MicroRNA-200 family modulation in distinct breast cancer phenotypes. - Wikidata - awgldk - TriplyDB

MicroRNA-200 family modulation in distinct breast cancer phenotypes.

MicroRNA-200 family modulation in distinct breast cancer phenotypes.

http://www.wikidata.org/entity/Q34462262

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MiRNAs and Other Epigenetic Changes as Biomarkers in Triple Negative Breast Cancer MicroRNAs: New Biomarkers for Diagnosis, Prognosis, Therapy Prediction and Therapeutic Tools for Breast Cancer Systematic enrichment analysis of microRNA expression profiling studies in endometriosis Functional Role of the microRNA-200 Family in Breast Morphogenesis and Neoplasia MicroRNAs and triple negative breast cancer MiR-200, a new star miRNA in human cancer Key nodes of a microRNA network associated with the integrated mesenchymal subtype of high-grade serous ovarian cancer The microRNA-200 family: small molecules with novel roles in cancer development, progression and therapy miR-200b as a prognostic factor in breast cancer targets multiple members of RAB family Metaplastic breast cancer: histologic characteristics, prognostic factors and systemic treatment strategies.Role of microRNA in epithelial to mesenchymal transition and metastasis and clinical perspectives.MiR-101 suppresses the epithelial-to-mesenchymal transition by targeting ZEB1 and ZEB2 in ovarian carcinoma Re-expression of miR-200c suppresses proliferation, colony formation and in vivo tumor growth of murine claudin-low mammary tumor cells.Computational analysis identifies a sponge interaction network between long non-coding RNAs and messenger RNAs in human breast cancer.microRNA-141 regulates BMI1 expression and induces senescence in human diploid fibroblasts.Overexpression of microRNA-200c predicts poor outcome in patients with PR-negative breast cancer.Reduced expression of miR-200 family members contributes to antiestrogen resistance in LY2 human breast cancer cells The role of miR-200a in mammalian epithelial cell transformation.Glabridin attenuates the migratory and invasive capacity of breast cancer cells by activating microRNA-200c.Dysregulation of microRNAs in breast cancer and their potential role as prognostic and predictive biomarkers in patient management.Identification of estrogen receptor proteins in breast cancer cells using matrix-assisted laser desorption/ionization time of flight mass spectrometry (Review).Prognostic Value and Clinicopathology Significance of MicroRNA-200c Expression in Cancer: A Meta-Analysis.An improved sequencing-based strategy to estimate locus-specific DNA methylation.SPOCK1 Is a Novel Transforming Growth Factor-β-Induced Myoepithelial Marker That Enhances Invasion and Correlates with Poor Prognosis in Breast Cancer.Dual regulation by microRNA-200b-3p and microRNA-200b-5p in the inhibition of epithelial-to-mesenchymal transition in triple-negative breast cancer miR-34a Silences c-SRC to Attenuate Tumor Growth in Triple-Negative Breast Cancer.MicroRNA transcriptomes relate intermuscular adipose tissue to metabolic risk Activation of miR200 by c-Myb depends on ZEB1 expression and miR200 promoter methylation Higher expression of circulating miR-182 as a novel biomarker for breast cancer.Oxidative stress associated to dysfunctional adipose tissue: a potential link between obesity, type 2 diabetes mellitus and breast cancer.The role of microRNAs in tumors.Aberrant DNA methylation of microRNA genes in human breast cancer - a critical appraisal.microRNAs in breast cancer: regulatory roles governing the hallmarks of cancer.Aberrantly expressed microRNAs in bladder cancer and renal cell carcinoma.MicroRNA-Mediated Post-Transcriptional Regulation of Epithelial to Mesenchymal Transition in Cancer.Induction of the mesenchymal to epithelial transition by demethylation- activated microRNA-200c is involved in the anti-migration/invasion effects of arsenic trioxide on human breast cancer cells.A core microRNA signature associated with inducers of the epithelial-to-mesenchymal transition.Epigenetic silencing of miR-200c in breast cancer is associated with aggressiveness and is modulated by ZEB1.Tamoxifen reverses epithelial-mesenchymal transition by demethylating miR-200c in triple-negative breast cancer cells.Therapeutic impacts of microRNAs in breast cancer by their roles in regulating processes involved in this disease.

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MicroRNA-200 family modulation in distinct breast cancer phenotypes.

http://www.wikidata.org/entity/Q34462262

description

2012 nî lūn-bûn

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2012 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2012 թվականի հոտեմբերին 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

MicroRNA-200 family modulation in distinct breast cancer phenotypes.

@ast

MicroRNA-200 family modulation in distinct breast cancer phenotypes.

@en

MicroRNA-200 family modulation in distinct breast cancer phenotypes.

@nl

type

label

MicroRNA-200 family modulation in distinct breast cancer phenotypes.

@ast

MicroRNA-200 family modulation in distinct breast cancer phenotypes.

@en

MicroRNA-200 family modulation in distinct breast cancer phenotypes.

@nl

prefLabel

MicroRNA-200 family modulation in distinct breast cancer phenotypes.

@ast

MicroRNA-200 family modulation in distinct breast cancer phenotypes.

@en

MicroRNA-200 family modulation in distinct breast cancer phenotypes.

@nl

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MicroRNA-200 family modulation in distinct breast cancer phenotypes.

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Begoña Vieites

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Clare M Isacke

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David Sarrió

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José Palacios

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Juan Díaz-Martín

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María Ángeles Castilla

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María Ángeles López-García

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Michele Biscuola

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Susana Ramiro-Fuentes

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P2860

MicroRNAs: target recognition and regulatory functions

The ZEB/miR-200 feedback loop--a motor of cellular plasticity in development and cancer?

Epithelial-mesenchymal transition in cancer: parallels between normal development and tumor progression

A collection of breast cancer cell lines for the study of functionally distinct cancer subtypes

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

The epithelial-mesenchymal transition generates cells with properties of stem cells

The miR-200 and miR-221/222 microRNA families: opposing effects on epithelial identity

Epithelial-mesenchymal transitions in development and disease

Gene expression patterns of breast carcinomas distinguish tumor subclasses with clinical implications

The miR-200 family and miR-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1

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Laura Romero-Pérez

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