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Jene Choi

Researcher at University of Ulsan

Publications -  53
Citations -  1334

Jene Choi is an academic researcher from University of Ulsan. The author has contributed to research in topics: Phosphatase & Mesenchymal stem cell. The author has an hindex of 22, co-authored 51 publications receiving 1157 citations. Previous affiliations of Jene Choi include Asan Medical Center.

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Deregulated expression of microRNA-221 with the potential for prognostic biomarkers in surgically resected hepatocellular carcinoma

TL;DR: The potential of microRNA-221 dysregulation for predicting local recurrence and distant metastasis after curative surgery is proposed and the possible role of microRNAs-221, micro RNA-222, micro RNAs-21, and microRNA -155 dysregulation in hepatocarcinogenesis is proposed.
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Overexpression of the wip1 gene abrogates the p38 MAPK/p53/Wip1 pathway and silences p16 expression in human breast cancers.

TL;DR: First report showing that Wip1 overexpression abrogates the homeostatic balance maintained through the p38–p53-Wip1 pathway, and contributes to malignant progression by inactivating wild-type p53 and p38 MAPK as well as decreasing p16 protein levels in human breast tissues.
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Umbilical Cord Mesenchymal Stromal Cells Affected by Gestational Diabetes Mellitus Display Premature Aging and Mitochondrial Dysfunction

TL;DR: It is reported intriguing and novel evidence that maternal metabolic derangement during gestation affects the biological properties of fetal cells, which may be a component of fetal programming.
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Umbilical cord-derived mesenchymal stem cell extracts reduce colitis in mice by re-polarizing intestinal macrophages

TL;DR: It is shown that MSC-Ex treatment can be a potent approach to overcome severe refractory IBD and was more potent than that with MSC in reducing DAI, the histological score, and nitrite levels.
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Pulmonary benign metastasizing leiomyoma associated with intravenous leiomyomatosis of the uterus: clinical behavior and genomic changes supporting a transportation theory.

TL;DR: The 2 lesions showed significantly overlapping, if not identical, complex genomic changes in the comparative genomic hybridization, suggesting that the 2 lesions are closely related to each other.