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X-linked microtubule-associated protein, Mid1, regulates axon development

X-linked microtubule-associated protein, Mid1, regulates axon development

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmed_primary_24194544

X-linked microtubule-associated protein, Mid1, regulates axon development

About this item

Full title

X-linked microtubule-associated protein, Mid1, regulates axon development

Publisher

Washington, DC: National Academy of Sciences

Journal title

Proceedings of the National Academy of Sciences - PNAS, 2013-11, Vol.110 (47), p.19131-19136

Language

English

Formats

Publication information

Publisher

Washington, DC: National Academy of Sciences

More information

Scope and Contents

Contents

Opitz syndrome (OS) is a genetic neurological disorder. The gene responsible for the X-linked form of OS, Midline-1 (MID1), encodes an E3 ubiquitin ligase that regulates the degradation of the catalytic subunit of protein phosphatase 2A (PP2Ac). However, how Mid1 functions during neural development is largely unknown. In this study, we provide data...

Alternative Titles

Full title

X-linked microtubule-associated protein, Mid1, regulates axon development

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmed_primary_24194544

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmed_primary_24194544

Other Identifiers

ISSN

0027-8424

E-ISSN

1091-6490

DOI

10.1073/pnas.1303687110

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