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Sökning: WFRF:(Zhong Zhuo)

  • Resultat 1-8 av 8
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2.
  • Menkveld, Albert J., et al. (författare)
  • Nonstandard Errors
  • 2024
  • Ingår i: JOURNAL OF FINANCE. - : Wiley-Blackwell. - 0022-1082 .- 1540-6261. ; 79:3, s. 2339-2390
  • Tidskriftsartikel (refereegranskat)abstract
    • In statistics, samples are drawn from a population in a data-generating process (DGP). Standard errors measure the uncertainty in estimates of population parameters. In science, evidence is generated to test hypotheses in an evidence-generating process (EGP). We claim that EGP variation across researchers adds uncertainty-nonstandard errors (NSEs). We study NSEs by letting 164 teams test the same hypotheses on the same data. NSEs turn out to be sizable, but smaller for more reproducible or higher rated research. Adding peer-review stages reduces NSEs. We further find that this type of uncertainty is underestimated by participants.
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3.
  • Ge, Rongbin, et al. (författare)
  • Metformin represses cancer cells via alternate pathways in N-cadherin expressing vs. N-cadherin deficient cells.
  • 2015
  • Ingår i: Oncotarget. - : Impact Journals, LLC. - 1949-2553. ; 6:30
  • Tidskriftsartikel (refereegranskat)abstract
    • Metformin has emerged as a potential anticancer agent. Here, we demonstrate that metformin plays an anti-tumor role via repressing N-cadherin, independent of AMPK, in wild-type N-cadherin cancer cells. Ectopic-expression of N-cadherin develops metformin-resistant cancer cells, while suppression of N-cadherin sensitizes cancer to metformin. Manipulation of AMPK expression does not alter sensitivity of cancer to metformin. We show that NF-kappaB is a downstream molecule of N-cadherin and metformin regulates NF-kappaB signaling via suppressing N-cadherin. Moreover, we also suggest that TWIST1 is an upstream molecule of N-cadherin/NF-kappaB signaling and manipulation of TWIST1 expression changes the sensitivity of cancer cells to metformin. In contrast to the cells that express N-cadherin, in N-cadherin deficient cells, metformin plays an anti-tumor role via activation of AMPK. Ectopic expression of N-cadherin makes cancer more resistant to metformin. Therefore, we suggest that metformin's anti-cancer therapeutic effect is mediated through different molecular mechanism in wild-type vs. deficient N-cadherin cancer cells. At last, we selected 49 out of 984 patients' samples with prostatic cancer after radical prostatectomy (selection criteria: Gleason score ≥ 7 and all patients taking metformin) and showed levels of N-cadherin, p65 and AMPK could predict post-surgical recurrence in prostate cancer after treatment of metformin.
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4.
  • Li, Zhuo, et al. (författare)
  • Atomic Structure and Electron Magnetic Circular Dichroism of Individual Rock Salt Structure Antiphase Boundaries in Spinel Ferrites
  • 2021
  • Ingår i: Advanced Functional Materials. - : John Wiley & Sons. - 1616-301X .- 1616-3028. ; 31:21
  • Tidskriftsartikel (refereegranskat)abstract
    • Spinel ferrites are an important class of materials, whose magnetic properties are of interest for industrial applications. The antiphase boundaries (APBs) that are commonly observed in spinel ferrite films can hinder their applications in spintronic devices and sensors, as a result of their influence on magnetic degradation and magnetoresistance of the materials. However, it is challenging to correlate magnetic properties with atomic structure in individual APBs due to the limited spatial resolution of most magnetic imaging techniques. Here, aberration-corrected scanning transmission electron microscopy and electron energy-loss magnetic chiral dichroism are used to measure the atomic structure and electron magnetic circular dichroism (EMCD) of a single APB in NiFe2O4 that takes the form of a rock salt structure interlayer and is associated with a crystal translation of (1/4)a[011]. First principles density functional theory calculations are used to confirm that this specific APB introduces antiferromagnetic coupling and a significant decrease in the magnitude of the magnetic moments, which is consistent with an observed decrease in EMCD signal at the APB. The results provide new insight into the physical origins of magnetic coupling at an individual defect on the atomic scale.
