BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

270 related articles for article (PubMed ID: 7636233)

  • 1. Novel dipeptide aldehydes are proteasome inhibitors and block the MHC-I antigen-processing pathway.
    Harding CV; France J; Song R; Farah JM; Chatterjee S; Iqbal M; Siman R
    J Immunol; 1995 Aug; 155(4):1767-75. PubMed ID: 7636233
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The generation of MHC class I-associated peptides is only partially inhibited by proteasome inhibitors: involvement of nonproteasomal cytosolic proteases in antigen processing?
    Vinitsky A; Antón LC; Snyder HL; Orlowski M; Bennink JR; Yewdell JW
    J Immunol; 1997 Jul; 159(2):554-64. PubMed ID: 9218569
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cloned dendritic cells can present exogenous antigens on both MHC class I and class II molecules.
    Shen Z; Reznikoff G; Dranoff G; Rock KL
    J Immunol; 1997 Mar; 158(6):2723-30. PubMed ID: 9058806
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Selective involvement of proteasomes and cysteine proteases in MHC class I antigen presentation.
    López D; Del Val M
    J Immunol; 1997 Dec; 159(12):5769-72. PubMed ID: 9550370
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Proteasome activity limits the assembly of MHC class I molecules after IFN-gamma stimulation.
    Benham AM; Neefjes JJ
    J Immunol; 1997 Dec; 159(12):5896-904. PubMed ID: 9550386
    [TBL] [Abstract][Full Text] [Related]  

  • 6. MHC-encoded proteasome subunits LMP2 and LMP7 are not required for efficient antigen presentation.
    Yewdell J; Lapham C; Bacik I; Spies T; Bennink J
    J Immunol; 1994 Feb; 152(3):1163-70. PubMed ID: 8301122
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dissociation of proteasomal degradation of biosynthesized viral proteins from generation of MHC class I-associated antigenic peptides.
    Antón LC; Snyder HL; Bennink JR; Vinitsky A; Orlowski M; Porgador A; Yewdell JW
    J Immunol; 1998 May; 160(10):4859-68. PubMed ID: 9590233
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Nonionic triblock copolymers facilitate delivery of exogenous proteins into the MHC class I and class II processing pathways.
    Ke Y; McGraw CL; Hunter RL; Kapp JA
    Cell Immunol; 1997 Mar; 176(2):113-21. PubMed ID: 9073383
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Allelic differences in the relationship between proteasome activity and MHC class I peptide loading.
    Benham AM; Grommé M; Neefjes J
    J Immunol; 1998 Jul; 161(1):83-9. PubMed ID: 9647210
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Antigen secreted from noncytosolic Listeria monocytogenes is processed by the classical MHC class I processing pathway.
    Zwickey HL; Potter TA
    J Immunol; 1999 Jun; 162(11):6341-50. PubMed ID: 10352246
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Specific proteolytic cleavages limit the diversity of the pool of peptides available to MHC class I molecules in living cells.
    Serwold T; Shastri N
    J Immunol; 1999 Apr; 162(8):4712-9. PubMed ID: 10202012
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Electroporation of exogenous antigen into the cytosol for antigen processing and class I major histocompatibility complex (MHC) presentation: weak base amines and hypothermia (18 degrees C) inhibit the class I MHC processing pathway.
    Harding CV
    Eur J Immunol; 1992 Jul; 22(7):1865-9. PubMed ID: 1623927
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Effects of protease inhibitors on binding of sperm to the vitelline coat of ascidian eggs: implications for participation of a proteasome (multicatalytic proteinase complex).
    Takizawa S; Sawada H; Someno T; Saitoh Y; Yokosawa H; Hoshi M
    J Exp Zool; 1993 Sep; 267(1):86-91. PubMed ID: 8376953
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Gamma-interferon and expression of MHC genes regulate peptide hydrolysis by proteasomes.
    Gaczynska M; Rock KL; Goldberg AL
    Nature; 1993 Sep; 365(6443):264-7. PubMed ID: 8396732
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Rate of antigen degradation by the ubiquitin-proteasome pathway influences MHC class I presentation.
    Grant EP; Michalek MT; Goldberg AL; Rock KL
    J Immunol; 1995 Oct; 155(8):3750-8. PubMed ID: 7561079
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Isolation of low molecular mass polypeptide complementary DNA clones from primitive vertebrates. Implications for the origin of MHC class I-restricted antigen presentation.
    Kandil E; Namikawa C; Nonaka M; Greenberg AS; Flajnik MF; Ishibashi T; Kasahara M
    J Immunol; 1996 Jun; 156(11):4245-53. PubMed ID: 8666794
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Kinetic studies of the branched chain amino acid preferring peptidase activity of the 20S proteasome: development of a continuous assay and inhibition by tripeptide aldehydes and clasto-lactacystin beta-lactone.
    McCormack TA; Cruikshank AA; Grenier L; Melandri FD; Nunes SL; Plamondon L; Stein RL; Dick LR
    Biochemistry; 1998 May; 37(21):7792-800. PubMed ID: 9601040
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Inhibitors of the proteasome block the degradation of most cell proteins and the generation of peptides presented on MHC class I molecules.
    Rock KL; Gramm C; Rothstein L; Clark K; Stein R; Dick L; Hwang D; Goldberg AL
    Cell; 1994 Sep; 78(5):761-71. PubMed ID: 8087844
    [TBL] [Abstract][Full Text] [Related]  

  • 19. MHC-linked low-molecular mass polypeptide subunits define distinct subsets of proteasomes. Implications for divergent function among distinct proteasome subsets.
    Brown MG; Driscoll J; Monaco JJ
    J Immunol; 1993 Aug; 151(3):1193-204. PubMed ID: 8335924
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Two new proteases in the MHC class I processing pathway.
    Stoltze L; Schirle M; Schwarz G; Schröter C; Thompson MW; Hersh LB; Kalbacher H; Stevanovic S; Rammensee HG; Schild H
    Nat Immunol; 2000 Nov; 1(5):413-8. PubMed ID: 11062501
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.