Molecular analyses of neurogenic defects in a human pluripotent stem cell model of fragile X syndrome-Reference-Cited by-同舟云学术

Molecular analyses of neurogenic defects in a human pluripotent stem cell model of fragile X syndrome

Published:2017-01-29 Issue: Volume: Page:aww357
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

Boland Michael J.,Nazor Kristopher L.,Tran Ha T.,Szücs Attila,Lynch Candace L.,Paredes Ryder,Tassone Flora,Sanna Pietro Paolo,Hagerman Randi J.,Loring Jeanne F.

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/140/3/582/18245308/aww357.pdf

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1. Local functions for FMRP in axon growth cone motility and activity-dependent regulation of filopodia and spine synapses

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4. Phenotypic differences in hiPSC NPCs derived from patients with schizophrenia

5. Microarray Identification of FMRP-Associated Brain mRNAs and Altered mRNA Translational Profiles in Fragile X Syndrome

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