High content image analysis identifies novel regulators of synaptogenesis in a high-throughput RNAi screen of primary neurons
PLoS ONE, ISSN: 1932-6203, Vol: 9, Issue: 3, Page: e91744
2014
- 34Citations
- 131Captures
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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.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations34
- Citation Indexes32
- 32
- CrossRef24
- Policy Citations2
- Policy Citation2
- Captures131
- Readers131
- 131
Article Description
The formation of synapses, the specialized points of chemical communication between neurons, is a highly regulated developmental process fundamental to establishing normal brain circuitry. Perturbations of synapse formation and function causally contribute to human developmental and degenerative neuropsychiatric disorders, such as Alzheimer's disease, intellectual disability, and autism spectrum disorders. Many genes controlling synaptogenesis have been identified, but lack of facile experimental systems has made systematic discovery of regulators of synaptogenesis challenging. Thus, we created a high-throughput platform to study excitatory and inhibitory synapse development in primary neuronal cultures and used a lentiviral RNA interference library to identify novel regulators of synapse formation. This methodology is broadly applicable for high-throughput screening of genes and drugs that may rescue or improve synaptic dysfunction associated with cognitive function and neurological disorders. © 2014 Nieland et al.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84897973093&origin=inward; http://dx.doi.org/10.1371/journal.pone.0091744; http://www.ncbi.nlm.nih.gov/pubmed/24633176; https://dx.plos.org/10.1371/journal.pone.0091744; https://dx.doi.org/10.1371/journal.pone.0091744; https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0091744
Public Library of Science (PLoS)
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