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April 30, 2015

  • Date:08SundayApril 201811WednesdayApril 2018

    EMBO workshop on Noncoding RNAs in Development and Cell Differentiation

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    Time
    08:00 - 08:00
    Location
    The David Lopatie Conference Centre
    Chairperson
    Igor Ulitsky
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    Conference
  • Date:08SundayApril 2018

    Behind the Scenes of Scientific Publishing at EMBO

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    Time
    10:00 - 11:00
    Location
    Max and Lillian Candiotty Building
    LecturerDr. Anne Nielsen
    Organizer
    Department of Immunology and Regenerative Biology
    Contact
    AbstractShow full text abstract about Publishing research papers is a cornerstone of working in li...»
    Publishing research papers is a cornerstone of working in life sciences, but do you know what actually happens to your manuscript once it is submitted to a scientific journal? Anne Nielsen – scientific editor for The EMBO journal – will take you behind the scenes of scientific publishing at EMBO and explain how editors make decisions, find referees and work with authors to improve the revised manuscript. She will also discuss some of the challenges faced by the current publishing landscape, talk about the efforts EMBO is making to prevent errors and fraud from entering the literature, and offer advice on manuscript writing and submission.
    Lecture
  • Date:08SundayApril 2018

    From kB to kB: Universal and efficient entropy estimation using a compression algorithm

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    Time
    11:00 - 12:00
    Location
    Perlman Chemical Sciences Building
    LecturerProf. Roy Beck
    School of Physics and Astronomy, TAU
    Organizer
    Department of Molecular Chemistry and Materials Science
    Contact
    AbstractShow full text abstract about Entropy and free-energy estimation are key in thermodynamic ...»
    Entropy and free-energy estimation are key in thermodynamic characterization of simulated systems ranging from spin models through polymers, colloids, protein structure, and drug-design. Current techniques suffer from being model specific, requiring abundant computation resources and simulation at conditions far from the studied realization. In this talk, I will present a novel universal scheme to calculate entropy using lossless compression algorithms and validate it on simulated systems of increasing complexity. Our results show accurate entropy values compared to benchmark calculations while being computationally effective. In molecular-dynamics simulations of protein folding, we exhibit unmatched detection capability of the folded states by measuring previously undetectable entropy fluctuations along the simulation timeline. Such entropy evaluation opens a new window onto the dynamics of complex systems and allows efficient free-energy calculations.
    Lecture
  • Date:08SundayApril 2018

    Molecular Genetics Departmental Seminars 2017-2018

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    Time
    13:00 - 13:00
    Title
    Adaptive evolution of noise-buffering through transcription-factor duplication
    Location
    Arthur and Rochelle Belfer Building for Biomedical Research
    LecturerMichal Chapal
    Organizer
    Department of Molecular Genetics
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    Lecture
  • Date:08SundayApril 2018

    Islet 3D chromatin architecture provides insights into personalized medicine for type 2 diabetes

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    Time
    15:00 - 16:00
    Location
    Arthur and Rochelle Belfer Building for Biomedical Research
    LecturerProf. Jorge Ferrer
    Department of Medicine, Imperial College London, UK
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    Lecture
  • Date:09MondayApril 2018

    "Inorganic nanotubes and fullerene-like nanoparticles at the crossroad between materials science and nanotechnology and their applications"

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    Time
    11:00 - 12:15
    Location
    Gerhard M.J. Schmidt Lecture Hall
    LecturerProf. Reshef Tenne
    Department of Materials and Interfaces, WIS
    Organizer
    Faculty of Chemistry
    Contact
    AbstractShow full text abstract about After almost 100 years of research inorganic layered (2D) ma...»
    After almost 100 years of research inorganic layered (2D) materials, like MoS2, are currently used as catalysts, lubricants, and perhaps most importantly in rechargeable Li- ion batteries. After a short briefing on the history of 2D materials research,1 the concepts which lead to the first synthesis of hollow-cage nanostructures, including nanotubes (INT) and fullerene-like (IF) nanoparticles from 2D compounds, will be presented. The progress with the high-temperature synthesis and characterization of new inorganic nanotubes (INT) and fullerene-like (IF) nanoparticles (NP) will be presented. In particular, the synthesis and structure of nanotubes from the ternary “misfit” layered compounds (MLC), like LnS-TaS2 (Ln= La, Ce, Gd, Ho, Er), CaCoO-CoO2 and numerous other MLC were elucidated. More recently nanotubes (and nanoscrolls) from quaternary MLC were reported.
    Major progress has been achieved in elucidating the structure of INT and IF using advanced microscopy techniques, like aberration corrected TEM and related techniques. Mechanical, electrical and optical measurements of individual WS2 nanotubes reveal their unique quasi-1D characteristics. This analysis demonstrate their different behavior compared to the bulk phase. Applications of the IF/INT as superior solid lubricants and for reinforcement of variety of polymers and light metal alloys was demonstrated. Few recent studies indicate that this brand of nanoparticles is less toxic than most nanoparticles. With expanding product lines, manufacturing and sales, these nanomaterials are gradually becoming an industrial commodity.
    1. L. Panchakarla, B. Visic and R. Tenne, “Perspective”, J. Am. Chem. Soc. 2017, 139, 12865-12878.
    Colloquia
  • Date:09MondayApril 2018

