A Dynamic Memory Systems Framework for Sex Differences in Fear Memory

2019 ◽  
Vol 42 (10) ◽  
pp. 680-692 ◽  
Author(s):  
Natalie C. Tronson ◽  
Ashley A. Keiser
2019 ◽  
Vol 161 ◽  
pp. 26-36 ◽  
Author(s):  
Adam J. Kirry ◽  
Deven J. Durigan ◽  
Robert C. Twining ◽  
Marieke R. Gilmartin

2013 ◽  
Vol 44 (3) ◽  
pp. 314-321
Author(s):  
Nan SUN ◽  
Yi-Ming WEI ◽  
Qian LI ◽  
Xi-Fu ZHENG

2016 ◽  
Vol 25 (10) ◽  
pp. 1630006
Author(s):  
Sungkyung Park ◽  
Chester Sungchung Park

Frequency dividers are used in frequency synthesizers to generate specific frequencies or clock (CK) waveforms. As consequences of their operating principles, frequency dividers often produce output waveforms that exhibit duty cycles other than 50%. However, some circuits and systems, including dynamic memory systems and data converters, which accommodate frequency divider outputs, may need symmetric or 50%-duty-cycle clock waveforms to optimize timing margins or to obtain sufficient timing reliability. In this review paper, design principles and methods are studied to produce symmetric waveforms for the in-phase (I) and quadrature (Q) outputs of high-speed CMOS frequency dividers with design considerations from the logic gate level down to the transistor level in terms of speed, reliability, noise, and latency. A compact and robust multi-gigahertz frequency divider with moduli 12, 14, and 16 to provide I and Q outputs with 50% duty cycle is proposed and designed using a 90-nm digital CMOS process technology with 1.2-V supply.


2015 ◽  
Vol 50 (8) ◽  
pp. 87-96 ◽  
Author(s):  
Alexandro Baldassin ◽  
Edson Borin ◽  
Guido Araujo

Author(s):  
Yaroslav Felipe Kalle Kossio ◽  
Sven Goedeke ◽  
Christian Klos ◽  
Raoul-Martin Memmesheimer

Change is ubiquitous in living beings. In particular, the connectome and neural representations can change. Nevertheless behaviors and memories often persist over long times. In a standard model, memories are represented by assemblies of strongly interconnected neurons. For faithful storage these assemblies are assumed to consist of the same neurons over time. Here we propose a contrasting memory model with complete temporal remodeling of assemblies, based on experimentally observed changes of connections and neural representations. The assemblies drift freely as spontaneous synaptic turnover or random activity induce neuron exchange. The gradual exchange allows activity dependent and homeostatic plasticity to conserve the representational structure and keep inputs, outputs and assemblies consistent. This leads to persistent memory. Our findings explain recent experimental results on the temporal evolution of fear memory representations and suggest that memory systems need to be understood in their completeness as individual parts may constantly change.


2018 ◽  
Author(s):  
Nicholas Diamond ◽  
Brian Levine

In this chapter, we summarize the literature on the role of the PFC in memory tasks. For other, more targeted reviews, see Fletcher and Henson (2001), Simons and Spiers (2003), Szczepanski and Knight (2014), and Nyhus and Badre (2015). Here, we focus our summary of the literature on work not already covered in depth in these reviews; we also cast a wider net, integrating findings from humanand animal research across frontal subregions and experimental paradigms. The task is challenging, given the breadth of memory-related processes attributed to the PFC. The psychological and neural architecture of memory has been fractionated into distinct processes and systems (e.g., short-term vs. long-term, encoding vs. retrieval, episodic vs. semantic memory). However, there is evidence that supposedly system- and process-specific neural activity transcends categorical distinctions in the memory literature, as demonstrated by neuroimaging (Ranganath, Johnson, & D’Esposito, 2003) and human and animal lesion studies (reviewed in Fuster, 1995). Furthermore, there are inconsistencies across studies in the division of the PFC. While strict assignment of discrete functions to PFC subregions is questionable (see Duncan, 2001; Wilson, Gaffan, Browning, & Baxter, 2010), some models of the functional organization of the frontal lobes both within memory (e.g., Fletcher & Henson, 2001) and in cognition more broadly (Badre & D’Esposito, 2009) have proven successful in generating new questions and holding up to new evidence. When possible, we highlight commonalities across tasks and paradigms, adopting a component processing framework (Cabeza & Moscovitch, 2013); yet our review also reflects the literature as it stands, much of which operates from a memory systems framework. We also emphasize recent memory-related research on PFC–MTL interactions and the participation of the PFC in large-scale functional networks, highlighting distributed oscillatory interactions as a mechanism of dynamic network coordination in the service of memory function. We begin by discussing overall functional contributions of the PFC to working, episodic and autobiographical memory tasks. We then discuss distinct PFC subregions and processes that they implement across these measures of memory.


2012 ◽  
Vol 36 (8) ◽  
pp. 3096-3102 ◽  
Author(s):  
J. P. ter Horst ◽  
A. P. Carobrez ◽  
M. H. van der Mark ◽  
E. R. de Kloet ◽  
M. S. Oitzl

2011 ◽  
Vol 71 ◽  
pp. e270
Author(s):  
Shingo Matsuda ◽  
Daisuke Matuzawa ◽  
Daisuke Ishii ◽  
Haruna Tomizawa ◽  
Chihiro Sutoh ◽  
...  
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