Last revised 11/15/2008. Please report additions and corrections to ted dot carnevale at yale dot edu
NEURON users who have teaching obligations should note the education-oriented posters by Grisham et al. (224.7, UU34) and Carver (225.4, UU53), as well as Moore and Stuart's latest version of Neurons in Action 2 (on display at the Sinauer booth).
Time & Place |
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Abstract Title |
Sat PM |
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2 - 3 WCC A-C |
36.2 |
F2 |
A. NÖRENBERG1, *M. BARTOS2, I. VIDA3, H. HU1, P. JONAS1; 1Dept. I, Physiological Inst., Freiburg, Germany; 2Inst. of Med. Sci., Univ. Aberdeen, Aberdeen, United Kingdom; 3Div. of Neurosci. and Biomed. Systems, Fac. of Biomed. and Life Sciences, Univ. of Glasgow West, Glasgow, United Kingdom |
Detailed cable models of fast-spiking basket cells in the
dentate gyrus |
3 - 4 WCC A-C |
36.3 |
F3 |
H. HU1,2, *P. M. JONAS1; 1Dept. I, Physiological Inst., Freiburg, Germany; 2Physiol., Inst. of Basal Medicine, Ctr. for Mol. Biol. and Neuroscience, Univ. of Oslo, Oslo, Norway |
Propagation of action potentials in the dendrites of
fast-spiking basket cells in the dentate gryus |
1 - 2 WCC A-C |
36.9 |
F9 |
*Y. WEI1, B. W. MEL2; |
Nonlinear synaptic integration depends on relative values and
timing of NMDA and AMPA conductances |
2 - 3 WCC A-C |
36.10 |
F10 |
*B. LOSAVIO, P. SAGGAU; Baylor Col. Med., Houston, TX |
Non-linear synaptic summation in different types of central
neurons |
3 - 4 WCC A-C |
36.19 |
G7 |
T. BRANCO, *B. A. CLARK, M. HAUSSER; WIBR, UCL, London, United Kingdom |
Directional selectivity in basal dendrites of cortical
pyramidal neurons |
4 - 5 WCC A-C |
41.16 |
O3 |
*T. SHINOZAKI1, H. CATEAU1, A. REYES2, M. OKADA3,1; 1Brain Sci. Inst., RIKEN, Wako, Japan; 2Ctr. for Neural Sci., New York Univ., New York, NY; 3Dept. of Complexity Sci. and Engin., Univ. of Tokyo, Kashiwa, Japan |
Preceding inhibition stabilizes propagation of synfire chain
in silico and in vitro |
2 - 3 WCC A-C |
43.2 |
R5 |
*S. DRUCKMANN1, H. MARKRAM2, I. SEGEV1; 1Hebrew Univ., Jerusalem, Israel; 2EPFL, Lausanne, Switzerland |
Objective assessment and automated modeling of the different
electrical classes of neurons in the neocortex |
2 - 3 WCC A-C |
43.10 |
S1 |
*H. KUBA, H. OHMORI; Dept Physiol, Fac Med, Kyoto Univ., Kyoto, Japan |
Distribution of axonal Na channels for precise spike timing in
an auditory relay neuron |
4 - 5 WCC A-C |
43.20 |
S11 |
A. YADAV1, *C. M. WEAVER1, Y. Z.
GAO1, J. I. LUEBKE2, S. L. WEARNE1;
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Altered mechanisms of calcium handling with age in neocortical
neurons: The role of spine size and background synaptic
activity |
2 - 3 WCC A-C |
43.22 |
T1 |
*S. A. PRESCOTT1, S. RATTÉ1, Y. DE KONINCK2, T. J. SEJNOWSKI3,4; 1Neurobio., Univ. of Pittsburgh, Pittsburgh, PA; 2CRULRG, Quebec, QC, Canada; 3Salk Institute, HHMI, La Jolla, CA; 4UCSD, La Jolla, CA |
How pyramidal neurons switch from integrators in vitro to
resonators under in vivo-like conditions |
1 - 2 WCC A-C |
44.5 |
T11 |
*J. L. BAKER1, T. PEREZ2, M. MIGLIORE3, G. BARRIONUEVO2, G. A. ASCOLI1; 1Krasnow Inst. Advanced Study, George Mason Univ., Fairfax, VA; 2Dept. of Neurosci., Univ. of Pittsburgh, Pittsburgh, PA; 3Inst. of Biophysics, Natl. Res. Council, Palermo, Italy |
Computer simulation of minimally evoked recurrent collateral
and perforant path excitatory synaptic responses in hippocampal