    Neural circuits for defensive responses

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    Time
    12:45 - 12:45
    Location
    Nella and Leon Benoziyo Building for Brain Research
    LecturerDr. Philip Tovote
    Institute of Clinical Neurobiology, Wurzburg University, Germany
    Organizer
    Department of Brain Sciences
    Contact
    AbstractShow full text abstract about Behavioral responses to threat encompass evolutionarily cons...»
    Behavioral responses to threat encompass evolutionarily conserved active or passive defensive motor responses, such as flight and freezing, respectively. Brain-wide distributed neural circuits mediate top-down control of the defense reaction and interact with ascending pathways that transmit interoceptive information from the periphery. Defensive action selection has been modelled around the concept of threat imminence, but the circuit mechanisms mediating different defensive behaviors and the switch between them remain unclear.
    The seminar will present a circuit-centered systems neuroscience approach to characterize the neural circuits for defensive responses with a focus on the central nucleus of the amygdala (CEA) and midbrain periaqueductal grey (PAG), whose output selection is mediated by integration of local microcircuit interactions and external inputs. Our findings demonstrate that defensive action selection is a cue- and context dependent, multi-site process involving complex functional motifs within evolutionary old, mammalian “survival circuits”.
    Lecture
  • Date:10TuesdayApril 2018

    Cell Penetration and Membrane Fusion: Two Sides of the Same Coin

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    Time
    10:00 - 11:00
    Location
    Nella and Leon Benoziyo Building for Biological Sciences
    LecturerProf. Pavel Jungwirth
    Institute of Organic Chemistry and Biochemistry of the CAS
    Organizer
    Department of Biomolecular Sciences
    Contact
    AbstractShow full text abstract about Cell penetrating peptides have a unique potential for target...»
    Cell penetrating peptides have a unique potential for targeted drug delivery, therefore, mechanistic understanding of their membrane action has been sought since their discovery over 20 years ago. While ATP-driven endocytosis is known to play a major role in their internalization, there has been also ample evidence for the importance of passive translocation for which the direct mechanism, where the peptide is thought to directly pass through the membrane via a temporary pore, has been widely advocated. In this talk, I will question this view and demonstrate that arginine-rich cell penetrating peptides can instead enter vesicles and cells by inducing multilamellarity and fusion, analogously to the action of calcium ions. The molecular picture of this penetration mode, which differs qualitatively from the previously proposed direct mechanism, is provided by molecular dynamics simulations. In addition, the kinetics of vesicle agglomeration and fusion by nonaarginine, nonalysine, and calcium ions are documented in real time by fluorescence techniques and the induction of multilamellar phases in vesicles and cells is revealed both via electron microscopy and fluorescence spectroscopy. We thus show that the newly identified passive cell penetration mechanism is analoguous to vesicle fusion induced by calcium ions, demonstrating that the two processes are of a common mechanistic origin.



    Lecture
  • Date:10TuesdayApril 2018

    Cyclodextrin Complexation: From Solution-State Complexes to Paper-Based Devices

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    Time
    11:00 - 12:00
    Location
    Helen and Milton A. Kimmelman Building
    LecturerProf. Mindy Levine
    University of Rhode Island
    Organizer
    Department of Molecular Chemistry and Materials Science
    Contact
    Lecture
  • Date:10TuesdayApril 2018

    SEMINAR CANCELLED: Foraminifera as bioindicators of marine environments

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    Time
    11:30 - 11:30
    LecturerProf. Sigal Abramovich
    Department of Geological and Environmental Sciences, Ben Gurion University of the Negev, Beer Sheva
    Organizer
    Department of Plant and Environmental Sciences
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    Lecture
  • Date:10TuesdayApril 2018

    Prof. Ehud Duchovni - From the largest to the smallest - What can be learned from the humongous LHC accelerator on the structure of matter?

