Memory phases in Drosophila
By W. G. Quinn, Y. Dudai. 1976
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
- Yoshinori Aso
- Ronald L. Davis
- P. Plaçais
- Jacob A. Berry
- Isaac Cervantes-Sandoval
- Stephan Knapek
- S. Waddell
- Liyuan Wang
Citations in the corpus
- Genetic dissection of mutual interference between two consecutive learning tasks in Drosophila (2022, background): “After 20 min, the memory performance of the proactive task partially declines and a consolidated memory component called anesthesiaresistant memory (ARM) is largely formed (Quinn and Dudai, 1976; Tully et al., 1994; Tully and Quinn, 1985; Zhang et al., 2016).”
- The restless engram: consolidations never end. (2012, background): “These elementary forms of learning produce distinct differences in the duration of memory storage (Carew et al., 1972; Pinsker et al., 1973; Quinn and Dudai, 1976).”
- Two independent mushroom body output circuits retrieve the six discrete components of Drosophila aversive memory. (2015, background): “Drosophila, which offer invaluable tools for neural network analysis, are capable of forming many different kinds of memory (Quinn and Dudai, 1976; Tempel et al., 1983; Tully et al., 1994; McBride et al., 1999; Liu et al., 2006; Colomb et al., 2009; Kaun et al., 2011).”
- Appetitive and Aversive Visual Learning in Freely Moving Drosophila (2009, background): “…this performance is rather short compared to memory duration found in appetitive olfactory memory lasting more than 24 h (Krashes and Waddell, 2008; Colomb et al., 2009), it might still allow the analysis of different memory components (see Quinn and Dudai, 1976; Honjo and Furukubo-Tokunaga, 2009).”
- Forgetting is regulated through Rac activity in Drosophila. (2010, unknown): “We first applied a cold shock amnesia treatment (Quinn and Dudai, 1976), which should disrupt anesthesia-sensitive labile early memory forms but not ARM.”
- Dissecting neural pathways for forgetting in Drosophila olfactory aversive memory (2015, background): “To test whether the decreased slope of memory decay arises because early memories are protected from forgetting or because memory consolidation is accelerated, we cold-anesthetized flies at 2 h after training, a treatment that eliminates early labile memory components but does not affect consolidate”
- Cdc42-Dependent Forgetting Regulates Repetition Effect in Prolonging Memory Retention. (2016, background): “Because ARM can be readily isolated from ASM through coldshock treatment and its formation is largely confined to the first hour after training (Quinn and Dudai, 1976; Tully et al., 1994), cold-shock treatments were applied at different time points within this first hour to determine the amount of A”
- Specific dopaminergic neurons for the formation of labile aversive memory (2010, unknown): “What type of memory is impaired by blocking MB-M3? Initially, labile odor memory in Drosophila is consolidated gradually and becomes resistant to retrograde amnesia [29, 30].”
- The molecular and systems biology of memory. (2014, unknown): “These elementary forms of learning produce distinct differences in the duration of memory storage (Carew et al., 1972; Pinsker et al., 1973; Quinn and Dudai, 1976).”
- Classical conditioning and retention in normal and mutantDrosophila melanogaster (1985, background): “Quinn and Dudai 1976; Dudai 1977; Tempel et al. 1983).”
- System-like consolidation of olfactory memories in Drosophila (2013, background): “Memories, shortly after they are acquired, are labile and susceptible to disruption by factors such as interference information, injuries, or amnesiac agents (Scoville and Milner, 1957; McGaugh and Alpern, 1966; Squire et al., 1975; Quinn and Dudai, 1976).”
- Active Protection: Learning-Activated Raf/MAPK Activity Protects Labile Memory from Rac1-Independent Forgetting. (2018, unknown): “In Drosophila, a single trial of aversive classical conditioning yields at least two identifiable memory components, which can be readily isolated using cold-shock anesthesia: a labile anesthesia-sensitive memory that largely decays in 3–6 hr, and a consolidated anesthesia-resistant memory that last”
- Bruchpilot, A Synaptic Active Zone Protein for Anesthesia-Resistant Memory (2011, background): “Therefore, ARM is built gradually after training, and STM consists mainly of ASM (Quinn and Dudai, 1976; Margulies et al., 2005).”
- Rapid Consolidation to a radish and Protein Synthesis-Dependent Long-Term Memory after Single-Session Appetitive Olfactory Conditioning in Drosophila (2008, background): “Appetitive LTM is rapidly consolidated within 2 h after training and requires radish The period of active memory consolidation in insects can be revealed by its sensitivity to cold-shock anesthesia (Erber, 1976; Quinn and Dudai, 1976; Tully et al., 1994).”