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.
22. The monocyte differentiation antigen, CD14, is anchored to the cell membrane by a phosphatidylinositol linkage. Haziot A; Chen S; Ferrero E; Low MG; Silber R; Goyert SM J Immunol; 1988 Jul; 141(2):547-52. PubMed ID: 3385210 [TBL] [Abstract][Full Text] [Related]
23. In vitro mutagenesis of a mouse MHC class I gene for the examination of structure-function relationships. Shiroishi T; Evans GA; Appella E; Ozato K J Immunol; 1985 Jan; 134(1):623-9. PubMed ID: 3964822 [TBL] [Abstract][Full Text] [Related]
24. I-Ak polymorphisms define a functionally dominant region for the presentation of hen egg lysozyme peptides. Rosloniec EF; Vitez LJ; Beck BN; Buerstedde JM; McKean DJ; Landais D; Benoist C; Mathis D; Freed JH J Immunol; 1989 Jul; 143(1):50-8. PubMed ID: 2786533 [TBL] [Abstract][Full Text] [Related]
25. A glycophospholipid anchor is required for Qa-2-mediated T cell activation. Robinson PJ; Millrain M; Antoniou J; Simpson E; Mellor AL Nature; 1989 Nov; 342(6245):85-7. PubMed ID: 2530453 [TBL] [Abstract][Full Text] [Related]
26. Site-specific mutagenesis of the class I regulatory element the Q10 gene allows expression in non-liver tissues. Handy DE; Burke PA; Ozato K; Coligan JE J Immunol; 1989 Feb; 142(3):1015-21. PubMed ID: 2913151 [TBL] [Abstract][Full Text] [Related]
27. The cytoplasmic and the transmembrane domains are not sufficient for class I MHC signal transduction. Gur H; Geppert TD; Wacholtz MC; Lipsky PE Cell Immunol; 1999 Feb; 191(2):105-16. PubMed ID: 9973532 [TBL] [Abstract][Full Text] [Related]
28. Analysis of hybrid H-2D and L antigens with reciprocally mismatched aminoterminal domains: functional T cell recognition requires preservation of fine structural determinants. McCluskey J; Boyd L; Foo M; Forman J; Margulies DH; Bluestone JA J Immunol; 1986 Dec; 137(12):3881-90. PubMed ID: 2431046 [TBL] [Abstract][Full Text] [Related]
29. Presentation of endogenous peptide/MHC class I complexes is profoundly influenced by specific C-terminal flanking residues. Shastri N; Serwold T; Gonzalez F J Immunol; 1995 Nov; 155(9):4339-46. PubMed ID: 7594593 [TBL] [Abstract][Full Text] [Related]
30. Expression cloning of the early activation antigen CD69, a type II integral membrane protein with a C-type lectin domain. Hamann J; Fiebig H; Strauss M J Immunol; 1993 Jun; 150(11):4920-7. PubMed ID: 8496594 [TBL] [Abstract][Full Text] [Related]
31. Identification of amino acids within the MHC molecule important for the interaction with the adenovirus protein E3/19K. Feuerbach D; Etteldorf S; Ebenau-Jehle C; Abastado JP; Madden D; Burgert HG J Immunol; 1994 Aug; 153(4):1626-36. PubMed ID: 8046235 [TBL] [Abstract][Full Text] [Related]
32. Aglycosylated and phosphatidylinositol-anchored MHC class I molecules are associated with calnexin. Evidence implicating the class I-connecting peptide segment in calnexin association. Carreno BM; Schreiber KL; McKean DJ; Stroynowski I; Hansen TH J Immunol; 1995 May; 154(10):5173-80. PubMed ID: 7730623 [TBL] [Abstract][Full Text] [Related]
33. Biosynthesis of a phosphatidylinositol-glycan-linked membrane protein: signals for posttranslational processing of the Ly-6E antigen. Su B; Bothwell AL Mol Cell Biol; 1989 Aug; 9(8):3369-76. PubMed ID: 2796989 [TBL] [Abstract][Full Text] [Related]
34. Molecular mapping of signals in the Qa-2 antigen required for attachment of the phosphatidylinositol membrane anchor. Waneck GL; Sherman DH; Kincade PW; Low MG; Flavell RA Proc Natl Acad Sci U S A; 1988 Jan; 85(2):577-81. PubMed ID: 3422441 [TBL] [Abstract][Full Text] [Related]
35. Selectivity at the cleavage/attachment site of phosphatidylinositol-glycan anchored membrane proteins is enzymatically determined. Micanovic R; Kodukula K; Gerber LD; Udenfriend S Proc Natl Acad Sci U S A; 1990 Oct; 87(20):7939-43. PubMed ID: 1700420 [TBL] [Abstract][Full Text] [Related]
36. Site-specific mutations in the COOH-terminus of placental alkaline phosphatase: a single amino acid change converts a phosphatidylinositol-glycan-anchored protein to a secreted protein. Lowe ME J Cell Biol; 1992 Feb; 116(3):799-807. PubMed ID: 1730777 [TBL] [Abstract][Full Text] [Related]
37. Biosynthesis of phosphatidylinositol-glycan (PI-G)-anchored membrane proteins in cell-free systems: cleavage of the nascent protein and addition of the PI-G moiety depend on the size of the COOH-terminal signal peptide. Kodukula K; Cines D; Amthauer R; Gerber L; Udenfriend S Proc Natl Acad Sci U S A; 1992 Feb; 89(4):1350-3. PubMed ID: 1531539 [TBL] [Abstract][Full Text] [Related]
38. Selectivity of the cleavage/attachment site of phosphatidylinositol-glycan-anchored membrane proteins determined by site-specific mutagenesis at Asp-484 of placental alkaline phosphatase. Micanovic R; Gerber LD; Berger J; Kodukula K; Udenfriend S Proc Natl Acad Sci U S A; 1990 Jan; 87(1):157-61. PubMed ID: 2153284 [TBL] [Abstract][Full Text] [Related]
39. Cell-free processing of nascent proteins destined to be linked to the plasma membrane by a phosphatidylinositol-glycan anchor. Udenfriend S; Kodukula K; Amthauer R Cell Mol Biol; 1992 Feb; 38(1):11-6. PubMed ID: 1559242 [TBL] [Abstract][Full Text] [Related]
40. COOH-terminal requirements for the correct processing of a phosphatidylinositol-glycan anchored membrane protein. Berger J; Howard AD; Brink L; Gerber L; Hauber J; Cullen BR; Udenfriend S J Biol Chem; 1988 Jul; 263(20):10016-21. PubMed ID: 3290206 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]