Double-blind photoarray administration as a safeguard against investigator bias.

[Correction Notice: An erratum for this article was reported in Vol 85(2) of Journal of Applied Psychology (see record 2007-17253-001). On page 947, the graphs within Figure 1 were incorrectly labeled. The corrected figure appears in this erratum.] This experiment examined whether a photoarray administrator's knowledge of a suspect's identity increased false identification rates. Fifty participant–administrators (PAs) presented 50 participant–witnesses (PWs) two perpetrator-absent photoarrays following a live staged crime involving two perpetrators. For one photoarray per trial, the experimenter revealed the suspect's identity to the PA. Each PA presented the photoarrays sequentially or simultaneously in the presence or absence of an observer. When the observer was present, PA knowledge of the suspect's identity had a biasing effect in sequential photoarrays only. This pattern did not emerge when the observer was absent. The experimental manipulations did not affect PAs' and PWs' ratings of photoarray fairness or PWs' ratings of pressure to make an identification. These data suggest that only administrators who are blind to the suspect's identity should present sequential photoarrays. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Minimum chemical requirements for adhesin activity of the acid-stable part of Candida albicans cell wall phosphomannoprotein complex

This study was conducted to define adhesive characteristics of the acid-stable moiety of the Candida albicans phosphomannoprotein complex (PMPC) on adherence of this fungus to marginal zone macrophages of the mouse spleen. Complete digestion of the acid-stable moiety (Fr.IIS) of the C. albicans PMPC with an alpha-mannosidase or hydrolysis with 0.6 N sulfuric acid destroyed adhesin activity, as determined by the inability of the soluble digests to inhibit yeast cell adherence to the splenic marginal zone. Fr.IIS adhesin activity was decreased following digestion with an alpha-1,2-specific mannosidase. Oligomannosyls consisting of one to six mannose units, which were isolated from the acid-stable part of the PMPC, did not inhibit yeast cell binding and thus do not function alone as adhesin sites in the PMPC. To gain more insight into the minimum requirements for adhesin activity, PMPCs were isolated from a Saccharomyces cerevisiae wild-type strain and from mutant strains mnn1, mnn2, and mnn4; the PMPCs were designated scwt/Fr.II, scmn1/Fr.II, scmn2/Fr.II, and scmn4/Fr.II, respectively. S. cerevisiae scmn2/Fr.II lacks oligomannosyl side chain branches from the outer core mannan, and scmn2/Fr.II was the only PMPC without adhesin activity. S. cerevisiae scwt/Fr.II, scmn1/Fr.II, and scmn4/Fr.II showed adhesin activities less than that of C. albicans Fr.II. These three S. cerevisiae PMPCs are generally similar to Fr. IIS, except that the S. cerevisiae structure has fewer and shorter side chains. Immunofluorescence microscopy show that the acid-stable part of the PMPC is displayed homogeneously on the C. albicans yeast cell surface, which would be expected for a surface adhesin. Our results indicate that both the mannan core and the oligomannosyl side chains are responsible for the adhesin activity of the acid-stable part of the PMPC.     

Identification of residues in the cysteine-rich domain of Raf-1 that control Ras binding and Raf-1 activity

We have identified mutations in Raf-1 that increase binding to Ras. The mutations were identified making use of three mutant forms of Ras that have reduced Raf-1 binding (Winkler, D. G., Johnson, J. C., Cooper, J. A., and Vojtek, A. B. (1997) J. Biol. Chem. 272, 24402-24409). One mutation in Raf-1, N64L, suppresses the Ras mutant R41Q but not other Ras mutants, suggesting that this mutation structurally complements the Ras R41Q mutation. Missense substitutions of residues 143 and 144 in the Raf-1 cysteine-rich domain were isolated multiple times. These Raf-1 mutants, R143Q, R143W, and K144E, were general suppressors of three different Ras mutants and had increased interaction with non-mutant Ras. Each was slightly activated relative to wild-type Raf-1 in a transformation assay. In addition, two mutants, R143W and K144E, were active when tested for induction of germinal vesicle breakdown in Xenopus oocytes. Interestingly, all three cysteine-rich domain mutations reduced the ability of the Raf-1 N-terminal regulatory region to inhibit Xenopus oocyte germinal vesicle breakdown induced by the C-terminal catalytic region of Raf-1. We propose that a direct or indirect regulatory interaction between the N- and C-terminal regions of Raf-1 is reduced by the R143W, R143Q, and K144E mutations, thereby increasing access to the Ras-binding regions of Raf-1 and increasing Raf-1 activity.     

