94 research outputs found
Multi-color optical monitoring of the quasar 3C 273 from 2005 to 2016
We have monitored the quasar 3C 273 in optical , and bands from
2005 to 2016. Intraday variability (IDV) is detected on seven nights. The
variability amplitudes for most of nights are less than 10\% and four nights
more than 20\%. When considering the nights with time spans hours, the
value of duty cycle (DC) is 14.17 per cent. Over the twelve years, the overall
magnitude and color index variabilities are ,
, , and
respectively. The largest clear IDV has an
amplitude of 42% over just 5.8 minutes and the weakest detected IDV is 5.4%
over 175 minutes. The BWB (bluer when brighter) chromatic trend is dominant for
3C 273 and appears at different flux levels on intraday timescales. The BWB
trend exists for short-term timescales and intermediate-term timescales but
different timescales have different correlations. There is no BWB trend for our
whole time-series data sets. A significant anti-correlation between BWB trend
and length of timescales is found. Combining with -band data from previous
works, we find a possible quasi-periodicity of days. The
possible explanations for the observed variability, BWB chromatic trend and
periodicity are discussed.Comment: 63 pages, 11 figures, 6 tables. Accepted for publication in ApJ
Text2Street: Controllable Text-to-image Generation for Street Views
Text-to-image generation has made remarkable progress with the emergence of
diffusion models. However, it is still a difficult task to generate images for
street views based on text, mainly because the road topology of street scenes
is complex, the traffic status is diverse and the weather condition is various,
which makes conventional text-to-image models difficult to deal with. To
address these challenges, we propose a novel controllable text-to-image
framework, named \textbf{Text2Street}. In the framework, we first introduce the
lane-aware road topology generator, which achieves text-to-map generation with
the accurate road structure and lane lines armed with the counting adapter,
realizing the controllable road topology generation. Then, the position-based
object layout generator is proposed to obtain text-to-layout generation through
an object-level bounding box diffusion strategy, realizing the controllable
traffic object layout generation. Finally, the multiple control image generator
is designed to integrate the road topology, object layout and weather
description to realize controllable street-view image generation. Extensive
experiments show that the proposed approach achieves controllable street-view
text-to-image generation and validates the effectiveness of the Text2Street
framework for street views
Control of Cyclin D1 and Breast Tumorigenesis by the EglN2 Prolyl Hydroxylase
Summary2-Oxoglutarate-dependent dioxygenases, including the EglN prolyl hydroxylases that regulate HIF, can be inhibited with drug-like molecules. EglN2 is estrogen inducible in breast carcinoma cells and the lone Drosophila EglN interacts genetically with Cyclin D1. Although EglN2 is a nonessential gene, we found that EglN2 inactivation decreases Cyclin D1 levels and suppresses mammary gland proliferation in vivo. Regulation of Cyclin D1 is a specific attribute of EglN2 among the EglN proteins and is HIF independent. Loss of EglN2 catalytic activity inhibits estrogen-dependent breast cancer tumorigenesis and can be rescued by exogenous Cyclin D1. EglN2 depletion also impairs the fitness of lung, brain, and hematopoietic cancer lines. These findings support the exploration of EglN2 inhibitors as therapeutics for estrogen-dependent breast cancer and other malignancies
Crystal structure of rhodopsin bound to arrestin by femtosecond X-ray laser.
G-protein-coupled receptors (GPCRs) signal primarily through G proteins or arrestins. Arrestin binding to GPCRs blocks G protein interaction and redirects signalling to numerous G-protein-independent pathways. Here we report the crystal structure of a constitutively active form of human rhodopsin bound to a pre-activated form of the mouse visual arrestin, determined by serial femtosecond X-ray laser crystallography. Together with extensive biochemical and mutagenesis data, the structure reveals an overall architecture of the rhodopsin-arrestin assembly in which rhodopsin uses distinct structural elements, including transmembrane helix 7 and helix 8, to recruit arrestin. Correspondingly, arrestin adopts the pre-activated conformation, with a ∼20° rotation between the amino and carboxy domains, which opens up a cleft in arrestin to accommodate a short helix formed by the second intracellular loop of rhodopsin. This structure provides a basis for understanding GPCR-mediated arrestin-biased signalling and demonstrates the power of X-ray lasers for advancing the frontiers of structural biology
Evaluation of a Novel Biphasic Culture Medium for Recovery of Mycobacteria: A Multi-Center Study
on L-J slants. Automated liquid culture systems are expensive. A low-cost culturing medium capable of rapidly indicating the presence of mycobacteria is needed. The aim of this study was to develop and evaluate a novel biphasic culture medium for the recovery of mycobacteria from clinical sputum specimens from suspected pulmonary tuberculosis patients.<0.001).
Robust estimation of bacterial cell count from optical density
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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