441 related articles for article (PubMed ID: 15634919)
21. ER-60, a chaperone with thiol-dependent reductase activity involved in MHC class I assembly.
Lindquist JA; Jensen ON; Mann M; Hämmerling GJ
EMBO J; 1998 Apr; 17(8):2186-95. PubMed ID: 9545232
[TBL] [Abstract][Full Text] [Related]
22. The role of tapasin in MHC class I antigen assembly.
Androlewicz MJ
Immunol Res; 1999; 20(2):79-88. PubMed ID: 10580633
[TBL] [Abstract][Full Text] [Related]
23. Mutant MHC class I molecules define interactions between components of the peptide-loading complex.
Paquet ME; Williams DB
Int Immunol; 2002 Apr; 14(4):347-58. PubMed ID: 11934871
[TBL] [Abstract][Full Text] [Related]
24. Hepatocytes express abundant surface class I MHC and efficiently use transporter associated with antigen processing, tapasin, and low molecular weight polypeptide proteasome subunit components of antigen processing and presentation pathway.
Chen M; Tabaczewski P; Truscott SM; Van Kaer L; Stroynowski I
J Immunol; 2005 Jul; 175(2):1047-55. PubMed ID: 16002705
[TBL] [Abstract][Full Text] [Related]
25. A single polymorphic residue within the peptide-binding cleft of MHC class I molecules determines spectrum of tapasin dependence.
Park B; Lee S; Kim E; Ahn K
J Immunol; 2003 Jan; 170(2):961-8. PubMed ID: 12517962
[TBL] [Abstract][Full Text] [Related]
26. Interaction of murine MHC class I molecules with tapasin and TAP enhances peptide loading and involves the heavy chain alpha3 domain.
Suh WK; Derby MA; Cohen-Doyle MF; Schoenhals GJ; Früh K; Berzofsky JA; Williams DB
J Immunol; 1999 Feb; 162(3):1530-40. PubMed ID: 9973410
[TBL] [Abstract][Full Text] [Related]
27. A major role for tapasin as a stabilizer of the TAP peptide transporter and consequences for MHC class I expression.
Garbi N; Tiwari N; Momburg F; Hämmerling GJ
Eur J Immunol; 2003 Jan; 33(1):264-73. PubMed ID: 12594855
[TBL] [Abstract][Full Text] [Related]
28. Dependence of peptide binding by MHC class I molecules on their interaction with TAP.
Grandea AG; Androlewicz MJ; Athwal RS; Geraghty DE; Spies T
Science; 1995 Oct; 270(5233):105-8. PubMed ID: 7569935
[TBL] [Abstract][Full Text] [Related]
29. Retention of empty MHC class I molecules by tapasin is essential to reconstitute antigen presentation in invertebrate cells.
Schoenhals GJ; Krishna RM; Grandea AG; Spies T; Peterson PA; Yang Y; Früh K
EMBO J; 1999 Feb; 18(3):743-53. PubMed ID: 9927434
[TBL] [Abstract][Full Text] [Related]
30. HLA-F surface expression on B cell and monocyte cell lines is partially independent from tapasin and completely independent from TAP.
Lee N; Geraghty DE
J Immunol; 2003 Nov; 171(10):5264-71. PubMed ID: 14607927
[TBL] [Abstract][Full Text] [Related]
31. Virus subversion of the MHC class I peptide-loading complex.
Lybarger L; Wang X; Harris MR; Virgin HW; Hansen TH
Immunity; 2003 Jan; 18(1):121-30. PubMed ID: 12530981
[TBL] [Abstract][Full Text] [Related]
32. The murine gamma-herpesvirus-68 MK3 protein causes TAP degradation independent of MHC class I heavy chain degradation.
Boname JM; May JS; Stevenson PG
Eur J Immunol; 2005 Jan; 35(1):171-9. PubMed ID: 15593121
[TBL] [Abstract][Full Text] [Related]
33. Tapasin is a facilitator, not an editor, of class I MHC peptide binding.
Zarling AL; Luckey CJ; Marto JA; White FM; Brame CJ; Evans AM; Lehner PJ; Cresswell P; Shabanowitz J; Hunt DF; Engelhard VH
J Immunol; 2003 Nov; 171(10):5287-95. PubMed ID: 14607930
[TBL] [Abstract][Full Text] [Related]
34. Tapasin-/- and TAP1-/- macrophages are deficient in vacuolar alternate class I MHC (MHC-I) processing due to decreased MHC-I stability at phagolysosomal pH.
Chefalo PJ; Grandea AG; Van Kaer L; Harding CV
J Immunol; 2003 Jun; 170(12):5825-33. PubMed ID: 12794107
[TBL] [Abstract][Full Text] [Related]
35. TAP- and tapasin-dependent HLA-E surface expression correlates with the binding of an MHC class I leader peptide.
Braud VM; Allan DS; Wilson D; McMichael AJ
Curr Biol; 1998 Jan; 8(1):1-10. PubMed ID: 9427624
[TBL] [Abstract][Full Text] [Related]
36. HLA-B27-restricted antigen presentation in the absence of tapasin reveals polymorphism in mechanisms of HLA class I peptide loading.
Peh CA; Burrows SR; Barnden M; Khanna R; Cresswell P; Moss DJ; McCluskey J
Immunity; 1998 May; 8(5):531-42. PubMed ID: 9620674
[TBL] [Abstract][Full Text] [Related]
37. Targeting tumour cells with defects in the MHC Class I antigen processing pathway with CD8+ T cells specific for hydrophobic TAP- and Tapasin-independent peptides: the requirement for directed access into the ER.
Aladin F; Lautscham G; Humphries E; Coulson J; Blake N
Cancer Immunol Immunother; 2007 Aug; 56(8):1143-52. PubMed ID: 17143611
[TBL] [Abstract][Full Text] [Related]
38. Increased efficiency of folding and peptide loading of mutant MHC class I molecules.
Beissbarth T; Sun J; Kavathas PB; Ortmann B
Eur J Immunol; 2000 Apr; 30(4):1203-13. PubMed ID: 10760810
[TBL] [Abstract][Full Text] [Related]
39. A transmembrane tail: interaction of tapasin with TAP and the MHC class I molecule.
Simone LC; Wang X; Solheim JC
Mol Immunol; 2009 Jun; 46(10):2147-50. PubMed ID: 19361863
[TBL] [Abstract][Full Text] [Related]
40. Tapasin is required for efficient peptide binding to transporter associated with antigen processing.
Li S; Paulsson KM; Chen S; Sjögren HO; Wang P
J Biol Chem; 2000 Jan; 275(3):1581-6. PubMed ID: 10636848
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
