MicroRNA-205inhibits cancer cell migration and invasion via modulation ofcentromere protein Fregulating pathways in prostate cancer

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Tumor-suppressivemicroRNA-218inhibits cancer cell migration and invasion via targeting ofLASP1in prostate cancer

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Tumour-suppressivemicroRNA-224inhibits cancer cell migration and invasion via targeting oncogenicTPD52in prostate cancer

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The tumor-suppressive microRNA-143/145 cluster inhibits cell migration and invasion by targeting GOLM1 in prostate cancer

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miR-205 regulates basement membrane deposition in human prostate: implications for cancer development

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Tumor suppressive microRNAs (miR-222 and miR-31) regulate molecular pathways based on microRNA expression signature in prostate cancer

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Epigenetic-induced repression of microRNA-205 is associated with MED1 activation and a poorer prognosis in localized prostate cancer

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Loss of p63 and its microRNA-205 target results in enhanced cell migration and metastasis in prostate cancer

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Tumour suppressors miR-1 and miR-133a target the oncogenic function of purine nucleoside phosphorylase (PNP) in prostate cancer

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Centromere protein F and survivin are associated with high risk and a poor prognosis in colorectal gastrointestinal stromal tumours

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MicroRNA-205-directed transcriptional activation of tumor suppressor genes in prostate cancer

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The ups and downs of miR-205: Identifying the roles of miR-205 in mammary gland development and breast cancer

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Castration-resistant Prostate Cancer: From New Pathophysiology to New Treatment Targets

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MicroRNAs in Cancer: Small Molecules With a Huge Impact

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Most mammalian mRNAs are conserved targets of microRNAs

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Mechanisms of post-transcriptional regulation by microRNAs: are the answers in sight?

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