Structural analysis of motion pictures as a symbol system

1968 ◽  
Vol 16 (4) ◽  
pp. 372-402 ◽  
Author(s):  
Calvin Pryluck
1974 ◽  
Vol 28 (1) ◽  
pp. 13-22 ◽  
Author(s):  
Barry Salt

2015 ◽  
Vol 2015 ◽  
pp. 1-8
Author(s):  
Marek Jóźwiak ◽  
Brian Po-Jung Chen ◽  
Bartosz Musielak ◽  
Jacek Fabiszak ◽  
Andrzej Grzegorzewski

This study presents how motion pictures illustrate a person with cerebral palsy (CP), the social impact from the media, and the possibility of cerebral palsy education by using motion pictures. 937 motion pictures were reviewed in this study. With the criteria of nondocumentary movies, possibility of disability classification, and availability, the total number of motion pictures about CP was reduced to 34. The geographical distribution of movie number ever produced is as follows: North America 12, Europe 11, India 2, East Asia 6, and Australia 3. The CP incidences of different motor types in real world and in movies, respectively, are 78–86%, 65% (Spastic); 1.5–6%, 9% (Dyskinetic); 6.5–9%, 26% (Mixed); 3%, 0% (Ataxic); 3-4%, 0% (Hypotonic). The CP incidences of different Gross Motor Function Classification System (GMFCS) levels in real world and in movies, respectively, are 40–51%, 47% (Level I + II); 14–19%, 12% (Level III); 34–41%, 41% (Level IV + V). Comparisons of incidence between the real world and the movies are surprisingly matching. Motion pictures honestly reflect the general public’s point of view to CP patients in our real world. With precise selection and medical professional explanations, motion pictures can play the suitable role making CP understood more clearly.


2018 ◽  
Vol 32 (19) ◽  
pp. 1840038
Author(s):  
Sung-Min Hong ◽  
Hyeon-Seok Kang ◽  
Do-Sik Shim ◽  
Hyeung-Sik Choi ◽  
Joon-Young Kim

This paper describes the dynamics modeling, structural analysis of UCR. First of all, the system configuration of UCR and structural analysis are introduced. After that, 3-DOF equation of UCR is introduced for an analysis of motion performance through a numerical simulation, and applying the LOS method at the UCR for path following. Finally, the performance of the proposed path tracking method is verified through simulation and experiments using small test platform.


PEDIATRICS ◽  
1966 ◽  
Vol 37 (1) ◽  
pp. 177-181

DESCENDED from the kymograph and odograph, the motion picture camera was conceived by E. J. Marey, whose attempts to study the locomotion of animals led first, in 1882, to his fusil photographique, a device making twelve consecutive exposures on a circular glass photographic plate in one second, and then to the chambre chronophotographique, the prototype of the modern cinema camera, in which a several meter strip of light sensitive paper moved intermittently across the lens of a camera at a controlled rate. This device was used for the further study of the locomotion of animals. During approximately the same period and working on a different tack, E. Muybridge, in association with Leland Stanford, the founder of Stanford University, isolated the components of movement in the gait of a race horse by consecutive photographs taken by a row of several cameras. This led to a studio in which similar multiple exposures, the consecutive rate of which could be controlled, were made of moving humans and animals. While the major activity in motion pictures soon became entertainment, the scientific use continued to be centered on that which had intrigued Marey and Muybridge: the analysis of motion. Gilbreth, in 1913, applied the motion picture to the analysis of the components of work to facilitate industrial management; Frisch, in 1926, investigated the communication of bees through examination of cinema sequences of their dance, and Wassink, in 1928, similarly studied abnormalities of walking. As equipment became more sophisticated, the use of high-speed cameras made analysis of more and more complex and rapidly moving processes practicable.


Author(s):  
W. H. Wu ◽  
R. M. Glaeser

Spirillum serpens possesses a surface layer protein which exhibits a regular hexagonal packing of the morphological subunits. A morphological model of the structure of the protein has been proposed at a resolution of about 25 Å, in which the morphological unit might be described as having the appearance of a flared-out, hollow cylinder with six ÅspokesÅ at the flared end. In order to understand the detailed association of the macromolecules, it is necessary to do a high resolution structural analysis. Large, single layered arrays of the surface layer protein have been obtained for this purpose by means of extensive heating in high CaCl2, a procedure derived from that of Buckmire and Murray. Low dose, low temperature electron microscopy has been applied to the large arrays.As a first step, the samples were negatively stained with neutralized phosphotungstic acid, and the specimens were imaged at 40,000 magnification by use of a high resolution cold stage on a JE0L 100B. Low dose images were recorded with exposures of 7-9 electrons/Å2. The micrographs obtained (Fig. 1) were examined by use of optical diffraction (Fig. 2) to tell what areas were especially well ordered.


Author(s):  
E. Loren Buhle ◽  
Pamela Rew ◽  
Ueli Aebi

While DNA-dependent RNA polymerase represents one of the key enzymes involved in transcription and ultimately in gene expression in procaryotic and eucaryotic cells, little progress has been made towards elucidation of its 3-D structure at the molecular level over the past few years. This is mainly because to date no 3-D crystals suitable for X-ray diffraction analysis have been obtained with this rather large (MW ~500 kd) multi-subunit (α2ββ'ζ). As an alternative, we have been trying to form ordered arrays of RNA polymerase from E. coli suitable for structural analysis in the electron microscope combined with image processing. Here we report about helical polymers induced from holoenzyme (α2ββ'ζ) at low ionic strength with 5-7 mM MnCl2 (see Fig. 1a). The presence of the ζ-subunit (MW 86 kd) is required to form these polymers, since the core enzyme (α2ββ') does fail to assemble into such structures under these conditions.


Author(s):  
Paul DeCosta ◽  
Kyugon Cho ◽  
Stephen Shemlon ◽  
Heesung Jun ◽  
Stanley M. Dunn

Introduction: The analysis and interpretation of electron micrographs of cells and tissues, often requires the accurate extraction of structural networks, which either provide immediate 2D or 3D information, or from which the desired information can be inferred. The images of these structures contain lines and/or curves whose orientation, lengths, and intersections characterize the overall network.Some examples exist of studies that have been done in the analysis of networks of natural structures. In, Sebok and Roemer determine the complexity of nerve structures in an EM formed slide. Here the number of nodes that exist in the image describes how dense nerve fibers are in a particular region of the skin. Hildith proposes a network structural analysis algorithm for the automatic classification of chromosome spreads (type, relative size and orientation).


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