Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Gwo-Bin Lee

dblp:38/3977 · DBLP profile ↗
← Back
2ranked-venue papers
1as first author
0since 2021 · last 2014
0000-0001-6910-9133ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Artificial intelligence and machine learning · 2 · 1 first-authorSystems, architecture and hardware · 2 · 1 first-author

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%
Computer graphics and multimedia
1 paper
Computational fabrication · 100%

Topics — the 1 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
cell patterning
0.212014
Regulating the mechanical properties of cells using a non-UV light-addressable hydrogel patterning process · ICRA 2014

Methods — techniques the papers use, named apart from their topics

photopolymerization · 0.4atomic force microscopy · 0.4PEGDA hydrogel · 0.4
YearPublicationVenuePosition
2014 Regulating the mechanical properties of cells using a non-UV light-addressable hydrogel patterning process
abstract
The determination of the mechanical properties of cells plays an important role in biological studies and has gained acceptance recently as a possible label-free biomarker for cell status determination or diseases detection. Investigations on how external cellular properties affect cell mechanics are helpful in understanding cell disease processes and cell morphogenesis, which are of large significance in medical science. Although most researchers have focused on individual cell mechanics, or the effect of substrate stiffness on cells, cell mechanical response due to interactions among cells is yet to be examined. A reason for this is that the study of cell mechanical response to cell shape requires one to use a cell patterning process. However, existing cell patterning methods are very complex and time-consuming. In this paper, we describe a practical and rapid technique that can easily pattern cells into desired shapes, which allows investigations of the effect of external environment on cell stiffness. In the new technique, Poly-(ethylene) glycol diacrylate (PEGDA) hydrogel film with thickness 70–100 nm is controllably patterned on a hydrogenated amorphous silicon (a-Si:H) substrate by polymerizing PEGDA molecules in-situ using programmable visual light patterns. The idea is to enable the confinement of cells cultured on the hydrogels into special areas. The elastic modulus of the patterned cells is measured using an atomic force microscope. Experimental results have demonstrated the versatility of the technique as a tool for cell pattering and exploration of cell mechanics under external mechanical stimuli.
Changlin Zhang, Lianqing Liu, Yuechao Wang, Gwo-Bin Lee, Wen Jung Li
ICRA5
2003 Platform technology for manipulation of cells, proteins and DNA
abstract
MEMS has been an enabling technology for biomedical applications recently. Not only does it provide an instrument to obtain information on molecular level, but it also allows us to manipulate bio-molecules efficiently. Micro devices and systems for manipulation of biological objects such as cells, proteins and DNA have been demonstrated. In this study, we report a technique using dielectrophoretic forces to manipulate micro particles. First, the concept of several manipulation techniques is reviewed. Then we focus on novel manipulation modes. With the help of these biochips, we are able to perform manipulation of micro particles/cells.
Gwo-Bin Lee, Long-Ming Fu
ICRA1