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5.
  • Ma, Zhuo, et al. (författare)
  • Deciphering early human pancreas development at the single-cell level
  • 2023
  • Ingår i: Nature Communications. - : NATURE PORTFOLIO. - 2041-1723. ; 14:1
  • Tidskriftsartikel (refereegranskat)abstract
    • Understanding pancreas development can provide clues for better treatments of pancreatic diseases. However, the molecular heterogeneity and developmental trajectory of the early human pancreas are poorly explored. Here, we performed large-scale single-cell RNA sequencing and single-cell assay for transposase accessible chromatin sequencing of human embryonic pancreas tissue obtained from first-trimester embryos. We unraveled the molecular heterogeneity, developmental trajectories and regulatory networks of the major cell types. The results reveal that dorsal pancreatic multipotent cells in humans exhibit different gene expression patterns than ventral multipotent cells. Pancreato-biliary progenitors that generate ventral multipotent cells in humans were identified. Notch and MAPK signals from mesenchymal cells regulate the differentiation of multipotent cells into trunk and duct cells. Notably, we identified endocrine progenitor subclusters with different differentiation potentials. Although the developmental trajectories are largely conserved between humans and mice, some distinct gene expression patterns have also been identified. Overall, we provide a comprehensive landscape of early human pancreas development to understand its lineage transitions and molecular complexity. Here, the authors revealed molecular heterogeneity, developmental trajectory and regulatory network of early human pancreas development, and depict the whole progression of pancreatic organogenesis during the first trimester at the single-cell level.
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6.
  • Qian, Zhen, et al. (författare)
  • Vectorized dataset of roadside noise barriers in China using street view imagery
  • 2022
  • Ingår i: Earth System Science Data. - : Copernicus GmbH. - 1866-3508 .- 1866-3516. ; 14:9, s. 4057-4076
  • Tidskriftsartikel (refereegranskat)abstract
    • Roadside noise barriers (RNBs) are important urban infrastructures to ensure that cities remain liveable. However, the absence of accurate and large-scale geospatial data on RNBs has impeded the increasing progress of rational urban planning, sustainable cities, and healthy environments. To address this problem, this study creates a vectorized RNB dataset in China using street view imagery and a geospatial artificial intelligence framework. First, intensive sampling is performed on the road network of each city based on OpenStreetMap, which is used as the georeference for downloading 6 x 10(6) Baidu Street View (BSV) images. Furthermore, considering the prior geographic knowledge contained in street view images, convolutional neural networks incorporating image context information (IC-CNNs) based on an ensemble learning strategy are developed to detect RNBs from the BSV images. The RNB dataset presented by polylines is generated based on the identified RNB locations, with a total length of 2667.02 km in 222 cities. Last, the quality of the RNB dataset is evaluated from two perspectives, i.e., the detection accuracy and the completeness and positional accuracy. Specifically, based on a set of randomly selected samples containing 10 000 BSV images, four quantitative metrics are calculated, with an overall accuracy of 98.61 %, recall of 87.14 %, precision of 76.44 %, and F-1 score of 81.44 %. A total length of 254.45 km of roads in different cities are manually surveyed using BSV images to evaluate the mileage deviation and overlap level between the generated and surveyed RNBs. The root mean squared error for the mileage deviation is 0.08 km, and the intersection over union for overlay level is 88.08% +/- 2.95 %. The evaluation results suggest that the generated RNB dataset is of high quality and can be applied as an accurate and reliable dataset for a variety of large-scale urban studies, such as estimating the regional solar photovoltaic potential, developing 3D urban models, and designing rational urban layouts. Besides that, the benchmark dataset of the labeled BSV images can also support more work on RNB detection, such as developing more advanced deep learning algorithms, fine-tuning the existing computer vision models, and analyzing geospatial scenes in BSV. The generated vectorized RNB dataset and the benchmark dataset of labeled BSV imagery are publicly available at https://doi.org/10.11888/Others.tpdc.271914 (Chen, 2021).
