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。

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

THE DESIGN AND ANALYSIS OF EXPERIMENTS. By Oscar Kempthorne. New York, John Wiley and Sons, Inc., 1952. 631 pp. $8.50. This book by a teacher of statistics (as well as a consultant for \"experimenters\") is a comprehensive study of the philosophical background for the statistical design of experiment. It is necessary to have some facility with algebraic notation and manipulation to be able to use the volume intelligently. The problems are presented from the theoretical point of view, without such practical examples as would be helpful for those not acquainted with mathematics. The mathematical justification for the techniques is given. As a somewhat advanced treatment of the design and analysis of experiments, this volume will be interesting and helpful for many who approach statistics theoretically as well as practically. With emphasis on the \"why,\" and with description given broadly, the author relates the subject matter to the general theory of statistics and to the general problem of experimental inference. MARGARET J. ROBERTSON

The Design and Analysis of Experiments

Co-Planar Stereotaxic Atlas of the Human Brain—3-Dimensional Proportional System: An Approach to Cerebral Imaging, J. Talairach, P. Tournoux. Georg Thieme Verlag, New York (1988), 122 pp., 130 figs. DM 268

I have developed "tennis elbow" from lugging this book around the past four weeks, but it is worth the pain, the effort, and the aspirin. It is also worth the (relatively speaking) bargain price. Including appendixes, this book contains 894 pages of text. The entire panorama of the neural sciences is surveyed and examined, and it is comprehensive in its scope, from genomes to social behaviors. The editors explicitly state that the book is designed as "an introductory text for students of biology, behavior, and medicine," but it is hard to imagine any audience, interested in any fragment of neuroscience at any level of sophistication, that would not enjoy this book. The editors have done a masterful job of weaving together the biologic, the behavioral, and the clinical sciences into a single tapestry in which everyone from the molecular biologist to the practicing psychiatrist can find and appreciate his or

Principles of Neural Science

Brains, it has recently been argued, are essentially prediction machines. They are bundles of cells that support perception and action by constantly attempting to match incoming sensory inputs with top-down expectations or predictions. This is achieved using a hierarchical generative model that aims to minimize prediction error within a bidirectional cascade of cortical processing. Such accounts offer a unifying model of perception and action, illuminate the functional role of attention, and may neatly capture the special contribution of cortical processing to adaptive success. This target article critically examines this "hierarchical prediction machine" approach, concluding that it offers the best clue yet to the shape of a unified science of mind and action. Sections 1 and 2 lay out the key elements and implications of the approach. Section 3 explores a variety of pitfalls and challenges, spanning the evidential, the methodological, and the more properly conceptual. The paper ends (sections 4 and 5) by asking how such approaches might impact our more general vision of mind, experience, and agency.

/pdf/whatever-next-predictive-brains-situated-agents-and-the-epj56cs868.pdf

Whatever next? Predictive brains, situated agents, and the future of cognitive science

Previous work investigating whether biological motion is supported by local second-order motion has been contradictory, with different groups finding either a difference or no difference in performance compared to that obtained with first-order stimuli. Here we show psychophysically, using randomized-polarity and contrast-modulated stimuli, that detection of second-order biological motion walkers is worse for stimuli defined by second-order cues, but this difference is explained by a difference in visibility of the local motion in the stimuli. By mixing first-order and second-order dots within the same stimulus, we show that, when the two types of dot are equally visible, first-order noise dots can mask a second-order walker, and vice-versa. We also show that direction-discrimination of normal, inverted and scrambled walkers follow the same pattern for second-order as that obtained with first-order stimuli. These results are consistent with biological motion being processed by a mechanism that is cue-invariant.

