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Research on flexible display at Ulsan National Institute of Science and Technology

npj Flexible Electronics 2017年第1期1卷 47-59页

作者： Jihun Park Sanghyun Heo Kibog Park Myoung Hoon Song Ju-Young Kim Gyouhyung Kyung rodney scott ruoff Jang-Ung Park Franklin Bien School of Materials Science and Engineering Ulsan National Institute of Science and Technology(UNIST)Ulsan Metropolitan City 44919Republic of Korea School of Electrical and Computer Engineering Ulsan National Institute of Science and Technology(UNIST)Ulsan Metropolitan City 44919Republic of Korea Department of Physics Ulsan National Institute of Science and Technology(UNIST)Ulsan Metropolitan City 44919Republic of Korea School of Design and Human Engineering Ulsan National Institute of Science and Technology(UNIST)Ulsan Metropolitan City 44919Republic of Korea Center for Multidimensional Carbon Materials Institute for Basic Science(IBS)Ulsan 44919Republic of Korea Department of Chemistry Ulsan National Institute of Science and Technology(UNIST)Ulsan 44919Republic of Korea

Displays represent information visually,so they have become the fundamental building block to visualize the data of current electronics including smartphones.Recently,electronics have been advanced toward flexible and wearable electronics that can be bent,folded,or stretched while maintaining their performance under various deformations.Here,recent advances in research to demonstrate flexible and wearable displays are reviewed.We introduce these results by dividing them into several categories according to the components of the display:active-matrix backplane,touch screen panel,light sources,integrated circuit for fingerprint touch screen panel,and characterization tests;and we also present mechanical tests in nano-meter scale and visual ergonomics research.

关键词： dividing electronics panel

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Gene Expression Profiling of Human Myeloid Leukemic MV4-11 Cells Treated with 5-Aza-2’-deoxycytidine

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Journal of Cancer Therapy 2012年第3期3卷 177-182页

作者： Kyu-Tae Kim David Mossman Donald Small rodney J. scott Division of Genetics Hunter Area Pathology Service John Hunter Hospital New Lambton Australia School of Biomedical Sciences and Pharmacy Faculty of Health University of Newcastle Callaghan Australia School of Medicine Johns Hopkins University Baltimore USA

The pyrimidine analog, 5-aza-2’-deoxycytidine (5-aza-dC) is a DNA methyltransferase inhibitor that triggers DNA demethylation leading to the reactivation of epigenetically silenced tumor suppressor genes. To understand the shift in gene expression which mediates the beneficial 5-aza-dC effects in leukemia, we have treated human myeloid derived leukemic cells with 5-aza-dC. Target genes were identified first in MV4-11 cells using a genome-wide gene expression profiling assay to detect differences in treated and untreated cells. From this analysis six genes were identified (HOXA4, HOXD4, HOXA8, HOXD12, CD9 and RGS2) as being significantly different expressed after treatment. To validate microarray data, we performed quantitative PCR on these genes from multiple leukemic cells. The results suggest that these genes are epigenetically regulated indicating that dysregulation of HOXA4, HOXD4, HOXA8, HOXD12, CD9 and RGS2 expression may play an important role in establishing the malignant phenotype in AML.

关键词： 5-Aza-2’-deoxycytidine Gene Expression Profile HOX CD9 RGS2

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