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Träfflista för sökning "WFRF:(Wang Gang) srt2:(2015-2019)"

Sökning: WFRF:(Wang Gang) > (2015-2019)

  • Resultat 11-20 av 62
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11.
  • Wang, Lu, et al. (författare)
  • Design of Chipless RFID Tag by Using Miniaturized Open-Loop Resonators
  • 2018
  • Ingår i: IEEE Transactions on Antennas and Propagation. - 0018-926X .- 1558-2221. ; 66:2, s. 618-626
  • Tidskriftsartikel (refereegranskat)abstract
    • In this paper, an open-loop resonator with fragment-loading structure is used for the first time in the design of radar cross section-based chipless radio-frequency identification (RFID) tag. By optimizing the distribution of fragment patches in an open loop, a microstrip open-loop resonator can be miniaturized so that the data capacity of the chipless RFID tag designed using such a miniaturized loop resonator can be significantly increased. Moreover, the resonant frequency of the fragment-loaded resonator can be adjusted conveniently by removing or disconnecting some fragment patches, which provides great flexibility for data encoding of the chipless RFID tag. The proposed chipless RFID tag with miniaturized open-loop resonators is designed and tested and can acquire 3.56 bits per resonator and a coding density of approximately 745.1bits/λg 2. Several experimental results validate the proposed design as well as its implementation in a realistic environment.
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12.
  • Wang, Lu, et al. (författare)
  • High-performance tight coupling microstrip directional coupler with fragment-type compensated structure
  • 2017
  • Ingår i: IET Microwaves, Antennas & Propagation. - : Institution of Engineering and Technology (IET). - 1751-8725 .- 1751-8733. ; 11:7, s. 1057-1063
  • Tidskriftsartikel (refereegranskat)abstract
    • In this study, a design scheme for high-performance tight coupling microstrip coupler is proposed by adding a fragment-type compensated structure between two loosely coupled lines. Owing to its flexibility and adaptability, the fragment-type compensated structure can not only provide a quarter-wavelength phase shift for coupling enhancement, but also compensate the difference in the phase velocities of the even- and odd-modes for high directivity. Design of the fragment-type compensated structure can be implemented by multi-objective optimisation searching with several design objectives characterising tight coupling couplers. A high-efficiency optimisation searching strategy by using two-dimensional median filtering operator is employed to improve the efficiency of multi-objective optimisation. For demonstration, a high-performance 3-dB tight coupling directional coupler operating at 2 GHz is designed. The measurement data demonstrates a maximum directivity of 47 dB, above 25 dB directivity in a 21.5% bandwidth, a maximum variation of 0.3 dB in the coupling level and a maximum power division ratio of 0.6 dB, which indicate the overall performance better than the previously reported 3-dB couplers. In addition, a simplified theoretical analysis of the proposed coupler and full-wave simulated results are provided for better understanding of the fragment-type compensated structure.
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13.
  • Wang, Suhao, et al. (författare)
  • A Chemically Doped Naphthalenediimide-Bithiazole Polymer for n-Type Organic Thermoelectrics
  • 2018
  • Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095. ; 30:31
  • Tidskriftsartikel (refereegranskat)abstract
    • The synthesis of a novel naphthalenediimide (NDI)-bithiazole (Tz2)-based polymer [P(NDI2OD-Tz2)] is reported, and structural, thin-film morphological, as well as charge transport and thermoelectric properties are compared to the parent and widely investigated NDI-bithiophene (T2) polymer [P(NDI2OD-T2)]. Since the steric repulsions in Tz2 are far lower than in T2, P(NDI2OD-Tz2) exhibits a more planar and rigid backbone, enhancing p-p chain stacking and intermolecular interactions. In addition, the electron-deficient nature of Tz2 enhances the polymer electron affinity, thus reducing the polymer donor-acceptor character. When n-doped with amines, P(NDI2OD-Tz2) achieves electrical conductivity (approximate to 0.1 S cm(-1)) and a power factor (1.5 mu W m(-1) K-2) far greater than those of P(NDI2OD-T2) (0.003 S cm(-1) and 0.012 mu W m(-1) K-2, respectively). These results demonstrate that planarized NDI-based polymers with reduced donor-acceptor character can achieve substantial electrical conductivity and thermoelectric response.
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14.
