McCluskey J - Search Results

1

Divergent T-cell receptor recognition modes of a HLA-I restricted extended tumour-associated peptide.

Chan KF, Gully BS, Gras S, Beringer DX, Kjer-Nielsen L, Cebon J, McCluskey J, Chen W, Rossjohn J. Chan KF, et al. Among authors: mccluskey j. Nat Commun. 2018 Mar 12;9(1):1026. doi: 10.1038/s41467-018-03321-w. Nat Commun. 2018. PMID: 29531227 Free PMC article.

2

Impaired expression of chimaeric major histocompatibility complex transgenes associated with plasmid sequences.

Kjer-Nielsen L, Holmberg K, Perera JD, McCluskey J. Kjer-Nielsen L, et al. Among authors: mccluskey j. Transgenic Res. 1992 Jul;1(4):182-7. doi: 10.1007/BF02522537. Transgenic Res. 1992. PMID: 1301211

3

Class II-restricted presentation of an endogenously derived immunodominant T-cell determinant of hen egg lysozyme.

Brooks A, Hartley S, Kjer-Nielsen L, Perera J, Goodnow CC, Basten A, McCluskey J. Brooks A, et al. Among authors: mccluskey j. Proc Natl Acad Sci U S A. 1991 Apr 15;88(8):3290-4. doi: 10.1073/pnas.88.8.3290. Proc Natl Acad Sci U S A. 1991. PMID: 1707537 Free PMC article.

4

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. Kjer-Nielsen L, et al. Among authors: mccluskey j. J Immunol. 1990 Apr 15;144(8):2915-24. J Immunol. 1990. PMID: 1969876

5

Structure function analysis of in vitro mutated CD4 and major histocompatibility complex class II gene products.

McCluskey J, Kjer-Nielsen L, Blok R. McCluskey J, et al. J Autoimmun. 1990 Apr;3 Suppl 1:91-6. doi: 10.1016/s0896-8411(09)90016-6. J Autoimmun. 1990. PMID: 2340062

6

The role of major histocompatibility molecules in antigen-specific immune responses.

McCluskey J, Blok R, Kjer-Nielsen L. McCluskey J, et al. Transplant Proc. 1989 Feb;21(1 Pt 1):591-4. Transplant Proc. 1989. PMID: 2495622 Review. No abstract available.

7

Determinant selection of major histocompatibility complex class I-restricted antigenic peptides is explained by class I-peptide affinity and is strongly influenced by nondominant anchor residues.

Chen W, Khilko S, Fecondo J, Margulies DH, McCluskey J. Chen W, et al. Among authors: mccluskey j. J Exp Med. 1994 Oct 1;180(4):1471-83. doi: 10.1084/jem.180.4.1471. J Exp Med. 1994. PMID: 7523572 Free PMC article.

8

Electroporation and commercial liposomes efficiently deliver soluble protein into the MHC class I presentation pathway. Priming in vitro and in vivo for class I-restricted recognition of soluble antigen.

Chen W, Carbone FR, McCluskey J. Chen W, et al. Among authors: mccluskey j. J Immunol Methods. 1993 Mar 15;160(1):49-57. doi: 10.1016/0022-1759(93)90007-t. J Immunol Methods. 1993. PMID: 7680698

9

The structural influence of individual residues located within peptide antigen depends upon their sequence context.

Chen W, Fecondo J, McCluskey J. Chen W, et al. Among authors: mccluskey j. Mol Immunol. 1994 Oct;31(14):1069-75. doi: 10.1016/0161-5890(94)90102-3. Mol Immunol. 1994. PMID: 7935498

10

Changes at peptide residues buried in the major histocompatibility complex (MHC) class I binding cleft influence T cell recognition: a possible role for indirect conformational alterations in the MHC class I or bound peptide in determining T cell recognition.

Chen W, McCluskey J, Rodda S, Carbone FR. Chen W, et al. Among authors: mccluskey j. J Exp Med. 1993 Mar 1;177(3):869-73. doi: 10.1084/jem.177.3.869. J Exp Med. 1993. PMID: 8436915 Free PMC article.

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