Motion estimation and video coding

Over the last ten years. research on the analysis of visual motion has come to play a key role in the fields of data compression for visual communication as well as computer vision. Enormous efforts have been made on the design of various motion estimation algorithms. One of the fundamental tasks in motion estimation is the accurate measurement of 2-D dense motion fields. For this purpose. we devise and present in this dissertation a multiattribute feedback computational framework. In this framework for each pixel in an image. instead of a single image intensity. multiple image attributes are computed as conservation information. To enhance the estimation accuracy. feedback technique is applied. Besides. the proposed algorithm needs less differentiation and thus is more robust to various noises. With these features. the estimation accuracy is improved considerably. Experiments have demonstrated that the proposed algorithm outperforms most of the existing techniques that compute 2-D dense motion fields in terms of accuracy. The estimation of 2-D block motion vector fields has been dominant among techniques in exploiting the temporal redundancy in video coding owing to its straightforward implementation and reasonable performance. But block matching is still a computational burden in real time video compression. Hence. efficient block matching techniques remain in demand. Existing block matching methods including full search and multiresolution techniques treat every region in an image domain indiscriminately no matter whether the region contains complicated motion or not. Motivated from this observation. we have developed two thresholding techniques for block matching in video coding. in which regions experiencing relatively uniform motion are withheld from further processing via thresholfing. thus saving compu­tation drastically. One is a thresholding multiresolution block matching. Extensive experiments show that the proposed algorithm has a consistent performance for sequences with different motion complexities. It reduces the processing time ranging from 14% to 20% while maintaining almost the same quality of the reconstructed image (only about 0.1 dB loss in PSNR). compared with the fastest existing multiresolution technique. The other is a thresholding hierarchical block matching where no pyramid is actually formed. Experiments indicate that for sequences with less motion such as videoconferencing sequences. this algorithm works faster and has much less motion vectors than the thresholding multiresolution block matching method

Anger Weakens Behavioral Inhibition Selectively in Contact Athletes

Studies have increasingly found that the aggression level of contact athletes is higher than that of non-athletes. Given that higher aggression levels are associated with worse behavioral inhibition and that athletes show better behavioral inhibition than non-athletes, it is unclear why contact athletes would exhibit higher aggression levels. Emotion, especially anger, is an important factor in the generation of aggressive behavior, and anger has been shown to affect behavioral inhibition. Thus, the present study examined the influence of anger on behavioral inhibition in contact athletes. An implicit emotional Go/No-go task was used that contained 50 anger-associated words and 50 neutral words as stimuli. Participants were asked to execute a key press depending on the explicit color of word and to ignore any (implicit) emotional information associated with the word. The results showed a significant interaction in performance accuracy on the No-go task between emotion (i.e., anger-associated words versus neutral words) and group (athlete versus non-athlete). The performance accuracy of the contact athletes on anger-associated stimuli was significantly lower than that for neutral stimuli. Evoked delta and theta oscillations were analyzed at the time windows 200–600 and 200–400 ms respectively in both groups. A time-frequency analysis indicated a significant interaction between group, emotion and task for both evoked delta and theta oscillations. Post hoc analyses showed that stronger evoked delta and theta oscillations were evoked during the presentation of anger-associated stimuli compared with neutral stimuli on the No-go task in athletes. By contrast, no other significant effect was found in the control group or between the control and athlete groups. These results indicate that time-frequency analysis can effectively distinguish conventional ERP components and that implicit anger significantly weakens behavioral inhibition in contact athletes but not in non-athletes

Potential molecular targets for intervention in pelvic organ prolapse

Pelvic organ prolapse (POP) is a concerning gynecological benign illness in middle-aged and senior women. Its etiology is complex, the incidence rate is high, symptoms are clinically subjective, and its influence tends to be polarized. At present, for those who need medical treatment, whether surgical or non-surgical, complications cannot be ignored, and treatment effect needs to be optimized. However, there is a lack of accurate molecular biological interventions for the prevention, diagnosis, progression delay, and treatment of POP. Here, we reviewed the current state of understanding of the molecular mechanisms and factors associated with POP etiology. These factors include cyclins, matrix metal peptidases/tissue inhibitors of metalloproteinases, microRNAs, homeobox A11, transforming growth factor β1, insulin-like growth factor 1, fibulin 5, lysyl oxidase-like 1, oxidative stress, inflammatory response, estrogen, and other potential biomarkers associated with POP. In addition, relevant molecular targets that may be used to intervene in POP are summarized. The aim of this review was to provide more information to identify accurate potential biomarkers and/or molecular targets for the prevention, diagnosis, progression delay, and treatment of POP, with the goal of improving medical treatment for patients at-risk for POP or having POP. Continued research is needed to identify additional details of currently accepted molecular mechanisms and to identify additional mechanisms that contribute to POP

Temporal Model Adaptation for Person Re-Identification

Person re-identification is an open and challenging problem in computer vision. Majority of the efforts have been spent either to design the best feature representation or to learn the optimal matching metric. Most approaches have neglected the problem of adapting the selected features or the learned model over time. To address such a problem, we propose a temporal model adaptation scheme with human in the loop. We first introduce a similarity-dissimilarity learning method which can be trained in an incremental fashion by means of a stochastic alternating directions methods of multipliers optimization procedure. Then, to achieve temporal adaptation with limited human effort, we exploit a graph-based approach to present the user only the most informative probe-gallery matches that should be used to update the model. Results on three datasets have shown that our approach performs on par or even better than state-of-the-art approaches while reducing the manual pairwise labeling effort by about 80%

