Paper · 468309
Differences in [3H]-thymidine uptake of lymph node cells stimulated by Con A and PHA in H-2 congenic mouse strains.
Bösze Z and 2 others. Immunology, 1979. Cited by 7 papers, by iCite.
11 sourcespapers-2026-11-12-0.1.0
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ConductScience Library. Differences in [3H]-thymidine uptake of lymph node cells stimulated by Con A and PHA in H-2 congenic mouse strains. Papers, record 468309. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/468309
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Paper
PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
- Title
- Differences in [3H]-thymidine uptake of lymph node cells stimulated by Con A and PHA in H-2 congenic mouse strains.
- PubMed
Topics15
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Concanavalin A | Major topic |
| H-2 Antigens | Major topic |
| Lectins | Major topic |
| Lymphocytes | Major topic |
| Thymidine | Major topic |
| Animals | |
| DNA | |
| Dose-Response Relationship, Drug | |
| In Vitro Techniques | |
| Kinetics | |
| Lymph Nodes | |
| Male | |
| Mice | |
| Mice, Inbred Strains | |
| Mitosis |
Source PubMed
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Trials0
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None in this release.
Comments and corrections0
PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.
None in this release.
References15
The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.
| Order | PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|---|
| 1 | 62,014 | Effects of anti-Ia sera on mitogenic responses. III. Mapping the genes controlling the expression of Ia determinants on concanavalin A-reactive cells to the I-J subregion of the H-2 gene complex. | J Exp Med | 1976 | https://conductscience.org/library/papers/62014 | PubMed |
| 2 | 300,750 | Evidence that Con A induces cytotoxicity in the same subclass of T cells as does alloimmunization. | J Immunol | 1977 | https://conductscience.org/library/papers/300750 | PubMed |
| 3 | 902,679 | Genetic control of two different types of antibody responses to oxazolone. | Eur J Immunol | 1977 | https://conductscience.org/library/papers/902679 | PubMed |
| 4 | 862,659 | Genetic control of contact sensitivity to oxazolone in inbred, H-2 congenic and intra-H-2 recombinant strains of mice. | Eur J Immunol | 1977 | https://conductscience.org/library/papers/862659 | PubMed |
| 5 | 848,890 | [Genetic selection of mice for quantitative responsiveness of lymphocytes to phytohemagglutinin]. | Ann Immunol (Paris) | 1977 | https://conductscience.org/library/papers/848890 | PubMed |
| 6 | 4,115,486 | Two new H-2 specificities: H-2.44 and H-2.45. | Folia Biol (Praha) | 1972 | https://conductscience.org/library/papers/4115486 | PubMed |
| 7 | 4,119,248 | Functional heterogeneity of murine lymphoid cells. 3. Differential responsiveness of T cells to phytohemagglutinin and concanavalin A as a probe for T cell subsets. | J Immunol | 1973 | https://conductscience.org/library/papers/4119248 | PubMed |
| 8 | 47,219 | The H-2 major histocompatibility complex and the I immune response region: genetic variation, function, and organization. | Adv Immunol | 1975 | https://conductscience.org/library/papers/47219 | PubMed |
| 9 | 4,275,202 | Genetic determinants of immunological responsiveness. | Adv Immunol | 1974 | https://conductscience.org/library/papers/4275202 | PubMed |
| 10 | 4,605,183 | Subpopulations of mouse spleen lymphocytes. I. Dissociation between the reactivities to different "non-specific" mitogens. | Immunology | 1974 | https://conductscience.org/library/papers/4605183 | PubMed |
1 to 10 of 15
See all 15 referencesCited by1
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 7 citations.
| PMID | Title | Journal | Year | In Papers |
|---|---|---|---|---|
| 6,974,136 | Genetic control of T-lymphocyte mitogenesis in chickens. | Immunogenetics | 1981 | https://conductscience.org/library/papers/6974136 |
Source PubMed
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- 2026-11-12
- Gene search
- 2026-11-11
- Pipelines
- 2026-09-18
Sources 11
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- 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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