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Träfflista för sökning "WFRF:(Lai Cheng) srt2:(2020-2023)"

Sökning: WFRF:(Lai Cheng) > (2020-2023)

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1.
  • Beal, Jacob, et al. (författare)
  • Robust estimation of bacterial cell count from optical density
  • 2020
  • Ingår i: Communications Biology. - : Springer Science and Business Media LLC. - 2399-3642. ; 3:1
  • Tidskriftsartikel (refereegranskat)abstract
    • Optical density (OD) is widely used to estimate the density of cells in liquid culture, but cannot be compared between instruments without a standardized calibration protocol and is challenging to relate to actual cell count. We address this with an interlaboratory study comparing three simple, low-cost, and highly accessible OD calibration protocols across 244 laboratories, applied to eight strains of constitutive GFP-expressing E. coli. Based on our results, we recommend calibrating OD to estimated cell count using serial dilution of silica microspheres, which produces highly precise calibration (95.5% of residuals <1.2-fold), is easily assessed for quality control, also assesses instrument effective linear range, and can be combined with fluorescence calibration to obtain units of Molecules of Equivalent Fluorescein (MEFL) per cell, allowing direct comparison and data fusion with flow cytometry measurements: in our study, fluorescence per cell measurements showed only a 1.07-fold mean difference between plate reader and flow cytometry data.
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  • Axfors, Cathrine, et al. (författare)
  • Mortality outcomes with hydroxychloroquine and chloroquine in COVID-19 from an international collaborative meta-analysis of randomized trials
  • 2021
  • Ingår i: Nature Communications. - : Springer Nature. - 2041-1723. ; 12:1
  • Tidskriftsartikel (refereegranskat)abstract
    • Substantial COVID-19 research investment has been allocated to randomized clinical trials (RCTs) on hydroxychloroquine/chloroquine, which currently face recruitment challenges or early discontinuation. We aim to estimate the effects of hydroxychloroquine and chloroquine on survival in COVID-19 from all currently available RCT evidence, published and unpublished. We present a rapid meta-analysis of ongoing, completed, or discontinued RCTs on hydroxychloroquine or chloroquine treatment for any COVID-19 patients (protocol: https://osf.io/QESV4/). We systematically identified unpublished RCTs (ClinicalTrials.gov, WHO International Clinical Trials Registry Platform, Cochrane COVID-registry up to June 11, 2020), and published RCTs (PubMed, medRxiv and bioRxiv up to October 16, 2020). All-cause mortality has been extracted (publications/preprints) or requested from investigators and combined in random-effects meta-analyses, calculating odds ratios (ORs) with 95% confidence intervals (CIs), separately for hydroxychloroquine and chloroquine. Prespecified subgroup analyses include patient setting, diagnostic confirmation, control type, and publication status. Sixty-three trials were potentially eligible. We included 14 unpublished trials (1308 patients) and 14 publications/preprints (9011 patients). Results for hydroxychloroquine are dominated by RECOVERY and WHO SOLIDARITY, two highly pragmatic trials, which employed relatively high doses and included 4716 and 1853 patients, respectively (67% of the total sample size). The combined OR on all-cause mortality for hydroxychloroquine is 1.11 (95% CI: 1.02, 1.20; I-2=0%; 26 trials; 10,012 patients) and for chloroquine 1.77 (95%CI: 0.15, 21.13, I-2=0%; 4 trials; 307 patients). We identified no subgroup effects. We found that treatment with hydroxychloroquine is associated with increased mortality in COVID-19 patients, and there is no benefit of chloroquine. Findings have unclear generalizability to outpatients, children, pregnant women, and people with comorbidities. Hydroxychloroquine and chloroquine have been investigated as a potential treatment for Covid-19 in several clinical trials. Here the authors report a meta-analysis of published and unpublished trials, and show that treatment with hydroxychloroquine for patients with Covid-19 was associated with increased mortality, and there was no benefit from chloroquine.
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  • Han, L., et al. (författare)
  • Cell transcriptomic atlas of the non-human primate Macaca fascicularis
  • 2022
  • Ingår i: Nature. - : Springer Nature. - 0028-0836 .- 1476-4687. ; 604:7907, s. 723-731
  • Tidskriftsartikel (refereegranskat)abstract
    • Studying tissue composition and function in non-human primates (NHPs) is crucial to understand the nature of our own species. Here we present a large-scale cell transcriptomic atlas that encompasses over 1 million cells from 45 tissues of the adult NHP Macaca fascicularis. This dataset provides a vast annotated resource to study a species phylogenetically close to humans. To demonstrate the utility of the atlas, we have reconstructed the cell–cell interaction networks that drive Wnt signalling across the body, mapped the distribution of receptors and co-receptors for viruses causing human infectious diseases, and intersected our data with human genetic disease orthologues to establish potential clinical associations. Our M. fascicularis cell atlas constitutes an essential reference for future studies in humans and NHPs. 