CA3b pyramidal cells |
4 - 5 WCC A-C |
44.16 |
U10 |
S. RIEUBLAND, J. T. DAVIE, *A. ROTH, M. HAUSSER; Wolfson Inst., Univ. Coll London, London, United Kingdom |
The dynamic current-voltage relation of cerebellar Purkinje
cells |
1 - 2 WCC A-C |
44.25 |
U19 |
*B. BATHELLIER1, T. W. MARGRIE2,
M. E. LARKUM1; |
Dendritic properties of olfatory cortex pyramidal
neurons |
4 - 5 WCC A-C |
44.28 |
U22 |
G. CELLOT1, S. CIPOLLONE2, L. GAMBAZZI3, H. MARKRAM3, M. PRATO2, *M. GIUGLIANO3, L. BALLERINI1; 1Physiol. and Pathology Department,, 2Univ. of Trieste, Trieste, Italy; 3Brain Mind Inst, Neural Micro, Ecole Polytech Fed d, Lausanne, Switzerland |
Interfacing neurons with carbon nanotubes boosts post spike
excitability |
3 - 4 WCC A-C |
58.11 |
CC26 |
*M. MIGLIORE1, C. CANNIA1, C. C. CANAVIER2; 1Inst. of Biophysics, Natl. Res. Council, Palermo, Italy; 2Neurosci. Ctr. of Excellence, LSU Hlth. Sci. Ctr., New Orleans, LA |
Getting sober with Ih: a possible pharmacological
target to mitigate the effects of ethanol on reward-related
dopaminergic signaling |
2 - 3 WCC A-C |
101.14 |
VV9 |
R. BRETTE1, J. GOMEZ GONZALEZ2, Z. PIWKOWSKA2, M. RUDOLPH-LILITH2, C. MONIER2, J. FOURNIER2, M. LEVY2, Y. FREGNAC2, T. BAL2, *A. DESTEXHE2; 1Ecole Normale Superieure, Paris, France; 2UNIC, CNRS, Gif-sur-Yvette Cedex, France |
Active Electrode Compensation for high-resolution
intracellular recordings in vitro and in vivo |
Sun AM |
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8 - 9 WCC A-C |
136.17 |
G2 |
*J. LIU1, D. V. BUONOMANO2; 1Dept. of Mathematics, 2Neurobiol & Psychol, UCLA, Los Angeles, CA |
Embedding multiple trajectories in recurrent neural networks
in a self-organizing manner |
10 - 11 WCC A-C |
139.7 |
L10 |
*A. CHATURVEDI1,3, C. R. BUTSON1, C. B. MAKS1, S. E. COOPER2, C. C. MCINTRYRE1,3,2; 1Biomed. Engin., 2Ctr. for Neurolog. Restoration, Cleveland Clin. Fndn., Cleveland, OH; 3Biomed. Engin., Case Western Reserve Univ., Cleveland, OH |
Integrating 3D brain atlases, fiber tractography, and axonal
activation models to build patient-specific models of deep brain
stimulation |
9 - 10 WCC A-C |
139.10 |
M1 |
*S. E. COOPER1, P. HAHN2, C. MCINTYRE2; 1Dept Neurol, 2Biomed. Engin., Cleveland Clin. Fndn., Cleveland, OH |
Synaptic plasticity in a subthalamopallidal network model of
deep brain stimulation |
Sun PM |
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1 - 2 WCC A-C |
237.17 |
D42 |
N. DOYON1, H. KROGER2, S. A. PRESCOTT3, *Y. DE KONINCK4; 1Cell. Neurobio., 2Laval Univ., Quebec, QC, Canada; 3Neurobio., Univ. of Pittsburgh, Pittsburgh, PA; 4Cell. Neurobiol, Laval Univ. / CRULRG, Quebec, Canada |
Impact of altered chloride extrusion capacity on cell
excitability |
4 - 5 WCC A-C |
240.4 |
E26 |
*B. A. MARCELIN1, L. CHAUVIÈRE1, A. BECKER2, M. MIGLIORE3, M. ESCLAPEZ1, C. BERNARD1; 1U751, INSERM, Marseilles, France; 2Dept. of Neuropathology & Natl. Brain Tumor Reference Ctr., Univ. of Bonn Med. Ctr., Bonn, Germany; 3Inst. of Biophysics, Palermo, Italy |
Alterations of Ih dynamics underlie a deficit of theta
oscillations in a rat model of temporal lobe
epilepsy |
3 - 4 WCC A-C |
250.15 |
V27 |
A. BOGAARD1, V. BOOTH2, *M. R. ZOCHOWSKI1; 1Physics, 2Dept. of Mathematics, Anasthesiology, Univ. of Michigan, Ann Arbor, MI |
Interaction of cellular and network mechanisms in
spatio-temporal pattern formation in neuronal networks and its
role in seizure generation |
3 - 4 WCC A-C |
