Paper · 56402
SPECIFIC positive and negative selection of rat lymphocytes reactive to strong histocompatibility antigens: activation with alloantigens in vitro and in vivo.
Wilson DB and 2 others. J Immunol, 1976. Cited by 27 papers, by iCite.
11 sourcespapers-2026-11-12-0.1.0
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ConductScience Library. SPECIFIC positive and negative selection of rat lymphocytes reactive to strong histocompatibility antigens: activation with alloantigens in vitro and in vivo. Papers, record 56402. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/56402
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PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
- Title
- SPECIFIC positive and negative selection of rat lymphocytes reactive to strong histocompatibility antigens: activation with alloantigens in vitro and in vivo.
- PubMed
Topics11
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Immunity, Cellular | Major topic |
| Lymphocytes | Major topic |
| Animals | |
| Epitopes | |
| Graft vs Host Reaction | |
| Lymphocyte Activation | |
| Lymphocyte Culture Test, Mixed | |
| Rats | |
| Rats, Inbred Strains | |
| Thoracic Duct | |
| Time Factors |
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Trials0
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Comments and corrections0
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References0
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Cited by13
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 27 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 6,973,003 | Induced tolerance in F1 rats to anti-major histocompatibility complex receptors on parental T cells. Implications for self tolerance. | J Exp Med | 1981 | https://conductscience.org/library/papers/6973003 | PubMed |
| 6,222,131 | Induction of cytotoxic T cell precursors in vivo. Role of T helper cells. | J Exp Med | 1983 | https://conductscience.org/library/papers/6222131 | PubMed |
| 6,216,134 | Spontaneous diabetes in BB rats: evidence for a T cell dependent immune response defect. | Diabetologia | 1982 | https://conductscience.org/library/papers/6216134 | PubMed |
| 3,875,095 | In vivo separation of two classes of T cells as determined by negative selection after the injection of UV-treated allogeneic lymphoid cells. | Proc Natl Acad Sci U S A | 1985 | https://conductscience.org/library/papers/3875095 | PubMed |
| 3,511,173 | Immunogenicity and crossreactivity of specificity-associated markers on alloreactive T cells. Confirmation based on the model of tolerance abolition by adoptive transfer. | J Exp Med | 1986 | https://conductscience.org/library/papers/3511173 | PubMed |
| 2,531,192 | Capacity of unprimed CD4+ and CD8+ T cells expressing V beta 11 receptors to respond to I-E alloantigens in vivo. | J Exp Med | 1989 | https://conductscience.org/library/papers/2531192 | PubMed |
| 2,117,641 | Selective expansion of T cells expressing V beta 2 in toxic shock syndrome. | J Exp Med | 1990 | https://conductscience.org/library/papers/2117641 | PubMed |
| 2,007,855 | Generation of T cells with lytic specificity for atypical antigens. III. Priming F1 animals with antigen-bearing cells also having reactivity for host alloantigens allows for potent lytic T cell responses. | J Exp Med | 1991 | https://conductscience.org/library/papers/2007855 | PubMed |
| 1,371,720 | Allogeneic tumor-specific cytotoxic T lymphocytes. | Cancer Immunol Immunother | 1992 | https://conductscience.org/library/papers/1371720 | PubMed |
| 301,550 | The generation of killer cells to trinitrophenyl-modified allogeneic targets by lymphocyte populations negatively selected to strong alloantigens. | J Exp Med | 1977 | https://conductscience.org/library/papers/301550 | PubMed |
1 to 10 of 13
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- 2026-11-12
- Gene search
- 2026-11-11
- Pipelines
- 2026-09-18
Sources 11
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- HGNCCC0
- iCiteCC BY 4.0
- NCBI GenePublic domain (US government)
- NIH RePORTER's grant and paper linksPublic domain
- Open TargetsCC0 1.0
- PMC's ID filePublic domain (US government)
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- HGNCCC0: https://www.genenames.org/about/license/
- iCiteCC BY 4.0
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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