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Journal Abstract Search
153 related items for PubMed ID: 7995932
1. Characterization of fibroblasts with a unique defect in processing antigens with disulfide bonds. Merkel BJ, Mandel R, Ryser HJ, McCoy KL. J Immunol; 1995 Jan 01; 154(1):128-36. PubMed ID: 7995932 [Abstract] [Full Text] [Related]
2. Defective antigen processing correlates with a low level of intracellular glutathione. Short S, Merkel BJ, Caffrey R, McCoy KL. Eur J Immunol; 1996 Dec 01; 26(12):3015-20. PubMed ID: 8977298 [Abstract] [Full Text] [Related]
3. Cytosolic targeting of hen egg lysozyme gives rise to a short-lived protein presented by class I but not class II major histocompatibility complex molecules. Calin-Laurens V, Forquet F, Mottez E, Kanellopoulos J, Godeau F, Kourilsky P, Gerlier D, Rabourdin-Combe C. Eur J Immunol; 1991 Mar 01; 21(3):761-9. PubMed ID: 2009914 [Abstract] [Full Text] [Related]
4. Processing of an endogenous protein can generate MHC class II-restricted T cell determinants distinct from those derived from exogenous antigen. Moreno J, Vignali DA, Nadimi F, Fuchs S, Adorini L, Hämmerling GJ. J Immunol; 1991 Nov 15; 147(10):3306-13. PubMed ID: 1658143 [Abstract] [Full Text] [Related]
5. Processing of endogenously synthesized hen egg-white lysozyme retained in the endoplasmic reticulum or in secretory form gives rise to a similar but not identical set of epitopes recognized by class II-restricted T cells. Adorini L, Guéry JC, Fuchs S, Ortiz-Navarrete V, Hämmerling GJ, Momburg F. J Immunol; 1993 Oct 01; 151(7):3576-86. PubMed ID: 7690807 [Abstract] [Full Text] [Related]
6. The extracellular domains of MHC class II molecules determine their processing requirements for antigen presentation. Kjer-Nielsen L, Perera JD, Boyd LF, Margulies DH, McCluskey J. J Immunol; 1990 Apr 15; 144(8):2915-24. PubMed ID: 1969876 [Abstract] [Full Text] [Related]
7. Selective processing of exogenous antigens by antigen-presenting cells with deleted MHC genes. Diment S, Shinde S. J Immunol; 1995 Jan 15; 154(2):530-5. PubMed ID: 7814866 [Abstract] [Full Text] [Related]
8. Intracellular location of cysteine transport activity correlates with productive processing of antigen disulfide. Gainey D, Short S, McCoy KL. J Cell Physiol; 1996 Aug 15; 168(2):248-54. PubMed ID: 8707860 [Abstract] [Full Text] [Related]
10. Class II-restricted presentation of a hen egg lysozyme determinant derived from endogenous antigen sequestered in the cytoplasm or endoplasmic reticulum of the antigen presenting cells. Brooks AG, McCluskey J. J Immunol; 1993 May 01; 150(9):3690-7. PubMed ID: 8473726 [Abstract] [Full Text] [Related]
12. Antigen presentation capacity of murine macrophages infected with Leishmania amazonensis amastigotes. Prina E, Jouanne C, de Souza Lão S, Szabo A, Guillet JG, Antoine JC. J Immunol; 1993 Aug 15; 151(4):2050-61. PubMed ID: 8102156 [Abstract] [Full Text] [Related]
13. Distinct effects of recombinant cholera toxin B subunit and holotoxin on different stages of class II MHC antigen processing and presentation by macrophages. Matousek MP, Nedrud JG, Harding CV. J Immunol; 1996 Jun 01; 156(11):4137-45. PubMed ID: 8666780 [Abstract] [Full Text] [Related]
17. Bone marrow-derived dendritic cells can process bacteria for MHC-I and MHC-II presentation to T cells. Svensson M, Stockinger B, Wick MJ. J Immunol; 1997 May 01; 158(9):4229-36. PubMed ID: 9126984 [Abstract] [Full Text] [Related]
18. Isotypic residues in the membrane proximal domain of MHC class II beta-chains control activation of CD4+ T cells. Sant AJ. J Immunol; 1993 Jun 15; 150(12):5299-310. PubMed ID: 8099935 [Abstract] [Full Text] [Related]
19. Antigen unfolding and disulfide reduction in antigen presenting cells. Jensen PE. Semin Immunol; 1995 Dec 15; 7(6):347-53. PubMed ID: 8775460 [Abstract] [Full Text] [Related]
20. Analysis of the interaction of peptide hen egg white lysozyme (34-45) with the I-Ak molecule. Lambert LE, Unanue ER. J Immunol; 1989 Aug 01; 143(3):802-7. PubMed ID: 2787347 [Abstract] [Full Text] [Related] Page: [Next] [New Search]