A putative gene located at the MHC class I region around the D6S105 marker contributes to the setting of CD8+ T-lymphocyte numbers in humans

2007 ◽  
Vol 34 (5) ◽  
pp. 359-367 ◽  
Author(s):  
J. Vieira ◽  
C. S. Cardoso ◽  
J. Pinto ◽  
K. Patil ◽  
P. Brazdil ◽  
...  
2005 ◽  
Vol 175 (9) ◽  
pp. 5986-5997 ◽  
Author(s):  
John T. Loffredo ◽  
John Sidney ◽  
Shari Piaskowski ◽  
Andrew Szymanski ◽  
Jessica Furlott ◽  
...  

2003 ◽  
Vol 39 (3) ◽  
pp. 279-286 ◽  
Author(s):  
Tanja Heintel ◽  
Frank Breinig ◽  
Manfred J Schmitt ◽  
Andreas Meyerhans

1993 ◽  
Vol 38 (1) ◽  
pp. 47-53 ◽  
Author(s):  
Corine Vernet ◽  
Marie-Th�r�se Ribouchon ◽  
Giovanna Chimini ◽  
Anne-Marie Jouanolle ◽  
Issa Sidib� ◽  
...  

2016 ◽  
Vol 65 (3) ◽  
pp. 261-271 ◽  
Author(s):  
Shiwen Peng ◽  
Austin Mattox ◽  
Simon R. Best ◽  
Anca M. Barbu ◽  
James A. Burns ◽  
...  

2008 ◽  
Vol 17 (8) ◽  
pp. 2074-2088 ◽  
Author(s):  
NATASJA G. DE GROOT ◽  
CORRINE M. C. HEIJMANS ◽  
NANINE DE GROOT ◽  
NEL OTTING ◽  
ANNEMIEK J. M. DE VOS-ROUWELER ◽  
...  

1990 ◽  
Vol 85 (5) ◽  
Author(s):  
DeirdreK. Lord ◽  
I. Dunham ◽  
R.Duncan Campbell ◽  
Adrian Bomford ◽  
Tom Strachan ◽  
...  

2005 ◽  
Vol 57 (8) ◽  
pp. 601-606 ◽  
Author(s):  
Shirley A. Ellis ◽  
W. Ivan Morrison ◽  
Niall D. MacHugh ◽  
James Birch ◽  
Alison Burrells ◽  
...  

1995 ◽  
Vol 182 (5) ◽  
pp. 1615-1619 ◽  
Author(s):  
J Hombach ◽  
H Pircher ◽  
S Tonegawa ◽  
R M Zinkernagel

Peptides presented by major histocompatibility complex (MHC) class I molecules are derived from intracellularly synthesized proteins. Cytosolic proteins are fragmented into peptides, which are subsequently transported via the transporter of antigen presentation (TAP) into the endoplasmic reticulum (ER), where they bind to MHC class I molecules. We have investigated the requirements for MHC class I presentation of the immunodominant gp33 cytotoxic T lymphocyte epitope of the lymphocytic choriomeningitis virus. This epitope is located within the leader peptide of the virus glycoprotein. Such an epitope is expected to be presented in a TAP-independent manner, since it is released into the ER by signal peptidase. Taking advantage of TAP1-/- mice, however, we show both in vitro and in vivo that, after virus infection, the presentation of the gp33 epitope is strictly dependent on a functional TAP heterodimer. The results are discussed with respect to peptide trimming processes in the ER.


AIDS ◽  
2001 ◽  
Vol 15 (1) ◽  
pp. 121-122
Author(s):  
Annette Oxenius ◽  
David A. Price ◽  
Sara J. Dawson ◽  
Tin Tun ◽  
Philippa J. Easterbrook ◽  
...  

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