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Caiwei Guo

Researcher at Baylor College of Medicine

Publications -  11
Citations -  515

Caiwei Guo is an academic researcher from Baylor College of Medicine. The author has contributed to research in topics: Neurofibrillary tangle & Transcriptome. The author has an hindex of 6, co-authored 8 publications receiving 319 citations. Previous affiliations of Caiwei Guo include Baylor University & Massachusetts Eye and Ear Infirmary.

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Journal ArticleDOI

Tau-Mediated Disruption of the Spliceosome Triggers Cryptic RNA Splicing and Neurodegeneration in Alzheimer's Disease.

TL;DR: It is shown that loss of function in SmB, encoding a core spliceosomal protein, causes decreased survival, progressive locomotor impairment, and neuronal loss, independent of Tau toxicity, and genetic disruption of these factors enhances Tau-mediated neurodegeneration in AD.
Journal ArticleDOI

Uncoupling neuronal death and dysfunction in Drosophila models of neurodegenerative disease

TL;DR: Interestingly, Tau and αSyn each cause prominent but distinct synaptotoxic profiles, including disorganization or enlargement of photoreceptor terminals, respectively, which highlight variable and dynamic properties of neurodegeneration triggered by these disease-relevant proteins in vivo.
Proceedings ArticleDOI

An ultra-fast and scalable quantification pipeline for transposable elements from next generation sequencing data.

TL;DR: SalmonTE, a fast and reliable pipeline for the quantification of TEs from RNA-seq data, is developed and benchmarked against TEtranscripts, a widely used TE quantification method, and three other quantification methods using several RNA- sequencing datasets from Drosophila melanogaster and human cell-line.
Journal ArticleDOI

Integrated analysis of the aging brain transcriptome and proteome in tauopathy

TL;DR: The results comprise a powerful, cross-species functional genomics resource for tauopathy, revealing Tau-mediated disruption of gene expression, including dynamic, age-dependent interactions between the brain transcriptome and proteome.