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    Time
    12:00 - 12:00
    Title
    From the largest to the smallest - What can be learned from the humongous LHC accelerator on the structure of matter?
    Location
    Dolfi and Lola Ebner Auditorium
    LecturerProf. Ehud Duchovni
    Organizer
    Communications and Spokesperson Department
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    Lecture
  • Date:10TuesdayApril 2018

    Emergence of behaviorally relevant motifs in the human cortex

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    Time
    12:30 - 12:30
    Location
    Gerhard M.J. Schmidt Lecture Hall
    LecturerDr. Tomer Livne
    Consultant, Prof. Dov Sagi Group Cortica Ltd, Tel Aviv
    Organizer
    Department of Brain Sciences
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    Lecture
  • Date:11WednesdayApril 2018

    Special Guest Seminar

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    Time
    11:00 - 11:00
    Title
    Apoptosis control by the unfolded protein response
    Location
    Arthur and Rochelle Belfer Building for Biomedical Research
    LecturerAvi Ashkenazi, PhD
    Senior Staff Scientist, Cancer Immunology, Genentech Inc.; and Adjunct Professor, Biochemistry and Biophysics, University of California, San Francisco, CA, USA
    Organizer
    Department of Molecular Genetics
    Contact
    AbstractShow full text abstract about Precise protein folding by the endoplasmic reticulum (ER) su...»
    Precise protein folding by the endoplasmic reticulum (ER) supports homeostasis, while cumulative protein misfolding causes ER stress and promotes disease. The kinases PERK and IRE1 help orchestrate the unfolded protein response (UPR) to alleviate ER stress; however, if stress persists, the UPR activates apoptosis to eliminate the damaged cell. We have previously shown that PERK drives cell death via transcriptional up-regulation of the pro-apoptotic death receptor DR5; we further showed that IRE1—which harbors both kinase and RNase modules—blocks apoptosis through regulated IRE1-dependent mRNA decay (RIDD) of DR5 (Lu et al, Science 2014). Recently, we turned to investigate the paradoxical observation that under irresolvable ER stress PERK activity persists, while IRE1 function attenuates. We discovered that PERK governs the attenuation of IRE1, through a phosphatase called RNA polymerase II-associated protein 2 (RPAP2). RPAP2 reverses IRE1 phosphorylation, inhibiting IRE1 RNase activation. This disrupts IRE1-dependent generation of the cytoprotective transcription factor XBP1s and dampens ER-associated degradation of misfolded proteins. Furthermore, it inhibits RIDD, thereby licensing DR5-mediated caspase activation and apoptotic cell death. Thus, under excessive ER stress, PERK attenuates IRE1 via RPAP2 to abort failed adaptation and trigger an apoptotic cell fate.
    Lecture
  • Date:11WednesdayApril 2018

    Special Guest Seminar

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    Time
    11:00 - 12:00
    Title
    “Apoptosis control by the unfolded protein response”
    Location
    Arthur and Rochelle Belfer Building for Biomedical Research
    LecturerDr. Avi Ashkenazi
    Senior Staff Scientist, Cancer Immunology, Genentech Inc.; and Adjunct Professor, Biochemistry and Biophysics, University of California, San Francisco, CA, USA
    Organizer
    Department of Molecular Genetics
    Contact
    AbstractShow full text abstract about Precise protein folding by the endoplasmic reticulum (ER) su...»
    Precise protein folding by the endoplasmic reticulum (ER) supports homeostasis, while cumulative protein misfolding causes ER stress and promotes disease. The kinases PERK and IRE1 help orchestrate the unfolded protein response (UPR) to alleviate ER stress; however, if stress persists, the UPR activates apoptosis to eliminate the damaged cell. We have previously shown that PERK drives cell death via transcriptional up-regulation of the pro-apoptotic death receptor DR5; we further showed that IRE1—which harbors both kinase and RNase modules—blocks apoptosis through regulated IRE1-dependent mRNA decay (RIDD) of DR5 (Lu et al, Science 2014). Recently, we turned to investigate the paradoxical observation that under irresolvable ER stress PERK activity persists, while IRE1 function attenuates. We discovered that PERK governs the attenuation of IRE1, through a phosphatase called RNA polymerase II-associated protein 2 (RPAP2). RPAP2 reverses IRE1 phosphorylation, inhibiting IRE1 RNase activation. This disrupts IRE1-dependent generation of the cytoprotective transcription factor XBP1s and dampens ER-associated degradation of misfolded proteins. Furthermore, it inhibits RIDD, thereby licensing DR5-mediated caspase activation and apoptotic cell death. Thus, under excessive ER stress, PERK attenuates IRE1 via RPAP2 to abort failed adaptation and trigger an apoptotic cell fate.
    Lecture
  • Date:12ThursdayApril 2018

    Memorial Ceremony for Holocaust Remembrance Day

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    Time
    10:00 - 10:45
    Contact
    Lecture
  • Date:12ThursdayApril 2018

