The exon junction complex in neural development and neurodevelopmental disease-Reference-Cited by-同舟云学术

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The exon junction complex in neural development and neurodevelopmental disease

Published:2016-04-09 Issue:1 Volume:55 Page:117-123
ISSN:0736-5748
Container-title:International Journal of Developmental Neuroscience
language:en
Short-container-title:Int. j. dev. neurosci.

Author:

McMahon J.J.¹,Miller E.E.¹,Silver D.L.¹²³⁴

Affiliation:

1. Department of Molecular Genetics and MicrobiologyDuke University Medical CenterDurhamNC27710United States

2. Department of Cell BiologyDuke University Medical CenterDurhamNC27710United States

3. Department of NeurobiologyDuke University Medical CenterDurhamNC27710United States

4. Duke Institute for Brain Sciences, Duke University Medical CenterDurhamNC27710United States

Funder

Silver lab for helpful discussions

Publisher

Wiley

Subject

Developmental Biology,Developmental Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1016/j.ijdevneu.2016.03.006

Reference63 articles.

1. A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders;Addington A.M.;Mol. Psychiatry,2011

2. An EJC factor RBM8a regulates anxiety behaviors;Alachkar A.;Curr. Mol. Med.,2013

3. Compound inheritance of a low‐frequency regulatory SNP and a rare null mutation in exon‐junction complex subunit RBM8A causes TAR syndrome;Albers C.A.;Nat. Genet.,2012

4. New insights into the genetic basis of TAR (thrombocytopenia‐ absent radii) syndrome;Albers C.A.;Curr. Opin. Genet. Dev.,2013

5. Full UPF3B function is critical for neuronal differentiation of neural stem cells;Alrahbeni T.;Mol. Brain BioMed. Central,2015

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