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Cited by 1,003

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Mutation-Specific Functional Impairments in Distinct Tau Isoforms of Hereditary FTDP-17

Hong, M.·1998·Science

Abstract

Tau proteins aggregate as cytoplasmic inclusions in a number of neurodegenerative diseases, including Alzheimer's disease and hereditary frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17). Over 10 exonic and intronic mutations in the tau gene have been identified in about 20 FTDP-17 families. Analyses of soluble and insoluble tau proteins from brains of FTDP-17 patients indicated that different pathogenic mutations differentially altered distinct biochemical properties and stoichiometry of brain tau isoforms. Functional assays of recombinant tau proteins with different FTDP-17 missense mutations implicated all but one of these mutations in disease pathogenesis by reducing the ability of tau to bind microtubules and promote microtubule assembly.

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Metadata

Authors
Hong, M.
Venue
Science
Published
1998-12-04
Volume
282
Issue
5395
Pages
1914-1917
ISSN
0036-8075 (ISSN-L)
OpenAlex
W2159643400
Cited by
1,003
References
2
FWCI
38.14
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Mutation-Specific Functional Impairments in Distinct Tau Isoforms of Hereditary FTDP-17. https://app.cochat.ai/papers/10.1126/science.282.5395.1914
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Hong, M. (1998). Mutation-Specific Functional Impairments in Distinct Tau Isoforms of Hereditary FTDP-17. Science. https://doi.org/10.1126/science.282.5395.1914

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

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.