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Paper · 62011

Ly phenotype of cytotoxic T cells for syngeneic tumor.

Shiku H and 4 others. J Exp Med, 1976. Cited by 93 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Ly phenotype of cytotoxic T cells for syngeneic tumor. Papers, record 62011. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/62011

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Paper

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

Title
Ly phenotype of cytotoxic T cells for syngeneic tumor.
PubMed
Journal
J Exp Med
PubMed
Year
1976
PubMed
Publication types
Journal Article, Research Support, U.S. Gov't, P.H.S.
PubMed
Citations, by iCite
93
iCite
Relative citation ratio, by iCite
2.4
iCite
Revised in PubMed
2019-05-08
PubMed

Authors5

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

OrderAuthorForenameKindORCID iD
1Shiku HH
2Takahashi TT
3Bean MAM A
4Old LJL J
5Oettgen HFH F

Source PubMed

Topics12

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

MeSH termMajor
PhenotypeMajor topic
T-LymphocytesMajor topic
Animals
Cytotoxicity Tests, Immunologic
Epitopes
Female
Mice
Mice, Inbred C57BL
Neoplasm Transplantation
Neoplasms, Experimental
Sarcoma
Transplantation, Isogeneic

Source PubMed

Grants0

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

None in this release.

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

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.

References5

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
11,078,839Expression of T-cell differentiation antigens on effector cells in cell-mediated cytotoxicity in vitro. Evidence for functional heterogeneity related to the surface phenotype of T cells.J Exp Med1975https://conductscience.org/library/papers/1078839PubMed
21,084,882Surface phenotype of nonadherent peritoneal cells effecting cell-mediated cytotoxicity in vitro for allogeneic and syngeneic murine sarcoma cells.Isr J Med Sci1976https://conductscience.org/library/papers/1084882PubMed
3234,178Ly antigens as markers for functionally distinct subpopulations of thymus-derived lymphocytes of the mouse.Nature1975https://conductscience.org/library/papers/234178PubMed
41,113,324Cytotoxic reactions of murine lymphoid cells studied with a tritiated proline microcytotoxicity test.J Natl Cancer Inst1975https://conductscience.org/library/papers/1113324PubMed
51,092,798Functional subclasses of T-lymphocytes bearing different Ly antigens. I. The generation of functionally distinct T-cell subclasses is a differentiative process independent of antigen.J Exp Med1975https://conductscience.org/library/papers/1092798PubMed

Cited by24

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 93 citations.

PMIDTitleJournalYearIn PapersSource
9,177,225Mutated mitogen-activated protein kinase: a tumor rejection antigen of mouse sarcoma.Proc Natl Acad Sci U S A1997https://conductscience.org/library/papers/9177225PubMed
6,982,847An analysis of T lymphocyte subsets in tumour-transplanted mice on the basis of Lyt antigenic markers and functions.Immunology1982https://conductscience.org/library/papers/6982847PubMed
6,974,221Eradication of disseminated murine leukemia by chemoimmunotherapy with cyclophosphamide and adoptively transferred immune syngeneic Lyt-1+2- lymphocytes.J Exp Med1981https://conductscience.org/library/papers/6974221PubMed
6,970,525The role of T cell sets in the rejection of a methylcholanthrene-induced sarcoma (S1509a) in syngeneic mice.Am J Pathol1981https://conductscience.org/library/papers/6970525PubMed
6,968,813Alloreactive and H-2-restricted Lyt 23 cytotoxic T lymphocytes derive from a common pool of antecedent Lyt 123 precursors.J Exp Med1980https://conductscience.org/library/papers/6968813PubMed
6,967,947Blocking effect of lyt-2 antibodies on T cell functions.J Exp Med1980https://conductscience.org/library/papers/6967947PubMed
6,967,215Alloantigen-induced T-cell proliferation: Lyt phenotype of responding cells and blocking of proliferation by Lyt antisera.Proc Natl Acad Sci U S A1980https://conductscience.org/library/papers/6967215PubMed
6,607,141Liposome facilitated xenogeneic approach for studying human colon cancer immunity: carrier and adjuvant effect of liposomes.Clin Exp Immunol1984https://conductscience.org/library/papers/6607141PubMed
6,454,744
Enhancement of T lymphocyte functions by Fc fragments of immunoglobulins. I. Augmentation of allogeneic mixed lymphocyte culture reactions requires I-A- or I-B-subregion differences between effector and stimulator cell populations.
J Exp Med1981https://conductscience.org/library/papers/6454744PubMed
6,293,112Regulation of the immune response to antigens on the malignant cell surface.Springer Semin Immunopathol1982https://conductscience.org/library/papers/6293112PubMed

1 to 10 of 24

See all 24 cited by

Genes2

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

GeneNCBI Gene IDLinked byIn GenesSource
CD8B926PubTator's text mininghttps://conductscience.org/library/genes/926NCBI Gene
THY17,070PubTator's text mininghttps://conductscience.org/library/genes/7070NCBI Gene

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

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

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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