Chris J. Mitchell

Bio: Chris J. Mitchell is an academic researcher from Royal Holloway, University of London. The author has contributed to research in topics: Authentication & Cryptography. The author has an hindex of 48, co-authored 397 publications receiving 10982 citations. Previous affiliations of Chris J. Mitchell include Johns Hopkins University & University of Portland.

Key Recovery and Forgery Attacks on the MacDES MAC Algorithm

Abstract: We describe a series of new attacks on a CBC-MAC algorithm due to Knudsen and Preneel including two key recovery attacks and a forgery attack. Unlike previous attacks, these techniques will work when the MAC calculation involves prefixing the data to be MACed with a 'length block'. These attack methods provide new (tighter) upper bounds on the level of security offered by the MacDES technique.

On the security of some password-based key agreement schemes

Abstract: In this paper we show that three potential security vulnerabilities exist in the strong password-only authenticated key exchange scheme due to Jablon. Two standardised schemes based on Jablon’s scheme, namely the first password-based key agreement mechanism in ISO/IEC FCD 11770-4 and the scheme BPKAS-SPEKE in IEEE P1363.2 also suffer from some of these security vulnerabilities. We further show that other password-based key agreement mechanisms, including those in ISO/IEC FCD 11770-4 and IEEE P1363.2, also suffer from these security vulnerabilities. Finally, we propose means to remove these security vulnerabilities.

Do Reaction Times in the Perruchet Effect Reflect Variations in the Strength of an Associative Link

Abstract: In 3 experiments, we examined Perruchet, Cleeremans, and Destrebecqz's (2006) double dissociation of cued reaction time (RT) and target expectancy. In this design, participants receive a tone on every trial and are required to respond as quickly as possible to a square presented on 50% of those trials (a partial reinforcement schedule). Participants are faster to respond to the square following many recent tone-square pairings and slower to respond following many tone-alone presentations. Of importance, expectancy of the square is highest when performance on the RT task is poorest-following many tone-alone trials. This finding suggests that RT performance is determined by the strength of a tone-square link and that this link is the product of a non-expectancy-based learning mechanism. The present experiments, however, provide evidence that the speeded RTs are not the consequence of the strengthening and weakening of a tone-square link. Thus, the RT Perruchet effect does not provide evidence for a non-expectancy-based link-formation mechanism.

I and i

Abstract: There is, I think, something ethereal about i —the square root of minus one. I remember first hearing about it at school. It seemed an odd beast at that time—an intruder hovering on the edge of reality. Usually familiarity dulls this sense of the bizarre, but in the case of i it was the reverse: over the years the sense of its surreal nature intensified. It seemed that it was impossible to write mathematics that described the real world in …

疟原虫var基因转换速率变化导致抗原变异[英]／Paul H, Robert P, Christodoulou Z, et al//Proc Natl Acad Sci U S A

Abstract: 抗原变异可使得多种致病微生物易于逃避宿主免疫应答。表达在感染红细胞表面的恶性疟原虫红细胞表面蛋白1（PfPMP1）与感染红细胞、内皮细胞、树突状细胞以及胎盘的单个或多个受体作用，在黏附及免疫逃避中起关键的作用。每个单倍体基因组var基因家族编码约60种成员，通过启动转录不同的var基因变异体为抗原变异提供了分子基础。

Handbook of Applied Cryptography

Abstract: From the Publisher: A valuable reference for the novice as well as for the expert who needs a wider scope of coverage within the area of cryptography, this book provides easy and rapid access of information and includes more than 200 algorithms and protocols; more than 200 tables and figures; more than 1,000 numbered definitions, facts, examples, notes, and remarks; and over 1,250 significant references, including brief comments on each paper.

Tissue-based map of the human proteome

Abstract: Resolving the molecular details of proteome variation in the different tissues and organs of the human body will greatly increase our knowledge of human biology and disease. Here, we present a map of the human tissue proteome based on an integrated omics approach that involves quantitative transcriptomics at the tissue and organ level, combined with tissue microarray-based immunohistochemistry, to achieve spatial localization of proteins down to the single-cell level. Our tissue-based analysis detected more than 90% of the putative protein-coding genes. We used this approach to explore the human secretome, the membrane proteome, the druggable proteome, the cancer proteome, and the metabolic functions in 32 different tissues and organs. All the data are integrated in an interactive Web-based database that allows exploration of individual proteins, as well as navigation of global expression patterns, in all major tissues and organs in the human body.

Differential Power Analysis

Abstract: Cryptosystem designers frequently assume that secrets will be manipulated in closed, reliable computing environments. Unfortunately, actual computers and microchips leak information about the operations they process. This paper examines specific methods for analyzing power consumption measurements to find secret keys from tamper resistant devices. We also discuss approaches for building cryptosystems that can operate securely in existing hardware that leaks information.