Global pattern and controls of soil microbial metabolic quotient

imbalanceThe microbial metabolic quotient (MMQ), microbial respiration per unit of biomass, is a fundamental factor controlling heterotrophic respiration, the largest carbon flux in soils. The magnitude and controls of MMQ at regional scale remain uncertain. We compiled a comprehensive data set of MMQ to investigate the global patterns and controls of MMQ in top 30 cm soils. Published MMQ values, generally measured in laboratory microcosms, were adjusted on ambient soil temperature using long-term (30 yr) average site soil temperature and a Q₁₀ = 2. The area-weighted global average of MMQ_Soil is estimated as 1.8 (1.5-2.2) (95% confidence interval) μmol C·h⁻¹·mmol⁻¹ microbial biomass carbon (MBC) with substantial variations across biomes and between cropland and natural ecosystems. Variation was most closely associated with biological factors, followed by edaphic and meteorological parameters. MMQ_Soil was greatest in sandy clay and sandy clay loam and showed a pH maximum of 6.7 ± 0.1 (mean ± se). At large scale, MMQ_Soil varied with latitude and mean annual temperature (MAT), and was negatively correlated with microbial N:P ratio, supporting growth rate theory. These trends led to large differences in MMQ_Soil between natural ecosystems and cropland. When MMQ was adjusted to 11°C (MMQ_Ref), the global MAT in the top 30 cm of soils, the area-weighted global averages of MMQ_Ref was 1.5 (1.3-1.8) μmol C·mmol MBC⁻¹·h⁻¹. The values, trends, and controls of MMQ_Soil add to our understanding of soil microbial influences on soil carbon cycling and could be used to represent microbial activity in global carbon models

MEIS2C and MEIS2D promote tumor progression via Wnt/β-catenin and hippo/YAP signaling in hepatocellular carcinoma

Abstract Background MEIS2 has been identified as one of the key transcription factors in the gene regulatory network in the development and pathogenesis of human cancers. Our study aims to identify the regulatory mechanisms of MEIS2 in hepatocellular carcinoma (HCC), which could be targeted to develop new therapeutic strategies. Methods The variation of MEIS2 levels were assayed in a cohort of HCC patients. The proliferation, clone-formation, migration, and invasion abilities of HCC cells were measured to analyze the effects of MEIS2C and MEIS2D (MEIS2C/D) knockdown with small hairpin RNAs in vitro and in vivo. Chromatin immunoprecipitation (ChIP) was performed to identify MEIS2 binding site. Immunoprecipitation and immunofluorescence assays were employed to detect proteins regulated by MEIS2. Results The expression of MEIS2C/D was increased in the HCC specimens when compared with the adjacent noncancerous liver (ANL) tissues. Moreover, MEIS2C/D expression negatively correlated with the prognosis of HCC patients. On the other hand, knockdown of MEIS2C/D could inhibit proliferation and diminish migration and invasion of hepatoma cells in vitro and in vivo. Mechanistically, MESI2C activated Wnt/β-catenin pathway in cooperation with Parafibromin (CDC73), while MEIS2D suppressed Hippo pathway by promoting YAP nuclear translocation via miR-1307-3p/LATS1 axis. Notably, CDC73 could directly either interact with MEIS2C/β-catenin or MEIS2D/YAP complex, depending on its tyrosine-phosphorylation status. Conclusions Our studies indicate that MEISC/D promote HCC development via Wnt/β-catenin and Hippo/YAP signaling pathways, highlighting the complex molecular network of MEIS2C/D in HCC pathogenesis. These results suggest that MEISC/D may serve as a potential novel therapeutic target for HCC.https://deepblue.lib.umich.edu/bitstream/2027.42/152244/1/13046_2019_Article_1417.pd

Retinoid-Induced Expression and Activity of an Immediate Early Tumor Suppressor Gene in Vascular Smooth Muscle Cells

Retinoids are used clinically to treat a number of hyper-proliferative disorders and have been shown in experimental animals to attenuate vascular occlusive diseases, presumably through nuclear receptors bound to retinoic acid response elements (RARE) located in target genes. Here, we show that natural or synthetic retinoids rapidly induce mRNA and protein expression of a specific isoform of A-Kinase Anchoring Protein 12 (AKAP12β) in cultured smooth muscle cells (SMC) as well as the intact vessel wall. Expression kinetics and actinomycin D studies indicate Akap12β is a retinoid-induced, immediate-early gene. Akap12β promoter analyses reveal a conserved RARE mildly induced with atRA in a region that exhibits hyper-acetylation. Immunofluorescence microscopy and protein kinase A (PKA) regulatory subunit overlay assays in SMC suggest a physical association between AKAP12β and PKA following retinoid treatment. Consistent with its designation as a tumor suppressor, inducible expression of AKAP12β attenuates SMC growth in vitro. Further, immunohistochemistry studies establish marked decreases in AKAP12 expression in experimentally-injured vessels of mice as well as atheromatous lesions in humans. Collectively, these results demonstrate a novel role for retinoids in the induction of an AKAP tumor suppressor that blocks vascular SMC growth thus providing new molecular insight into how retiniods may exert their anti-proliferative effects in the injured vessel wall