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Common mechanisms mediate synapse formation during development and synapse plasticity during learning and memory
Lecture
Monday, July 30, 2007
Hour: 12:00
Location:
Nella and Leon Benoziyo Building for Brain Research
Common mechanisms mediate synapse formation during development and synapse plasticity during learning and memory
Prof. Samuel Schacher
Center for Neurobiology & Behavior,
Columbia University College, New York, NY
"The Effects of Age-Related Morphologic Changes
Lecture
Sunday, July 29, 2007
Hour: 12:00
Location:
Nella and Leon Benoziyo Building for Brain Research
"The Effects of Age-Related Morphologic Changes
Dr. Doron Kabaso
Department of Biomathematical Sciences
Mount Sinai School of Medicine, New York, NY, USA
:3.14" A Constant That is Fundamental to Visual Cortex Design"
Lecture
Wednesday, July 18, 2007
Hour: 12:00
Location:
Nella and Leon Benoziyo Building for Brain Research
:3.14" A Constant That is Fundamental to Visual Cortex Design"
Prof. Fred Wolf
Research Group Theoretical Neurophysics
Max Planck Institute for Dynamics and Self-Organization
Gottingen, Germany
Circadian clocks in the limbic forebrain:
Lecture
Tuesday, July 10, 2007
Hour: 12:00
Location:
Nella and Leon Benoziyo Building for Brain Research
Circadian clocks in the limbic forebrain:
Prof. Shimon Amir
Concordia University Research Chair
Center for Studies in Behavioral Neurobiology
Department of Psychology
Concordia University, Montreal, Canada
"A Functional Circuit Underlying Male Sexual Behaviour Uncovered in
Lecture
Sunday, July 8, 2007
Hour: 12:00
Location:
Nella and Leon Benoziyo Building for Brain Research
"A Functional Circuit Underlying Male Sexual Behaviour Uncovered in
Dr. Tali Kimchi
Dept of Molecular & Cellular Biology, Howard Hughes Medical Institute, Cambridge, MA
Integrate & Play Theory of Hippocampal Function:
Lecture
Monday, July 2, 2007
Hour: 12:00
Location:
Nella and Leon Benoziyo Building for Brain Research
Integrate & Play Theory of Hippocampal Function:
Dr. Dori Derdikman
Centre for the Biology of Memory
Norwegian University of Science & Technology (NTNU)
Trondheim, Norway
An alternative model to the Declarative-Memory & Cognitive Map theories of the function of the hippocampus is suggested. the new model may explain the deficits described in the famous case of H.M., who displayed total anterograde amnesia following a surgery in which a bilateral dissection of the whole medial-temporal lobe (MTL) was perfromed (Scoville and Milner, 1957) . According to the model, the main functions of the MTL are: (1) to act as an integrator (2) to detect novelty. The integrator function is used, for example, for generation of the place-cell and grid-cell system. Normally, the MTL is integrating an episode until it detects a novel situation. Once the MTL detects such a novel situation, it sends the executive brain (perhaps the basal ganglia and/or prefrontal cortex) a message that it is time to play a novel behavioral game. In the case of H.M., where the MTL is missing, the executive brain never gets the message that an episode is novel, and thus continues to play "old games". In principle, at least, if this model is correct, H.M. could be cured from his memory problem, if the executive brain would have received the missing novelty signals artificially.
Itch more than scratching the surface
Lecture
Monday, June 25, 2007
Hour: 12:00
Location:
Nella and Leon Benoziyo Building for Brain Research
Itch more than scratching the surface
Prof. Gil Yosipovitch
Dept of Dermatology, Neurobiology & Anatomy, & Regenerative Medicine, Wake Forest University Health Sciences Winston-Salem, NC
Predicting odor pleasantness from odor structure:Pleasantness as a reflection of the physical world
Lecture
Monday, June 18, 2007
Hour: 12:00
Location:
Nella and Leon Benoziyo Building for Brain Research
Predicting odor pleasantness from odor structure:Pleasantness as a reflection of the physical world
Prof. Noam Sobel
Dept of Neurobiology, WIS
The cell biology of Alzheimer's disease: Intracellular pathways to pathogenesis
Lecture
Monday, June 11, 2007
Hour: 12:00 - 13:00
Location:
Nella and Leon Benoziyo Building for Brain Research
The cell biology of Alzheimer's disease: Intracellular pathways to pathogenesis
Prof. Scott A. Small
Columbia University, School of Physicians and Surgeons, New York, NY
The Hippocampus and Memory: Consolidation or Transformation?
Lecture
Tuesday, May 29, 2007
Hour: 12:00 - 13:00
Location:
Nella and Leon Benoziyo Building for Brain Research
The Hippocampus and Memory: Consolidation or Transformation?