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7.
  • Wan, Lu Ming, et al. (författare)
  • Heparanase Facilitates PMA-Induced Megakaryocytic Differentiation in K562 Cells via Interleukin 6/STAT3 Pathway
  • 2020
  • Ingår i: Thrombosis and Haemostasis. - : GEORG THIEME VERLAG KG. - 0340-6245 .- 2567-689X. ; 120:4, s. 647-657
  • Tidskriftsartikel (refereegranskat)abstract
    • Heparanase (HPSE) is an endo-beta-D-glucuronidase that cleaves heparan sulfate and hence participates in remodeling of the extracellular matrix, leading to release of cytokines that are immobilized by binding to heparan sulfate proteoglycans (HSPGs), and consequently activating signaling pathways. This function of HPSE is correlated to its expression level that is normally very low in majority of the tissues. Exceptionally, human platelets express high level of HPSE, suggesting a unique physiological role in this cell. Using K562 cell line, we found a progressive increase of HPSE during the megakaryocytic differentiation. Analysis of a series of megakaryocytic differentiation-related heparin-binding proteins (HBPs) in the cell culture medium revealed an exclusive positive correlation between the level of interleukin 6 (IL-6) and HPSE expression. IL-6 modulated megakaryocytic differentiation through activation of STAT3. Further, we demonstrated that overexpression of HPSE potentiates megakaryocytic differentiation, whereas elimination of HPSE led to a delayed differentiation. This function of HPSE is associated with its activity, as overexpression of inactive HPSE had no effect on IL-6 production and megakaryocytic differentiation. The role of HPSE is further supported by the observation in an umbilical cord blood CD34+ cells megakaryocytic differentiation model. Our data propose a novel role for HPSE in platelets production by a HPSE/IL-6/STAT3 positive feedback loop that specifically regulates megakaryocytes maturation.
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8.
  • Zhu, Zikai, et al. (författare)
  • Using a VAE-SOM architecture for anomaly detection of flexible sensors in limb prosthesis
  • 2023
  • Ingår i: Journal of Industrial Information Integration. - : Elsevier BV. - 2452-414X .- 2467-964X. ; 35
  • Tidskriftsartikel (refereegranskat)abstract
    • Flexible wearable sensor electronics, combined with advanced software functions, pave the way toward increasingly intelligent healthcare devices. One important application area is limb prosthesis, where printed flexible sensor solutions enable efficient monitoring and assessing of the actual intra-socket dynamic operation conditions in clinical and other more natural environments. However, the data collected by such sensors suffer from variations and errors, leading to difficulty in perceiving the actual operational conditions. This paper proposes a novel method for detecting anomalies in the data that are collected for measuring the intra-socket dynamic operation conditions by printed flexible wearable sensors. A discrete generative model based on Variational AutoEncoder (VAE) is used first to encode the collected multi-variant time-series data in terms of latent states. After that, a clustering method based on the Self-Organizing Map (SOM) is used to acquire discrete and interpretable representations of the VAE encoded latent states. An adaptive Markov chain is utilized to detect anomalies by quantifying state transitions and revealing temporal dependencies. The contributions of the proposed architecture conclude as follows: (1) Using the VAE-SOM hybrid model to regularize the continues data as discrete states, supporting interpreting the operational data to analytic models. (2) Employing adaptive Markov chains to generalize the transitions of these states, allowing to model the complex operational conditions. Compared with benchmark methods, our architecture is validated via two public datasets and achieves the best F1 scores. Moreover, we measure the run-time performance of this lightweight architecture. The results indicate that the proposed method performs low computational complexity, facilitating the applications on real-life productions.
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