Author

Sara Calabretta

Jewish General HospitalORCID 0009-0009-1859-3995Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Molecular Biology· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 1

Frequent Co-Authors

Baoyu CheniD· 1 shared Claudia L. KleinmaniD· 1 shared Daniel A. KrameriD· 1 shared Frédéric CharroniD· 1 shared Gillian Vogel· 1 shared Greg J. BashawiD· 1 shared Kaiyue ZhangiD· 1 shared Karina ChaudhariiD· 1 shared

Activity by Year

2018-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperNeuroscience

Baoyu ChenORCID

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintOct 13, 2022

A human DCC variant causing mirror movement disorder reveals an essential role for the Wave regulatory complex in Netrin/DCC signaling

Karina Chaudhari, Kaiyue Zhang, Patricia T. Yam…·Greg J. Bashaw

This paper identifies a DCC variant causing mirror movement disorder and shows it disrupts the DCC-WAVE regulatory complex interaction, essential for Netrin-1 signaling.

3 citations

humanexperimental assay

𝕏 PostBluesky

Molecular BiologyDevelopmental CellPeer-reviewedJul 26, 2018

Loss of PRMT5 promotes PDGFRα degradation during oligodendrocyte differentiation and myelination

Sara Calabretta, Gillian Vogel, Zhenbao Yu…·Stéphane Richard

The paper shows that reduced PRMT5 activity during oligodendrocyte differentiation leads to PDGFRα degradation, promoting myelination by altering Cbl binding.

59 citations

experimental assay

𝕏 PostBluesky