Possible open-charmed pentaquark molecule Ωc(3188)\Omega_c(3188) --- the DΞD \Xi bound state --- in the Bethe-Salpeter formalism

We study the $S$-wave $D\Xi$ bound state in the Bethe-Salpeter formalism in the ladder and instantaneous approximations. With the kernel generated by the hadronic effective Lagrangian, two open-charmed bound states, which quantum numbers are $I=0$, $J^P=(\frac{1}{2})^-$ and $I=1$, $J^P=(\frac{1}{2})^-$, respectively, are predicted as new candidates of hadronic pentaquark molecules in our formalism. If existing, they could contribute to the broad 3188 eV structure near the five new narrow $\Omega_c$ states observed recently by the LHCb Collaboration.Comment: 8 pages, 4 figures, accepted by Eur. Phys. J.

Development of Murine Hepatic NK Cells during Ontogeny: Comparison with Spleen NK Cells

The phenotype of developing liver NK cells (CD3−NK1.1+) was investigated during mouse ontogeny comparing with spleen NK cells. The highest percentage of hepatic CD27−CD11b− NK cells occurred at the fetal stage. After birth, the percentage of CD27−CD11b−NK cells in both the liver and spleen gradually decreased to their lowest level at 6 weeks. More CD27+CD11b−NK cells were detected in the liver than that in spleen from week 1 to 6. Expression of NKG2A on liver NK cells was decreased but still much higher than that of spleen NK cells after 1 week. The NKG2D expression on liver NK cells increased to its highest level and was significantly higher than on spleen NK cells till 4 weeks. During mouse ontogeny, weaker expression of NKp46 and CD2 and stronger expression of CD69, CD11c, 2B4, and CD73 were observed on liver NK cells. Furthermore, neonatal liver NK cells express higher IFN-γ and perforin than adult .These results suggest that the maturation process of NK cells is unique in the livers, and liver microenvironments might play critical roles to keep NK cells in an immature status

The peroxisome proliferator-activated receptor delta +294T > C polymorphism and alcohol consumption on serum lipid levels

<p>Abstract</p> <p>Background</p> <p>The single nucleotide polymorphism (SNP) of peroxisome proliferator-activated receptor delta (<it>PPARD</it>) gene affects serum lipid profiles, but to what extent alcohol consumption interferes with this association remains unknown. The present study was undertaken to compare the association of <it>PPARD </it>+294T > C (rs2016520) polymorphism and serum lipid levels in the nondrinkers and drinkers.</p> <p>Methods</p> <p>A total of 685 unrelated nondrinkers and 497 drinkers aged 15-82 were randomly selected from our previous stratified randomized cluster samples. Genotyping of the <it>PPARD </it>+294T > C was performed by polymerase chain reaction and restriction fragment length polymorphism. Interactions of the <it>PPARD </it>+294T > C genotypes and alcohol consumption on serum lipid levels were detected by using a factorial regression analysis after controlling for potential confounders.</p> <p>Results</p> <p>The levels of triglyceride (TG), high-density lipoprotein cholesterol (HDL-C), apolipoprotein (Apo) A1, and the ratio of ApoA1 to ApoB were higher in drinkers than in nondrinkers (<it>P </it>< 0.05-0.001). There were no significant differences in the levels of total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C) and ApoB between the two groups (<it>P </it>> 0.05 for all). The frequencies of TT, TC and CC genotypes were 56.0%, 36.4% and 7.6% in nondrinkers, and 57.2%, 38.0% and 4.8% in drinkers (<it>P </it>> 0.05); respectively. The frequencies of T and C alleles were 74.2% and 25.8% in nondrinkers, and 76.2% and 23.8% in drinkers (<it>P </it>> 0.05); respectively. There was also no significant difference in the genotypic and allelic frequencies between males and females in both groups (<it>P </it>> 0.05 for all). The levels of TC in nondrinkers were different among the three genotypes (<it>P </it>= 0.01), the C allele carriers had higher serum TC levels than the C allele noncarriers. The levels of all seven lipid traits in drinkers were not different among the three genotypes (P > 0.05 for all). The interactions of <it>PPARD </it>+294T > C genotypes and alcohol consumption on serum lipid levels were not detected in the drinkers (<it>P ></it>0.05 for all). Multiple linear regression analysis showed that serum TC, HDL-C, LDL-C, ApoA1, and ApoB levels were correlated with genotypes in drinkers but not in nondrinkers (<it>P </it>< 0.05-0.01).</p> <p>Conclusions</p> <p>These results suggest that the great majority of our study populations are beneficial from alcohol consumption. But there is no interaction between the <it>PPARD </it>+294T > C genotypes and alcohol consumption on serum lipid levels in the drinkers.</p

Detecting and removing visual distractors for video aesthetic enhancement

Personal videos often contain visual distractors, which are objects that are accidentally captured that can distract viewers from focusing on the main subjects. We propose a method to automatically detect and localize these distractors through learning from a manually labeled dataset. To achieve spatially and temporally coherent detection, we propose extracting features at the Temporal-Superpixel (TSP) level using a traditional SVM-based learning framework. We also experiment with end-to-end learning using Convolutional Neural Networks (CNNs), which achieves slightly higher performance than other methods. The classification result is further refined in a post-processing step based on graph-cut optimization. Experimental results show that our method achieves an accuracy of 81% and a recall of 86%. We demonstrate several ways of removing the detected distractors to improve the video quality, including video hole filling; video frame replacement; and camera path re-planning. The user study results show that our method can significantly improve the aesthetic quality of videos