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Journal Articles

Models of T cell anergy: is there a common molecular mechanism?

R H Schwartz

J Exp Med (1996) 184 (1): 1–8.

https://doi.org/10.1084/jem.184.1.1

Published: 01 July 1996

View articletitled, Models of T cell anergy: is there a common molecular mechanism?

Journal Articles

A quantitative analysis of antigen-presenting cell function: activated B cells stimulate naive CD4 T cells but are inferior to dendritic cells in providing costimulation.

D J Cassell, R H Schwartz

J Exp Med (1994) 180 (5): 1829–1840.

https://doi.org/10.1084/jem.180.5.1829

Published: 01 November 1994

View articletitled, A quantitative analysis of antigen-presenting cell function: activated B cells stimulate naive CD4 T cells but are inferior to dendritic cells in providing costimulation.

Journal Articles

Activation events during thymic selection.

A Bendelac, P Matzinger, R A Seder, W E Paul, R H Schwartz

J Exp Med (1992) 175 (3): 731–742.

https://doi.org/10.1084/jem.175.3.731

Published: 01 March 1992

View articletitled, Activation events during thymic selection.

Journal Articles

Early genetic events in T cell development analyzed by in situ hybridization.

D M Pardoll, B J Fowlkes, R I Lechler, R N Germain, R H Schwartz

J Exp Med (1987) 165 (6): 1624–1638.

https://doi.org/10.1084/jem.165.6.1624

Published: 01 June 1987

View articletitled, Early genetic events in T cell development analyzed by in situ hybridization.

Journal Articles

Antigen presentation by chemically modified splenocytes induces antigen-specific T cell unresponsiveness in vitro and in vivo.

M K Jenkins, R H Schwartz

J Exp Med (1987) 165 (2): 302–319.

https://doi.org/10.1084/jem.165.2.302

Published: 01 February 1987

View articletitled, Antigen presentation by chemically modified splenocytes induces antigen-specific T cell unresponsiveness in vitro and in vivo.

Journal Articles

Polyclonal stimulation of resting B lymphocytes by antigen-specific T lymphocytes.

A L DeFranco, J D Ashwell, R H Schwartz, W E Paul

J Exp Med (1984) 159 (3): 861–880.

https://doi.org/10.1084/jem.159.3.861

Published: 01 March 1984

View articletitled, Polyclonal stimulation of resting B lymphocytes by antigen-specific T lymphocytes.

Journal Articles

Antigen presentation by resting B cells. Radiosensitivity of the antigen-presentation function and two distinct pathways of T cell activation.

J D Ashwell, A L DeFranco, W E Paul, R H Schwartz

J Exp Med (1984) 159 (3): 881–905.

https://doi.org/10.1084/jem.159.3.881

Published: 01 March 1984

View articletitled, Antigen presentation by resting B cells. Radiosensitivity of the antigen-presentation function and two distinct pathways of T cell activation.

Journal Articles

T and B cells that recognize the same antigen do not transcribe similar heavy chain variable region gene segments.

E Kraig, M Kronenberg, J A Kapp, C W Pierce, A F Abruzzini, C M Sorensen, L E Samelson, R H Schwartz, L E Hood

J Exp Med (1983) 158 (1): 192–209.

https://doi.org/10.1084/jem.158.1.192

Published: 01 July 1983

View articletitled, T and B cells that recognize the same antigen do not transcribe similar heavy chain variable region gene segments.

Journal Articles

Immune response gene function correlates with the expression of an Ia antigen. I. Preferential association of certain Ae and E alpha chains results in a quantitative deficiency in expression of an Ae:E alpha complex.

J M McNicholas, D B Murphy, L A Matis, R H Schwartz, E A Lerner, C A Janeway, Jr, P P Jones

J Exp Med (1982) 155 (2): 490–507.

https://doi.org/10.1084/jem.155.2.490

Published: 01 February 1982

View articletitled, Immune response gene function correlates with the expression of an Ia antigen. I. Preferential association of certain Ae and E alpha chains results in a quantitative deficiency in expression of an Ae:E alpha complex.

Journal Articles

Monoclonal antibody against an Ir gene product?

E A Lerner, L A Matis, C A Janeway, Jr, P P Jones, R H Schwartz, D B Murphy

J Exp Med (1980) 152 (4): 1085–1101.

https://doi.org/10.1084/jem.152.4.1085

Published: 01 October 1980

View articletitled, Monoclonal antibody against an Ir gene product?

Journal Articles

Gene complementation. Neither Ir-GLphi gene need be present in the proliferative T cell to generate an immune response to Poly(Glu55Lys36Phe9)n.

D L Longo, R H Schwartz

J Exp Med (1980) 151 (6): 1452–1467.

https://doi.org/10.1084/jem.151.6.1452

Published: 01 June 1980

View articletitled, Gene complementation. Neither Ir-GLphi gene need be present in the proliferative T cell to generate an immune response to Poly(Glu55Lys36Phe9)n.

