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October 01, 2018

  • Date:23TuesdayOctober 2018

    Northern exposure – The study of host-virus interactions from the lab to the Norwegian Fjords

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    Time
    11:30 - 11:30
    Location
    Nella and Leon Benoziyo Building for Biological Sciences
    LecturerDr. Daniella Schatz
    Prof. Assaf Vardi's lab., Department of Plant and Environmental Sciences
    Organizer
    Department of Plant and Environmental Sciences
    Contact
    Lecture
  • Date:23TuesdayOctober 2018

    Synapsins regulate alpha-synuclein function

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    Time
    12:30 - 12:30
    Location
    Gerhard M.J. Schmidt Lecture Hall
    LecturerDr. Daniel Gitler
    Dept of Physiology and Cell Biology/Faculty of Health Sciences and Zlotowksi Center for Neuroscience Ben-Gurion University of the Negev
    Organizer
    Department of Brain Sciences
    Contact
    AbstractShow full text abstract about The normal function of alpha-synuclein, a protein involved i...»
    The normal function of alpha-synuclein, a protein involved in Parkinson's Disease and other synucleinopathies, remains elusive. Though recent studies suggest that alpha-synuclein is a physiological attenuator of synaptic vesicle recycling, mechanisms remain unclear. Our data show that synapsin – a cytosolic protein with established roles in synaptic vesicle mobilization and clustering – is required for alpha-synuclein function. Furthermore, we show that the two proteins interact in a reversible manner in the synapse and that in the absence of synapsins, the localization of alpha-synuclein to synapses is deficient. Our data suggest a model where alpha-synuclein and synapsin cooperate in clustering SVs and attenuating recycling.
    Lecture
  • Date:23TuesdayOctober 2018

    Chemical Approaches to Study Oxidative Protein Folding

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    Time
    14:00 - 15:00
    Location
    Helen and Milton A. Kimmelman Building
    LecturerDr. Norman Metanis
    Organizer
    Department of Chemical and Structural Biology
    Contact
    Lecture
  • Date:24WednesdayOctober 2018

    Transport and fate of Pt-based pharmaceuticals in natural soil-water environments

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    Time
    10:00 - 10:00
    Location
    Sussman Family Building for Environmental Sciences
    LecturerNatalia Chana Goykhman
    Department of Earth and Planetary Sciences Weizmann Institute of Science
    Organizer
    Department of Earth and Planetary Sciences
    Contact
    Lecture
  • Date:24WednesdayOctober 2018

    Spotlight on Science

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    Time
    12:00 - 12:00
    Title
    Detecting the Invisible: On Giant Detectors, Elusive Particles and Dark Matter
    Location
    Gerhard M.J. Schmidt Lecture Hall
    LecturerDr. Hagar Landsman
    Department of Particle Physics and Astrophysics
    Contact
    Lecture
  • Date:24WednesdayOctober 2018

    Emotional valence and implicit memory formation under anesthesia: Neural mechanisms in the amygdala and pre-frontal cortex

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    Time
    14:00 - 15:00
    Location
    Nella and Leon Benoziyo Building for Brain Research
    LecturerNir Samuel (PhD Thesis Defense),
    Rony Paz Lab, Dept of Neurobiology, WIS
    Organizer
    Department of Brain Sciences
    Contact
    AbstractShow full text abstract about Background: The aim of anaesthesia is to eliminate awareness...»
    Background: The aim of anaesthesia is to eliminate awareness and prevent memory of the various aversive stimuli of medical procedures. Yet in a portion of cases, patients can recall events that occurred during surgery resulting in risks of adverse psychological outcomes. Fear conditioning offers a robust behavioral model to study this phenomenon, while the abundant evidence implicating the amygdala-medial prefrontal cortex (mPFC) circuit in acquisition, consolidation and retrieval of these memories offers a natural hypothesis for the neural mechanisms.
    Objective: We aimed to study the effect of anaesthesia on stimulus valence, acquisition and memory and to identify the correlates in the mPFC-amygdala circuit using a primate model and clinically relevant doses of anesthesia.
    Materials and methods: Two non-human primates acquired aversive memories by tone-odor classical conditioning under anesthesia with different doses of ketamine, a non-competitive antagonist of NMDA and midazolam, a GABA agonist. Both agents are in wide clinical use. We simultaneously recorded single neurons in the BLA and mPFC. Analyses focused on behavioral and neural evidence suggesting maintained valence, acquisition and retention of memory.
    Results: Seventy-six full sessions from two non-human primates entered analysis. We recorded 172 amygdala and 189 dACC neurons respectively. We found evidence of successful aversive conditioning under both anesthetics and in all doses. Under anesthesia, we found behavioral evidence of retention in 46% of sessions matched by a complementary response of 16.2% and 18.7% of amygdala and mPFC neurons respectively. An increased and escalating amygdala and mPFC response during acquisition predicted later retention and correlated the behavioral result. The behavioral and neural representation of aversive valence was sufficient to drive learning and affected conditioning outcome.
    Conclusion: Our results suggest that under anesthesia, the perception of stimuli and implicit aversive memory formation may be maintained. We show patterns in the amygdala-mPFC circuit that precede and predict this phenomenon and that may serve future monitoring strategies of anesthetized patients. The use of a primate model and therapeutic doses of common anesthetics affecting both GABA and NMDA transmission improves the possible translation of our findings.

