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Paper40870

Differential elution of Clq, Clr and Cls from human Cl bound to immune aggregates. Use in the rapid purification of Cl subcomponents.

Arlaud GJ and 3 others. Mol Immunol, 1979. Cited by 141 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Differential elution of Clq, Clr and Cls from human Cl bound to immune aggregates. Use in the rapid purification of Cl subcomponents. Papers, record 40870. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/40870

Paper

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

Title
Differential elution of Clq, Clr and Cls from human Cl bound to immune aggregates. Use in the rapid purification of Cl subcomponents.
PubMed
Journal
Mol Immunol
PubMed
Year
1979
PubMed
Publication types
Journal Article
PubMed
Citations, by iCite
141
iCite
Relative citation ratio, by iCite
3.55
iCite
Revised in PubMed
2019-08-23
PubMed

Authors4

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

OrderAuthorForenameKindORCID iD
1Arlaud GJG J
2Sim RBR B
3Duplaa AMA M
4Colomb MGM G

Source PubMed

Topics9

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

MeSH termMajor
Complement C1Major topic
Complement Pathway, Classical
Electrophoresis, Polyacrylamide Gel
Humans
Hydrogen-Ion Concentration
Immunoglobulin G
Osmolar Concentration
Ovalbumin
Protein Binding

Source PubMed

Cited by51

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 141 citations.

PMIDTitleJournalYearIn PapersSource
41,176,693The fc fragment of IgMs binds C1q to activate the first step of the classical complement pathway, while inhibiting complement-dependent cytotoxicity.FEBS J2026https://conductscience.org/library/papers/41176693PubMed
38,911,852Revisiting the interaction between complement lectin pathway protease MASP-2 and SARS-CoV-2 nucleoprotein.Front Immunol2024https://conductscience.org/library/papers/38911852PubMed
35,685,087Biophysical Characterization of the Oligomeric States of Recombinant Immunoglobulins Type-M and Their C1q-Binding Kinetics by Biolayer Interferometry.Front Bioeng Biotechnol2022https://conductscience.org/library/papers/35685087PubMed
34,066,122Molecular Basis of Complement C1q Collagen-Like Region Interaction with the Immunoglobulin-Like Receptor LAIR-1.Int J Mol Sci2021https://conductscience.org/library/papers/34066122PubMed
33,193,398Complement C1q Interacts With LRP1 Clusters II and IV Through a Site Close but Different From the Binding Site of Its C1r and C1s-Associated Proteases.Front Immunol2020https://conductscience.org/library/papers/33193398PubMed
32,296,440Molecular and Cellular Interactions of Scavenger Receptor SR-F1 With Complement C1q Provide Insights Into Its Role in the Clearance of Apoptotic Cells.Front Immunol2020https://conductscience.org/library/papers/32296440PubMed
32,163,462Transient pentameric IgM fulfill biological function-Effect of expression host and transfection on IgM properties.PLoS One2020https://conductscience.org/library/papers/32163462PubMed
31,749,804C1R Mutations Trigger Constitutive Complement 1 Activation in Periodontal Ehlers-Danlos Syndrome.Front Immunol2019https://conductscience.org/library/papers/31749804PubMed
30,923,526Interaction of C1q With Pentraxin 3 and IgM Revisited: Mutational Studies With Recombinant C1q Variants.Front Immunol2019https://conductscience.org/library/papers/30923526PubMed
29,563,915C1q and Mannose-Binding Lectin Interact with CR1 in the Same Region on CCP24-25 Modules.Front Immunol2018https://conductscience.org/library/papers/29563915PubMed
29,209,066Interaction of Complement Defence Collagens C1q and Mannose-Binding Lectin with BMP-1/Tolloid-like Proteinases.Sci Rep2017https://conductscience.org/library/papers/29209066PubMed
26,973,654Structural and Functional Characterization of a Single-Chain Form of the Recognition Domain of Complement Protein C1q.Front Immunol2016https://conductscience.org/library/papers/26973654PubMed
23,861,840The serine protease domain of MASP-3: enzymatic properties and crystal structure in complex with ecotin.PLoS One2013https://conductscience.org/library/papers/23861840PubMed
23,650,384Expression of recombinant human complement C1q allows identification of the C1r/C1s-binding sites.Proc Natl Acad Sci U S A2013https://conductscience.org/library/papers/23650384PubMed
20,727,163Recombinant human complement component C2 produced in a human cell line restores the classical complement pathway activity in-vitro: an alternative treatment for C2 deficiency diseases.BMC Immunol2010https://conductscience.org/library/papers/20727163PubMed
20,592,021Mapping surface accessibility of the C1r/C1s tetramer by chemical modification and mass spectrometry provides new insights into assembly of the human C1 complex.J Biol Chem2010https://conductscience.org/library/papers/20592021PubMed
20,410,306Complement protein C1q forms a complex with cytotoxic prion protein oligomers.J Biol Chem2010https://conductscience.org/library/papers/20410306PubMed
20,008,834Analysis of human C1q by combined bottom-up and top-down mass spectrometry: detailed mapping of post-translational modifications and insights into the C1r/C1s binding sites.Mol Cell Proteomics2010https://conductscience.org/library/papers/20008834PubMed
19,494,295Analogous interactions in initiating complexes of the classical and lectin pathways of complement.J Immunol2009https://conductscience.org/library/papers/19494295PubMed
19,473,974Identification of the C1q-binding Sites of Human C1r and C1s: a refined three-dimensional model of the C1 complex of complement.J Biol Chem2009https://conductscience.org/library/papers/19473974PubMed

See all 51 cited by

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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  • 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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