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- W2064553451 abstract "A subset of frontotemporal dementia cases are neuropathologically defined by tau-negative, TAR DNA-binding protein-43, and ubiquitin-positive inclusions in the brain and are associated with mutations in the progranulin gene (GRN). Deep sequencing of families exhibiting late-onset dementia revealed several novel variants in GRN. Because of the small size of these families and limited availability of samples, it was not possible to determine whether the variants segregated with the disease. Furthermore, none of these families had autopsy confirmation of diagnosis. We sought to determine if these novel GRN variants alter progranulin (PGRN) protein stability, PGRN secretion, and PGRN cleavage in cultured cells. All the novel GRN variants behave like PGRN wild-type protein, suggesting that these variants represent rare polymorphisms. However, it remains possible that these variants affect other aspects of PGRN function or represent risk factors for dementia when combined with other modifying genes." @default.
- W2064553451 created "2016-06-24" @default.
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- W2064553451 date "2013-11-01" @default.
- W2064553451 modified "2023-09-26" @default.
- W2064553451 title "Novel progranulin variants do not disrupt progranulin secretion and cleavage" @default.
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- W2064553451 doi "https://doi.org/10.1016/j.neurobiolaging.2013.05.004" @default.
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