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Germanium-lead perovskite light-emitting diodes 期刊论文
Nature Communications, 2021
作者:  Dexin Yang;  Guoling Zhang;  Runchen Lai;  Yao Cheng;  Yaxiao Lian;  Min Rao;  Dexuan Huo;  Dongchen Lan;  Baodan Zhao;  Dawei Di
收藏  |  浏览/下载:15/0  |  提交时间:2021/07/27
Hydraulic transmissivity inferred from ice-sheet relaxation following Greenland supraglacial lake drainages 期刊论文
Nature Communications, 2021
作者:  Ching-Yao Lai;  Laura A. Stevens;  Danielle L. Chase;  Timothy T. Creyts;  Mark D. Behn;  Sarah B. Das;  Howard A. Stone
收藏  |  浏览/下载:10/0  |  提交时间:2021/07/27
Flexural Control of Basal Crevasse Opening Under Ice Shelves 期刊论文
Geophysical Research Letters, 2021
作者:  W. Roger Buck;  Ching‐;  Yao Lai
收藏  |  浏览/下载:5/0  |  提交时间:2021/04/12
Vulnerability of Antarctica鈥檚 ice shelves to meltwater-driven fracture 期刊论文
Nature, 2020
作者:  Ching-Yao Lai;  Jonathan Kingslake;  Martin G. Wearing;  Po-Hsuan Cameron Chen;  Pierre Gentine;  Harold Li;  Julian J. Spergel;  J. Melchior van Wessem
收藏  |  浏览/下载:16/0  |  提交时间:2020/09/08
Can atmospheric reanalyses (CRA and ERA5) represent cloud spatiotemporal characteristics? 期刊论文
Atmospheric Research, 2020
作者:  Bin Yao, Shiwen Teng, Ruize Lai, Xiaofeng Xu, ... Chao Liu
收藏  |  浏览/下载:9/0  |  提交时间:2020/06/09
Feedback generates a second receptive field in neurons of the visual cortex 期刊论文
NATURE, 2020
作者:  Shi, Enzheng;  Yuan, Biao;  Shiring, Stephen B.;  Gao, Yao;  Akriti;  Guo, Yunfan;  Su, Cong;  Lai, Minliang;  Yang, Peidong;  Kong, Jing;  Savoie, Brett M.;  Yu, Yi;  Dou, Letian
收藏  |  浏览/下载:45/0  |  提交时间:2020/07/03

Animals sense the environment through pathways that link sensory organs to the brain. In the visual system, these feedforward pathways define the classical feedforward receptive field (ffRF), the area in space in which visual stimuli excite a neuron(1). The visual system also uses visual context-the visual scene surrounding a stimulus-to predict the content of the stimulus(2), and accordingly, neurons have been identified that are excited by stimuli outside their ffRF(3-8). However, the mechanisms that generate excitation to stimuli outside the ffRF are unclear. Here we show that feedback projections onto excitatory neurons in the mouse primary visual cortex generate a second receptive field that is driven by stimuli outside the ffRF. The stimulation of this feedback receptive field (fbRF) elicits responses that are slower and are delayed in comparison with those resulting from the stimulation of the ffRF. These responses are preferentially reduced by anaesthesia and by silencing higher visual areas. Feedback inputs from higher visual areas have scattered receptive fields relative to their putative targets in the primary visual cortex, which enables the generation of the fbRF. Neurons with fbRFs are located in cortical layers that receive strong feedback projections and are absent in the main input layer, which is consistent with a laminar processing hierarchy. The observation that large, uniform stimuli-which cover both the fbRF and the ffRF-suppress these responses indicates that the fbRF and the ffRF are mutually antagonistic. Whereas somatostatin-expressing inhibitory neurons are driven by these large stimuli, inhibitory neurons that express parvalbumin and vasoactive intestinal peptide have mutually antagonistic fbRF and ffRF, similar to excitatory neurons. Feedback projections may therefore enable neurons to use context to estimate information that is missing from the ffRF and to report differences in stimulus features across visual space, regardless of whether excitation occurs inside or outside the ffRF. By complementing the ffRF, the fbRF that we identify here could contribute to predictive processing.


Feedback projections onto neurons of the mouse primary visual cortex generate a second excitatory receptive field that is driven by stimuli outside of the classical feedforward receptive field, with responses mediated by higher visual areas.


  
Notch signalling drives synovial fibroblast identity and arthritis pathology 期刊论文
NATURE, 2020, 582 (7811) : 259-+
作者:  Han, Xiaoping;  Zhou, Ziming;  Fei, Lijiang;  Sun, Huiyu;  Wang, Renying;  Chen, Yao;  Chen, Haide;  Wang, Jingjing;  Tang, Huanna;  Ge, Wenhao;  Zhou, Yincong;  Ye, Fang;  Jiang, Mengmeng;  Wu, Junqing;  Xiao, Yanyu;  Jia, Xiaoning;  Zhang, Tingyue;  Ma, Xiaojie;  Zhang, Qi;  Bai, Xueli;  Lai, Shujing;  Yu, Chengxuan;  Zhu, Lijun;  Lin, Rui;  Gao, Yuchi;  Wang, Min;  Wu, Yiqing;  Zhang, Jianming;  Zhan, Renya;  Zhu, Saiyong;  Hu, Hailan;  Wang, Changchun;  Chen, Ming;  Huang, He;  Liang, Tingbo;  Chen, Jianghua;  Wang, Weilin;  Zhang, Dan;  Guo, Guoji
收藏  |  浏览/下载:44/0  |  提交时间:2020/07/03

NOTCH3 signalling is shown to be the underlying driver of the differentiation and expansion of a subset of synovial fibroblasts implicated in the pathogenesis of rheumatoid arthritis.


The synovium is a mesenchymal tissue composed mainly of fibroblasts, with a lining and sublining that surround the joints. In rheumatoid arthritis the synovial tissue undergoes marked hyperplasia, becomes inflamed and invasive, and destroys the joint(1,2). It has recently been shown that a subset of fibroblasts in the sublining undergoes a major expansion in rheumatoid arthritis that is linked to disease activity(3-5)  however, the molecular mechanism by which these fibroblasts differentiate and expand is unknown. Here we identify a critical role for NOTCH3 signalling in the differentiation of perivascular and sublining fibroblasts that express CD90 (encoded by THY1). Using single-cell RNA sequencing and synovial tissue organoids, we found that NOTCH3 signalling drives both transcriptional and spatial gradients-emanating from vascular endothelial cells outwards-in fibroblasts. In active rheumatoid arthritis, NOTCH3 and Notch target genes are markedly upregulated in synovial fibroblasts. In mice, the genetic deletion of Notch3 or the blockade of NOTCH3 signalling attenuates inflammation and prevents joint damage in inflammatory arthritis. Our results indicate that synovial fibroblasts exhibit a positional identity that is regulated by endothelium-derived Notch signalling, and that this stromal crosstalk pathway underlies inflammation and pathology in inflammatory arthritis.


  
DNA-induced 2 ' 3 '-cGAMP enhances haplotype-specific human STING cleavage by dengue protease 期刊论文
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2020, 117 (27) : 15947-15954
作者:  Su, Chan-, I;  Kao, Yu-Ting;  Chang, Chao-Chen;  Chang, Yao;  Ho, Tzong-shiann;  Sun, H. Sunny;  Lin, Yi-Ling;  Lai, Michael M. C.;  Liu, Yu-Huei;  Yu, Chia-Yi
收藏  |  浏览/下载:10/0  |  提交时间:2020/02/17
STING  DENV protease  SNP  2 '  3 '  -cGAMP  cGAS