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Hideki Enokida

Researcher at Kagoshima University

Publications -  224
Citations -  12728

Hideki Enokida is an academic researcher from Kagoshima University. The author has contributed to research in topics: microRNA & Cancer. The author has an hindex of 65, co-authored 196 publications receiving 11432 citations. Previous affiliations of Hideki Enokida include San Francisco VA Medical Center & University of California, San Francisco.

Papers
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Small dsRNAs induce transcriptional activation in human cells

TL;DR: A more diverse role for small RNA molecules in the regulation of gene expression than previously recognized is revealed and a potential therapeutic use for dsRNA in targeted gene activation is identified.
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miR-145, miR-133a and miR-133b: Tumor-suppressive miRNAs target FSCN1 in esophageal squamous cell carcinoma

TL;DR: The identification of tumor‐suppressive miRNAs,miR‐145, miR‐133a and miR-133b, directly control oncogenic FSCN1 gene, and could provide new insights into potential mechanisms of ESCC carcinogenesis.
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Identification of novel microRNA targets based on microRNA signatures in bladder cancer.

TL;DR: The target search algorithm and gene‐expression profiling in BCs revealed that Keratin7 (KRT7) mRNA was a common target of the downregulated miRNAs, and the mRNA expression levels of KRT7 were significantly higher inBCs than in NBEs.
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miR-145 and miR-133a function as tumour suppressors and directly regulate FSCN1 expression in bladder cancer

TL;DR: Tumour suppressivemiR-145 and miR-133a directly control oncogenic FSCN1 in BC, and both microRNAs repressed the mRNA and protein expression of F SCN1.
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Durvalumab alone and durvalumab plus tremelimumab versus chemotherapy in previously untreated patients with unresectable, locally advanced or metastatic urothelial carcinoma (DANUBE): a randomised, open-label, multicentre, phase 3 trial

Thomas Powles, +206 more
- 01 Dec 2020 - 
TL;DR: The overall survival of patients who received durvalumab (a PD-L1 inhibitor), with or without tremelimumab ( a CTLA-4 inhibitor), as a first-line treatment for metastatic urothelial carcinoma was assessed.