Paper · 302173

Selective expression of separate I-region loci in functionally different lymphocyte subpopulations.

Murphy DB and 4 others. Cold Spring Harb Symp Quant Biol, 1977. Cited by 29 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

Cite this record

ConductScience Library. Selective expression of separate I-region loci in functionally different lymphocyte subpopulations. Papers, record 302173. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/302173

On this page

Paper

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

Title: Selective expression of separate I-region loci in functionally different lymphocyte subpopulations.; PubMed
Journal: Cold Spring Harb Symp Quant Biol; PubMed
Year: 1977; PubMed
Publication types: Journal Article, Research Support, U.S. Gov't, P.H.S.; PubMed
PubMed: https://pubmed.ncbi.nlm.nih.gov/302173/; PubMed
DOI: https://doi.org/10.1101/sqb.1977.041.01.057; PubMed
The journal: https://conductscience.org/library/journal-index/1256107; PubMed
Citations, by iCite: 29; iCite
Relative citation ratio, by iCite: 0.73; iCite
Revised in PubMed: 2019-08-23; PubMed

Authors5

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

Order	Author	Forename
1	Murphy DB	D B
2	Okumura K	K
3	Herzenberg LA	L A
4	Herzenberg LA	L A
5	McDevitt HO	H O

Source PubMed

Topics11

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

MeSH term	Major
B-Lymphocytes	Major topic
Genes	Major topic
Histocompatibility Antigens	Major topic
T-Lymphocytes	Major topic
Animals
Antibody Formation
Lymphocyte Activation
Mice
Mice, Inbred BALB C
Mice, Inbred Strains
Phenotype

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 by10

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 29 citations.

PMID	Title	Journal	Year	In Papers	Source
7,373,222	Generation of primary cytotoxic lymphocytes against non-major histocompatibility complex antigens by anti-Ia serum plus complement-treated lymphocytes.	J Exp Med	1980	https://conductscience.org/library/papers/7373222	PubMed
6,168,576	T cells in a suppressor circuit and non-T:non-B cells bear different I-J determinants.	Immunogenetics	1981	https://conductscience.org/library/papers/6168576	PubMed
2,971,754	Thymic selection of H-2-incompatible bone marrow cells in SCID mice. Differences in T help for induction of B cell IgG responses versus cytotoxic T cells.	J Exp Med	1988	https://conductscience.org/library/papers/2971754	PubMed
2,417,235	Association of I-J determinants with lipomodulin/macrocortin.	Proc Natl Acad Sci U S A	1986	https://conductscience.org/library/papers/2417235	PubMed
448,292	Evidence for two homologous, but nonidentical, Ia molecules determined by the I-EC subregion.	J Exp Med	1979	https://conductscience.org/library/papers/448292	PubMed
418,135	In vitro analysis of allogeneic lymphocyte interaction. II. I-region control of the activity of a B-cell-derived H-2-restricted allogeneic effect factor and its receptor during B-cell activation.	J Exp Med	1978	https://conductscience.org/library/papers/418135	PubMed
288,078	Clonal evolution of myeloma cells leads to quantitative changes in immunoglobulin secretion and surface antigen expression.	Proc Natl Acad Sci U S A	1979	https://conductscience.org/library/papers/288078	PubMed
117,075	Functional analysis of T cells expressing Ia antigens. I. Demonstration of helper T-cell heterogeneity.	J Exp Med	1979	https://conductscience.org/library/papers/117075	PubMed
82,605	Immunological dissection of human Ia molecules.	J Exp Med	1978	https://conductscience.org/library/papers/82605	PubMed
33,223	The role of H-2 and Ia antigens in graft-versus-host reactions (GVHR). Presence of host alloantigens on donor cells after GVHR and suppression of GVHR with an anti-Ia antiserum against hose Ia antigens.	J Exp Med	1979	https://conductscience.org/library/papers/33223	PubMed

Genes2

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

Gene	NCBI Gene ID	Linked by	In Genes	Source
INSM1	3,642	PubTator's text mining	https://conductscience.org/library/genes/3642	NCBI Gene
ITGA4	3,676	PubTator's text mining	https://conductscience.org/library/genes/3676	NCBI 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.

For software

Read this paper from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/papers/v1/302173

GET https://conductscience.org/api/papers/v1/302173/authors

API reference For AI assistants