Dr. Gordon Winocur
Rotman Research Institute, Toronto, Ontario, Canada
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Conversion of sensory signals into perceptual decisions
Lecture
Monday, January 8, 2007
Hour: 14:00
Location:
Arthur and Rochelle Belfer Building for Biomedical Research
Conversion of sensory signals into perceptual decisions
Prof. Ranulfo Romo
National Autonomous University of Mexico
Multi-regional Interactions support memory formation: modulation of the Rhinal cortices by the Amygdala and the mPFC
Lecture
Monday, January 8, 2007
Hour: 12:00
Location:
Nella and Leon Benoziyo Building for Brain Research
Multi-regional Interactions support memory formation: modulation of the Rhinal cortices by the Amygdala and the mPFC
Dr. Rony Paz
Center for Molecular & Behavioral Neuroscience, Rutgert University, New-Jersey
When is it worth working: Behavioral, physiological, genetic, and modeling experiments investigating motivation and reward expectancy
Lecture
Sunday, January 7, 2007
Hour: 10:00 - 11:00
Location:
Nella and Leon Benoziyo Building for Brain Research
When is it worth working: Behavioral, physiological, genetic, and modeling experiments investigating motivation and reward expectancy
Dr. Barry J. Richmond
Chief, Section on Neural Coding and Computation Laboratory of Neuropsychology, National Institute of Mental Health,
NIH, DHHS, USA
The intensity or vigor of goal-directed behavior is a correlate of the motivation underlying it. Motivation is related to the subjective value of rewards and is moderated, or even completely dissipated, if the perceived effort or discomfort seems too great. Under what circumstances do we seek a goal or a reward? To study motivated behavior in monkeys, we use several variants of a task in which monkeys must perform some work, in this case detecting when a target spot turns from red-to-green, to obtain a drop of juice. We use another visual stimulus, a cue, to indicate how much discomfort must be endured, e.g., the number of trials to be worked, to obtain the reward. The monkeys learn about the cues quickly, often after just a few trials. The number of errors becomes proportional to amount of work remaining before reward, achieving our goal of manipulating motivation. This is a behavior in which the monkeys decrease their performance in response to an increased predicted workload. Temporal difference models have provided an important framework for interpreting goal directed-behavior, and in economics, game theory has been used to model choice behavior. A key concept in these models is to determine how the value of the reward is modulated by some parameter of the experiment, such as changing the reward size, or the amount of time needed to obtain the reward. In learning or adaptation the TD algorithm predicts that behavior should be (and in artificial systems is) adapted to maximize long-term reward. By examining the influence of reward size, waiting time, and amount of work, we can examine in what ways different model succeed and fail. Our data show that performances depend on work completed since preceding reward (sunk cost effect), and accumulated reward (over whole sessions) and work. In addition this behavior can be used to learn about categorization and rule learning. Using single neuronal recording, regional ablation, and molecular ablation of the D2 receptor we show that dopamine-rich brain regions have signals related to the balance between reward and work.
Stress and the Brain – a Molecular View
Lecture
Tuesday, January 2, 2007
Hour: 12:00 - 13:15
Location:
Nella and Leon Benoziyo Building for Brain Research
Stress and the Brain – a Molecular View
Dr. Daniela Kaufer
Department of Integrative Biology
Helen Wills Neuroscience Institute, University of California
Berkeley, CA
My lab studies the molecular basis of neural and hormonal mechanisms of stress responses. Using interdisciplinary multilevel approach we look at the plasticity of the brain in dealing with physiological and pathological events. In this talk I will describe three current projects: Hormonal Regulation of Neural Stem Cells. Determining the environmental and internal cues that control the proliferation and fate choices of stem cells in the adult hippocampus, and their role in functional plasticity. RNA Regulatory Mechanisms in Neural Stress Responses. RNA regulation, specifically, alternative splicing and microRNA expression as a fine tuning neural stress mechanism. The Molecular Mechanisms of post-trauma Epileptogenesis. Determine the mechanism underlying epileptogenesis following blood brain barrier damage.
Synaptic maintenance - Insights from live imaging experiments
Lecture
Monday, January 1, 2007
Hour: 12:00
Location:
Nella and Leon Benoziyo Building for Brain Research
Synaptic maintenance - Insights from live imaging experiments
Dr. Noam Ziv
Dept of Physiology, Faculty of Medicine, Technion
Recent studies suggest that central nervous system (CNS) synapses persist
for many weeks, months and even lifetimes, yet little is
known on the mechanisms that allow these structures to persist for so
long despite the many deconstructive processes acting at biological
systems and neurons in particular. As a step toward a better
understanding of synaptic maintenance we set out to examine some of the
deconstructive and reconstructive forces acting at individual CNS
synapses. To that end we studied the molecular dynamics of several
presynaptic and postsynaptic cytomatrix molecules. Fluorescence
recovery after photobleaching (FRAP) and photoactivation experiments
revealed that these molecules are continuously incorporated into and lost
from individual synaptic structures within tens of minutes.
Moreover, these dynamics can be accelerated by synaptic activity.
Finally, we find that synaptic molecules are continuously exchanged
between nearby synaptic structures at similar rates and that these rates
greatly exceed the rates at which synapses are replenished with molecules
arriving from somatic sources. Our findings indicate that the dynamics of
key synaptic matrix molecules may be dominated by local protein exchange
and redistribution, whereas protein synthesis and degradation serve to
maintain and regulate the sizes of local, shared pools of these proteins.
The nature of these dynamics raises intriguing questions as to how
synapses manage to maintain their
individual, use-dependent structural and functional characteristics over
long durations.
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