| Literature DB >> 16098136 |
D C Zarnescu1, G Shan, S T Warren, P Jin.
Abstract
The past few years have seen an increased number of articles using Drosophila as a model system to study fragile X syndrome. Phenotypic analyses have demonstrated an array of neuronal and behavioral defects similar to the phenotypes reported in mouse models as well as human patients. The availability of both cellular and molecular tools along with the power of genetics makes the tiny fruit fly a premiere model in elucidating the molecular basis of fragile X syndrome. Here, we summarize the advances made in recent years in the characterization of fragile X Drosophila models and the identification of new molecular partners in neural development.Entities:
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Year: 2005 PMID: 16098136 DOI: 10.1111/j.1601-183X.2005.00136.x
Source DB: PubMed Journal: Genes Brain Behav ISSN: 1601-183X Impact factor: 3.449