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Items: 1 to 20 of 930

1.

Human cytomegalovirus-encoded US2 differentially affects surface expression of MHC class I locus products and targets membrane-bound, but not soluble HLA-G1 for degradation.

Barel MT, Ressing M, Pizzato N, van Leeuwen D, Le Bouteiller P, Lenfant F, Wiertz EJ.

J Immunol. 2003 Dec 15;171(12):6757-65.

2.

Subtle sequence variation among MHC class I locus products greatly influences sensitivity to HCMV US2- and US11-mediated degradation.

Barel MT, Pizzato N, Le Bouteiller P, Wiertz EJ, Lenfant F.

Int Immunol. 2006 Jan;18(1):173-82. Epub 2005 Dec 16.

PMID:
16361314
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Differential down-modulation of HLA-G and HLA-A2 or -A3 cell surface expression following human cytomegalovirus infection.

Pizzato N, Garmy-Susini B, Le Bouteiller P, Lenfant F.

J Reprod Immunol. 2004 Jun;62(1-2):3-15.

PMID:
15288176
6.

NK cell activity during human cytomegalovirus infection is dominated by US2-11-mediated HLA class I down-regulation.

Falk CS, Mach M, Schendel DJ, Weiss EH, Hilgert I, Hahn G.

J Immunol. 2002 Sep 15;169(6):3257-66.

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A structural determinant of human cytomegalovirus US2 dictates the down-regulation of class I major histocompatibility molecules.

Oresic K, Noriega V, Andrews L, Tortorella D.

J Biol Chem. 2006 Jul 14;281(28):19395-406. Epub 2006 May 10.

10.

Down-regulation of HLA-G1 cell surface expression in human cytomegalovirus infected cells.

Pizzato N, Garmy-Susini B, Le Bouteiller P, Lenfant F.

Am J Reprod Immunol. 2003 Oct;50(4):328-33.

PMID:
14672336
11.

Signal peptide peptidase is required for dislocation from the endoplasmic reticulum.

Loureiro J, Lilley BN, Spooner E, Noriega V, Tortorella D, Ploegh HL.

Nature. 2006 Jun 15;441(7095):894-7. Epub 2006 May 31.

PMID:
16738546
12.

Human cytomegalovirus-encoded US2 and US11 target unassembled MHC class I heavy chains for degradation.

Barel MT, Hassink GC, van Voorden S, Wiertz EJ.

Mol Immunol. 2006 Mar;43(8):1258-66. Epub 2005 Aug 10.

PMID:
16098592
13.

Binding of human cytomegalovirus US2 to major histocompatibility complex class I and II proteins is not sufficient for their degradation.

Chevalier MS, Daniels GM, Johnson DC.

J Virol. 2002 Aug;76(16):8265-75. Erratum in: J Virol 2002 Dec;76(24):13126.

14.

Ubiquitinylation of the cytosolic domain of a type I membrane protein is not required to initiate its dislocation from the endoplasmic reticulum.

Furman MH, Loureiro J, Ploegh HL, Tortorella D.

J Biol Chem. 2003 Sep 12;278(37):34804-11. Epub 2003 Jun 27.

15.

Surface expression of HLA-E, an inhibitor of natural killer cells, enhanced by human cytomegalovirus gpUL40.

Tomasec P, Braud VM, Rickards C, Powell MB, McSharry BP, Gadola S, Cerundolo V, Borysiewicz LK, McMichael AJ, Wilkinson GW.

Science. 2000 Feb 11;287(5455):1031.

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Ubiquitination of MHC class I heavy chains is essential for dislocation by human cytomegalovirus-encoded US2 but not US11.

Hassink GC, Barel MT, Van Voorden SB, Kikkert M, Wiertz EJ.

J Biol Chem. 2006 Oct 6;281(40):30063-71. Epub 2006 Jul 29.

18.

The short forms of HLA-G are unlikely to play a role in pregnancy because they are not expressed at the cell surface.

Bainbridge DR, Ellis SA, Sargent IL.

J Reprod Immunol. 2000 May;47(1):1-16.

PMID:
10779586
20.

Peptides with dual binding specificity for HLA-A2 and HLA-E are encoded by alternatively spliced isoforms of the antioxidant enzyme peroxiredoxin 5.

Sensi M, Pietra G, Molla A, Nicolini G, Vegetti C, Bersani I, Millo E, Weiss E, Moretta L, Mingari MC, Anichini A.

Int Immunol. 2009 Mar;21(3):257-68. doi: 10.1093/intimm/dxn141. Epub 2009 Jan 30.

PMID:
19181932

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