Localization of a Stable Neural Correlate of Associative Memory
By L. Reijmers, Brian L Perkins, Naoki Matsuo, M. Mayford. 2007
785 citations recorded by the source corpus.
Subfields: Cellular and Molecular Neuroscience, Cognitive Neuroscience, Social Psychology
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
- S. Tonegawa
- Y. Dudai
- E. Kandel
- Paul W. Frankland
- M. Mayford
- T. Kitamura
- M. Yokoyama
- Blake Aaron Richards
In Cognitive Neuroscience
- Y. Dudai
- S. Tonegawa
- E. Kandel
- Paul W. Frankland
- M. Mayford
- T. Kitamura
- Blake Aaron Richards
- M. Yokoyama
In Social Psychology
Citations in the corpus
- Loss of Ensemble Segregation in Dentate Gyrus, but not in Somatosensory Cortex, during Contextual Fear Memory Generalization (2016, methodology): “The generation of cfos-transactivator (tTA) × tetO-tau lacZ double transgenic mice has been described previously (Reijmers et al., 2007).”
- The molecular biology of memory: cAMP, PKA, CRE, CREB-1, CREB-2, and CPEB (2012, methodology): “memory has a stable neural correlate [119].”
- Transgenic mice for intersectional targeting of neural sensors and effectors with high specificity and performance (2015, positive): “…been used in mice for inducible expression of genes from the TRE (tetracycline response element, also called tetO) promoter in response to tTA (Tet-Off) or rtTA (Tet-On) activation (Garner et al., 2012; Gossen and Bujard, 1992; Mayford et al., 1996; Reijmers et al., 2007; Urlinger et al., 2000).”
- Noninvasive deep brain stimulation via temporally interfering electric fields (2017, positive): “…immediate early gene c-fos as a marker of neural activity, as has been used previously to gauge the focality of brain stimulation, since c-fos functions in the mouse cortex and hippocampus as an indicator of activated neurons (Chen et al., 2015; Dragunow and Robertson 1987; Reijmers et al., 2007).”
- Entorhinal Cortical Ocean Cells Encode Specific Contexts and Drive Context-Specific Fear Memory. (2015, positive): “For this purpose, we injected AAV2/9-TRE-mCherry into CA3 of c-fos tTA mice (Reijmers et al., 2007) and exposed them to Context A while off Dox so as to label activated CA3 cells with mCherry (Ramirez et al., 2013).”
- Permanent Genetic Access to Transiently Active Neurons via TRAP: Targeted Recombination in Active Populations (2013, methodology): “TetTag also suffers from relatively high background levels of tagging, even in mice that are maintained on doxycycline (Liu et al., 2012; Reijmers et al., 2007) and in mice that have only the tTA* and reporter transgenes without the Fos-tTA component (K.M., unpublished data).”
- Memory Engram Cells Have Come of Age. (2015, positive): “…of a fear memory were preferentially reactivated during the recall of that memory in different areas of the mouse brain, such as the amygdala (Reijmers et al., 2007), the hippocampus (Deng et al., 2013; Tayler et al., 2013), multiple layer II cortical areas including the sensory cortex (Xie…”
- The molecular and systems biology of memory. (2014, positive): “One useful approach uses the cfos promoter to link the natural patterns of sensory evoked neural activity to genetic alteration such that the pattern of neurons activated during a behavioral session can be specifically altered to express essentially any desired protein (Reijmers et al., 2007).”