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  • 2021
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  • Huang, Jianpan, et al. (författare)
  • Altered d-glucose in brain parenchyma and cerebrospinal fluid of early Alzheimer's disease detected by dynamic glucose-enhanced MRI
  • 2020
  • Ingår i: Science Advances. - : American Association for the Advancement of Science (AAAS). - 2375-2548. ; 6:20
  • Tidskriftsartikel (refereegranskat)abstract
    • Altered cerebral glucose uptake is one of the hallmarks of Alzheimer's disease (AD). A dynamic glucose-enhanced (DGE) magnetic resonance imaging (MRI) approach was developed to simultaneously monitor d-glucose uptake and clearance in both brain parenchyma and cerebrospinal fluid (CSF). We observed substantially higher uptake in parenchyma of young (6 months) transgenic AD mice compared to age-matched wild-type (WT) mice. Notably lower uptakes were observed in parenchyma and CSF of old (16 months) AD mice. Both young and old AD mice had an obviously slower CSF clearance than age-matched WT mice. This resembles recent reports of the hampered CSF clearance that leads to protein accumulation in the brain. These findings suggest that DGE MRI can identify altered glucose uptake and clearance in young AD mice upon the emergence of amyloid plaques. DGE MRI of brain parenchyma and CSF has potential for early AD stratification, especially at 3T clinical field strength MRI.
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  • Liu, Xiuyu, et al. (författare)
  • Structure-function analysis of CYP719As involved in methylenedioxy bridge-formation in the biosynthesis of benzylisoquinoline alkaloids and its de novo production
  • 2023
  • Ingår i: Microbial Cell Factories. - : Springer Science and Business Media LLC. - 1475-2859. ; 22:1
  • Tidskriftsartikel (refereegranskat)abstract
    • Benzylisoquinoline alkaloids (BIAs) are a type of secondary metabolite with clinical application value. (S)-stylopine is a special BIA which contains methylenedioxy bridge structures. CYP719As could catalyze the methylenedioxy bridge-formation on the A or D rings of protoberberine alkaloids, while displaying significant substrate regiospecificity. To explore the substrate preference of CYP719As, we cloned and identified five CyCYP719A candidates from Corydalis yanhusuo. Two CyCYP719As (CyCYP719A39 and CyCYP719A42) with high catalytic efficiency for the methylenedioxy bridge-formation on the D or A rings were characterized, respectively. The residues (Leu 294 for CyCYP719A42 and Asp 289 for CyCYP719A39) were identified as the key to controlling the regioselectivity of CYP719As affecting the methylenedioxy bridge-formation on the A or D rings by homology modeling and mutation analysis. Furthermore, for de novo production of BIAs, CyCYP719A39, CyCYP719A42, and their mutants were introduced into the (S)-scoulerine-producing yeast to produce 32 mg/L (S)-stylopine. These results lay a foundation for understanding the structure-function relationship of CYP719A-mediated methylenedioxy bridge-formation and provide yeast strains for the BIAs production by synthetic biology.
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  • Lu, Yichen, et al. (författare)
  • Analytical Method of Traffic Conflict at Urban Road Intersections Based on Risk Region
  • 2021
  • Ingår i: Tongji Daxue Xuebao/Journal of Tongji University. - 0253-374X. ; 49:7, s. 941-948
  • Tidskriftsartikel (refereegranskat)abstract
    • A two-stage method of traffic conflict analysis was proposed based on risk region. By using the inD dataset, traffic conflicts were recognized with the calculation of time to risk region(tTTR), and then the degree of traffic conflict risk was judged by risk region duration. Compared with the method based on time-to-collision(tTTC), the proposed method can not only identify rear-end conflicts and crossing conflicts more effectively, but also characterize the degree of traffic conflict risk at different times.
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  • Zheng, Lai, et al. (författare)
  • Investigating consecutive conflicts of pedestrian crossing at unsignalized crosswalks using the bivariate logistic approach
  • 2021
  • Ingår i: Accident Analysis and Prevention. - : Elsevier BV. - 0001-4575. ; 162
  • Tidskriftsartikel (refereegranskat)abstract
    • Pedestrians confront risky situations at unsignalized crosswalks when they are consecutively interacting with motorized vehicles and non-motorized vehicles while crossing. This study aims to investigate the safety of pedestrians with a new perspective that focuses on consecutive conflicts occurring during pedestrian crossing. Based on about 9 h video data collected by an unmanned aerial vehicle from six unsignalized crosswalks of a roundabout, consecutive conflicts were identified, and an integrated severity index that combines post encroachment time, jerk and yaw rate ratio was proposed to measure the severity of consecutive conflicts. Moreover, bivariate logistic models that account for and not account for the correlation between the pedestrian-motorized vehicle (P-MV) conflict and the pedestrian-non-motorized vehicle (P-NV) conflict of a consecutive conflict were developed, and speed-, count-, time to zebra-related factors and other factors of involved road users were considered in the models. A total of 899 consecutive conflicts were identified and on average one in six pedestrians encountered consecutive conflicts. The bivariate logistic modeling results show that the model accounting for the correlation significantly outperform its counterpart. A negative correlation is found between the severities of P-MV conflict and P-NV conflict, and the P-NV conflict is more likely to be the serious one. It is also found that speed of motorized vehicle and time to zebra for the first conflicting subject are the common factors that affect the severities of both P-NV conflicts and P-MV conflicts, while speed of pedestrian, speed of non-motorized vehicle, number of motorized vehicles, number of non-motorized vehicles, group and direction of pedestrians have significant effects on the severity of either P-MV conflicts or P-NV conflicts.
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