Cellular and Circuitry Bases of Autism: Lessons Learned from the Temporospatial Manipulation of Autism Genes in the Brain
Neuroscience Bulletin, ISSN: 1995-8218, Vol: 33, Issue: 2, Page: 205-218
2017
- 14Citations
- 78Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations14
- Citation Indexes14
- 14
- CrossRef9
- Captures78
- Readers78
- 78
Review Description
Transgenic mice carrying mutations that cause Autism Spectrum Disorders (ASDs) continue to be valuable for determining the molecular underpinnings of the disorders. Recently, researchers have taken advantage of such models combined with Cre-loxP and similar systems to manipulate gene expression over space and time. Thus, a clearer picture is starting to emerge of the cell types, circuits, brain regions, and developmental time periods underlying ASDs. ASD-causing mutations have been restricted to or rescued specifically in excitatory or inhibitory neurons, different neurotransmitter systems, and cells specific to the forebrain or cerebellum. In addition, mutations have been induced or corrected in adult mice, providing some evidence for the plasticity and reversibility of core ASD symptoms. The limited availability of Cre lines that are highly specific to certain cell types or time periods provides a challenge to determining the cellular and circuitry bases of autism, but other technological advances may eventually overcome this obstacle.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85014531487&origin=inward; http://dx.doi.org/10.1007/s12264-017-0112-7; http://www.ncbi.nlm.nih.gov/pubmed/28271437; http://link.springer.com/10.1007/s12264-017-0112-7; https://dx.doi.org/10.1007/s12264-017-0112-7; https://link.springer.com/article/10.1007/s12264-017-0112-7; http://sciencechina.cn/gw.jsp?action=cited_outline.jsp&type=1&id=5954014&internal_id=5954014&from=elsevier
Springer Science and Business Media LLC
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