Paper · 71240

Isolated hapten-binding receptors of sensitized lymphocytes. I. Receptors from nylon wool-enriched mouse T lymphocytes lack serological markers of immunoglobulin constant domains but express heavy chain variable portions.

Krawinkel U and 5 others. Eur J Immunol, 1977. Cited by 77 papers, by iCite.

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ConductScience Library. Isolated hapten-binding receptors of sensitized lymphocytes. I. Receptors from nylon wool-enriched mouse T lymphocytes lack serological markers of immunoglobulin constant domains but express heavy chain variable portions. Papers, record 71240. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/71240

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Paper

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

Title: Isolated hapten-binding receptors of sensitized lymphocytes. I. Receptors from nylon wool-enriched mouse T lymphocytes lack serological markers of immunoglobulin constant domains but express heavy chain variable portions.; PubMed
Journal: Eur J Immunol; PubMed
Year: 1977; PubMed
Publication types: Journal Article; PubMed
PubMed: https://pubmed.ncbi.nlm.nih.gov/71240/; PubMed
DOI: https://doi.org/10.1002/eji.1830070814; PubMed
The journal: https://conductscience.org/library/journal-index/1273201; PubMed
Citations, by iCite: 77; iCite
Relative citation ratio, by iCite: 1.46; iCite
Revised in PubMed: 2011-11-17; PubMed

Authors6

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

Order	Author	Forename
1	Krawinkel U	U
2	Cramer M	M
3	Imanishi-Kari T	T
4	Jack RS	R S
5	Rajewsky K	K
6	Mäkelä O	O

Source PubMed

Topics15

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

MeSH term	Major
Binding Sites, Antibody	Major topic
Epitopes	Major topic
Genes	Major topic
Haptens	Major topic
Immunoglobulin Heavy Chains	Major topic
Immunoglobulin Variable Region	Major topic
T-Lymphocytes	Major topic
Animals
Antibodies, Anti-Idiotypic
Antibody Specificity
Genotype
Mice
Mice, Inbred C57BL
Mice, Inbred CBA
Nitrobenzenes

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.

References0

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

None in this release.

Cited by23

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 77 citations.

PMID	Title	Journal	Year	In Papers	Source
6,976,417	Tthyd, a new thymocyte alloantigen linked to Igh-1. Implications for a switch mechanism for T cell antigen receptors.	J Exp Med	1982	https://conductscience.org/library/papers/6976417	PubMed
6,967,947	Blocking effect of lyt-2 antibodies on T cell functions.	J Exp Med	1980	https://conductscience.org/library/papers/6967947	PubMed
6,808,074	Regulatory idiotypes. T helper cells recognize a shared VH idiotope on phosphorylcholine-specific antibodies.	J Exp Med	1982	https://conductscience.org/library/papers/6808074	PubMed
6,792,727	Helper and suppressor T cell factors.	Springer Semin Immunopathol	1980	https://conductscience.org/library/papers/6792727	PubMed
6,791,163	Expression of an antigen receptor on T cells does not require recombination at the immunoglobulin JH-C mu locus.	Proc Natl Acad Sci U S A	1981	https://conductscience.org/library/papers/6791163	PubMed
6,235,521	Internal complementarities in the immune system: regulation of the expression of helper T-cell idiotypes.	Proc Natl Acad Sci U S A	1984	https://conductscience.org/library/papers/6235521	PubMed
6,190,977	T and B cells that recognize the same antigen do not transcribe similar heavy chain variable region gene segments.	J Exp Med	1983	https://conductscience.org/library/papers/6190977	PubMed
6,189,953	Presence of IgT-C and I-A subregion-encoded determinants on distinct chains of monoclonal antigen-specific augmenting factor derived from a T cell hybridoma.	J Exp Med	1983	https://conductscience.org/library/papers/6189953	PubMed
6,180,436	T-cell proliferative response to hapten-modified self-immunoglobulins: recognition of conjugate-specific determinants.	Proc Natl Acad Sci U S A	1982	https://conductscience.org/library/papers/6180436	PubMed
6,168,565	T-cell hybridomas producing hapten-specific suppressor factors.	Immunology	1981	https://conductscience.org/library/papers/6168565	PubMed

1 to 10 of 23

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Genes0

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

None in this release.

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

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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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