Channelrhodopsin-2–assisted circuit mapping of long-range callosal projections
By Leopoldo T. Petreanu, Daniel Huber, A. Sobczyk, Karel Svoboda. Nature Neuroscience, 2007
920 citations recorded by the source corpus.
Subfields: Cellular and Molecular Neuroscience, Cognitive Neuroscience
View Paper: https://www.semanticscholar.org/paper/7504e8db794e20d9aee8ebfee1df28d5ccaeb2c4
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cellular and Molecular Neuroscience
- Karl Deisseroth
- György Buzsáki
- Ofer Yizhar
- Lief Ericsson Fenno
- K. Tye
- Ed Boyden
- Logan Grosenick
- Karel Svoboda
In Cognitive Neuroscience
- Karl Deisseroth
- György Buzsáki
- Logan Grosenick
- James H. Marshel
- Lief Ericsson Fenno
- Ed Boyden
- Ofer Yizhar
- Karel Svoboda
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”
- Spatiotemporal dynamics of cortical sensorimotor integration in behaving mice. (2007, result): “The paucity of callosal axons terminating in the barrel cortex of the opposite hemisphere is also in good agreement with recent mouse data showing that only a small very lateral portion of the barrel field is innervated by supragranular callosal axons (Petreanu et al., 2007).”
- Imaging neural activity in worms, flies and mice with improved GCaMP calcium indicators (2009, methodology): “L2/3 progenitor cells were transfected via in utero electroporation in C57BL/6Crl pregnant mice at E16 with a plasmid expressing CRE recombinase under the CAGS promoter as previously describe”
- Diaschisis: past, present, future. (2014, background): “sin ChR2 in slice (Petreanu et al., 2007) and in living animals (Lim”
- The functional organization of the barrel cortex. (2007, background): “Callosal connectivity between the barrel cortices on opposite hemispheres appears to be limited to the representation of the most medial A-row whiskers (Petreanu et al., 2007).”
- Closed-loop and activity-guided optogenetic control. (2015, positive): “…developmental stage (e.g., birth date) as in the case of in utero electroporation to target specific layers in cortex (Saito and Nakatsuji, 2001; Gradinaru et al., 2007; Petreanu et al., 2007) and by promoter-based strategies and viral tropism (Adamantidis et al., 2007; Nathanson et al., 2009).”
- A Sensorimotor Circuit in Mouse Cortex for Visual Flow Predictions. (2017, neutral): “(F) Left: Injection scheme for CRACM.”
- Genetically encoded calcium indicators for multi-color neural activity imaging and combination with optogenetics (2013, background): “…non-overlapping imaging/optogenetics will enable qualitatively new sorts of neuroscience experiments, such as mapping projections of numerous single neurons through brain tissue, akin to an “all-optical” channelrhodopsin-assisted circuit mapping (CRACM) experiment (Petreanu et al., 2007).”
- A toolbox of Cre-dependent optogenetic transgenic mice for light-induced activation and silencing (2012, methodology): “ChR2(H134R)-tdTomato was synthesized based on the hChR2 sequence 26 , and ChR2(H134R)-EYFP was synthesized based on the ChR2 sequence 3 .”
- Genetic dissection of neural circuits. (2008, methodology): “Remarkably, even ChR2-positive axons that are severed from their parent somatacanbephotostimulated to fire actionpotentials (Petreanu et al., 2007).”
- The Development and Application of Optogenetics (2011, methodology): “Optogenetic tools have been well tolerated when electroporated in utero into mouse embryos (Adesnik & Scanziani 2010, Gradinaru et al. 2007, Lewis et al. 2009, Petreanu et al. 2007); IUE may www.annualreviews.org • The Development and Application of Optogenetics 399 A nn u.”
- 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…”