Evaluating robustness in a two layer simulated robot architecture

Many two layer robot architectures have been proposed and implemented. While justification for the design can be well argued, how does one know it is really a good idea? In this paper, one describes a two layer architecture (reinforcement learning in the bottom layer and POMDP planning at the top) for a simulated robot and summarize a set of three experiments in which one evaluated the design. To address the many difficulties of evaluating robot architectures, one advocates an experimental approach in which design criteria are elucidated and then form the basis for the evaluation experiments. In our case, one tests the implementation for its reliability and generalization (our design criteria) by comparing our architecture to one in which a key component is substituted; in these experiments, one demonstrates significant performance gains on the design criteria for our architecture.     

Biomarkers for cardiovascular risk assessment in autoimmune diseases

Autoimmune diseases, such as antiphospholipid syndrome, systemic lupus erythematosus, and rheumatoid arthritis, are characterized by a high prevalence of cardiovascular (CV) disease (CVD), which constitutes the leading causes of morbidity and mortality among such patients. Although such effects are partly explained by a higher prevalence of traditional CV risk factors, many studies indicate that such factors do not fully explain the enhanced CV risk in these patients. In addition, risk stratification algorithms based upon traditional CV risk factors are not as predictive in autoimmune diseases as in the general population. For these reasons, the timely and accurate assessment of CV risk in these high-risk populations still remains an unmet clinical need. An enhanced contribution of different inflammatory components of the immune response, as well as autoimmune elements (e.g. autoantibodies, autoantigens, and cellular response), has been proposed to underlie the incremental CV risk observed in these populations. Recent advances in proteomic tools have contributed to the discovery of proteins involved in CVDs, including some that may be suitable to be used as biological markers. In this review we summarize the main markers in the field of CVDs associated with autoimmunity, as well as the recent advances in proteomic technology and their application for biomarker discovery in autoimmune disease.     

Virtual Human versus Human Administration of Photographic Lineups

One solution to mistaken identification by a crime's victims and eyewitnesses is to use a virtual officer to conduct identification procedures. Results from a study comparing a virtual officer with a live human investigator indicate that the virtual officer performs comparably to the human in terms of identification accuracy, emotional affect, and ease of use.     

Effect of the hydroxyl content and molecular weight of polyvinyl butyral on tape properties

Despite the desire to replace organics with water in tape casting systems, thick films often use solvent in order to speed up drying rates. Polyvinyl butyral having hydroxyl contents ranging between 11 and 20% and molecular weights between 40,000 and 120,000 g/mol was plasticized with butyl benzyl phthalate at solids contents between 62 and 75 vol.% La_0.5Sr_0.5CoO₃ once the toluene/ethanol solvent was evaporated. High-hydroxyl content was more important than high molecular weight in increasing the Young's modulus, yield strength, and tensile strength of the tapes at room temperature. Annealing tapes at low temperatures (65 °C) for short times (10 min) relaxed stresses and tended to equalize modulus, strength, and ductility. Low hydroxyl content and low molecular weight enhanced particle packing, which resulted in cracking as tape thickness increased from 0.2 mm to 0.7 mm at higher solids contents. Crack-free tapes were made at all solids contents when the hydroxyl content was greater than 18%. Lower molecular weight at high-hydroxyl content, along with high solids content, was important for minimizing the amount of solvent used.