    Lecture
  • Date:24WednesdayOctober 2018

    Emotional valence and implicit memory formation under anesthesia: Neural mechanisms in the amygdala and pre-frontal cortex

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    Time
    14:00 - 15:00
    Location
    Nella and Leon Benoziyo Building for Brain Research
    LecturerNir Samuel (PhD Thesis Defense)
    Rony Paz Lab, Dept of Neurobiology, WIS
    Organizer
    Department of Brain Sciences
    Contact
    AbstractShow full text abstract about Background: The aim of anaesthesia is to eliminate awareness...»
    Background: The aim of anaesthesia is to eliminate awareness and prevent memory of the various aversive stimuli of medical procedures. Yet in a portion of cases, patients can recall events that occurred during surgery resulting in risks of adverse psychological outcomes. Fear conditioning offers a robust behavioral model to study this phenomenon, while the abundant evidence implicating the amygdala-medial prefrontal cortex (mPFC) circuit in acquisition, consolidation and retrieval of these memories offers a natural hypothesis for the neural mechanisms.
    Objective: We aimed to study the effect of anaesthesia on stimulus valence, acquisition and memory and to identify the correlates in the mPFC-amygdala circuit using a primate model and clinically relevant doses of anesthesia.
    Materials and methods: Two non-human primates acquired aversive memories by tone-odor classical conditioning under anesthesia with different doses of ketamine, a non-competitive antagonist of NMDA and midazolam, a GABA agonist. Both agents are in wide clinical use. We simultaneously recorded single neurons in the BLA and mPFC. Analyses focused on behavioral and neural evidence suggesting maintained valence, acquisition and retention of memory.
    Results: Seventy-six full sessions from two non-human primates entered analysis. We recorded 172 amygdala and 189 dACC neurons respectively. We found evidence of successful aversive conditioning under both anesthetics and in all doses. Under anesthesia, we found behavioral evidence of retention in 46% of sessions matched by a complementary response of 16.2% and 18.7% of amygdala and mPFC neurons respectively. An increased and escalating amygdala and mPFC response during acquisition predicted later retention and correlated the behavioral result. The behavioral and neural representation of aversive valence was sufficient to drive learning and affected conditioning outcome.
    Conclusion: Our results suggest that under anesthesia, the perception of stimuli and implicit aversive memory formation may be maintained. We show patterns in the amygdala-mPFC circuit that precede and predict this phenomenon and that may serve future monitoring strategies of anesthetized patients. The use of a primate model and therapeutic doses of common anesthetics affecting both GABA and NMDA transmission improves the possible translation of our findings.

    Lecture
  • Date:25ThursdayOctober 2018

    Bose-Einstein condensation of photons

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    Time
    11:15 - 12:30
    Location
    Edna and K.B. Weissman Building of Physical Sciences
    LecturerMartin Weitz
    Institut für Angewandte Physik, Universität Bonn
    Organizer
    Faculty of Physics
    Contact
    AbstractShow full text abstract about Bose-Einstein condensation has been observed in several phys...»
    Bose-Einstein condensation has been observed in several physical systems, including cold atomic gases, exciton-polaritons, and magnons. Photons usually show no Bose-Einstein con-densation, since for Planck’s blackbody radiation the particle number is not conserved and the photons at low temperatures vanish in the system walls. I here describe experiments with a dye-filled optical microresonator experimentally observing Bose-Einstein condensation of pho-tons. Thermalization is achieved in a number conserving way by repeated absorption re-emission cycles on the dye molecules, and the cavity mirrors provide both an effective photon mass and a confining potential. More recently, we have investigated calorimetric properties of the trapped photon gas, and determined both the heat capacity and the entropy around the phase transition. In other work, we have realized lattice potentials for photons in the dye mi-crocavity. In my talk, I will begin with a general introduction and give an account of current work and future plans of the Bonn photon gas experiment.
    Colloquia
  • Date:25ThursdayOctober 2018

