Measurement-device-independent QKD with Modified Coherent State

The measurement-device-independent quantum key distribution (MDI-QKD) protocol has been proposed for the purpose of removing the detector side channel attacks. Due to the multi-photon events of coherent states sources, real-life implementations of MDI-QKD protocol must employ decoy states to beat the photon-number-splitting attack. Decoy states for MDI-QKD based on the weak coherent states have been studied recently. In this paper, we propose to perform MDI-QKD protocol with modified coherent states (MCS) sources. We simulate the performance of MDI-QKD with the decoy states based on MCS sources. And our simulation indicates that both the secure-key rate and transmission distance can be improved evidently with MCS sources.The physics behind this improvement is that the probability of multi-photon events of the MCS is lower than that of weak coherent states while at the same time the probability of single-photon is higher

M^2-3DLaneNet: Multi-Modal 3D Lane Detection

Estimating accurate lane lines in 3D space remains challenging due to their sparse and slim nature. In this work, we propose the M^2-3DLaneNet, a Multi-Modal framework for effective 3D lane detection. Aiming at integrating complementary information from multi-sensors, M^2-3DLaneNet first extracts multi-modal features with modal-specific backbones, then fuses them in a unified Bird's-Eye View (BEV) space. Specifically, our method consists of two core components. 1) To achieve accurate 2D-3D mapping, we propose the top-down BEV generation. Within it, a Line-Restricted Deform-Attention (LRDA) module is utilized to effectively enhance image features in a top-down manner, fully capturing the slenderness features of lanes. After that, it casts the 2D pyramidal features into 3D space using depth-aware lifting and generates BEV features through pillarization. 2) We further propose the bottom-up BEV fusion, which aggregates multi-modal features through multi-scale cascaded attention, integrating complementary information from camera and LiDAR sensors. Sufficient experiments demonstrate the effectiveness of M^2-3DLaneNet, which outperforms previous state-of-the-art methods by a large margin, i.e., 12.1% F1-score improvement on OpenLane dataset

Measurement-device-independent quantum key distribution with uncharacterized qubit sources

Measurement-device-independent quantum key distribution (MDIQKD) is proposed to be secure against any possible detection attacks. The security of the original proposal relies on the assumption that the legitimate users can fully characterize the encoding systems including sources. Here, we propose a MDIQKD protocol where we allow uncharacterized encoding systems as long as qubit sources are used. A security proof of the MDIQKD protocol is presented that does not need the knowledge of the encoding states. Simulation results show that the scheme is practical

Haplotype of gene Nedd4 binding protein 2 associated with sporadic nasopharyngeal carcinoma in the Southern Chinese population

<p>Abstract</p> <p>Background</p> <p>Bcl-3 as an oncoprotein is overexpressed in nasopharyngeal carcinoma (NPC). Nedd4 binding protein 2 (N4BP2), which is located in the NPC susceptibility locus, is a Bcl-3 binding protein. This study is aimed to explore the association between N4BP2 genetic polymorphism and the risk of NPC.</p> <p>Methods</p> <p>We performed a hospital-based case-control study, including 531 sporadic NPC and 480 cancer-free control subjects from southern China. PCR-sequencing was carried out on Exons, promoter region and nearby introns of the N4BP2 gene. The expression pattern of N4BP2 and Bcl-3 was also analyzed.</p> <p>Results</p> <p>We observed a statistically significant difference in haplotype blocks ATTA and GTTG between cases and controls. In addition, three novel SNPs were identified, two of which were in exons (loc123-e3l-snp2, position 39868005, A/G, Met171Val; RS17511668-SNP2, position 39926432, G/A, Glu118Lys), and one was in the intron6 (RS794001-SNP1, position 39944127, T/G). Moreover, N4BP2 was at higher levels in a majority of tumor tissues examined, relative to paired normal tissues.</p> <p>Conclusion</p> <p>These data suggest that haplotype blocks ATTA and GTTG of N4BP2 is correlation with the risk of sporadic nasopharyngeal carcinoma in the Southern Chinese population and N4BP2 has a potential role in the development of NPC.</p

Mismatched-basis statistics enable quantum key distribution with uncharacterized qubit sources

In the postprocessing of quantum key distribution, the raw key bits from the mismatched-basis measurements, where two parties use different bases, are normally discarded. Here, we propose a postprocessing method that exploits measurement statistics from mismatched-basis cases, and prove that incorporating these statistics enables uncharacterized qubit sources to be used in the measurement-device-independent quantum key distribution protocol and the Bennett-Brassard 1984 protocol, a case which is otherwise impossible.Comment: Part of this article contains a significant improvement over arXiv:1309.381

The expression of p63 is associated with the differential stage in nasopharyngeal carcinoma and EBV infection

BACKGROUND: Nasopharyngeal carcinoma (NPC) is common among Southern Chinese and the main histology is the undifferentiated carcinoma associated with Epstein-Barr virus (EBV) infection. p63 is a recently proved member of the p53 family based on the structural similarity to p53, but its function in NPC is still unknown. This study was aimed to investigate the association between p63 and NPC. RESULTS: p63 was expressed in 100%(202/202) of nasopharyngeal carcinoma (NPC) tissues but not in 29 nasopharynx inflammation and 17 non-cancerous nasopharyngeal epidermises on a tissue microarray by immunohistostaining. Further investigation suggested that the p63 expression was associated with the differential stage of NPC: p63 strong staining in Keratinizing squamous cell carcinoma, differentiated non-keratinizing NPC and undifferentiated non-keratinizing NPC presented the percentage of 5/8 (62.5%), 43/48 (92.5%) and 50/50 (100%), respectively. A significant difference (p = 0.001) existed between the keratinizing and non-keratinizing groups. No pathogenic mutations were detected in p63 gene in 12 primary NPC tissues and matched peripheral blood lymphocytes (PBL). Half-life measurement study revealed distinct stability of p63 protein in the different cell lines, especially between the carcinoma cell lines with EBV infection and the non-cancerous cell lines. The results of immunoprecipitation suggested a direct interaction between Epstein-Barr virus nuclear antigen 5 (EBNA-5) and p63 protein in NPC, and this binding would increase the stability of p63. CONCLUSION: Our data suggested p63 might be used as an adjunct diagnostic marker of NPC and contributed a new way to understand the contribution of the EBV in the pathogenesis of NPC