges.MiRNA genes constitute new targets for microsatellite instability in colorectal cancer Specific alterations of the microRNA transcriptome and global network structure in colorectal cancer after treatment with MAPK/ERK inhibitors.Regulation of microRNAs by natural agents: an emerging field in chemoprevention and chemotherapy research.microRNA-221 and microRNA-18a identification in stool as potential biomarkers for the non-invasive diagnosis of colorectal carcinoma.Serum microRNA panel as biomarkers for early diagnosis of colorectal adenocarcinoma Tumor suppressor p53 meets microRNAs.MicroRNA-18a attenuates DNA damage repair through suppressing the expression of ataxia telangiectasia mutated in colorectal cancer The miR-221/222 cluster, miR-10b and miR-92a are highly upregulated in metastatic minimally invasive follicular thyroid carcinoma.microRNA-92a promotes lymph node metastasis of human esophageal squamous cell carcinoma via E-cadherin.Identification and evaluation of plasma microRNAs for early detection of colorectal cancer.miRNAs as biomarkers for management of patients with colorectal cancer.Reversible, interrelated mRNA and miRNA expression patterns in the transcriptome of Rasless fibroblasts: functional and mechanistic implications Serum miRNA profiling identifies miR-150/30a as potential biomarker for workers with damaged nerve fibers from carbon disulfide miR-18a inhibits CDC42 and plays a tumour suppressor role in colorectal cancer cells.Genome wide copy number analysis of paediatric Burkitt lymphoma using formalin-fixed tissues reveals a subset with gain of chromosome 13q and corresponding miRNA over expression Pathway Regulation of p63, a Director of Epithelial Cell Fate Implications of microRNAs in colorectal cancer development, diagnosis, prognosis, and therapeutics.MicroRNAs: promising biomarkers for diagnosis and therapeutic targets in human colorectal cancer metastasis.Developmental regulation of microRNA expression in Schwann cells

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P2860

MiR-17-92 cluster is associated with 13q gain and c-myc expression during colorectal adenoma to adenocarcinoma progression

http://www.wikidata.org/entity/Q24643470

description

2009 nî lūn-bûn

@nan

2009 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի օգոստոսին 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-17-92 cluster is associate ...... to adenocarcinoma progression

@ast

MiR-17-92 cluster is associate ...... to adenocarcinoma progression

@en

MiR-17-92 cluster is associate ...... to adenocarcinoma progression

@nl

type

label

MiR-17-92 cluster is associate ...... to adenocarcinoma progression

@ast

MiR-17-92 cluster is associate ...... to adenocarcinoma progression

@en

MiR-17-92 cluster is associate ...... to adenocarcinoma progression

@nl

prefLabel

MiR-17-92 cluster is associate ...... to adenocarcinoma progression

@ast

MiR-17-92 cluster is associate ...... to adenocarcinoma progression

@en

MiR-17-92 cluster is associate ...... to adenocarcinoma progression

@nl

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P2860

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

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

microRNAs exhibit high frequency genomic alterations in human cancer

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

Targeted deletion reveals essential and overlapping functions of the miR-17 through 92 family of miRNA clusters

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

Widespread microRNA repression by Myc contributes to tumorigenesis

Lymphoproliferative disease and autoimmunity in mice with increased miR-17-92 expression in lymphocytes

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

RAS is regulated by the let-7 microRNA family

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