361 |
Generic Bi-directional Real-time Neural Interface (Zrenner et al. 2010) |
362 |
Genetic, biochemical and bioelectrical dynamics in pattern regulation (Pietak & Levin 2017) |
363 |
Global and multiplexed dendritic computations under in vivo-like conditions (Ujfalussy et al 2018) |
364 |
Global structure, robustness, and modulation of neuronal models (Goldman et al. 2001) |
365 |
Globus pallidus multi-compartmental model neuron with realistic morphology (Gunay et al. 2008) |
366 |
Globus pallidus neuron models with differing dendritic Na channel expression (Edgerton et al., 2010) |
367 |
Glutamate mediated dendritic and somatic plateau potentials in cortical L5 pyr cells (Gao et al '20) |
368 |
Goldfish Mauthner cell (Medan et al 2017) |
369 |
GP Neuron, somatic and dendritic phase response curves (Schultheiss et al. 2011) |
370 |
GPi/GPe neuron models (Johnson and McIntyre 2008) |
371 |
Granule Cells of the Olfactory Bulb (Simoes_De_Souza et al. 2014) |
372 |
Grid cell oscillatory interference with noisy network oscillators (Zilli and Hasselmo 2010) |
373 |
Grid cells from place cells (Castro & Aguiar, 2014) |
374 |
HERG K+ channels spike-frequency adaptation (Chiesa et al 1997) |
375 |
HH model neuron of the Suprachiasmatic Nucleus including a persistent Na+ channel (Paul et al 2016) |
376 |
High entrainment constrains synaptic depression in a globular bushy cell (Rudnicki & Hemmert 2017) |
377 |
High frequency stimulation of the Subthalamic Nucleus (Rubin and Terman 2004) |
378 |
Hippocampal CA1 pyramidal cell demonstrating dynamic mode switching (Berteau & Bullock 2020) |
379 |
Hippocampal CA3 network and circadian regulation (Stanley et al. 2013) |
380 |
Hippocampus CA1 Interneuron Specific 3 (IS3) in vivo-like virtual NN simulations (Luo et al 2020) |
381 |
Hippocampus CA1 pyramidal model with Na channel exhibiting slow inactivation (Menon et al. 2009) |
382 |
Hodgkin-Huxley model of persistent activity in PFC neurons (Winograd et al. 2008) (NEURON python) |
383 |
Hodgkin-Huxley model of persistent activity in prefrontal cortex neurons (Winograd et al. 2008) |
384 |
Hodgkin-Huxley models of different classes of cortical neurons (Pospischil et al. 2008) |
385 |
Hodgkin-Huxley simplifed 2D and 3D models (Lundstrom et al. 2009) |
386 |
Hodgkin-Huxley with dynamic ion concentrations (Hubel and Dahlem, 2014) |
387 |
Homeostatic synaptic plasticity (Rabinowitch and Segev 2006a,b) |
388 |
Hotspots of dendritic spine turnover facilitates new spines and NN sparsity (Frank et al 2018) |
389 |
How adaptation makes low firing rates robust (Sherman & Ha 2017) |
390 |
Human tactile FA1 neurons (Hay and Pruszynski 2020) |
391 |
Hyperbolic model (Daneshzand et al 2017) |
392 |
I A in Kenyon cells resemble Shaker currents (Pelz et al 1999) |
393 |
I&F recurrent networks with current- or conductance-based synapses (Cavallari et al. 2014) |
394 |
IA and IT interact to set first spike latency (Molineux et al 2005) |
395 |
Ih levels roles in bursting and regular-spiking subiculum pyramidal neurons (van Welie et al 2006) |
396 |
Impact of dendritic atrophy on intrinsic and synaptic excitability (Narayanan & Chattarji, 2010) |
397 |
Impact of dendritic size and topology on pyramidal cell burst firing (van Elburg and van Ooyen 2010) |
398 |
Impact of fast Na channel inact. on AP threshold & synaptic integration (Platkiewicz & Brette 2011) |
399 |
Impedance spectrum in cortical tissue: implications for LFP signal propagation (Miceli et al. 2017) |
400 |
INa and IKv4.3 heterogeneity in canine LV myocytes (Flaim et al 2006) |