    Hierarchical dynamics of visual inference

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    Time
    12:30 - 12:30
    Location
    Nella and Leon Benoziyo Building for Brain Research
    LecturerProf. Jochen Braun
    Institute of Biology Otto-von-Guericke Unversity, Magdeburg
    Organizer
    Department of Brain Sciences
    Contact
    AbstractShow full text abstract about Visual input is noisy, variable, and ambiguous. Optimal inf...»
    Visual input is noisy, variable, and ambiguous. Optimal inference of physical causes is challenging even for a restricted set of causes (e.g., orientations and spatial frequencies). It is well understood (e.g., Veliz-Cuba et al., 2016) that stochastic dynamical systems can approximate optimal inference by continuously accumulating and evaluating visual evidence. I will argue that the dynamics of multi-stable perception is consistent with just such an inference mechanism. Its psychophysically observable characteristics fully constrain a hierarchical dynamics with three levels, the lowest of which may conceivably correspond to cortical columns or clusters of columns. Given suitable inputs, this hierarchical dynamics accumulates and evaluates noisy evidence to make nearly optimal categorical discriminations. Moreover, its dynamical features seem to afford functional benefits in a volatile world, such as balancing stability and sensitivity of inference.

    References:
    Cao, Pastukhov, Mattia, Braun (2016) Collective activity of many bistable assemblies reproduces characteristic dynamics of multistable perception. J. Neurosci., 36: 6957-72.

    Veliz-Cuba, Kilpatrick, Josic (2016) Stochastic models of evidence accumulation in changing environments. SIAM Review, 58: 264-289.

    Lecture
  • Date:25ThursdayOctober 2018

    Development of placenta-derived (PLX) cell therapy- from bench- to bedside

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    Time
    14:00 - 15:00
    Title
    Special Guest Lecture
    Location
    Max and Lillian Candiotty Building
    LecturerDr. Racheli Ofir
    Vice President Research & Intellectual Property, {Pluristem, MATAM, Haifa
    Organizer
    Department of Immunology and Regenerative Biology
    Contact
    AbstractShow full text abstract about PLacental expanded (PLX) cells are placenta-derived, mesench...»
    PLacental expanded (PLX) cells are placenta-derived, mesenchymal-like adherent stromal cells expanded using a bioreactor system which provides a three dimensional (3D) micro-environment enabling tightly controlled expansion. Accumulated data from multiple in vitro and in vivo experiments indicate that these cells act via a paracrine or endocrine manner to facilitate healing of damaged tissue.
    Pluristem’s two lead placenta-derived cell products, PLX-PAD and PLX-R18, are each in clinical development for several indications. PLX-Immune is in non-clinical development stages for Cancer. Data from non-clinical as well as clinical studies will be presented.
    Lecture
  • Date:25ThursdayOctober 2018

    Pelletron meeting - by invitation only

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    Time
    16:00 - 17:30
    Contact
    Lecture
  • Date:28SundayOctober 201802FridayNovember 2018

    International Board SAAC Review

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    Time
    All day
    Contact
    Academic Events
  • Date:28SundayOctober 201801ThursdayNovember 2018

    SAAC meeting

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    Time
    All day
    Title
    Scientific and Academic Advisory Committee meeting 2018
    Contact
    International Board
  • Date:28SundayOctober 2018

    Pre SAAC Symposium on Recent Progress in Chemistry and in Advanced Materials

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    Time
    08:30 - 16:30
    Location
    The David Lopatie Conference Centre
    Chairperson
    Jacob Klein
    Homepage
    Conference
  • Date:28SundayOctober 2018

    Pre-SAAC Symposium on High Energy Physics

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    Time
    10:00 - 15:45
    Location
    Edna and K.B. Weissman Building of Physical Sciences
    LecturerProf. Beate Heinemann, Prof. Joanna Stachel, Prof. Marumi Kado, Prof. Michael Dine, Prof. Michelangelo L. Mangano
    Organizer
    Faculty of Physics
    Contact
    Lecture
  • Date:28SundayOctober 2018

