(Q41725380)

8 October 2017

The alpha 1 domain of the HLA-DR molecule is essential for high-affinity binding of the toxic shock syndrome toxin-1. (English)

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8 October 2017

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Karp DR

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8 October 2017

Teletski CL

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8 October 2017

Scholl P

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8 October 2017

Geha R

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8 October 2017

Long EO

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8 October 2017

language of work or name

English

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publication date

1 August 1990

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8 October 2017

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8 October 2017

346

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474-476

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8 October 2017

6283

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https://scigraph.springernature.com/pub.10.1038/346474a0

8 October 2017

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cites work

Analysis of the mitogenic effects of toxic shock toxin on human peripheral blood mononuclear cells in vitro

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7 January 2021

T cell stimulation by staphylococcal enterotoxins. Clonally variable response and requirement for major histocompatibility complex class II molecules on accessory or target cells

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7 January 2021

Class II MHC molecules are specific receptors for staphylococcus enterotoxin A

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7 January 2021

High-affinity binding of staphylococcal enterotoxins A and B to HLA-DR

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7 January 2021

Interaction of Staphylococcus aureus toxin "superantigens" with human T cells

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7 January 2021

V beta-specific stimulation of human T cells by staphylococcal toxins.

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7 January 2021

Toxic shock syndrome toxin 1 binds to major histocompatibility complex class II molecules

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7 January 2021

Structural requirements for pairing of alpha and beta chains in HLA-DR and HLA-DP molecules

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7 January 2021

Structure-activity relationship of toxic-shock-syndrome toxin-1: derivation and characterization of immunologically and biologically active fragments

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7 January 2021

A hypothetical model of the foreign antigen binding site of class II histocompatibility molecules

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7 January 2021

Degenerate binding of immunogenic peptides to HLA-DR proteins on B cell Srfaces

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7 January 2021

Gamma ray-induced loss of expression of HLA and glyoxalase I alleles in lymphoblastoid cells

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7 January 2021

The effects of MHC gene dosage and allelic variation on T cell receptor selection

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7 January 2021

Further characterization of HLA-DS molecules: implications for studies assessing the role of human Ia molecules in cell interactions and disease susceptibility

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7 January 2021

Identifiers

DOI

10.1038/346474A0

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Dimensions Publication ID

8 October 2017

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