    Jew Süss: Between Truth and Fiction

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    Time
    11:15 - 12:30
    Location
    Edna and K.B. Weissman Building of Physical Sciences
    LecturerYair Mintzker
    Princeton
    Organizer
    Faculty of Physics
    Contact
    AbstractShow full text abstract about Joseph Süss Oppenheimer—"Jew Süss"—is one of the m...»
    Joseph Süss Oppenheimer—"Jew Süss"—is one of the most iconic figures in the history of an-ti-Semitism. Originally from Heidelberg, in 1733 Oppenheimer became the "court Jew" of the duke of the small German state of Württemberg. When the duke died unexpectedly a few years later, the Württemberg authorities arrested Oppenheimer, put him on trial, and con-demned him to death for unspecified "misdeeds." On February 4, 1738, Oppenheimer was hanged in front of a large crowd just outside Stuttgart. It was one of the most sensational exe-cutions of the entire eighteenth century.

    This lecture by Prof. Yair Mintzker (Princeton University) is based on his new book, “The Many Deaths of Jew Süss: The Notorious Trial and Execution of an Eighteen Century Court Jew” (Princeton UP, 2017). It will concentrate on the tension between the historical figure of “Jew Süss” as reflected in eighteenth-century sources on the one hand, and, on the other hand, the widespread and often cynical use of this figure in later works of fiction, chief among them the vicious Nazi propaganda movie "Jew Süss,” which was made in 1940 at the behest of Joseph Goebbels.
    Colloquia
  • Date:12ThursdayApril 2018

    Identifying and targeting

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    Time
    14:00 - 15:00
    Title
    Cancer Research Club Seminar
    Location
    Max and Lillian Candiotty Building
    LecturerProf. Eyal Gottlieb
    The Ruth and Bruce Rappaport Faculty of Medicine,Technion - Israel Institute of Technology, Haifa
    Organizer
    Department of Immunology and Regenerative Biology
    Contact
    Lecture
  • Date:15SundayApril 2018

    Understanding the response of the atmospheric circulation to climate change from an energetic perspective

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    Time
    11:00 - 11:00
    Location
    Sussman Family Building for Environmental Sciences
    LecturerOrli Lachmy (The Open University of Israel), The Open University of Israel
    Organizer
    Department of Earth and Planetary Sciences
    Contact
    AbstractShow full text abstract about The atmospheric circulation determines the structure of Eart...»
    The atmospheric circulation determines the structure of Earth’s climate. Changes in the circulation, such as meridional shifts in the circulation patterns can lead to dramatic changes in the local climate. Increased greenhouse gas emission is expected to change the vertical and meridional temperature profile and affect the atmospheric circulation. Climate models predict that greenhouse gas-induced climate change would cause a warming of the troposphere and cooling of the stratosphere, as well as a poleward and upward shift of the midlatitude jet stream and storm tracks - the major components of the extratropical circulation. The response of the atmospheric circulation to climate change is difficult to explain, due to nonlinear dynamical feedbacks within the system. Previous studies have attempted to explain the poleward shift of the jet stream in response to climate change based on different dynamical mechanisms. Here we propose an alternative approach of connecting the energy and momentum flux in order to explain the jet shift based on energy balance considerations.

    Lecture
  • Date:15SundayApril 2018

    Is mesoscopic resolution for BOLD fMRI enough? MR Imaging of electrical properties as a more direct probe of neuronal activation

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    Time
    12:30 - 12:30
    Location
    Gerhard M.J. Schmidt Lecture Hall
    LecturerDr. Rita Schmidt
    C.J. Gorter Center for High Field MRI, Leiden University Medical Center, Leiden, Netherlands
    Organizer
    Department of Brain Sciences
    Contact
    AbstractShow full text abstract about Current state of the art ultra-high field MRI scanners have ...»
    Current state of the art ultra-high field MRI scanners have already achieved submillimeter resolution in 3D imaging of the human brain. Studies of the functional activity in the brain - by Blood Oxygen Level Dependent (BOLD) technique - have utilized this capability to observe mesoscopic (200-300µm) structures in humans. However, does BOLD tell us the full story? With current state of the art in mind, we are looking for the next step forward to better understand the brain physiology. I will share an on-going research on the mapping of electrical properties, aimed at studying functional activity in the human brain and offering a more direct probe of neuronal activity. The research includes a new computational technique for estimating electrical properties from an MR experiment, as well as the implementation of fast acquisition techniques. I will also show a correlation between changes in the electrical conductivity and basic activation paradigms (visual or motor) demonstrating faster response versus BOLD signal.
    Lecture
  • Date:15SundayApril 2018

    Molecular Genetics Departmental Seminars 2017-2018

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    Time
    13:00 - 13:00
    Title
    Programmed cell death in early embryonic development: a myth or reality?
    Location
    Arthur and Rochelle Belfer Building for Biomedical Research
    LecturerRivi Halimi
    Organizer
    Department of Molecular Genetics
    Contact
    Lecture

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