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Institution

National Cheng Kung University

EducationTainan City, Taiwan
About: National Cheng Kung University is a education organization based out in Tainan City, Taiwan. It is known for research contribution in the topics: Population & Thin film. The organization has 49723 authors who have published 69799 publications receiving 1437420 citations. The organization is also known as: NCKU.


Papers
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Journal ArticleDOI
TL;DR: It is concluded that targeting microglial signaling might lead to more effective treatments for devastating chronic pain after diabetic neuropathy, viral infection, cancer, and major surgeries, partly via improving the analgesic efficacy of opioids.

187 citations

Journal ArticleDOI
TL;DR: In this paper, different p-type Cu2O powders were prepared from electrodeposition and subjected to analysis of their photocatalytic activity in water reduction, showing that the electrodeposited powders showed higher photocatalysis activity than a commercially available Cu 2O powder.

187 citations

Journal ArticleDOI
TL;DR: An A-->T (+12 position in intron 2) mutation was found in the CYP2C9 sequencing process and was found to create a NIa III site in most Chinese subjects.
Abstract: Cytochrome P450 (CYP) 2C9 catalyses the metabolism of a wide range of drugs Previous studies have shown the differences in the amino acid composition among CYP2C9 variants at Cys144/Arg, Tyr358/Cys, Leu359/Ile, and Gly417/Asp PCR-endonuclease digestion methods have been developed to detect these four possible polymorphisms The T416-->C mutation in exon 3 of CYP2C9 (Cys144-->Arg) creates an Ava II site In the 135 subjects we tested, all leukocyte DNA samples showed a complete Ava II digestion indicating homozygous C416 (Arg144) A Tyr358-->Cys mutation will create a Nsi I site at codon 1057-1063 in exon 7 In 40 subjects tested, all samples showed negative results DNA sequencing on a few samples showed Tyr358Ile359 A mismatched PCR primer pair was then designed to detect codon C1061-->A (Leu359-->Ile) mutation In 115 subjects tested, 111 samples showed a complete Nsi I digestion (Ile359) and four samples showed heterozygous results Another mismatched PCR primer pair was used to confirm the C1061 codon in heterozygous subjects The four heterozygous subjects showed partial digestion with endonuclease Kpn I, which confirmed the heterozygous Ile/Leu at amino acid 359 The G1236-->A mutation in exon 8 of CYP2C9 (Gly417-->Asp) creates a Hph I site In all 46 subjects, homozygous G1236 (Gly417) was found Most Chinese subjects actually have Arg144 Tyr358 Ile359 Gly417 in CYP2C9 as previously reported human-2 Furthermore, we found an A-->T (+12 position in intron 2) mutation in our CYP2C9 sequencing process The mutation creates a NIa III site(ABSTRACT TRUNCATED AT 250 WORDS)

186 citations

Journal ArticleDOI
TL;DR: A framework for designing a telerobotic system controller designed so the dynamic behaviors of the master robot and the slave robot are functions of each other, and a control architecture is proposed to achieve these functions.
Abstract: A framework for designing a telerobotic system controller is presented. This controller is designed so the dynamic behaviors of the master robot and the slave robot are functions of each other. These functions, which the designer chooses based upon the application, are described, and a control architecture is proposed to achieve these functions. To guarantee that the specified functions and proposed architecture govern the system behavior, H/sub infinity / control theory and model reduction techniques are used. Several experiments were conducted to verify the theoretical derivations. This control method is unique, because it does not require any transfer of either position or velocity information between the master robot and the slave robot; it only requires the transfer of forces. Although this property leads to a wider communication bandwidth between the master and slave robots, the entire system may still suffer from a positional error buildup between the master robot and slave robot. >

186 citations

Journal ArticleDOI
TL;DR: In this paper, RNA analysis and SWEET17-β-glucuronidase/-GREEN FLUORESCENT PROTEIN fusions expressed in Arabidopsis (Arabidopsis thaliana) reveal that SWEet17 is highly expressed in the cortex of roots and localizes to the tonoplast of root cells.
Abstract: Fructose (Fru) is a major storage form of sugars found in vacuoles, yet the molecular regulation of vacuolar Fru transport is poorly studied. Although SWEET17 (for SUGARS WILL EVENTUALLY BE EXPORTED TRANSPORTERS17) has been characterized as a vacuolar Fru exporter in leaves, its expression in leaves is low. Here, RNA analysis and SWEET17-β-glucuronidase/-GREEN FLUORESCENT PROTEIN fusions expressed in Arabidopsis (Arabidopsis thaliana) reveal that SWEET17 is highly expressed in the cortex of roots and localizes to the tonoplast of root cells. Expression of SWEET17 in roots was inducible by Fru and darkness, treatments that activate accumulation and release of vacuolar Fru, respectively. Mutation and ectopic expression of SWEET17 led to increased and decreased root growth in the presence of Fru, respectively. Overexpression of SWEET17 specifically reduced the Fru content in leaves by 80% during cold stress. These results intimate that SWEET17 functions as a Fru-specific uniporter on the root tonoplast. Vacuoles overexpressing SWEET17 showed increased [14C]Fru uptake compared with the wild type. SWEET17-mediated Fru uptake was insensitive to ATP or treatment with NH4Cl or carbonyl cyanide m-chlorophenyl hydrazone, indicating that SWEET17 functions as an energy-independent facilitative carrier. The Arabidopsis genome contains a close paralog of SWEET17 in clade IV, SWEET16. The predominant expression of SWEET16 in root vacuoles and reduced root growth of mutants under Fru excess indicate that SWEET16 also functions as a vacuolar transporter in roots. We propose that in addition to a role in leaves, SWEET17 plays a key role in facilitating bidirectional Fru transport across the tonoplast of roots in response to metabolic demand to maintain cytosolic Fru homeostasis.

186 citations


Authors

Showing all 49872 results

NameH-indexPapersCitations
Yi Chen2174342293080
Yang Yang1642704144071
R. E. Hughes1541312110970
Mercouri G. Kanatzidis1521854113022
Thomas J. Smith1401775113919
Hui Li1352982105903
Gerald M. Reaven13379980351
Chi-Huey Wong129122066349
Joseph P. Vacanti11944150739
Kai Nan An10995351638
Ding-Shinn Chen10477446068
James D. Neaton10133164719
David C. Christiani100105255399
Jo Shu Chang9963937487
Yu Shyr9854239527
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202373
2022315
20213,425
20203,154
20192,895
20182,764