Hippocampal neuronal polarity specified by spatially localized mPar3/mPar6 and PI 3-kinase activity.
By S. Shi, L. Jan, Y. Jan. Cell, 2003
625 citations recorded by the source corpus.
Subfields: Aging, Cell Biology, Cellular and Molecular Neuroscience
View Paper: https://www.semanticscholar.org/paper/d677b6593c016790e11dc185683fb9829e30a758
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Citations in the corpus
- Rho GTPases: biochemistry and biology. (2005, background): “Cdc42 and the Par3/Par6/aPKC complex are specifically enriched in the developing axon and disruption of their activity results in polarity defects, leading to zero or multiple axons (Schwamborn & Puschel 2004, Shi et al. 2003).”
- Neuronal polarity: from extracellular signals to intracellular mechanisms (2007, background): “Accumulating evidence indicates the importance of PI3K and its lipid product, phosphatidylinositol-3,4,5-trisphosphate (PtdIns(3,4,5)P 3 ), in neuronal polarizatio”
- Microtubule assembly, organization and dynamics in axons and dendrites (2009, background): “PI3K signalling also plays an important part in neuronal polarizatio”
- Regulation of Dendritic Morphogenesis by Ras–PI3K–Akt–mTOR and Ras–MAPK Signaling Pathways (2005, background): “DOI:10.1523/JNEUROSCI.2284-05.2005 Copyright © 2005 Society for Neuroscience 0270-6474/05/2511288-12$15.00/0 tion of neuronal polarity and axonal growth (Markus et al., 2002; Shi et al., 2003; Jiang et al., 2005) have been revealed.”
- The role of the Rho GTPases in neuronal development. (2005, background): “2002), it was suggested that a positive feedback loop may amplify growth cone signaling to break the symmetrical distribution of mPar proteins and promote neuronal polarization (Shi et al. 2003).”
- The PAR proteins: fundamental players in animal cell polarization. (2007, background): “Also, dominant-interfering fragments of PAR-3, or inhibition of aPKC, can block axon specification (Shi et al., 2003).”