224.7 |
UU34 |
W. E. GRISHAM, N. A. SCHOTTLER, F. B. KRASNE; Dept Psychol, UCLA, Los Angeles, CA |
SWIMMY: inquiry-based, free software providing experience with
basic neurophysiology and mechanisms of motor pattern
generation |
4 - 5 WCC A-C |
225.4 |
UU53 |
*S. G. CARVER; |
Bringing the research frontier to the classroom: teaching
neural modeling through system identification |
Mon AM |
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8 - 9 WCC A-C |
368.5 |
JJ30 |
*A. M. TAN, P. ZHAO, Y.-W. CHENG, S. STAMBOULIAN, J. CHOI, A. B. HAINS, S. G. WAXMAN, B. C. HAINS; Neurol., Yale Univ. Sch. of Med., West Haven, CT |
This presenter will not attend |
10 - 11 WCC A-C |
376.23 |
PP16 |
T. S. ANDERSON1,2, R. FOGLYANO1, P. J. THOMAS3,4, *C. G. WILSON1; 1Dept Pediatrics, 2Sch. of Med., 3Mathematics, 4Biol., CWRU, Cleveland, OH |
Changing external potassium conditions elicits periodic
modulation of respiratory rhythm in a preBötzinger complex
network model while other methods of boosting neural excitability
do not |
Mon PM |
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2 - 3 WCC A-C |
435.6 |
H11 |
*S. OZEN1, A. M. SIROTA1, C. A. ANASTASSIOU2, C. KOCH2, G. BUZSAKI1; 1Cntr for Neurosci, Rutgers Univ., Newark, NJ; 2Div. of Biol., Caltech, Pasadena, CA |
Entrainment of the cortical slow oscillation by extra-cranial
weak electric fields |
4 - 5 WCC A-C |
435.8 |
I1 |
C. A. ANASTASSIOU1, S. M. MONTGOMERY2, M. BARAHONA3, *G. BUZSAKI2, C. KOCH1; 1Div. of Biol., Caltech, Pasadena, CA; 2Ctr. for Molec & Behav Neurosci, Rutgers Univ., Newark, NJ; 3Dept. of Bioengineering, Imperial Col. London, London, United Kingdom |
Effects of spatially inhomogeneous extracellular fields on the
membrane potential of single neurons |
4 - 5 WCC A-C |
437.8 |
K4 |
*R. H. CUDMORE1,2, P. GIRAUD1,2, D. DEBANNE1,2; 1INSERM U641, Marseille, France; 2Univ. de la Méditerranée, Marseille, France |
Spike time precision and network synchrony are controlled by
the homeostatic regulation of IA/ID |
3 - 4 WCC A-C |
445.19 |
W24 |
*S. M. ELBASIOUNY1, C. J. HECKMAN2; 1Dept Physiol, 2Departments of Physiol. and Physical Med. and Rehabil., Northwestern Univ., Chicago, IL |
Upregulation of active conductances and persistent inward
currents in mutant SOD1 motoneurons: Insights from computer
simulations |
3:20 - 3:55 PM WCC Blrm B |
399.5 |
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A. Destexhe; UNIC, CNRS, Gif-sur-Yvette Cedex, FRANCE. |
Modulation of information transfer by network
activity |
Tue AM |
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8 - 8:15 AM WCC 140A |
517.1 |
*P. N. STEINMETZ1,2, S. C. BELLINGER1; 1Bioengineering, Arizona St Univ., Tempe, AZ; 2Neurol., Barrow Neurolog. Inst., Phoenix, AZ |
Submyelin potassium accumulation may functionally block
subsets of local axons during deep brain stimulation: a modeling
study |
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8 - 9 WCC A-C |
535.1 |
D62 |
*J. AMBROS-INGERSON1, L. M. GROVER2, W. R. HOLMES1; 1Dept Biol Sci., Ohio Univ., Athens, OH; 2Dept of Pharmacology, Physiol. and Toxicology, Marshall Univ. Sch. of Med., Huntington, WV |
The upstroke of the action potential has two events that
suggest initiation occurs at the nodes of Ranvier in hippocampal
CA1 pyramidal cells |
9 - 10 WCC A-C |
578.10 |
QQ12 |
*J. T. MOYER1, B. L. HALTERMAN1, L. H. FINKEL1, J. A. WOLF2; 1Dept Bioengineering, 2Dept Psychiatry, Univ. Pennsylvania, Philadelphia, PA |
