The subcellular organization of neocortical excitatory connections

By Leopoldo T. Petreanu, Tianyi Mao, Scott Sternson, Karel Svoboda. Nature, 2009

1,028 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Cognitive Neuroscience

View Paper: https://www.semanticscholar.org/paper/b4702f87376fd6d5f45b83e961843b6b3b9ee06e

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In Cellular and Molecular Neuroscience

In Cognitive Neuroscience

Citations in the corpus

Optogenetic investigation of neural circuits underlying brain disease in animal models (2012, background): “, several elegant optogenetic studies have already made substantial advances in detailed circuit mappin”
Three Groups of Interneurons Account for Nearly 100% of Neocortical GABAergic Neurons (2011, background): “Although the functional connectivity of long-range cortical inputs to pyramidal neurons in superficial layers in primary S1 has been mapped (Petreanu et al., 2009), the long-range cortical projection to interneurons has not been studied.”
Burst-dependent synaptic plasticity can coordinate learning in hierarchical circuits (2020, background): “There is evidence for this structure [82], but also some data showing 426 that it is not always this way [107].”
Molecular and cellular approaches for diversifying and extending optogenetics. (2010, background): “…species such as rats and primates), as with earlier projection-based targeting methods that are not transcellular (Gradinaru et al., 2007, 2009; Petreanu et al., 2007, 2009; Lima et al., 2009); but, if needed, such additional genetic refinements can be readily added (for example, both the…”
All-optical electrophysiology in mammalian neurons using engineered microbial rhodopsins (2014, methodology): “With extension to multiple genetically specified cells, Optopatch measurements in tissue may provide a useful tool for functional circuit mapping 2 .”
Synaptic Plasticity Forms and Functions. (2020, background): “The dependence of reward-motivated behavior on dopamine (DA) neuron activity and DA receptor activation is a well-documented example (Schultz 2007, Steinberg et al. 2013, Pignatelli & Bonci 2015, Berke 2018).”
Active properties of neocortical pyramidal neuron dendrites. (2013, background): “Basals and proximal obliques can be further collapsed together functionally, depending on the layer specificity of inputs (Briggs & Callaway 2005, Lübke & Feldmeyer 2007, Petreanu et al. 2009, Schubert et al. 2001).”
Intact-Brain Analyses Reveal Distinct Information Carried by SNc Dopamine Subcircuits (2015, background): “…potassium channel antagonist 4-AP (100 mM) to isolate monosynaptic inputs by preventing disynaptic disinhibitory responses through the GABAergic cells of the SNr (with TTX) while enabling ChR2 to drive neurotransmitter release in the absence of action potentials (with 4-AP) (Petreanu et al., 2009).”