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CryoET Reveals Organelle Phenotypes in Huntington Disease Patient iPSC-Derived and Mouse Primary Neurons

2022-03-27

Abstract excerpt

Huntington’s Disease (HD) is caused by an expanded CAG repeat in the huntingtin gene, yielding a Huntingtin protein with an expanded polyglutamine tract. Patient-derived induced pluripotent stem cells (iPSCs) can help understand disease; however, defining pathological biomarkers is challenging. Here, we used cryogenic electron tomography to visualize neurites in HD patient iPSC-derived neurons with varying CAG rep...

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Literature Corpus work
b6220de0-3701-5214-bb03-7f7cbe0c4f59
DOI
10.1101/2022.03.26.485912
Open publication

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CryoET Reveals Organelle Phenotypes in Huntington Disease Patient iPSC-Derived and Mouse Primary NeuronsDOI 10.1101/2022.03.26.485912
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