170 related articles for article (PubMed ID: 8186195)
21. Multiple roles of the invariant chain in MHC class II function.
Stumptner-Cuvelette P; Benaroch P
Biochim Biophys Acta; 2002 Jan; 1542(1-3):1-13. PubMed ID: 11853874
[No Abstract] [Full Text] [Related]
22. Structural analysis of proteolytic products of MHC class II-invariant chain complexes generated in vivo.
Newcomb JR; Cresswell P
J Immunol; 1993 Oct; 151(8):4153-63. PubMed ID: 8409392
[TBL] [Abstract][Full Text] [Related]
23. Delivery of nascent MHC class II-invariant chain complexes to lysosomal compartments and proteolysis of invariant chain by cysteine proteases precedes peptide binding in B-lymphoblastoid cells.
Morton PA; Zacheis ML; Giacoletto KS; Manning JA; Schwartz BD
J Immunol; 1995 Jan; 154(1):137-50. PubMed ID: 7995933
[TBL] [Abstract][Full Text] [Related]
24. Attenuation of HLA-DR expression by mononuclear phagocytes infected with Mycobacterium tuberculosis is related to intracellular sequestration of immature class II heterodimers.
Hmama Z; Gabathuler R; Jefferies WA; de Jong G; Reiner NE
J Immunol; 1998 Nov; 161(9):4882-93. PubMed ID: 9794422
[TBL] [Abstract][Full Text] [Related]
25. Poor loading of major histocompatibility complex class II molecules with endogenously synthesized short peptides in the absence of invariant chain.
Busch R; Vturina IY; Drexler J; Momburg F; Hämmerling GJ
Eur J Immunol; 1995 Jan; 25(1):48-53. PubMed ID: 7843252
[TBL] [Abstract][Full Text] [Related]
26. Inhibition of invariant chain (Ii)-calnexin interaction results in enhanced degradation of Ii but does not prevent the assembly of alpha beta Ii complexes.
Romagnoli P; Germain RN
J Exp Med; 1995 Dec; 182(6):2027-36. PubMed ID: 7500048
[TBL] [Abstract][Full Text] [Related]
27. Major histocompatibility complex class II compartments in human B lymphoblastoid cells are distinct from early endosomes.
Peters PJ; Raposo G; Neefjes JJ; Oorschot V; Leijendekker RL; Geuze HJ; Ploegh HL
J Exp Med; 1995 Aug; 182(2):325-34. PubMed ID: 7629497
[TBL] [Abstract][Full Text] [Related]
28. The MHC class II-associated invariant chain contains two endosomal targeting signals within its cytoplasmic tail.
Pieters J; Bakke O; Dobberstein B
J Cell Sci; 1993 Nov; 106 ( Pt 3)():831-46. PubMed ID: 8308066
[TBL] [Abstract][Full Text] [Related]
29. Intracellular and cell surface heterotypic associations of human leukocyte antigen-DR and human invariant chain.
Triantafilou K; Triantafilou M; Wilson KM; Cherry RJ; Fernandez N
Hum Immunol; 1999 Nov; 60(11):1101-12. PubMed ID: 10600008
[TBL] [Abstract][Full Text] [Related]
30. Structural analysis of invariant chain subsets as a function of their association with MHC class II chains.
Nguyen QV; Reyes VE; Humphreys RE
Arch Biochem Biophys; 1995 Feb; 317(1):128-32. PubMed ID: 7872774
[TBL] [Abstract][Full Text] [Related]
31. The CLIP region of invariant chain plays a critical role in regulating major histocompatibility complex class II folding, transport, and peptide occupancy.
Romagnoli P; Germain RN
J Exp Med; 1994 Sep; 180(3):1107-13. PubMed ID: 8064228
[TBL] [Abstract][Full Text] [Related]
32. Acquisition of peptides by MHC class II polypeptides in the absence of the invariant chain.
Hitzel C; van Endert P; Koch N
J Immunol; 1995 Feb; 154(3):1048-56. PubMed ID: 7822782
[TBL] [Abstract][Full Text] [Related]
33. Intracellular transport of class II MHC molecules directed by invariant chain.
Lotteau V; Teyton L; Peleraux A; Nilsson T; Karlsson L; Schmid SL; Quaranta V; Peterson PA
Nature; 1990 Dec; 348(6302):600-5. PubMed ID: 2250716
[TBL] [Abstract][Full Text] [Related]
34. Efficient internalization of MHC class II-invariant chain complexes is not sufficient for invariant chain proteolysis and class II antigen presentation.
Swier K; Miller J
J Immunol; 1995 Jul; 155(2):630-43. PubMed ID: 7608541
[TBL] [Abstract][Full Text] [Related]
35. Phosphorylation regulates the delivery of MHC class II invariant chain complexes to antigen processing compartments.
Anderson HA; Roche PA
J Immunol; 1998 May; 160(10):4850-8. PubMed ID: 9590232
[TBL] [Abstract][Full Text] [Related]
36. Direct transport of newly synthesized HLA-DR from the trans-Golgi network to major histocompatibility complex class II containing compartments (MIICS) demonstrated using a novel tyrosine-sulfated chimera.
Davidson HW
J Biol Chem; 1999 Sep; 274(38):27315-22. PubMed ID: 10480952
[TBL] [Abstract][Full Text] [Related]
37. An N-terminal double-arginine motif maintains type II membrane proteins in the endoplasmic reticulum.
Schutze MP; Peterson PA; Jackson MR
EMBO J; 1994 Apr; 13(7):1696-705. PubMed ID: 8157008
[TBL] [Abstract][Full Text] [Related]
38. GTP-bound forms of rab6 induce the redistribution of Golgi proteins into the endoplasmic reticulum.
Martinez O; Antony C; Pehau-Arnaudet G; Berger EG; Salamero J; Goud B
Proc Natl Acad Sci U S A; 1997 Mar; 94(5):1828-33. PubMed ID: 9050864
[TBL] [Abstract][Full Text] [Related]
39. Cathepsin B cleavage and release of invariant chain from MHC class II molecules follow a staged pattern.
Xu M; Capraro GA; Daibata M; Reyes VE; Humphreys RE
Mol Immunol; 1994 Jul; 31(10):723-31. PubMed ID: 8035834
[TBL] [Abstract][Full Text] [Related]
40. Interferon-gamma-stimulated human keratinocytes express the genes necessary for the production of peptide-loaded MHC class II molecules.
Albanesi C; Cavani A; Girolomoni G
J Invest Dermatol; 1998 Feb; 110(2):138-42. PubMed ID: 9457908
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
