Clinical and Molecular Analysis of Stargardt Disease With Preserved Foveal Structure and Function

2013 ◽  
Vol 156 (3) ◽  
pp. 487-501.e1 ◽  
Author(s):  
Kaoru Fujinami ◽  
Panagiotis I. Sergouniotis ◽  
Alice E. Davidson ◽  
Genevieve Wright ◽  
Ravinder K. Chana ◽  
...  
Physiology ◽  
1988 ◽  
Vol 3 (5) ◽  
pp. 206-211
Author(s):  
PG FitzGerald

Gap junctions are nearly ubiquitous structures that ionically and metabolically couple adjacent cells. Molecular analysis of junctional proteins is establishing the presence of families of unique but homologous junctional proteins, opening the door to an explanation of tissue specificity in gap junction structure and function.


2003 ◽  
Vol 26 (12) ◽  
pp. 937-943 ◽  
Author(s):  
Shin-ichiro MIURA ◽  
Keijiro SAKU ◽  
Sadashiva S KARNIK

2001 ◽  
Vol 65 (3) ◽  
pp. 951-960 ◽  
Author(s):  
Bonnie S. Dunbar ◽  
Therese M. Timmons ◽  
Sheri M. Skinner ◽  
Sarvamangala V. Prasad

2002 ◽  
Vol 292 (2) ◽  
pp. 127-137 ◽  
Author(s):  
Fahd K. Majiduddin ◽  
Isabel C. Materon ◽  
Timothy G. Palzkill

Author(s):  
Peter Sterling

The synaptic connections in cat retina that link photoreceptors to ganglion cells have been analyzed quantitatively. Our approach has been to prepare serial, ultrathin sections and photograph en montage at low magnification (˜2000X) in the electron microscope. Six series, 100-300 sections long, have been prepared over the last decade. They derive from different cats but always from the same region of retina, about one degree from the center of the visual axis. The material has been analyzed by reconstructing adjacent neurons in each array and then identifying systematically the synaptic connections between arrays. Most reconstructions were done manually by tracing the outlines of processes in successive sections onto acetate sheets aligned on a cartoonist's jig. The tracings were then digitized, stacked by computer, and printed with the hidden lines removed. The results have provided rather than the usual one-dimensional account of pathways, a three-dimensional account of circuits. From this has emerged insight into the functional architecture.


Author(s):  
K.E. Krizan ◽  
J.E. Laffoon ◽  
M.J. Buckley

With increase use of tissue-integrated prostheses in recent years it is a goal to understand what is happening at the interface between haversion bone and bulk metal. This study uses electron microscopy (EM) techniques to establish parameters for osseointegration (structure and function between bone and nonload-carrying implants) in an animal model. In the past the interface has been evaluated extensively with light microscopy methods. Today researchers are using the EM for ultrastructural studies of the bone tissue and implant responses to an in vivo environment. Under general anesthesia nine adult mongrel dogs received three Brånemark (Nobelpharma) 3.75 × 7 mm titanium implants surgical placed in their left zygomatic arch. After a one year healing period the animals were injected with a routine bone marker (oxytetracycline), euthanized and perfused via aortic cannulation with 3% glutaraldehyde in 0.1M cacodylate buffer pH 7.2. Implants were retrieved en bloc, harvest radiographs made (Fig. 1), and routinely embedded in plastic. Tissue and implants were cut into 300 micron thick wafers, longitudinally to the implant with an Isomet saw and diamond wafering blade [Beuhler] until the center of the implant was reached.


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