Paper · 89088
Isolation and characterization of homogeneous heat-labile enterotoxins with high specific activity from Escherichia coli cultures.
Clements JD and 1 other. Infect Immun, 1979. Cited by 296 papers, by iCite.
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ConductScience Library. Isolation and characterization of homogeneous heat-labile enterotoxins with high specific activity from Escherichia coli cultures. Papers, record 89088. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/89088
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Paper
PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
- Title
- Isolation and characterization of homogeneous heat-labile enterotoxins with high specific activity from Escherichia coli cultures.
- PubMed
Topics9
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Bacterial Toxins | Major topic |
| Enterotoxins | Major topic |
| Escherichia coli | Major topic |
| Amino Acids | |
| Animals | |
| Biological Assay | |
| Cholera Toxin | |
| Epitopes | |
| Rabbits |
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.
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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
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References22
The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.
| Order | PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|---|
| 1 | 3,214 | The arrangement of subunits in cholera toxin. | Biochemistry | 1976 | https://conductscience.org/library/papers/3214 | PubMed |
| 2 | 83,301 | Demonstration of shared and unique immunological determinants in enterotoxins from Vibrio cholerae and Escherichia coli. | Infect Immun | 1978 | https://conductscience.org/library/papers/83301 | PubMed |
| 3 | 103,838 | Purification of heat-labile enterotoxin from four Escherichia coli strains by affinity immunoadsorbent: evidence for similar subunit structure. | Infect Immun | 1978 | https://conductscience.org/library/papers/103838 | PubMed |
| 4 | 241,754 | Escherichia coli enterotoxin. Purification and partial characterization. | J Biol Chem | 1975 | https://conductscience.org/library/papers/241754 | PubMed |
| 5 | 361,573 | Immunological cross-reactivity between a heat-labile enterotoxin(s) of Escherichia coli and subunits of Vibrio cholerae enterotoxin. | Infect Immun | 1978 | https://conductscience.org/library/papers/361573 | PubMed |
| 6 | 786,881 | Partial purification and characterization of a heat-labile enterotoxin of Escherichia coli. | Infect Immun | 1976 | https://conductscience.org/library/papers/786881 | PubMed |
| 7 | 803,978 | Studies on toxinogenesis in Vibrio cholerae. III. Characterization of nontoxinogenic mutants in vitro and in experimental animals. | J Clin Invest | 1975 | https://conductscience.org/library/papers/803978 | PubMed |
| 8 | 942,051 | A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. | Anal Biochem | 1976 | https://conductscience.org/library/papers/942051 | PubMed |
| 9 | 955,672 | Subunit structure and N-terminal amino acid sequence of the three chains of cholera enterotoxin. | Immunochemistry | 1976 | https://conductscience.org/library/papers/955672 | PubMed |
| 10 | 1,089,601 | Test for enterotoxigenic Escherichia coli using Y-1 adrenal cells in miniculture. | Infect Immun | 1975 | https://conductscience.org/library/papers/1089601 | PubMed |
1 to 10 of 22
See all 22 referencesCited by151
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 296 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 42,088,495 | The case for evaluation of double mutant heat-labile toxin as an adjuvant to improve oral cholera vaccine immunogenicity. | Front Immunol | 2026 | https://conductscience.org/library/papers/42088495 | PubMed |
| 41,727,468 | MVA-Spike encoding the A subunit of dmLT safely enhances systemic and mucosal immune responses. | Front Immunol | 2026 | https://conductscience.org/library/papers/41727468 | PubMed |
| 40,788,160 | ETEC biofilms are regulated by magnesium and lactate bioavailability. | Infect Immun | 2025 | https://conductscience.org/library/papers/40788160 | PubMed |
| 37,258,506 | Establishment of isotype-switched, antigen-specific B cells in multiple mucosal tissues using non-mucosal immunization. | NPJ Vaccines | 2023 | https://conductscience.org/library/papers/37258506 | PubMed |
| 31,427,449 | Intradermal or Sublingual Delivery and Heat-Labile Enterotoxin Proteins Shape Immunologic Responses to a CFA/I Fimbria-Derived Subunit Antigen Vaccine against Enterotoxigenic Escherichia coli. | Infect Immun | 2019 | https://conductscience.org/library/papers/31427449 | PubMed |
| 30,045,966 | The Mucosal Vaccine Adjuvant LT(R192G/L211A) or dmLT. | mSphere | 2018 | https://conductscience.org/library/papers/30045966 | PubMed |
| 27,735,786 | Animal Enterotoxigenic Escherichia coli. | EcoSal Plus | 2016 | https://conductscience.org/library/papers/27735786 | PubMed |
| 26,754,836 | Case-control study of pathogens involved in piglet diarrhea. | BMC Res Notes | 2016 | https://conductscience.org/library/papers/26754836 | PubMed |
| 26,305,793 | Evaluating the A-Subunit of the Heat-Labile Toxin (LT) As an Immunogen and a Protective Antigen Against Enterotoxigenic Escherichia coli (ETEC). | PLoS One | 2015 | https://conductscience.org/library/papers/26305793 | PubMed |
| 25,287,923 | Simultaneous exposure to Escherichia coli heat-labile and heat-stable enterotoxins increases fluid secretion and alters cyclic nucleotide and cytokine production by intestinal epithelial cells. | Infect Immun | 2014 | https://conductscience.org/library/papers/25287923 | PubMed |
1 to 10 of 151
See all 151 cited byGenes0
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- 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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