  • Xiao, Chao, et al. (författare)
  • RBBP6 increases radioresistance and serves as a therapeutic target for preoperative radiotherapy in colorectal cancer
  • 2018
  • Ingår i: Cancer Science. - : Blackwell Publishing. - 1347-9032 .- 1349-7006. ; 109:4, s. 1075-1087
  • Tidskriftsartikel (refereegranskat)abstract
    • Radiotherapy (RT) can be used as preoperative treatment to downstage initially unresectable locally rectal carcinoma, but the radioresistance and recurrence remain significant problems. Retinoblastoma binding protein 6 (RBBP6) has been implicated in the regulation of cell cycle, apoptosis and chemoresistance both in vitro and in vivo. This study investigated whether the inhibition of RBBP6 expression would improve radiosensitivity in human colorectal cancer cells. After SW620 and HT29 cells were exposed to radiation, the levels of RBBP6 mRNA and protein increased over time in both two cells. Moreover, a significant reduction in clonogenic survival and a decrease in cell viability in parallel with an obvious increase in cell apoptosis were demonstrated in irradiated RBBP6-knockdown cells. Besides, transfection with RBBP6 shRNA improved levels of G2-M phase arrest which blocked the cells in a more radiosensitive period of the cell cycle. These observations indicated that cell cycle and apoptosis mechanisms may be connected with tumor cell survival following radiotherapy. In vivo, tumor growth rate of nude mice in RBBP6-knockdown group was significantly slower than that in other groups. These results indicated that RBBP6 overexpression could resist colorectal cancer cells against radiation by regulating cell cycle and apoptosis pathways, and inhibition of RBBP6 could enhance radiosensitivity of human colorectal cancer.
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15.
  • Xu, Shuang Feng, et al. (författare)
  • Lactoferrin ameliorates dopaminergic neurodegeneration and motor deficits in MPTP-treated mice
  • 2019
  • Ingår i: Redox Biology. - : Elsevier BV. - 2213-2317. ; 21
  • Tidskriftsartikel (refereegranskat)abstract
    • Brain iron accumulation is common in patients with Parkinson's disease (PD). Iron chelators have been investigated for their ability to prevent neurodegenerative diseases with features of iron overload. Given the non-trivial side effects of classical iron chelators, lactoferrin (Lf), a multifunctional iron-binding globular glycoprotein, was screened to identify novel neuroprotective pathways against dopaminergic neuronal impairment. We found that Lf substantially ameliorated PD-like motor dysfunction in the subacute 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced mouse model of PD. We further showed that Lf could alleviate MPTP-triggered apoptosis of DA neurons, neuroinflammation, and histological alterations. As expected, we also found that Lf suppressed MPTP-induced excessive iron accumulation and the upregulation of divalent metal transporter (DMT1) and transferrin receptor (TFR), which is the main intracellular iron regulation protein, and subsequently improved the activity of several antioxidant enzymes. We probed further and determined that the neuroprotection provided by Lf was involved in the upregulated levels of brain-derived neurotrophic factor (BDNF), hypoxia-inducible factor 1α (HIF-1α) and its downstream protein, accompanied by the activation of extracellular regulated protein kinases (ERK) and cAMP response element binding protein (CREB), as well as decreased phosphorylation of c-Jun N-terminal kinase (JNK) and mitogen activated protein kinase (MAPK)/P38 kinase in vitro and in vivo. Our findings suggest that Lf may be an alternative safe drug in ameliorating MPTP-induced brain abnormalities and movement disorder.
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16.
  • Zhuang, Ting, et al. (författare)
  • SHARPIN stabilizes estrogen receptor a and promotes breast cancer cell proliferation
  • 2017
  • Ingår i: Oncotarget. - : Impact Journals, LLC. - 1949-2553. ; 8:44, s. 77137-77151
  • Tidskriftsartikel (refereegranskat)abstract
    • Estrogen receptor a is expressed in the majority of breast cancers and promotes estrogen-dependent cancer progression. In our study, we identified the novel E3 ubiquitin ligase SHARPIN function to facilitate ERα signaling. SHARPIN is highly expressed in human breast cancer and correlates with ERα protein level by immunohistochemistry. SHARPIN expression level correlates with poor prognosis in ERα positive breast cancer patients. SHARPIN depletion based RNA-sequence data shows that ERα signaling is a potential SHARPIN target. SHARPIN depletion significantly decreases ERα protein level, ERα target genes expression and estrogen response element activity in breast cancer cells, while SHARPIN overexpression could reverse these effects. SHARPIN depletion significantly decreases estrogen stimulated cell proliferation in breast cancer cells, which effect could be further rescued by ERα overexpression. Further mechanistic study reveals that SHARPIN mainly localizes in the cytosol and interacts with ERα both in the cytosol and the nuclear. SHARPIN regulates ERα signaling through protein stability, not through gene expression. SHARPIN stabilizes ERα protein via prohibiting ERα protein poly-ubiquitination. Further study shows that SHARPIN could facilitate the mono-ubiquitinaiton of ERα at K302/303 sites and facilitate ERE luciferase activity. Together, our findings propose a novel ERα modulation mechanism in supporting breast cancer cell growth, in which SHARPIN could be one suitable target for development of novel therapy for ERα positive breast cancer.