    Interactive Microscopy Image Analysis with IMARIS

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    Time
    10:30 - 10:30
    Location
    Max and Lillian Candiotty Building
    LecturerGeorgia Golfis
    BITPLANE
    Organizer
    Department of Life Sciences Core Facilities
    Contact
    Lecture
  • Date:28SundayOctober 2018

    Convergence of hunger and thirst in the insular cortex

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    Time
    11:00 - 11:00
    Location
    Arthur and Rochelle Belfer Building for Biomedical Research
    LecturerDr. Yoav Livneh
    Beth Israel Deaconess Medical Center and Harvard Medical School
    Organizer
    Department of Brain Sciences
    Contact
    Lecture
  • Date:28SundayOctober 2018

    Ozone waves in the stratosphere and the early winter mid-latitude QBO signal

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    Time
    11:00 - 11:00
    Location
    Sussman Family Building for Environmental Sciences
    LecturerVered Silverman
    Earth and Planetary Sciences Weizmann Institute of Science
    Organizer
    Department of Earth and Planetary Sciences
    Contact
    Lecture
  • Date:28SundayOctober 2018

    Unravelling the tumor immune microenvironment by multiplexed imaging

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    Time
    15:00 - 15:00
    Location
    Arthur and Rochelle Belfer Building for Biomedical Research
    LecturerDr. Leeat Yankielowicz-Keren
    Department of Pathology, School of Medicine, Stanford University
    Organizer
    Department of Systems Immunology , Department of Molecular Cell Biology , Department of Molecular Genetics
    Contact
    Lecture
  • Date:28SundayOctober 2018

    Ultrahigh Field MR Imaging in the Mesosphere Where Physics, Life Sciences, Computer Sciences and Medicine Meet

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    Time
    16:30 - 17:30
    Location
    Gerhard M.J. Schmidt Lecture Hall
    LecturerProf. Thoralf Niendorf
    Berlin Ultrahigh Field Facility (B.U.F.F.), Max-Delbrueck Center for Molecular Medicine
    Organizer
    Department of Molecular Chemistry and Materials Science
    Contact
    AbstractShow full text abstract about The development of ultrahigh field magnetic resonance (UHF-M...»
    The development of ultrahigh field magnetic resonance (UHF-MR) is moving forward at an amazing speed that is breaking through technical barriers almost as fast as they appear. UHF-MR has a staggering number of potential uses in neuroscience, neurology, radiology, cardiology, internal medicine, physiology, oncology, nephrology, ophthalmology and other related clinical fields. With over 50,000 MR examinations already performed at 7.0 Tesla, the reasons for moving UHF-MR into clinical applications are more compelling than ever. The value UHF-MR has already proven itself many times over at lower field strengths; now 7.0 T has opened a window on tissues, organs, and (patho)physiological processes that have been largely inaccessible in the past. Images from these instruments have revealed new aspects of the anatomy, functions and physio-metabolic characteristics of the brain, heart, joints, kidneys, liver, eye, and other organs/tissues, at an unparalleled quality. 50,000 sounds like a large number, but in fact we have barely cracked open the door and have yet to truly assess what lies on the other side. To this end this presentation documents advances and progress of UHF-MR with the goal to engage the interest of clinical adopters, basic scientists, engineers, and translational researchers from many areas. To meet this goal the traits, challenges and opportunities for discovery of human UHF-MRI will be surveyed. The considerations run from technical advances to early clinical applications. Examples of UHF-MR strategies are demonstrated. Their added value over the kindred counterparts at lower fields is explored along with an outline of research promises. Encouraging developments into enabling multiple channel radiofrequency (RF) antennae concepts (Figure 1) are reviewed. Frontier applications of MR at 7.0 T are surveyed including cardiac imaging (Figure 1), ophthalmic MRI and high spatial resolution MRI of the brain. Heteronuclear UHF-MR applications are explored with a focus on in vivo mapping of electrolytes including potassium MRI and sodium MRI (Figure 1). Practical obstacles of UHF MR are outlined including MR safety. Insights into RF heating induced by conductive stents and implants are provided. Current trends in UHF-MR are considered together with their clinical implications. A concluding section ventures a glance beyond the horizon including explorations into Extreme Field MR (EF-MR) which envisions human MR at 20 Tesla, which is an important leap of the imagination because it aims to fill a crucial "resolution gap" in our understanding of human biology (39, 40). It is the speakers hope that this presentation will convey the seeds of this vision and inspire the audience to become pioneers in these amazingly promising new areas of biomedical research: ultrahigh field and extreme field MR..
    Lecture

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