Molecular basis of bluetongue virus neutralization.

1983 ◽  
Vol 48 (3) ◽  
pp. 627-632 ◽  
Author(s):  
J Kahlon ◽  
K Sugiyama ◽  
P Roy
Science ◽  
2016 ◽  
Vol 351 (6279) ◽  
pp. 1343-1346 ◽  
Author(s):  
J. Misasi ◽  
M. S. A. Gilman ◽  
M. Kanekiyo ◽  
M. Gui ◽  
A. Cagigi ◽  
...  

1991 ◽  
Vol 57 (1) ◽  
pp. 37-42 ◽  
Author(s):  
Franziska B. Grieder ◽  
Kevin T. Schultz

1988 ◽  
Vol 41 (4) ◽  
pp. 553 ◽  
Author(s):  
JM Sharp ◽  
I R Littlejohns ◽  
T D St George

Using antigens prepared from cell cultures infected by bluetongue (BLU) virus type 20 (BLU-20), and sera from cattle which had recovered from experimental infection by that virus, two distinct precipitin reactions were demonstrated by immunodiffusion. Two distinct gel diffusion precipitin tests were developed based on these reactions. The antigen of one was common to BLU-20 and two other Australian BLU isolates, CSIRO 154 (BLU-21) and CSIRO 156 (BLU-l). It was therefore concluded to be a group-specific test. The antigen of the second appeared to be unique to BLU-20. The test based on this antigen correlated well with the virus neutralization test for BLU-20 and it was therefore concluded to be type-specific.


1987 ◽  
Vol 68 (11) ◽  
pp. 2967-2973 ◽  
Author(s):  
A. Fukusho ◽  
G. D. Ritter ◽  
P. Roy

Author(s):  
Ben O. Spurlock ◽  
Milton J. Cormier

The phenomenon of bioluminescence has fascinated layman and scientist alike for many centuries. During the eighteenth and nineteenth centuries a number of observations were reported on the physiology of bioluminescence in Renilla, the common sea pansy. More recently biochemists have directed their attention to the molecular basis of luminosity in this colonial form. These studies have centered primarily on defining the chemical basis for bioluminescence and its control. It is now established that bioluminescence in Renilla arises due to the luciferase-catalyzed oxidation of luciferin. This results in the creation of a product (oxyluciferin) in an electronic excited state. The transition of oxyluciferin from its excited state to the ground state leads to light emission.


Author(s):  
Darcy B. Kelley ◽  
Martha L. Tobias ◽  
Mark Ellisman

Brain and muscle are sexually differentiated tissues in which masculinization is controlled by the secretion of androgens from the testes. Sensitivity to androgen is conferred by the expression of an intracellular protein, the androgen receptor. A central problem of sexual differentiation is thus to understand the cellular and molecular basis of androgen action. We do not understand how hormone occupancy of a receptor translates into an alteration in the developmental program of the target cell. Our studies on sexual differentiation of brain and muscle in Xenopus laevis are designed to explore the molecular basis of androgen induced sexual differentiation by examining how this hormone controls the masculinization of brain and muscle targets.Our approach to this problem has focused on a highly androgen sensitive, sexually dimorphic neuromuscular system: laryngeal muscles and motor neurons of the clawed frog, Xenopus laevis. We have been studying sex differences at a synapse, the laryngeal neuromuscular junction, which mediates sexually dimorphic vocal behavior in Xenopus laevis frogs.


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