Matches in SemOpenAlex for { <https://semopenalex.org/work/W2086021621> ?p ?o ?g. }
- W2086021621 endingPage "9168" @default.
- W2086021621 startingPage "9155" @default.
- W2086021621 abstract "Intracellular tau deposits are characteristic of several neurodegenerative disorders called tauopathies. The tau protein regulates the stability and assembly of microtubules by binding to microtubules through three or four microtubule-binding repeats (3R and 4R). The number of microtubule-binding repeats is determined by the inclusion or exclusion of the second microtubule-binding repeat encoded by exon 10 of the TAU gene. TAU gene mutations that alter the inclusion of exon 10, and hence the 4R:3R ratio, are causal in the tauopathy frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17). A mutation located in exon 10 has been identified in several FTDP-17 families that present with increased exon 10 inclusion in both mRNA and protein, parkinsonism, movement disorders, and dementia. We have engineered a human tau minigene construct that was designed to allow alternative splicing of the tau exon 10. Here we demonstrate that transgenic mice expressing human tau protein with this mutation develop neurodegeneration as result of aberrant splicing. The mice recapitulate many of the disease hallmarks that are seen in patients with this mutation, including increased tau exon 10 inclusion in both mRNA and protein, motor and behavioral deficits, and tau protein accumulation in neurons and tufted astrocytes. Furthermore, these mice present with degeneration of the nigrostriatal dopaminergic pathway, suggesting a possible mechanism for parkinsonism in FTDP-17. Additionally, activated caspase-3 immunoreactivity in both neurons and astrocytes implicates the involvement of the apoptotic pathway in the pathology of these mice." @default.
- W2086021621 created "2016-06-24" @default.
- W2086021621 creator A5000594249 @default.
- W2086021621 creator A5033086401 @default.
- W2086021621 creator A5045138056 @default.
- W2086021621 creator A5089286114 @default.
- W2086021621 date "2007-08-22" @default.
- W2086021621 modified "2023-09-27" @default.
- W2086021621 title "The Tau N279K Exon 10 Splicing Mutation Recapitulates Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17 Tauopathy in a Mouse Model" @default.
- W2086021621 cites W126426573 @default.
- W2086021621 cites W1509571186 @default.
- W2086021621 cites W150987474 @default.
- W2086021621 cites W1511517753 @default.
- W2086021621 cites W1556490889 @default.
- W2086021621 cites W1561023982 @default.
- W2086021621 cites W1565807488 @default.
- W2086021621 cites W1588125132 @default.
- W2086021621 cites W1600934558 @default.
- W2086021621 cites W1621971853 @default.
- W2086021621 cites W173382140 @default.
- W2086021621 cites W1769834022 @default.
- W2086021621 cites W1823494905 @default.
- W2086021621 cites W183718668 @default.
- W2086021621 cites W1893543180 @default.
- W2086021621 cites W1944699774 @default.
- W2086021621 cites W1966001133 @default.
- W2086021621 cites W1968813853 @default.
- W2086021621 cites W1970186069 @default.
- W2086021621 cites W1971775491 @default.
- W2086021621 cites W1974322112 @default.
- W2086021621 cites W1974760231 @default.
- W2086021621 cites W1975040221 @default.
- W2086021621 cites W1975321314 @default.
- W2086021621 cites W1976452550 @default.
- W2086021621 cites W1978400690 @default.
- W2086021621 cites W1979345939 @default.
- W2086021621 cites W1982228171 @default.
- W2086021621 cites W1984305500 @default.
- W2086021621 cites W1984770038 @default.
- W2086021621 cites W1985002125 @default.
- W2086021621 cites W1985131940 @default.
- W2086021621 cites W1985811907 @default.
- W2086021621 cites W1987093796 @default.
- W2086021621 cites W1987114379 @default.
- W2086021621 cites W1988884999 @default.
- W2086021621 cites W1989301820 @default.
- W2086021621 cites W1989335631 @default.
- W2086021621 cites W1989856924 @default.
- W2086021621 cites W1992380863 @default.
- W2086021621 cites W1992589625 @default.
- W2086021621 cites W1994030229 @default.
- W2086021621 cites W1998319561 @default.
- W2086021621 cites W1999486169 @default.
- W2086021621 cites W1999895781 @default.
- W2086021621 cites W2000303735 @default.
- W2086021621 cites W2002347888 @default.
- W2086021621 cites W2005311608 @default.
- W2086021621 cites W2011246846 @default.
- W2086021621 cites W2012531638 @default.
- W2086021621 cites W2013475161 @default.
- W2086021621 cites W2015563160 @default.
- W2086021621 cites W2021590064 @default.
- W2086021621 cites W2025256992 @default.
- W2086021621 cites W2025765615 @default.
- W2086021621 cites W2027582763 @default.
- W2086021621 cites W2033867506 @default.
- W2086021621 cites W2036008741 @default.
- W2086021621 cites W2041922475 @default.
- W2086021621 cites W2042644489 @default.
- W2086021621 cites W2045671840 @default.
- W2086021621 cites W2047304481 @default.
- W2086021621 cites W2051233811 @default.
- W2086021621 cites W2053216332 @default.
- W2086021621 cites W2057732851 @default.
- W2086021621 cites W2057862759 @default.
- W2086021621 cites W2057894590 @default.
- W2086021621 cites W2059618864 @default.
- W2086021621 cites W2060148395 @default.
- W2086021621 cites W2062360332 @default.
- W2086021621 cites W2065426913 @default.
- W2086021621 cites W2066068917 @default.
- W2086021621 cites W2068151389 @default.
- W2086021621 cites W2069933213 @default.
- W2086021621 cites W2070446123 @default.
- W2086021621 cites W2070463563 @default.
- W2086021621 cites W2070971554 @default.
- W2086021621 cites W2072963607 @default.
- W2086021621 cites W2075791440 @default.
- W2086021621 cites W2076836926 @default.
- W2086021621 cites W2081319561 @default.
- W2086021621 cites W2081451333 @default.
- W2086021621 cites W2082429191 @default.
- W2086021621 cites W2083434553 @default.
- W2086021621 cites W2088073407 @default.
- W2086021621 cites W2089364726 @default.
- W2086021621 cites W2089480603 @default.
- W2086021621 cites W2093822807 @default.
- W2086021621 cites W2096623085 @default.