Functional roles of lateral and feedforward inhibition in the
striatum |
Tue PM |
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1 - 2 WCC A-C |
631.5 |
D41 |
O. WAROUX1, M. BONJEAN2, G.
DRION3, D. ENGEL4, R. SEPULCHRE3,
*V. M. SEUTIN4; |
Modulation of burst firing by KCNQ channels in dopaminergic
neurons: further mechanistic modelling and experimental
findings |
2 - 3 WCC A-C |
641.2 |
R12 |
*C. C. MCINTYRE1, P. J. HAHN1, M. J. LOWE2, M. D. PHILLIPS2; 1Biomed Engin., 2Radiology, Cleveland Clin. Fndn., Cleveland, OH |
Integration of patient-specific network models and fMRI
activation during deep brain stimulation |
3 - 4 WCC A-C |
641.3 |
S1 |
*P. J. HAHN, C. C. MCINTYRE; Biomed. Engr, Cleveland Clin. Lerner Resch Inst., Cleveland, OH |
Training a subthalamopallidal network model of deep brain
stimulation using experimental data |
3 - 4 WCC A-C |
641.27 |
U1 |
*T. J. FOUTZ1,2, S. MIOCINOVIC1,2, C. C. MCINTYRE1,2; 1Dept of Biomed. Engin., Case Western Reserve Univ., Cleveland, OH; 2Dept of Biomed. Engin., Cleveland Clin. Fndn., Cleveland, OH |
Evaluation of novel stimulus waveforms for subthalamic deep
brain stimulation |
4 - 5 WCC A-C |
690.12 |
TT85 |
*S. A. NEYMOTIN1, A. V. OLYPHER5, H.-Y. KAO2, E. KELEMEN2, A. E. JOZWICKA2, W. W. LYTTON3, A. A. FENTON4; 1Biomed. Engin. Program, 2Neural and Behavioral Sci. Program, 3Physiol. & Pharmacology, Neurology, Biomed. Engin., 4Physiol. & Pharmacol., SUNY Downstate, Brooklyn, NY; 5Biol., Emory Univ., Atlanta, GA |
Standardized assessment of extracellular single unit isolation
quality |
3 - 4 WCC A-C |
694.20 |
UU80 |
A. HAJJ, *P. A. FORTIER; Dept Cell & Molec Med., Univ. Ottawa, Ottawa, ON, Canada |
Simulation of retinal triadic circuitry and signal
transmission along the early visual pathway |
Wed AM |
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9 - 10 WCC A-C |
738.10 |
N1 |
*M. FERRANTE1, M. MIGLIORE3,4, G. A. ASCOLI2; 1Krasnow Inst., 2Dept. of Mol. Neurosci., George Mason Univ., fairfax, VA; 3Yale Univ., New Haven, CT; 4Inst. of Biophysics, Natl. Res. Council, Palermo, Italy |
Feed-forward inhibition as a buffer of the neuronal
input-output relation |
8 - 9 WCC A-C |
769.25 |
KK31 |
S. A. NEYMOTIN1, D. J. UHLRICH3, *W. W. LYTTON2; 1Program in Biomed. Engin., 2Physiol, Pharmacol, Neurol, SUNY Downstate, Brooklyn, NY; 3Anat., U. Wisconsin, Madison, WI |
Virtual slice simulation of resonance in a layered cortical
model |
10 - 11 WCC A-C |
775.19 |
OO12 |
B. GUCLU1, G. K. MAHONEY2, L. PAWSON2, *A. PACK3, R. L. SMITH2; 1Biomed. Engin. Inst., Bogazici Univ., Istanbul, Turkey; 2Inst. for Sensory Res., Syracuse, NY; 3Biol., Utica Col., Utica, NY |
Computational model predicts directional sensitivity and
voltage-sensitive channels in slowly-adapting Type I
mechanoreceptive neurites |
9 - 10 WCC A-C |
798.14 |
VV7 |
*M. L. HINES1, F. SCHUERMANN2, H. MARKRAM2; 1Computer Sci., Yale Univ., New Haven, CT; 2Brain Mind Inst., EPFL, Lausanne, Switzerland |
Threads on multicore workstations allow a good balance between
computational efficiency and ease of use in the NEURON Simulation
Environment |
Wed PM |
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2 - 3 WCC A-C |
823.6 |
C19 |
*S. MANITA, W. N. ROSS; |
IP3 production and IP3 diffusion regulate the time window of
synergistic Ca2+ release by backpropagating action potentials and
mGluR activation in the apical dendrites of CA1 pyramidal
neurons |
2 - 3 WCC A-C |
849.2 |
BB10 |
M. FERRANTE1, K. T. BLACKWELL1, M. MIGLIORE2,3, *G. A. ASCOLI1; 1Krasnow Inst. Advanced Studies, George Mason Univ., Fairfax, VA; 2Inst. of Biophysics, Natl. Res. Council, Palermo, Italy; 3Dept. of Neurobio., Yale Univ., New Haven, CT |
Computational models of neuronal biophysics and the
characterization of potential neuropharmacological
targets |