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Cahir J. O'Kane

Researcher at University of Cambridge

Publications -  101
Citations -  16453

Cahir J. O'Kane is an academic researcher from University of Cambridge. The author has contributed to research in topics: Autophagy & Gene. The author has an hindex of 50, co-authored 99 publications receiving 15391 citations. Previous affiliations of Cahir J. O'Kane include Université libre de Bruxelles & University of Basel.

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Inhibition of mTOR induces autophagy and reduces toxicity of polyglutamine expansions in fly and mouse models of Huntington disease.

TL;DR: This work shows that mammalian target of rapamycin (mTOR) is sequestered in polyglutamine aggregates in cell models, transgenic mice and human brains, and provides proof-of-principle for the potential of inducing autophagy to treat Huntington disease.
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Targeted expression of tetanus toxin light chain in Drosophila specifically eliminates synaptic transmission and causes behavioral defects

TL;DR: To further the study of synaptic function in a genetically tractable organism and to generate a tool to disable neuronal communication for behavioural studies, a gene encoding tetanus toxin light chain is expressed in Drosophila.
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Detection in situ of genomic regulatory elements in Drosophila.

TL;DR: The P-lacZ fusion gene is an efficient tool for the recovery of elements that may regulate gene expression in Drosophila and for the generation of a wide variety of cell-type-specific markers.
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Novel targets for Huntington's disease in an mTOR-independent autophagy pathway

TL;DR: A cyclical mTOR-independent pathway regulating autophagy is revealed, in which cAMP regulates IP3 levels, influencing calpain activity, which completes the cycle by cleaving and activating G(s)alpha, which regulates cAMP levels.
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Lysosomal positioning coordinates cellular nutrient responses

TL;DR: It is reported that lysosomal positioning coordinates anabolic and catabolic responses with changes in nutrient availability by orchestrating early plasma-membrane signalling events, mTORC1 signalling and autophagy.