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Items: 1 to 20 of 102

1.
2.

Association of tapasin and COPI provides a mechanism for the retrograde transport of major histocompatibility complex (MHC) class I molecules from the Golgi complex to the endoplasmic reticulum.

Paulsson KM, Kleijmeer MJ, Griffith J, Jevon M, Chen S, Anderson PO, Sjogren HO, Li S, Wang P.

J Biol Chem. 2002 May 24;277(21):18266-71. Epub 2002 Mar 7.

3.

Tapasin enhances peptide-induced expression of H2-M3 molecules, but is not required for the retention of open conformers.

Lybarger L, Yu YY, Chun T, Wang CR, Grandea AG 3rd, Van Kaer L, Hansen TH.

J Immunol. 2001 Aug 15;167(4):2097-105.

5.

Inhibition of the MHC class II antigen presentation pathway by human cytomegalovirus.

Johnson DC, Hegde NR.

Curr Top Microbiol Immunol. 2002;269:101-15. Review.

PMID:
12224504
6.

Distinct functions of tapasin revealed by polymorphism in MHC class I peptide loading.

Peh CA, Laham N, Burrows SR, Zhu Y, McCluskey J.

J Immunol. 2000 Jan 1;164(1):292-9.

7.

Assembly of tapasin-associated MHC class I in the absence of the transporter associated with antigen processing (TAP).

Paulsson KM, Anderson PO, Chen S, Sjögren HO, Ljunggren HG, Wang P, Li S.

Int Immunol. 2001 Jan;13(1):23-9.

PMID:
11133831
8.

A short isoform of human cytomegalovirus US3 functions as a dominant negative inhibitor of the full-length form.

Shin J, Park B, Lee S, Kim Y, Biegalke BJ, Kang S, Ahn K.

J Virol. 2006 Jun;80(11):5397-404.

9.

Human cytomegalovirus: host immune modulation by the viral US3 gene.

Liu Z, Winkler M, Biegalke B.

Int J Biochem Cell Biol. 2009 Mar;41(3):503-6. doi: 10.1016/j.biocel.2008.10.012. Epub 2008 Oct 18. Review.

PMID:
18992841
10.

A single polymorphic residue within the peptide-binding cleft of MHC class I molecules determines spectrum of tapasin dependence.

Park B, Lee S, Kim E, Ahn K.

J Immunol. 2003 Jan 15;170(2):961-8. Erratum in: J Immunol. 2003 May 1;170(9):4869.

12.
13.

Retention of empty MHC class I molecules by tapasin is essential to reconstitute antigen presentation in invertebrate cells.

Schoenhals GJ, Krishna RM, Grandea AG 3rd, Spies T, Peterson PA, Yang Y, Früh K.

EMBO J. 1999 Feb 1;18(3):743-53.

14.
15.

Structural and functional dissection of human cytomegalovirus US3 in binding major histocompatibility complex class I molecules.

Lee S, Yoon J, Park B, Jun Y, Jin M, Sung HC, Kim IH, Kang S, Choi EJ, Ahn BY, Ahn K.

J Virol. 2000 Dec;74(23):11262-9.

16.

Tapasin and ERp57 form a stable disulfide-linked dimer within the MHC class I peptide-loading complex.

Peaper DR, Wearsch PA, Cresswell P.

EMBO J. 2005 Oct 19;24(20):3613-23. Epub 2005 Sep 29.

17.

Optimization of the MHC class I peptide cargo is dependent on tapasin.

Williams AP, Peh CA, Purcell AW, McCluskey J, Elliott T.

Immunity. 2002 Apr;16(4):509-20.

18.

A major role for tapasin as a stabilizer of the TAP peptide transporter and consequences for MHC class I expression.

Garbi N, Tiwari N, Momburg F, Hämmerling GJ.

Eur J Immunol. 2003 Jan;33(1):264-73.

19.

An essential function of tapasin in quality control of HLA-G molecules.

Park B, Ahn K.

J Biol Chem. 2003 Apr 18;278(16):14337-45. Epub 2003 Feb 11.

20.

Human cytomegalovirus disrupts the major histocompatibility complex class I peptide-loading complex and inhibits tapasin gene transcription.

Halenius A, Hauka S, Dölken L, Stindt J, Reinhard H, Wiek C, Hanenberg H, Koszinowski UH, Momburg F, Hengel H.

J Virol. 2011 Apr;85(7):3473-85. doi: 10.1128/JVI.01923-10. Epub 2011 Jan 19.

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