Journal Articles

T-lymphocyte response to cytochrome c. I. Demonstration of a T-cell heteroclitic proliferative response and identification of a topographic antigenic determinant on pigeon cytochrome c whose immune recognition requires two complementing major histocompatibility complex-linked immune response genes.

A M Solinger, M E Ultee, E Margoliash, R H Schwartz

J Exp Med (1979) 150 (4): 830–848.

https://doi.org/10.1084/jem.150.4.830

Published: 01 October 1979

View articletitled, T-lymphocyte response to cytochrome c. I. Demonstration of a T-cell heteroclitic proliferative response and identification of a topographic antigenic determinant on pigeon cytochrome c whose immune recognition requires two complementing major histocompatibility complex-linked immune response genes.

Journal Articles

Gene complementation in the T-lymphocyte proliferative response to poly (Glu55Lys36Phe9)n. A demonstration that both immune response gene products must be expressed in the same antigen-presenting cell.

R H Schwartz, A Yano, J H Stimpfling, W E Paul

J Exp Med (1979) 149 (1): 40–57.

https://doi.org/10.1084/jem.149.1.40

Published: 01 January 1979

View articletitled, Gene complementation in the T-lymphocyte proliferative response to poly (Glu55Lys36Phe9)n. A demonstration that both immune response gene products must be expressed in the same antigen-presenting cell.

Journal Articles

T-lymphocyte-enriched murine peritoneal exudate cells. IV. Genetic control of cross-stimulation at the T-cell level.

R H Schwartz, C L Horton, W E Paul

J Exp Med (1977) 145 (2): 327–343.

https://doi.org/10.1084/jem.145.2.327

Published: 01 February 1977

View articletitled, T-lymphocyte-enriched murine peritoneal exudate cells. IV. Genetic control of cross-stimulation at the T-cell level.

Journal Articles

The requirement for two complementing Ir-GLphi immune response genes in the T-lymphocyte proliferative response to poly-(Glu53Lys36Phe11).

R H Schwartz, M E Dorf, B Benacerraf, W E Paul

J Exp Med (1976) 143 (4): 897–905.

https://doi.org/10.1084/jem.143.4.897

Published: 01 April 1976

View articletitled, The requirement for two complementing Ir-GLphi immune response genes in the T-lymphocyte proliferative response to poly-(Glu53Lys36Phe11).

Journal Articles

T-lymphocyte-enriched murine peritoneal exudate cells. II. Genetic control of antigen-induced T-lymphocyte proliferation.

R H Schwartz, W E Paul

J Exp Med (1976) 143 (3): 529–540.

https://doi.org/10.1084/jem.143.3.529

Published: 01 March 1976

View articletitled, T-lymphocyte-enriched murine peritoneal exudate cells. II. Genetic control of antigen-induced T-lymphocyte proliferation.

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Models of T cell anergy: is there a common molecular mechanism?

A quantitative analysis of antigen-presenting cell function: activated B cells stimulate naive CD4 T cells but are inferior to dendritic cells in providing costimulation.

Activation events during thymic selection.

Early genetic events in T cell development analyzed by in situ hybridization.

Antigen presentation by chemically modified splenocytes induces antigen-specific T cell unresponsiveness in vitro and in vivo.

Polyclonal stimulation of resting B lymphocytes by antigen-specific T lymphocytes.

Antigen presentation by resting B cells. Radiosensitivity of the antigen-presentation function and two distinct pathways of T cell activation.

T and B cells that recognize the same antigen do not transcribe similar heavy chain variable region gene segments.

Immune response gene function correlates with the expression of an Ia antigen. I. Preferential association of certain Ae and E alpha chains results in a quantitative deficiency in expression of an Ae:E alpha complex.

Monoclonal antibody against an Ir gene product?

Gene complementation. Neither Ir-GLphi gene need be present in the proliferative T cell to generate an immune response to Poly(Glu55Lys36Phe9)n.

T-lymphocyte response to cytochrome c. I. Demonstration of a T-cell heteroclitic proliferative response and identification of a topographic antigenic determinant on pigeon cytochrome c whose immune recognition requires two complementing major histocompatibility complex-linked immune response genes.

Gene complementation in the T-lymphocyte proliferative response to poly (Glu55Lys36Phe9)n. A demonstration that both immune response gene products must be expressed in the same antigen-presenting cell.

T-lymphocyte-enriched murine peritoneal exudate cells. IV. Genetic control of cross-stimulation at the T-cell level.

The requirement for two complementing Ir-GLphi immune response genes in the T-lymphocyte proliferative response to poly-(Glu53Lys36Phe11).

T-lymphocyte-enriched murine peritoneal exudate cells. II. Genetic control of antigen-induced T-lymphocyte proliferation.

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