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Fragile X syndrome patient-derived neurons developing in the mouse brain show FMR1 -dependent phenot...

Fragile X syndrome patient-derived neurons developing in the mouse brain show FMR1 -dependent phenot...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2577220050

Fragile X syndrome patient-derived neurons developing in the mouse brain show FMR1 -dependent phenotypes

About this item

Full title

Fragile X syndrome patient-derived neurons developing in the mouse brain show FMR1 -dependent phenotypes

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

Journal title

bioRxiv, 2021-09

Language

English

Formats

Publication information

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

More information

Scope and Contents

Contents

Abnormal neuronal development in Fragile X syndrome (FXS) is poorly understood. Data on FXS patients remain scarce and FXS animal models have failed to yield successful therapies. In vitro models do not fully recapitulate the morphology and function of human neurons. Here, we co-injected neural precursor cells (NPCs) from FXS patient-derived and co...

Alternative Titles

Full title

Fragile X syndrome patient-derived neurons developing in the mouse brain show FMR1 -dependent phenotypes

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_2577220050

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2577220050

Other Identifiers

E-ISSN

2692-8205

DOI

10.1101/2021.09.27.461739