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Paper · 41865294

Membrane-Based Assembly and Interactions in Immune Receptors.

Call ME and 1 other. Chem Rev, 2026. Cited by 1 paper, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Membrane-Based Assembly and Interactions in Immune Receptors. Papers, record 41865294. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/41865294

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Paper

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

Title
Membrane-Based Assembly and Interactions in Immune Receptors.
PubMed
Journal
Chem Rev
PubMed
Year
2026
PubMed
Publication types
Journal Article, Review
PubMed
Citations, by iCite
1
iCite
Revised in PubMed
2026-08-13
PubMed

Authors2

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

OrderAuthorForenameKindORCID iD
1Call MEMatthew Ehttps://orcid.org/0000-0001-5846-6469
2Call MJMelissa J

Source PubMed

Topics6

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

MeSH termMajor
Receptors, ImmunologicMajor topic
Cell MembraneMajor topic
Humans
Animals
Lipid Bilayers
Signal Transduction

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.

References339

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

OrderPMIDTitleJournalYearIn PapersSource
128,893,902The cytosolic domain of T-cell receptor ζ associates with membranes in a dynamic equilibrium and deeply penetrates the bilayer.J Biol Chem2017https://conductscience.org/library/papers/28893902PubMed
210,359,120
NKp46 is the major triggering receptor involved in the natural cytotoxicity of fresh or cultured human NK cells. Correlation between surface density of NKp46 and natural cytotoxicity against autologous, allogeneic or xenogeneic target cells.
Eur J Immunol1999https://conductscience.org/library/papers/10359120PubMed
318,425,106Up on the tightrope: natural killer cell activation and inhibition.Nat Immunol2008https://conductscience.org/library/papers/18425106PubMed
410,943,843The Sec61p complex mediates the integration of a membrane protein by allowing lipid partitioning of the transmembrane domain.Cell2000https://conductscience.org/library/papers/10943843PubMed
514,530,327The tetraspanin CD81 regulates the expression of CD19 during B cell development in a postendoplasmic reticulum compartment.J Immunol2003https://conductscience.org/library/papers/14530327PubMed
626,824,389Mutational scanning reveals the determinants of protein insertion and association energetics in the plasma membrane.Elife2016https://conductscience.org/library/papers/26824389PubMed
716,834,459MPLW515L is a novel somatic activating mutation in myelofibrosis with myeloid metaplasia.PLoS Med2006https://conductscience.org/library/papers/16834459PubMed
82,421,164Transfer of specificity by murine alpha and beta T-cell receptor genes.Nature1986https://conductscience.org/library/papers/2421164PubMed
940,254,394MARC, a novel modular chimeric antigen receptor, improves T cell-based cancer immunotherapies by preventing early T cell exhaustion and enhancing persistence.J Immunother Cancer2025https://conductscience.org/library/papers/40254394PubMed
1032,814,900An intramembrane chaperone complex facilitates membrane protein biogenesis.Nature2020https://conductscience.org/library/papers/32814900PubMed

Cited by0

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 1 citation.

None in this release.

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

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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