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Institution

Hong Kong Baptist University

EducationHong Kong, China
About: Hong Kong Baptist University is a education organization based out in Hong Kong, China. It is known for research contribution in the topics: Population & China. The organization has 7811 authors who have published 18919 publications receiving 555274 citations. The organization is also known as: Hong Kong Baptist College & HKBU.


Papers
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Journal ArticleDOI
TL;DR: Diosgenin inhibits K562 cell proliferation via cell cycle G2/M arrest and apoptosis, with disruption of Ca2+ homeostasis and mitochondrial dysfunction playing vital roles.
Abstract: Diosgenin is a steroidal sapogenin with estrogenic and antitumor properties. In order to elucidate the mechanism of its antiproliferative activity, we investigated its effects on the cell cycle and apoptosis in human chronic myelogenous leukemia K562 cells. Cell viability was assessed via an MTT assay. Apoptosis was investigated in terms of nuclear morphology, DNA fragmentation, and phosphatidylserine externalization. Cell cycle analysis was performed via PI staining and flow cytometry (FCM). Western blotting and immunofluorescence methods were used to determine the levels of p53, cell cycle-related proteins and Bcl-2 family members. FCM was also used to estimate the changes in mitochondrial membrane potential (MMP), intracellular Ca2+ concentration and reactive oxygen species (ROS) generation. Cell cycle analysis showed that diosgenin caused G2/M arrest independently of p53. The levels of cyclin B1 and p21Cip1/Waf1 were decreased, whereas cdc2 levels were increased. Subsequent apoptosis was demonstrated with the dramatic activation of caspase-3. A dramatic decline in intracellular Ca2+ concentration was observed as an initiating event in the process of cell cycle arrest and apoptosis, which was followed by the hyperpolarization and depolarization of MMP. Generation of ROS was observed in the progression of apoptosis. The antiapoptotic Bcl-2 and Bcl-xL proteins were downregulated, whereas the proapoptotic Bax was upregulated. Diosgenin inhibits K562 cell proliferation via cell cycle G2/M arrest and apoptosis, with disruption of Ca2+ homeostasis and mitochondrial dysfunction playing vital roles.

172 citations

Journal ArticleDOI
TL;DR: In this review, different mechanisms of white-light emission from a single molecule and the performance of single-molecule-based WOLEDs are collected and expounded, hoping to light up the interesting subject on single-Molecule white- light-emitting materials, which have great potential aswhite-light emitters for illumination and lighting applications in the world.
Abstract: White organic light-emitting diodes (WOLEDs) are superior to traditional incandescent light bulbs and compact fluorescent lamps in terms of their merits in ensuring pure white-light emission, low-energy consumption, large-area thin-film fabrication, etc. Unfortunately, WOLEDs based on multilayered or multicomponent (red, green, and blue (RGB)) emissive layers can suffer from some remarkable disadvantages, such as intricate device fabrication and voltage-dependent emission color, etc. Single molecules, which can emit white light, can be used to replace multiple emitters, leading to a simplified fabrication process, stable and reproducible WOLEDs. Recently, the performance of WOLEDs by using single molecules is catching up with that of the state-of-the-art devices fabricated by multicomponent emitters. Therefore, an increasing attention has been paid on single white-light-emitting materials for efficient WOLEDs. In this review, different mechanisms of white-light emission from a single molecule and the performance of single-molecule-based WOLEDs are collected and expounded, hoping to light up the interesting subject on single-molecule white-light-emitting materials, which have great potential as white-light emitters for illumination and lighting applications in the world.

