The expression of tenascin and fibronectin in keratoconus, scarred and normal human cornea

1997 ◽  
Vol 235 (4) ◽  
pp. 222-229 ◽  
Author(s):  
Antti Tuori ◽  
Ismo Virtanen ◽  
Esko Aine ◽  
Hannu Uusitalo
Keyword(s):  
Human Cornea ◽  
Normal Human

Confocal microscopy of the normal human cornea

2001 ◽  
Vol 24 (1) ◽  
pp. 16-24 ◽  
Author(s):  
Nathan Efron ◽  
Inma Perez-Gomez ◽  
Haliza A. Mutalib ◽  
Jo Hollingsworth
Keyword(s):  
Confocal Microscopy ◽  
Human Cornea ◽  
Normal Human

Confocal microscopy of the normal human cornea

2001 ◽  
Vol 24 (2) ◽  
pp. 83-85
Author(s):  
Nathan Efron ◽  
Inma Perez-Gomez ◽  
Haliza A. Mutalib ◽  
Jo Hollingsworth
Keyword(s):  
Confocal Microscopy ◽  
Human Cornea ◽  
Normal Human

Expression of the interleukin 1 receptor antagonist in the normal human cornea

1994 ◽  
Vol 2 (4) ◽  
pp. 217-222 ◽  
Author(s):  
Paulo Torres ◽  
Alex F. de Vos ◽  
Ruth van der Gaag ◽  
Aize Kijlstra
Keyword(s):  
Receptor Antagonist ◽  
Interleukin 1 ◽  
Human Cornea ◽  
Interleukin 1 Receptor Antagonist ◽  
Normal Human

scholarly journals Scanning Slit Confocal Microscopy of the Living Eye

1994 ◽  
Vol 2 (8) ◽  
pp. 3-4
Author(s):  
Barry D. Masters
Keyword(s):  
Real Time ◽  
Optical Design ◽  
Front Surface ◽  
Confocal Microscope ◽  
Human Cornea ◽  
The Real ◽  
Human Eye ◽  
Time Scanning ◽  
Normal Human

The living human eye is in constant motion. The cornea, which is the transparent front surface of the eyeball, is a formidable specimen for microscopy. How can we use a microscope to obtain sufficient contrast in order to observe cellular and subcellular details on a moving, transparent specimen? Although the normal human cornea is free of blood vessels, there are many nerves within the 500 μm thickness of this tissue. How can we observe these nerves in the living human eye?To accomplish these aims, use a new real-time, scanning slit confocal microscope that was developed by Dr. A. Thaer for imaging the in vivo human cornea. The optical design of the real-time, scanning slit confocal microscope is shown as follows in Figure 1. The confocal microscope is a modification of the real-time, scanning slit confocal microscope based on an oscillating too-sided mirror (bi-lateral scanning) which was designed and first constructed in 1969 by G. M. Svishchev in Lenningrad.

scholarly journals T lymphocytes of the normal human cornea.

1987 ◽  
Vol 71 (5) ◽  
pp. 384-386 ◽  
Author(s):  
O F Scheiffarth ◽  
F H Stefani ◽  
N Gabriel ◽  
O E Lund
Keyword(s):  
T Lymphocytes ◽  
Human Cornea ◽  
Normal Human

Imaging of Keratoconic and normal human cornea with a Brillouin imaging system (Conference Presentation)

2016 ◽  
Author(s):  
Sebastien Besner ◽  
Peng Shao ◽  
Giuliano Scarcelli ◽  
Roberto Pineda ◽  
Seok-Hyun (Andy) Yun
Keyword(s):  
Imaging System ◽  
Human Cornea ◽  
Normal Human

The effect of moxifloxacin on the normal human cornea

2006 ◽  
Vol 22 (10) ◽  
pp. 2073-2078 ◽  
Author(s):  
Kendall E. Donaldson ◽  
Fabiana B. Marangon ◽  
Lauren Schatz ◽  
Anna S. Venkatraman ◽  
Eduardo C. Alfonso
Keyword(s):  
Human Cornea ◽  
Normal Human
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