These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 11068758)

  • 21. Prominence of beta 2-microglobulin, class I heavy chain conformation, and tapasin in the interactions of class I heavy chain with calreticulin and the transporter associated with antigen processing.
    Solheim JC; Harris MR; Kindle CS; Hansen TH
    J Immunol; 1997 Mar; 158(5):2236-41. PubMed ID: 9036970
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The N-terminal region of tapasin is required to stabilize the MHC class I loading complex.
    Bangia N; Lehner PJ; Hughes EA; Surman M; Cresswell P
    Eur J Immunol; 1999 Jun; 29(6):1858-70. PubMed ID: 10382748
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The related molecular chaperones calnexin and calreticulin differentially associate with nascent T cell antigen receptor proteins within the endoplasmic reticulum.
    Van Leeuwen JE; Kearse KP
    J Biol Chem; 1996 Oct; 271(41):25345-9. PubMed ID: 8810299
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Chaperone properties of calreticulin.
    Svaerke C; Houen G
    Acta Chem Scand (Cph); 1998 Jul; 52(7):942-9. PubMed ID: 9661269
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Accessory proteins that control the assembly of MHC molecules with peptides.
    Van Kaer L
    Immunol Res; 2001; 23(2-3):205-14. PubMed ID: 11444385
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Assembly, peptide loading, and transport of MHC class I molecules in a calnexin-negative cell line.
    Sadasivan BK; Cariappa A; Waneck GL; Cresswell P
    Cold Spring Harb Symp Quant Biol; 1995; 60():267-75. PubMed ID: 8824400
    [No Abstract]   [Full Text] [Related]  

  • 28. Overexpression of calreticulin increases the Ca2+ capacity of rapidly exchanging Ca2+ stores and reveals aspects of their lumenal microenvironment and function.
    Bastianutto C; Clementi E; Codazzi F; Podini P; De Giorgi F; Rizzuto R; Meldolesi J; Pozzan T
    J Cell Biol; 1995 Aug; 130(4):847-55. PubMed ID: 7642702
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Assembly and export of MHC class I peptide ligands.
    Antoniou AN; Powis SJ; Elliott T
    Curr Opin Immunol; 2003 Feb; 15(1):75-81. PubMed ID: 12495737
    [No Abstract]   [Full Text] [Related]  

  • 30. Oligosaccharide binding characteristics of the molecular chaperones calnexin and calreticulin.
    Vassilakos A; Michalak M; Lehrman MA; Williams DB
    Biochemistry; 1998 Mar; 37(10):3480-90. PubMed ID: 9521669
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A set of endoplasmic reticulum proteins possessing properties of molecular chaperones includes Ca(2+)-binding proteins and members of the thioredoxin superfamily.
    Nigam SK; Goldberg AL; Ho S; Rohde MF; Bush KT; Sherman MYu
    J Biol Chem; 1994 Jan; 269(3):1744-9. PubMed ID: 8294423
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Analysis of the early biogenesis of CD1b: involvement of the chaperones calnexin and calreticulin, the proteasome and beta(2)-microglobulin.
    Hüttinger R; Staffler G; Majdic O; Stockinger H
    Int Immunol; 1999 Oct; 11(10):1615-23. PubMed ID: 10508179
    [TBL] [Abstract][Full Text] [Related]  

  • 33. An extensive region of an MHC class I alpha 2 domain loop influences interaction with the assembly complex.
    Yu YY; Turnquist HR; Myers NB; Balendiran GK; Hansen TH; Solheim JC
    J Immunol; 1999 Oct; 163(8):4427-33. PubMed ID: 10510384
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Accessory molecules in the assembly of major histocompatibility complex class I/peptide complexes: how essential are they for CD8(+) T-cell immune responses?
    Garbi N; Tanaka S; van den Broek M; Momburg F; Hämmerling GJ
    Immunol Rev; 2005 Oct; 207():77-88. PubMed ID: 16181328
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A charged amino acid residue in the transmembrane/cytoplasmic region of tapasin influences MHC class I assembly and maturation.
    Petersen JL; Hickman-Miller HD; McIlhaney MM; Vargas SE; Purcell AW; Hildebrand WH; Solheim JC
    J Immunol; 2005 Jan; 174(2):962-9. PubMed ID: 15634919
    [TBL] [Abstract][Full Text] [Related]  

  • 36. TAP-translocated peptides specifically bind proteins in the endoplasmic reticulum, including gp96, protein disulfide isomerase and calreticulin.
    Spee P; Neefjes J
    Eur J Immunol; 1997 Sep; 27(9):2441-9. PubMed ID: 9341791
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Lectins of the ER quality control machinery.
    Jakob CA; Chevet E; Thomas DY; Bergeron JJ
    Results Probl Cell Differ; 2001; 33():1-17. PubMed ID: 11190669
    [No Abstract]   [Full Text] [Related]  

  • 38. Interactions of HLA-B27 with the peptide loading complex as revealed by heavy chain mutations.
    Harris MR; Lybarger L; Myers NB; Hilbert C; Solheim JC; Hansen TH; Yu YY
    Int Immunol; 2001 Oct; 13(10):1275-82. PubMed ID: 11581172
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Structural features of MHC class I molecules that might facilitate alternative pathways of presentation.
    Hansen T; Balendiran G; Solheim J; Ostrov D; Nathenson S
    Immunol Today; 2000 Feb; 21(2):83-8. PubMed ID: 10652466
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Rubella virus glycoprotein interaction with the endoplasmic reticulum calreticulin and calnexin.
    Nakhasi HL; Ramanujam M; Atreya CD; Hobman TC; Lee N; Esmaili A; Duncan RC
    Arch Virol; 2001; 146(1):1-14. PubMed ID: 11266204
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.