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Cited by 687

The DOI matches its Crossref record; 41 of the 41 references it cites were found in a registry or an index.

Expression of human beta-amyloid peptide in transgenic Caenorhabditis elegans.

Open access
Link, C D·1995·Proceedings of the National Academy of Sciences

Abstract

Transgenic Caenorhabditis elegans nematodes have been engineered to express potentially amyloidic human proteins. These animals contain constructs in which the muscle-specific unc-54 promoter/enhancer of C. elegans drives the expression of the appropriate coding regions derived from human cDNA clones. Animals containing constructs expressing the 42-amino acid beta-amyloid peptide (derived from human amyloid precursor protein cDNA) produce muscle-specific deposits immunoreactive with anti-beta-amyloid polyclonal and monoclonal antibodies. A subset of these deposits also bind the amyloid-specific dye thioflavin S, indicating that these deposits have the tinctural characteristics of classic amyloid. Co-expression of beta-peptide and transthyretin, a protein implicated in preventing the formation of insoluble beta-amyloid, leads to a dramatic reduction in the number of dye-reactive deposits. These results suggest that this invertebrate model may be useful for in vivo investigation of factors that modulate amyloid formation.

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Metadata

Authors
Link, C. D.
Venue
Proceedings of the National Academy of Sciences
Published
1995-09-26
Volume
92
Issue
20
Pages
9368-9372
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W1975595547
Cited by
687
References
41
FWCI
0.42
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Expression of human beta-amyloid peptide in transgenic Caenorhabditis elegans. https://app.cochat.ai/papers/10.1073/pnas.92.20.9368
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Link, C. D. (1995). Expression of human beta-amyloid peptide in transgenic Caenorhabditis elegans. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.92.20.9368

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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