Methods to study the roles of Rho GTPases in dendritic tree complexity
Methods in Molecular Biology, ISSN: 1064-3745, Vol: 1821, Page: 297-317
2018
- 2Citations
- 3Captures
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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
- Citations2
- Citation Indexes2
- Captures3
- Readers3
Book Chapter Description
Most neurons elaborate a characteristic dendritic arbor which is physiologically important for receiving and processing of synaptic inputs. Pathologically, disturbances in the regulation of dendritic tree complexity are often associated with mental retardation and other neurological deficits. Rho GTPases are major players in the regulation of dendritic tree complexity. They are involved in many signal transduction cascades, activated at the neuronal plasma membrane, and relayed to intracellular proteins that directly rearrange the cytoskeleton. The use of siRNA technology combined with morphometric and imaging techniques allows the roles of individual Rho GTPases, such as Rac1, in dendritic branching to be examined. In this chapter we describe the establishment, transfection, and processing of a primary hippocampal cell culture. Methods to assess the complexity of dendritic arbors like the Sholl analysis, and techniques to investigate Rac1 activity in hippocampal cells, and specifically in neuronal dendrites, such as fluorescence resonance energy transfer (FRET) imaging are presented.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85051084681&origin=inward; http://dx.doi.org/10.1007/978-1-4939-8612-5_21; http://www.ncbi.nlm.nih.gov/pubmed/30062421; http://link.springer.com/10.1007/978-1-4939-8612-5_21; https://dx.doi.org/10.1007/978-1-4939-8612-5_21; https://link.springer.com/protocol/10.1007/978-1-4939-8612-5_21
Springer Nature America, Inc
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