scholarly journals Cell surface molecules that bind fibronectin's matrix assembly domain

1991 ◽  
Vol 266 (15) ◽  
pp. 9697-9702 ◽  
Author(s):  
A.H. Limper ◽  
B.J. Quade ◽  
R.M. LaChance ◽  
T.M. Birkenmeier ◽  
T.S. Rangwala ◽  
...  
Neuroscience ◽  
1996 ◽  
Vol 73 (1) ◽  
pp. 161-169 ◽  
Author(s):  
G. Gopinath ◽  
V. Sable ◽  
K. Sailaja ◽  
P.N. Tandon

2011 ◽  
Vol 134 (2) ◽  
pp. 113-121 ◽  
Author(s):  
Laia Llinàs ◽  
Adriana Lázaro ◽  
Jose de Salort ◽  
Jessica Matesanz-Isabel ◽  
Jordi Sintes ◽  
...  

Author(s):  
D. N. J. Hart ◽  
G. J. Clark ◽  
J. W. Dekker ◽  
D. B. Fearnley ◽  
M. Kato ◽  
...  

Hybridoma ◽  
1983 ◽  
Vol 2 (1) ◽  
pp. 39-47 ◽  
Author(s):  
DEBRA M. MORIARITY ◽  
NILES FOX ◽  
DAVID P. ADEN ◽  
JOHN R. HOYER ◽  
BARBARA B. KNOWLES

1983 ◽  
Vol 4 (9) ◽  
pp. 256-259 ◽  
Author(s):  
Jeffrey A Bluestone ◽  
Richard J Hodes

2001 ◽  
Vol 65 (3) ◽  
pp. 371-389 ◽  
Author(s):  
Julie Overbaugh ◽  
A. Dusty Miller ◽  
Maribeth V. Eiden

SUMMARY In the past few years, many retrovirus receptors, coreceptors, and cofactors have been identified. These molecules are important for some aspects of viral entry, although in some cases it remains to be determined whether they are required for binding or postbinding stages in entry, such as fusion. There are certain common features to the molecules that many retroviruses use to gain entry into the cell. For example, the receptors for most mammalian oncoretroviruses are multiple membrane-spanning transport proteins. However, avian retroviruses use single-pass membrane proteins, and a sheep retrovirus uses a glycosylphosphatidylinositol-anchored molecule as its receptor. For some retroviruses, particularly the lentiviruses, two cell surface molecules are required for efficient entry. More recently, a soluble protein that is required for viral entry has been identified for a feline oncoretrovirus. In this review, we will focus on the various strategies used by mammalian retroviruses to gain entry into the cell. The choice of receptors will also be discussed in light of pressures that drive viral evolution and persistence.


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