Vignali KM - Search Results

1

Distinct TCR signaling pathways drive proliferation and cytokine production in T cells.

Guy CS, Vignali KM, Temirov J, Bettini ML, Overacre AE, Smeltzer M, Zhang H, Huppa JB, Tsai YH, Lobry C, Xie J, Dempsey PJ, Crawford HC, Aifantis I, Davis MM, Vignali DA. Guy CS, et al. Among authors: vignali da, vignali km. Nat Immunol. 2013 Mar;14(3):262-70. doi: 10.1038/ni.2538. Epub 2013 Feb 3. Nat Immunol. 2013. PMID: 23377202 Free PMC article.

2

T cell receptor recognition of MHC class II-bound peptide flanking residues enhances immunogenicity and results in altered TCR V region usage.

Carson RT, Vignali KM, Woodland DL, Vignali DA. Carson RT, et al. Among authors: vignali da, vignali km. Immunity. 1997 Sep;7(3):387-99. doi: 10.1016/s1074-7613(00)80360-x. Immunity. 1997. PMID: 9324359 Free article.

3

Immunoregulation of Th cells by naturally processed peptide antagonists.

Carson RT, Desai DD, Vignali KM, Vignali DA. Carson RT, et al. Among authors: vignali da, vignali km. J Immunol. 1999 Jan 1;162(1):1-4. J Immunol. 1999. PMID: 9886362

4

Profound enhancement of T cell activation mediated by the interaction between the TCR and the D3 domain of CD4.

Vignali DA, Vignali KM. Vignali DA, et al. Among authors: vignali km. J Immunol. 1999 Feb 1;162(3):1431-9. J Immunol. 1999. PMID: 9973399

5

The majority of immunogenic epitopes generate CD4+ T cells that are dependent on MHC class II-bound peptide-flanking residues.

Arnold PY, La Gruta NL, Miller T, Vignali KM, Adams PS, Woodland DL, Vignali DA. Arnold PY, et al. Among authors: vignali da, vignali km. J Immunol. 2002 Jul 15;169(2):739-49. doi: 10.4049/jimmunol.169.2.739. J Immunol. 2002. PMID: 12097376

6

Reliable generation and use of MHC class II:gamma2aFc multimers for the identification of antigen-specific CD4(+) T cells.

Arnold PY, Vignali KM, Miller TB, La Gruta NL, Cauley LS, Haynes L, Scott Adams P, Swain SL, Woodland DL, Vignali DA. Arnold PY, et al. Among authors: vignali da, vignali km. J Immunol Methods. 2002 Dec 20;271(1-2):137-51. doi: 10.1016/s0022-1759(02)00343-5. J Immunol Methods. 2002. PMID: 12445737

7

Cutting edge: virus-specific CD4+ memory T cells in nonlymphoid tissues express a highly activated phenotype.

Cauley LS, Cookenham T, Miller TB, Adams PS, Vignali KM, Vignali DA, Woodland DL. Cauley LS, et al. Among authors: vignali da, vignali km. J Immunol. 2002 Dec 15;169(12):6655-8. doi: 10.4049/jimmunol.169.12.6655. J Immunol. 2002. PMID: 12471092

8

Correction of multi-gene deficiency in vivo using a single 'self-cleaving' 2A peptide-based retroviral vector.

Szymczak AL, Workman CJ, Wang Y, Vignali KM, Dilioglou S, Vanin EF, Vignali DA. Szymczak AL, et al. Among authors: vignali da, vignali km. Nat Biotechnol. 2004 May;22(5):589-94. doi: 10.1038/nbt957. Epub 2004 Apr 4. Nat Biotechnol. 2004. PMID: 15064769

9

The CD3epsilon proline-rich sequence, and its interaction with Nck, is not required for T cell development and function.

Szymczak AL, Workman CJ, Gil D, Dilioglou S, Vignali KM, Palmer E, Vignali DA. Szymczak AL, et al. Among authors: vignali da, vignali km. J Immunol. 2005 Jul 1;175(1):270-5. doi: 10.4049/jimmunol.175.1.270. J Immunol. 2005. PMID: 15972658

10

Rapid analysis of T-cell selection in vivo using T cell-receptor retrogenic mice.

Holst J, Vignali KM, Burton AR, Vignali DA. Holst J, et al. Among authors: vignali da, vignali km. Nat Methods. 2006 Mar;3(3):191-7. doi: 10.1038/nmeth858. Nat Methods. 2006. PMID: 16489336

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