171 citations

Journal ArticleDOI
TL;DR: In this article, the authors modeled an aggregation of EVs with a queueing network, whose structure allows them to estimate the capacities for regulation-up and regulation-down separately, which can be used for establishing a regulation contract between an aggregator and the grid operator, and facilitating a new business model for V2G.
Abstract: Due to various green initiatives, renewable energy will be massively incorporated into the future smart grid. However, the intermittency of the renewables may result in power imbalance, thus adversely affecting the stability of a power system. Frequency regulation may be used to maintain the power balance at all times. As electric vehicles (EVs) become popular, they may be connected to the grid to form a vehicle-to-grid (V2G) system. An aggregation of EVs can be coordinated to provide frequency regulation services. However, V2G is a dynamic system where the participating EVs come and go independently. Thus, it is not easy to estimate the regulation capacities for V2G. In a preliminary study, we modeled an aggregation of EVs with a queueing network, whose structure allows us to estimate the capacities for regulation-up and regulation-down separately. The estimated capacities from the V2G system can be used for establishing a regulation contract between an aggregator and the grid operator, and facilitating a new business model for V2G. In this paper, we extend our previous development by designing a smart charging mechanism that can adapt to given characteristics of the EVs and make the performance of the actual system follow the analytical model.

171 citations

Journal ArticleDOI
TL;DR: A dual-path network with a novel bi-directional dual-constrained top-ranking (BDTR) loss to learn discriminative feature representations and the extensive experiments on two cross-modality re-ID datasets demonstrate the superiority of the proposed method compared to the state-of-the-arts.
Abstract: Visible thermal person re-identification (VT-REID) is a task of matching person images captured by thermal and visible cameras, which is an extremely important issue in night-time surveillance applications. Existing cross-modality recognition works mainly focus on learning sharable feature representations to handle the cross-modality discrepancies. However, apart from the cross-modality discrepancy caused by different camera spectrums, VT-REID also suffers from large cross-modality and intra-modality variations caused by different camera environments and human poses, and so on. In this paper, we propose a dual-path network with a novel bi-directional dual-constrained top-ranking (BDTR) loss to learn discriminative feature representations. It is featured in two aspects: 1) end-to-end learning without extra metric learning step and 2) the dual-constraint simultaneously handles the cross-modality and intra-modality variations to ensure the feature discriminability. Meanwhile, a bi-directional center-constrained top-ranking (eBDTR) is proposed to incorporate the previous two constraints into a single formula, which preserves the properties to handle both cross-modality and intra-modality variations. The extensive experiments on two cross-modality re-ID datasets demonstrate the superiority of the proposed method compared to the state-of-the-arts.

171 citations

Journal ArticleDOI
TL;DR: A water-soluble nucleolin aptamer-paclitaxel conjugate that selectively accumulates in ovarian tumor issues displaying reduced toxicity and improved activity profiles is reported.
Abstract: Paclitaxel (PTX) is among the most commonly used first-line drugs for cancer chemotherapy. However, its poor water solubility and indiscriminate distribution in normal tissues remain clinical challenges. Here we design and synthesize a highly water-soluble nucleolin aptamer-paclitaxel conjugate (NucA-PTX) that selectively delivers PTX to the tumor site. By connecting a tumor-targeting nucleolin aptamer (NucA) to the active hydroxyl group at 2' position of PTX via a cathepsin B sensitive dipeptide bond, NucA-PTX remains stable and inactive in the circulation. NucA facilitates the uptake of the conjugated PTX specifically in tumor cells. Once inside cells, the dipeptide bond linker of NucA-PTX is cleaved by cathepsin B and then the conjugated PTX is released for action. The NucA modification assists the selective accumulation of the conjugated PTX in ovarian tumor tissue rather than normal tissues, and subsequently resulting in notably improved antitumor activity and reduced toxicity.

171 citations


Authors

Showing all 7946 results

NameH-indexPapersCitations
Weihong Tan14089267151
Bin Liu138218187085
Jun Lu135152699767
John P. Giesy114116262790
Qiang Yang112111771540
Ming Hung Wong10371039738
Wei Wang95354459660
Jianhua Zhang9241528085
Xiaojun Wu91108831687
Guibin Jiang8885034633
Shu Tao8763927304
Paul K.S. Lam8748525614
Cheng-Yong Su8758132322
Hai-Long Jiang8619830946
Baowen Li8347723080
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202346
2022246
20211,655
20201,479
20191,244
20181,093