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17.
  • Aldrin-Kirk, Patrick, et al. (författare)
  • DREADD Modulation of Transplanted DA Neurons Reveals a Novel Parkinsonian Dyskinesia Mechanism Mediated by the Serotonin 5-HT6 Receptor
  • 2016
  • Ingår i: Neuron. - : Elsevier BV. - 0896-6273. ; 90:5, s. 955-968
  • Tidskriftsartikel (refereegranskat)abstract
    • Transplantation of DA neurons is actively pursued as a restorative therapy in Parkinson's disease (PD). Pioneering clinical trials using transplants of fetal DA neuroblasts have given promising results, although a number of patients have developed graft-induced dyskinesias (GIDs), and the mechanism underlying this troublesome side effect is still unknown. Here we have used a new model where the activity of the transplanted DA neurons can be selectively modulated using a bimodal chemogenetic (DREADD) approach, allowing either enhancement or reduction of the therapeutic effect. We show that exclusive activation of a cAMP-linked (Gs-coupled) DREADD or serotonin 5-HT6 receptor, located on the grafted DA neurons, is sufficient to induce GIDs. These findings establish a mechanistic link between the 5-HT6 receptor, intracellular cAMP, and GIDs in transplanted PD patients. This effect is thought to be mediated through counteraction of the D2 autoreceptor feedback inhibition, resulting in a dysplastic DA release from the transplant.
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18.
  • Andersson, Anna, et al. (författare)
  • The landscape of somatic mutations in infant MLL-rearranged acute lymphoblastic leukemias.
  • 2015
  • Ingår i: Nature Genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 47:4, s. 192-330
  • Tidskriftsartikel (refereegranskat)abstract
    • Infant acute lymphoblastic leukemia (ALL) with MLL rearrangements (MLL-R) represents a distinct leukemia with a poor prognosis. To define its mutational landscape, we performed whole-genome, exome, RNA and targeted DNA sequencing on 65 infants (47 MLL-R and 18 non-MLL-R cases) and 20 older children (MLL-R cases) with leukemia. Our data show that infant MLL-R ALL has one of the lowest frequencies of somatic mutations of any sequenced cancer, with the predominant leukemic clone carrying a mean of 1.3 non-silent mutations. Despite this paucity of mutations, we detected activating mutations in kinase-PI3K-RAS signaling pathway components in 47% of cases. Surprisingly, these mutations were often subclonal and were frequently lost at relapse. In contrast to infant cases, MLL-R leukemia in older children had more somatic mutations (mean of 6.5 mutations/case versus 1.3 mutations/case, P = 7.15 × 10(-5)) and had frequent mutations (45%) in epigenetic regulators, a category of genes that, with the exception of MLL, was rarely mutated in infant MLL-R ALL.
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19.
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20.
  • Chen, Gang, et al. (författare)
  • EDF-VD Scheduling of Flexible Mixed-Criticality System With Multiple-Shot Transitions
  • 2018
  • Ingår i: IEEE Transactions on Computer-Aided Design of Integrated Circuits and Systems. - 0278-0070 .- 1937-4151. ; 37:11, s. 2393-2403
  • Tidskriftsartikel (refereegranskat)abstract
    • The existing mixed-criticality (MC) real-time task models assume that once any high-criticality task overruns, all high-criticality jobs execute up to their most pessimistic WCET estimations simultaneously in a one-shot manner. This is very pessimistic in the sense of unnecessary resource overbooking. In this paper, we propose a more generalized mixed-critical real-time task model, called flexible MC model with multiple-shot transitions (FMC-MST), to address this problem. In FMC-MST, high-criticality tasks can transit multiple intermediate levels to handle less pessimistic overruns independently and to nonuni-formly scale the deadline on each level. We develop a run-time schedulability analysis for FMC-MST under EDF-VD scheduling, in which a better tradeoff between the penalties of low-criticality tasks and the overruns of high-criticality tasks is achieved to improve the service quality of low-criticality tasks. We also develop a resource optimization technique to find resource-efficient level-insertion configurations for FMC-MST task systems under MC timing constraints. Experiments demonstrate the effectiveness of FMC-MST compared with the state-of-the-art techniques.
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