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Zero-Correlation Linear Cryptanalysis of Reduced Round ARIA with Partial-sum and FFT
( Wen-tan Yi ),( Shao-zhen Chen ),( Kuan-yang Wei ) 한국인터넷정보학회 2015 KSII Transactions on Internet and Information Syst Vol.9 No.1
Block cipher ARIA was first proposed by some South Korean experts in 2003, and later, it was established as a Korean Standard block cipher algorithm by Korean Agency for Technology and Standards. In this paper, we focus on the security evaluation of ARIA block cipher against the recent zero-correlation linear cryptanalysis. In addition, Partial-sum technique and FFT (Fast Fourier Transform) technique are used to speed up the cryptanalysis, respectively. We first introduce some 4-round linear approximations of ARIA with zero-correlation, and then present some key-recovery attacks on 6/7-round ARIA-128/256 with the Partial-sum technique and FFT technique. The key-recovery attack with Partial-sum technique on 6-round ARIA-128 needs 2<sup>123.6</sup> known plaintexts (KPs), 2<sup>121</sup>encryptions and 2<sup>90.3</sup> bytes memory, and the attack with FFT technique requires 2<sup>124.1</sup>KPs, 2<sup>121.5</sup> encryptions and 2<sup>90.3</sup> bytes memory. Moreover, applying Partial-sum technique, we can attack 7-round ARIA-256 with 2<sup>124.6</sup>KPs, 2<sup>203.5</sup> encryptions and 2<sup>152</sup> bytes memory and 7-round ARIA-256 employing FFT technique, requires 2<sup>124.7</sup>KPs, 2<sup>209.5</sup> encryptions and 2<sup>152</sup> bytes memory . Our results are the first zero-correlation linear cryptanalysis results on ARIA.
Multidimensional Differential-Linear Cryptanalysis of ARIA Block Cipher
Wen-Tan Yi,Jiongjiong Ren,Shao-Zhen Chen 한국전자통신연구원 2017 ETRI Journal Vol.39 No.1
ARIA is a 128-bit block cipher that has been selected as a Korean encryption standard. Similar to AES, it is robust against differential cryptanalysis and linear cryptanalysis. In this study, we analyze the security of ARIA against differential-linear cryptanalysis. We present five rounds of differential-linear distinguishers for ARIA, which can distinguish five rounds of ARIA from random permutations using only 284.8 chosen plaintexts. Moreover, we develop differential-linear attacks based on six rounds of ARIA-128 and seven rounds of ARIA-256. This is the first multidimensional differential-linear cryptanalysis of ARIA and it has lower data complexity than all previous results. This is a preliminary study and further research may obtain better results in the future.
Lack of Influence of an XRCC3 Gene Polymorphism on Oral Cancer Susceptibility: Meta-analysis
Zhang, En-Jiao,Cui, Zhi-Gang,Xu, Zhong-Fei,Duan, Wei-Yi,Huang, Shao-Hui,Tan, Xue-Xin,Yin, Zhi-Hua,Sun, Chang-Fu,Lu, Li Asian Pacific Journal of Cancer Prevention 2014 Asian Pacific journal of cancer prevention Vol.15 No.23
Background: To systematically summarize the association between the X-ray repair cross complementing 3 (XRCC3) gene polymorphism and oral cancer susceptibility by meta-analysis. Materials and Methods: Databases including PubMed, EMbase, CNKI, VIP and WanFang Data were searched to identify case-control studies concerning the association between an XRCC3 gene polymorphism and the risk of oral cancer from the inception to June 2014. Two reviewers independently screened the literature according to the criteria, extracted the data and assessed the quality. Then meta-analysis was performed using Stata 11.0 software. Results: Seven published case-control studies including 775 patients with oral cancer and 1922 controls were selected. Associations between the rs861539 polymorphism and overall oral cancer risk were not statistically significant in all kinds of comparison models (CT vs CC: OR=0.94, 95%CI=0.74-1.18; TT vs CC: OR=0.94, 95%CI=0.64-1.38; dominant model: OR=0.95, 95%CI=0.76-1.18; recessive model: OR=0.94, 95%CI=0.69-1.29; allele T vs C: OR=0.97, 95%CI=0.84-1.11). In the stratified analysis by ethnicity, no significant associations were found among Asians and Caucasians. On stratification by tumor type, no significant associations were found for cancer and oral premalignant lesions. Conclusions: The XRCC3 gene polymorphism was not found to be associated with the risk of oral cancer. Considering the limited quality of the included case-control studies, more high quality studies with large sample size are needed to verify the above conclusion.