B7-1 and B7-2 selectively recruit CTLA-4 and CD28 to the immunological synapse (Q46346021)

21 December 2017

title

B7-1 and B7-2 selectively recruit CTLA-4 and CD28 to the immunological synapse (English)

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21 December 2017

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James P Allison

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Jackson Egen

object named as

Jackson G Egen

series ordinal

2

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author name string

Tsvetelina Pentcheva-Hoang

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1

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21 December 2017

Kathleen Wojnoonski

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3

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21 December 2017

language of work or name

English

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publication date

1 September 2004

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21 December 2017

published in

Immunity

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21 December 2017

volume

21

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21 December 2017

issue

3

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21 December 2017

page(s)

401-413

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21 December 2017

Crystal structure of the B7-1/CTLA-4 complex that inhibits human immune responses

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Blockade of costimulation through B7/CD28 inhibits experimental autoimmune uveoretinitis, but does not induce long-term tolerance.

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Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

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B7.1 and B7.2 co-stimulatory molecules regulate crescentic glomerulonephritis

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Complementarity determining region 1 (CDR1)- and CDR3-analogous regions in CTLA-4 and CD28 determine the binding to B7-1.

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CTLA-4: new insights into its biological function and use in tumor immunotherapy

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12 October 2022

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Episomal vectors rapidly and stably produce high-titer recombinant retrovirus

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12 October 2022

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Structural basis for co-stimulation by the human CTLA-4/B7-2 complex

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12 October 2022

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A new member of the immunoglobulin superfamily--CTLA-4

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12 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/J.IMMUNI.2004.06.017

Identifiers

DOI

10.1016/J.IMMUNI.2004.06.017

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21 December 2017

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21 December 2017