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dc.contributor.authorVila, Olaia F
dc.contributor.authorUzel, Sebastien Guy Marcel
dc.contributor.authorMa, Stephen P
dc.contributor.authorWilliams, Damian
dc.contributor.authorPak, Joseph
dc.contributor.authorKamm, Roger Dale
dc.contributor.authorVunjak-Novakovic, Gordana
dc.date.accessioned2022-07-05T12:57:14Z
dc.date.available2021-10-27T20:10:49Z
dc.date.available2022-07-05T12:57:14Z
dc.date.issued2019
dc.identifier.urihttps://hdl.handle.net/1721.1/135122.2
dc.description.abstract© Ivyspring International Publisher. The study of human neuromuscular diseases has traditionally been performed in animal models, due to the difficulty of performing studies in human subjects. Despite the unquestioned value of animal models, inter-species differences hamper the translation of these findings to clinical trials. Tissue-engineered models of the neuromuscular junction (NMJ) allow for the recapitulation of the human physiology in tightly controlled in vitro settings. Methods: Here we report the first human patient-specific tissue-engineered model of the neuromuscular junction (NMJ) that combines stem cell technology with tissue engineering, optogenetics, microfabrication and image processing. The combination of custom-made hardware and software allows for repeated, quantitative measurements of NMJ function in a user-independent manner. Results: We demonstrate the utility of this model for basic and translational research by characterizing in real time the functional changes during physiological and pathological processes. Principal Conclusions: This system holds great potential for the study of neuromuscular diseases and drug screening, allowing for the extraction of quantitative functional data from a human, patient-specific system.en_US
dc.language.isoen
dc.publisherIvyspring International Publisheren_US
dc.relation.isversionof10.7150/THNO.25735en_US
dc.rightsCreative Commons Attribution NonCommercial License 4.0en_US
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/en_US
dc.sourceTheranosticsen_US
dc.titleQuantification of human neuromuscular function through optogeneticsen_US
dc.typeArticleen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.relation.journalTheranosticsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2020-08-17T17:32:28Z
dspace.orderedauthorsVila, OF; Uzel, SGM; Ma, SP; Williams, D; Pak, J; Kamm, RD; Vunjak-Novakovic, Gen_US
dspace.date.submission2020-08-17T17:32:30Z
mit.journal.volume9en_US
mit.journal.issue5en_US
mit.licensePUBLISHER_CC
mit.metadata.statusPublication Information Neededen_US


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