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dc.contributor.authorBilican, B
dc.contributor.authorSerio, A
dc.contributor.authorBarmada, SJ
dc.contributor.authorNishimura, AL
dc.contributor.authorSullivan, GJ
dc.contributor.authorCarrasco, M
dc.contributor.authorPhatnani, HP
dc.contributor.authorPuddifoot, CA
dc.contributor.authorStory, D
dc.contributor.authorFletcher, J
dc.contributor.authorPark, I-H
dc.contributor.authorFriedman, BA
dc.contributor.authorDaley, GQ
dc.contributor.authorWyllie, DJA
dc.contributor.authorHardingham, GE
dc.contributor.authorWilmut, I
dc.contributor.authorFinkbeiner, S
dc.contributor.authorManiatis, T
dc.contributor.authorShaw, CE
dc.contributor.authorChandran, S
dc.date.accessioned2024-01-04T14:28:22Z
dc.date.available2024-01-04T14:28:22Z
dc.date.issued2013-06-05
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/93379
dc.description.abstractEgawa et al. recently showed the value of patient-specific induced pluripotent stem cells (iPSCs) for modeling amyotrophic lateral sclerosis in vitro. Their study and our work highlight the need for complementary assays to detect small, but potentially important, phenotypic differences between control iPSC lines and those carrying disease mutations.en_US
dc.format.extent188le2 - ?
dc.languageeng
dc.publisherAmerican Association for the Advancement of Scienceen_US
dc.relation.ispartofSci Transl Med
dc.subjectAmyotrophic Lateral Sclerosisen_US
dc.subjectDrug Evaluation, Preclinicalen_US
dc.subjectHumansen_US
dc.subjectInduced Pluripotent Stem Cellsen_US
dc.subjectMotor Neuronsen_US
dc.titleComment on "Drug screening for ALS using patient-specific induced pluripotent stem cells".en_US
dc.typeArticleen_US
dc.identifier.doi10.1126/scitranslmed.3005065
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/23740897en_US
pubs.issue188en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume5en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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