Three-dimensional electron microscopic studies of the transitional oligodendrocyte associated with the initial stage of myelination in developing rat hippocampal fimbria

2004 ◽  
Vol 148 (2) ◽  
pp. 207-212 ◽  
Author(s):  
Tokiko Ogawa ◽  
Mitsuru Suzuki ◽  
Koichi Matoh ◽  
Katsuya Sasaki
Keyword(s):  
Three Dimensional ◽  
Dimensional Electron ◽  
Electron Microscopic ◽  
Initial Stage ◽  
Microscopic Studies ◽  
Developing Rat

The effects of an antiserum to the contractile proteins of the heart on the developing rat embryo

Development ◽  
1971 ◽  
Vol 25 (2) ◽  
pp. 203-212
Author(s):  
Colin L. Berry
Keyword(s):  
Rat Heart ◽  
Contractile Proteins ◽  
Degenerative Changes ◽  
Foetal Death ◽  
Rat Embryo ◽  
Electron Microscopic ◽  
Microscopic Studies ◽  
Specific Reactivity ◽  
Developing Rat ◽  
Isolated Rat

An antiserum with specific reactivity against the contractile proteins of the rat heart has been raised in the rabbit. Fractions of the serum have been shown to enter the isolated rat embryo by electron-microscopic studies with ferritin, where they bind to the myocardium, producing degenerative changes. Both IgG and IgM fractions are toxic, producing foetal death in a large proportion of explanted embryos.

A Relatively Inexpensive Microprocessor-Linked Digital Plamimeter for Electron Microscopic Morphometry

1981 ◽  
Vol 39 ◽  
pp. 266-269
Author(s):  
Lee D. Peachey
Keyword(s):  
Theoretical Basis ◽  
Structural Parameters ◽  
Three Dimensional ◽  
Structural Data ◽  
Large Set ◽  
Dimensional Electron ◽  
Electron Microscopic ◽  
Morphometric Methods ◽  
Electron Microscopic Morphometry ◽  
Separate Step

Stereology provides a theoretical basis for powerful morphometric methods for the estimation of three-dimensional structural parameters from two-dimensional electron micrographs of cells and tissues. These methods assume at the start that one has a sufficiently large set of micrographs containing valid structural data. The task of obtaining from these micrographs the large quantity of data needed to get statistically valid results has been eased in two general ways. Sampling of data in the micrograph can be done rapidly by point and intersection counting methods. An alternate method, planimetry, obtains all the data in the micrograph, but in general is more time-consuming than point and intersection counting. Some of the relative inefficiency of planimetry is compensated when a digital planimeter is coupled with a computer. Areas and lengths can be computed simultaneously as fast as profiles are traced. Furthermore, rapid and numerically accurate compilation and statistical analysis of the data can be done automatically as the planimetry is done, not as a separate step after the data have been obtained.

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