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Paper77781

Antigen-induced proliferation assay for mouse T lymphocytes. Response to a monovalent antigen.

Alkan SS. Eur J Immunol, 1978. Cited by 64 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Antigen-induced proliferation assay for mouse T lymphocytes. Response to a monovalent antigen. Papers, record 77781. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/77781

Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
Antigen-induced proliferation assay for mouse T lymphocytes. Response to a monovalent antigen.
PubMed
Journal
Eur J Immunol
PubMed
Year
1978
PubMed
Publication types
Journal Article
PubMed
Citations, by iCite
64
iCite
Relative citation ratio, by iCite
1.36
iCite
Revised in PubMed
2013-11-21
PubMed

Authors1

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Alkan SSS S

Source PubMed

Topics17

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
AntigensMajor topic
Lymphocyte ActivationMajor topic
T-LymphocytesMajor topic
Animals
Antilymphocyte Serum
Cell Separation
Dose-Response Relationship, Immunologic
Epitopes
Female
Kinetics
Lymph Nodes
Mice
Mice, Inbred BALB C
Mice, Nude
Tyrosine
gamma-Globulins
p-Azobenzenearsonate

Source PubMed

Cited by15

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 64 citations.

PMIDTitleJournalYearIn PapersSource
7,452,148Systemic tolerance and secretory immunity after oral immunization.J Exp Med1980https://conductscience.org/library/papers/7452148PubMed
6,970,169Antigen-induced proliferation assay for rabbit T lymphocytes. I. Characteristics of the response.Immunology1980https://conductscience.org/library/papers/6970169PubMed
6,800,945Selection of H-2 molecules for the context of antigen recognition by T lymphocytes.Immunogenetics1981https://conductscience.org/library/papers/6800945PubMed
6,800,943Genetic analysis of immune suppression. I. Gene complementation is required for suppression of antigen-specific proliferative responses by T-cell derived factors.Immunogenetics1981https://conductscience.org/library/papers/6800943PubMed
6,791,162A novel type of T-T cell interaction removes the requirement for I-B region in the H-2 complex.Proc Natl Acad Sci U S A1981https://conductscience.org/library/papers/6791162PubMed
6,421,725Characterization of three new intra-I region recombinant mouse strains, B10.ASR7 (H-2as3), B10.BAR4 (H-2h6), and B10.BASR1 (H-2as4).Immunogenetics1984https://conductscience.org/library/papers/6421725PubMed
6,195,108RT1-linked Ir and Is genes control the immune response to bovine insulin in the rat.Immunogenetics1983https://conductscience.org/library/papers/6195108PubMed
6,086,092Genetic control of T-cell proliferative responses to poly(glu40ala60) and poly(glu51lys34tyr15): subregion-specific inhibition of the responses with monoclonal Ia antibodies.Immunogenetics1980https://conductscience.org/library/papers/6086092PubMed
3,117,691Genetic control of immune response to staphylococcal exfoliative toxin A in mice.Infect Immun1987https://conductscience.org/library/papers/3117691PubMed
2,412,742Ability of isoprinosine to restore interleukin-2 production and T cell proliferation in autoimmune mice.Clin Exp Immunol1985https://conductscience.org/library/papers/2412742PubMed
2,396,988Transforming growth factor beta 2 differentially modulates interleukin-1 beta- and tumour-necrosis-factor-alpha-stimulated phospholipase A2 and prostaglandin E2 synthesis in rat renal mesangial cells.Biochem J1990https://conductscience.org/library/papers/2396988PubMed
1,373,200Identification of T-helper epitopes in the VP1 capsid protein of poliovirus.J Virol1992https://conductscience.org/library/papers/1373200PubMed
389,784Interaction of subpopulations of murine lymph node lymphocytes in antigen-induced [14C]-thymidine incorporation: T and B cell synergy in the response to antigen.Immunology1979https://conductscience.org/library/papers/389784PubMed
159,935Immune responses during pregnancy. Evidence of suppressor cells for splenic antibody response.J Exp Med1979https://conductscience.org/library/papers/159935PubMed
93,081Inhibition of antigen-induced lymph node cell proliferation by murine amniotic fluid and its components.Immunology1979https://conductscience.org/library/papers/93081PubMed

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

None in this release

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  • References
  • Genes
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  • Data

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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