/pdf/biological-motion-perception-is-cue-invariant-ecqal0hu41.pdf

Biological motion perception is cue-invariant

Phase information is a fundamental aspect of visual stimuli. However, the nature of the binocular combination of stimuli defined by modulations in contrast, so-called second-order stimuli, is presently not clear. To address this issue, we measured binocular combination for first- (luminance modulated) and second-order (contrast modulated) stimuli using a binocular phase combination paradigm in seven normal adults. We found that the binocular perceived phase of second-order gratings depends on the interocular signal ratio as has been previously shown for their first order counterparts; the interocular signal ratios when the two eyes were balanced was close to 1 in both first- and second-order phase combinations. However, second-order combination is more linear than previously found for first-order combination. Furthermore, binocular combination of second-order stimuli was similar regardless of whether the carriers in the two eyes were correlated, anti-correlated, or uncorrelated. This suggests that, in normal adults, the binocular phase combination of second-order stimuli occurs after the monocular extracting of the second-order modulations. The sensory balance associated with this second-order combination can be obtained from binocular phase combination measurements.

/pdf/binocular-combination-of-second-order-stimuli-4xc93el4pf.pdf

Binocular combination of second-order stimuli.

Spatial scale invariance of the amblyopic global motion deficit

The internal noise present in a linear system can be quantified by the equivalent noise method. By measuring the effect that applying external noise to the system’s input has on its output one can estimate the variance of this internal noise. By applying this simple “linear amplifier” model to the human visual system, one can entirely explain an observer’s detection performance by a combination of the internal noise variance and their efficiency relative to an ideal observer. Studies using this method rely on two crucial factors: firstly that the external noise in their stimuli behaves like the visual system’s internal noise in the dimension of interest, and secondly that the assumptions underlying their model are correct (e.g. linearity). Here we explore the effects of these two factors while applying the equivalent noise method to investigate the contrast sensitivity function (CSF). We compare the results at 0.5 and 6 c/deg from the equivalent noise method against those we would expect based on pedestal masking data collected from the same observers. We find that the loss of sensitivity with increasing spatial frequency results from changes in the saturation constant of the gain control nonlinearity, and that this only masquerades as a change in internal noise under the equivalent noise method. Part of the effect we find can be attributed to the optical transfer function of the eye. The remainder can be explained by either changes in effective input gain, divisive suppression, or a combination of the two. Given these effects the efficiency of our observers approaches the ideal level. We show the importance of considering these factors in equivalent noise studies.

/pdf/what-do-contrast-threshold-equivalent-noise-studies-actually-3uxdtxd393.pdf

What Do Contrast Threshold Equivalent Noise Studies Actually Measure? Noise vs. Nonlinearity in Different Masking Paradigms.

The detection of a luminance-defined Gabor is improved by two high contrast, aligned, flanking Gabors, an effect termed collinear facilitation. We investigate whether this facilitation also occurs for isoluminant chromatic stimuli, and whether it can occur for chromatic targets with luminance flanks and vice versa. We measured collinear facilitation for Gabor stimuli (0.75 cpd, 1 octave bandwidth) of three different contrast types: achromatic, red-green that isolates the L/M-cone opponent mechanism, and blue-yellow that isolates the S-cone opponent mechanism. Three conditions were investigated: (1) target and flanks all of the same contrast type and spatial phase; (2) target and flanks of the same contrast type but opposite phases (0- and 180-); and (3) target and flanks of different contrast types (chromatic with achromatic contrast) and two opposite phase combinations. We find that a similar degree of collinear facilitation occurs for the isoluminant chromatic stimuli as for the achromatic stimuli, and all exhibit phase dependency. Facilitation did not occur, however, between chromatic and achromatic target and flanking stimuli. This suggests that at the level of collinear facilitation, the chromatic and the achromatic postreceptoral mechanisms have their own spatial interactions that are segregated from one another.

/pdf/collinear-facilitation-in-color-vision-1oyxtcxkyq.pdf

Robert F. Hess

Papers

Biological motion perception is cue-invariant

Binocular combination of second-order stimuli.

Spatial scale invariance of the amblyopic global motion deficit

What Do Contrast Threshold Equivalent Noise Studies Actually Measure? Noise vs. Nonlinearity in Different Masking Paradigms.

Collinear facilitation in color vision.