Publications by authors named "Yingzhi Tang"

Burkholderia cenocepacia is an opportunistic pathogen that causes severe infections of the cystic fibrosis (CF) lung. To acquire iron, B. cenocepacia secretes the Fe(III)-binding compound, ornibactin.

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Person reidentification (Re-ID) aims at recognizing the same identity across different camera views. However, the cross resolution of images [high resolution (HR) and low resolution (LR)] is unavoidable in a realistic scenario due to the various distances among cameras and pedestrians of interest, thus leading to cross-resolution person Re-ID problems. Recently, most cross-resolution person Re-ID methods focus on solving the resolution mismatch problem, while the distribution mismatch between HR and LR images is another factor that significantly impacts the person Re-ID performance.

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Person re-identification (re-ID) is a technique aiming to recognize person cross different cameras. Although some supervised methods have achieved favorable performance, they are far from practical application owing to the lack of labeled data. Thus, unsupervised person re-ID methods are in urgent need.

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Compared with face recognition, the performance of person re-identification (re-ID) is still far from practical application. Among various interferences, there are two factors seriously limiting the performance improvement, i.e.

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OrbS and PvdS are extracytoplasmic function (ECF) σ factors that regulate transcription of operons required for the biosynthesis of the siderophores ornibactin and pyoverdine in the complex and spp., respectively. Here we show that promoter recognition by OrbS requires specific tetrameric -35 and -10 element sequences that are strikingly similar to those of the consensus PvdS-dependent promoter.

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Upon starvation for glucose or any other macronutrient, yeast cells exit from the mitotic cell cycle and acquire a set of characteristics that are specific to quiescent cells to ensure longevity. Little is known about the molecular determinants that orchestrate quiescence entry and lifespan extension. Using starvation-specific gene reporters, we screened a subset of the yeast deletion library representing the genes encoding 'signaling' proteins.

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Upon starvation for glucose or any other core nutrient, yeast cells exit from the mitotic cell cycle and acquire a set of G0-specific characteristics to ensure long-term survival. It is not well understood whether or how cell cycle progression is coordinated with the acquisition of different G0-related features during the transition to stationary phase (SP). Here, we identify the yeast GSK-3 homologue Mck1 as a key regulator of G0 entry and reveal that Mck1 acts in parallel to Rim15 to activate starvation-induced gene expression, the acquisition of stress resistance, the accumulation of storage carbohydrates, the ability of early SP cells to exit from quiescence, and their chronological lifespan.

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