Digital cinema--an environment for multi-threaded stories

Thesis (M.S.)--Massachusetts Institute of Technology, Program in Media Arts & Sciences, 1993.Includes bibliographical references (leaves 85-86).by Mark David Halliday.M.S

The therapeutic value of formic acid in diphtheria in i. cardiac failure; ii. paralysis; iii. albuminuria

It is difficult not to conclude that results, such as these, are sufficiently successful as to at least warrant a thorough and prolonged trial.It may be urged that the influence of antitoxin has not been given the prominence due to it, but has purposely been disregarded as being in the same proportion for the Control Cases.Treatment would, therefore, appear to resolve itself into:-1. Adequate and early doses of Antitoxin;2. Rest in proportion to the severity of the case;3. Gradual and proportionate stimulation by Non -blood- pressure raising drugs;4. The use of Formic Acid and the Formates;and until proof positive negatives it, that, with such results, a thorough trial of such lines of treatment must be made at the expense of the older treatment which relied for stimulation solely on an increase of blood pressure, while it would seem to be the case that Formic Acid and the Formates, by their influence on every complication of importance in diphtheria, render them, in that disease, drugs of the greatest importance

Application of point-process system identification techniques to complex physiological systems

This thesis is concerned with the application of system identification techniques to the analysis of complex physiological systems. The techniques are applied to neuronal spike-train data obtained from elements of the neuromuscular system. A brief description of the neuromuscular system is given in chapter 1, along with a more detailed discussion of the muscle spindle, which is the component of the neuromuscular system which this study deals with. In addition, some possibilities for system identification studies of the muscle spindle are discussed. The identification procedure is based on statistical methods for the treatment of point-process data. The point-process representation of a spike-train is introduced in chapter 2 with definitions of time and frequency domain point-process parameters. Estimates for these parameters are given, along with expressions for their asymptotic distributions. The linear point-process system identification model is introduced and estimates are described for the model parameters in terms of the previously defined point-process parameters. These point-process and linear parameter estimates are applied to muscle spindle spike-train data. In the analysis of a single spike-train certain important features only show up in the frequency domain, and for input and output spike-trains a linear transfer function type description is constructed in the frequency domain. The mathematical model of this transfer function is used as the basis for an analogue computer simulation of a subsystem of the muscle spindle. This consists of a linear first order filter followed by an encoder which generates output spikes. Data logged from the simulation is processed in the same manner as experimental data, and the effect of varying the simulation parameters on the linear model estimates is looked at. It is shown that in general the linear model description reflects the properties of the linear filter in the simulation, and varying the simulation parameters can be used to accurately match results from simulated data with those obtained from real data. Chapter 3 compares the point-process approach with a more conventional filtering and sampled data approach to estimate power spectra. The filtering of spike-trains with broad band spectra is investigated, and this shows up a pitfall in the choice of filter cut-off frequency. It is concluded that the point-process approach is preferable due to shorter computational times, and the well documented statistical propeties of the point-process estimates. The application of the point-process techniques described in chapter 2 to the analysis of more general spike-train data is considered in chapter 4. Three techniques for measuring the degree of coupling between two spike-trains are compared, and the point-process frequency domain measure is found to be the most sensitive. This measure is also applied to a data set containing a strong single periodicity, and the ability to detect coupling at a single harmonic is demonstrated. The analysis of coupling between spike-trains in the frequency domain is extended to deal with multiple spike-trains, and the ability to distinguish genuine coupling from the effect of a common input is shown to be a powerful tool which can be used to investigate communications pathways in neural systems. Finally, one special feature of the muscle spindle response to a spike-train input is analysed using the simulation. It is demonstrated that the point-process approach can produce results about a particular phenomenon from a single experiment much more rapidly than using a repetitive trial and error approach. Chapter 5 considers the extension of the linear point-process identification model introduced in chapter 2. Higher order time and frequency domain point-process parameters are defined and estimates given. In the time domain, a new technique for rapidly generating higher order time domain parameters is developed. The quadratic point-process model is introduced and solutions for its parameters given. These estimates are applied to muscl

Single-trial multiwavelet coherence in application to neurophysiological time series

A method of single-trial coherence analysis is presented, through the application of continuous muldwavelets. Multiwavelets allow the construction of spectra and bivariate statistics such as coherence within single trials. Spectral estimates are made consistent through optimal time-frequency localization and smoothing. The use of multiwavelets is considered along with an alternative single-trial method prevalent in the literature, with the focus being on statistical, interpretive and computational aspects. The multiwavelet approach is shown to possess many desirable properties, including optimal conditioning, statistical descriptions and computational efficiency. The methods. are then applied to bivariate surrogate and neurophysiological data for calibration and comparative study. Neurophysiological data were recorded intracellularly from two spinal motoneurones innervating the posterior,biceps muscle during fictive locomotion in the decerebrated cat

Apolipoprotein-E forms dimers in human frontal cortex and hippocampus

<p>Abstract</p> <p>Background</p> <p>Apolipoprotein-E (apoE) plays important roles in neurobiology and the apoE4 isoform increases risk for Alzheimer's disease (AD). ApoE3 and apoE2 are known to form disulphide-linked dimers in plasma and cerebrospinal fluid whereas apoE4 cannot form these dimers as it lacks a cysteine residue. Previous in vitro research indicates dimerisation of apoE3 has a significant impact on its functions related to cholesterol homeostasis and amyloid-beta peptide degradation. The possible occurrence of apoE dimers in cortical tissues has not been examined and was therefore assessed. Human frontal cortex and hippocampus from control and AD post-mortem samples were homogenised and analysed for apoE by western blotting under both reducing and non-reducing conditions.</p> <p>Results</p> <p>In apoE3 homozygous samples, ~12% of apoE was present as a homodimer and ~2% was detected as a 43 kDa heterodimer. The level of dimerisation was not significantly different when control and AD samples were compared. As expected, these dimerised forms of apoE were not detected in apoE4 homozygous samples but were detected in apoE3/4 heterozygotes at a level approximately 60% lower than seen in the apoE3 homozygous samples. Similar apoE3 dimers were also detected in lysates of SK-N-SH neuroblastoma cells and in freshly prepared rabbit brain homogenates. The addition of the thiol trapping agent, iodoacetamide, to block reactive thiols during both human and rabbit brain sample homogenisation and processing did not reduce the amount of apoE homodimer recovered. These data indicate that the apoE dimers we detected in the human brain are not likely to be post-mortem artefacts.</p> <p>Conclusion</p> <p>The identification of disulphide-linked apoE dimers in human cortical and hippocampal tissues represents a distinct structural difference between the apoE3 and apoE4 isoforms that may have functional consequences.</p

A Review of Very Large Vapor Cloud Explosions

Presentatio