Preview. Angelman syndrome: finding the lost arc

Tai, H. C.; Schuman, Erin M.

doi:10.1016/j.cell.2010.02.019

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Preview. Angelman syndrome: finding the lost arc

Tai, H. C., & Schuman, E. M. (2010). Preview. Angelman syndrome: finding the lost arc. Cell, 140(5), 608-610. doi:10.1016/j.cell.2010.02.019.

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Item Permalink: https://hdl.handle.net/21.11116/0000-0007-EF28-0 Version Permalink: https://hdl.handle.net/21.11116/0000-000B-6B34-3

Genre: Journal Article

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https://www.ncbi.nlm.nih.gov/pubmed/20211128 (Any fulltext) Open Access status unknown

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Creators:
Tai, H. C., Author
Schuman, Erin M.¹, Author

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1Synaptic Plasticity Department, Max Planck Institute for Brain Research, Max Planck Society, ou_2461710

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Abstract: Angelman syndrome is a neurodevelopmental disorder caused by mutations in the maternally inherited UBE3A gene, which encodes a ubiquitin ligase. Greer et al. (2010) now identify a UBE3A substrate called Arc that promotes endocytosis of neuronal AMPA receptors, providing insight into synaptic defects that may underlie the cognitive deficits in Angelman syndrome.

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Dates: Date issued: 2010-03-10

Publication Status: Issued

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Identifiers: PMID: 20211128
DOI: 10.1016/j.cell.2010.02.019
ISSN: 1097-4172 (Electronic)0092-8674 (Linking)

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Title: Cell

Source Genre: Journal

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Publ. Info: Cambridge, Mass. : Cell Press

Pages: - Volume / Issue: 140 (5) Sequence Number: - Start / End Page: 608 - 610 Identifier: ISSN: 0092-8674
CoNE: https://pure.mpg.de/cone/journals/resource/954925463183