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September 01, 2016

  • Date:02FridaySeptember 2016

    Nathan's Friends - Greek love

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    Time
    20:00 - 22:45
    Title
    With Dionysis
    Location
    Michael Sela Auditorium
    Contact
    Cultural Events
  • Date:04SundaySeptember 2016

    Guest Seminar

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    Time
    10:00 - 11:00
    Title
    "The role of Stablin-1 in fibrogenesis and repair"
    Location
    Wolfson Building for Biological Research
    LecturerDr. Shishir Shetty
    entre for liver research, Institute of Immunotherapy and Immunology, University of Birmingham
    Organizer
    Department of Systems Immunology
    Contact
    Lecture
  • Date:06TuesdaySeptember 2016

    The Self and the Friend in Space

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    Time
    12:30 - 12:30
    Location
    Gerhard M.J. Schmidt Lecture Hall
    LecturerDr. Pia Rotshtein
    School of Psychology, Birmingham University Imaging Centre, University of Birmingham UK
    Organizer
    Department of Brain Sciences
    Contact
    AbstractShow full text abstract about Understanding the Self has fascinated artists, writers, phil...»
    Understanding the Self has fascinated artists, writers, philosophers and psychologist for generation. In the past two decades cognitive and neurocognitive tools have been applied to the study of the Self. The talk will present research on the Self and the Friend. Not surprisingly, it is consistently found that our brain prioritize the Self. For example, deciding whether a face looks to the left or right is faster on one’s own face than on a face of a friend. This prioritization transcend time, showing similar prioritization to one’s face in the past as in the present. Lesions to the fusiform gyrus hinders Self facilitation, while lesions to lateral frontal cortices amplifies it. Associating a simple geometric shape to oneself is done much more efficiently than to a stranger an effect that is mediated via the left STS, medial and lateral frontal cortices. Participants are also better at judging a perspective of an avatar if it is tagged as them than as a stranger. But in all these studies the Friend is also prioritized relative to a stranger. Why is the friend prioritized, is it because it is relevant, or because it is liked? In a simple shape-identity matching task, we manipulated orthogonally the valence and relevance of familiar identities. We found that prioritization is given based on relevance and valence in Western culture, but primarily based on valance in Asian cultures. Using spatial maps to represent the social space, we observed consistent representation of social relations as physical distances. Physical distance between identities was affected by the valence and relevance factors, though this was modulated by the participants’ culture. Finally, presenting participants with incongruent spatial maps of their social relations, resulted in increase and decrease responses in a large network of regions including the Amygdala and superior temporal structure known to play a rule in social cognition. Taken together this body of work highlight neurocognitive mechanism by which our brain prioritize information based on social rules.

    Lecture
  • Date:07WednesdaySeptember 2016

    G-INCPM - Special Seminar - Prof. Eran Hornstein, the Dept. of Molecular Genetics, Weizmann - "MicroRNA Dysfunction in Neurodegeneration"

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    Time
    11:00 - 12:30
    Location
    Edna and K.B. Weissman Building of Physical Sciences
    LecturerDept. of Molecular Genetics, Weizmann, Prof. Eran Hornstein
    Organizer
    Department of Biomolecular Sciences
    Contact
    AbstractShow full text abstract about Interest in RNA dysfunction in ALS recently aroused upon dis...»
    Interest in RNA dysfunction in ALS recently aroused upon discovering causative mutations in RNA-binding protein genes. Focusing on the causes and consequences of miRNA dysregulation in amyotrophic lateral sclerosis (ALS) we will understand how advances in sequencing and molecular technologies enable deciphering the contribution of noncoding RNAs to Neurodegeneration. In the past, we identified extensive down-regulation of miRNA levels is a common molecular denominator for multiple forms of human ALS. We further demonstrated that pathogenic ALS-causing mutations are sufficient to inhibit miRNA biogenesis at the Dicing step. These works position miRNAs downstream of the initiating mutations that drive ALS and encourage testing what are the specific miRNAs that play roles in motor neurons and whether mutations in miRNA genes will be able to causatively initiate the disease.


    Lecture
  • Date:07WednesdaySeptember 2016

    "The Formation and Light Manipulation Properties of Biogenic Guanine Based Photonic Crystal"

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    Time
    13:00 - 13:00
    Location
    Michael Sela Auditorium
    LecturerDr. Dvir Gur
    Organizer
    Department of Chemical and Structural Biology
    Contact
    Lecture
  • Date:07WednesdaySeptember 2016

    Kidnapped

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    Time
    21:00 - 21:00
    Title
    Family drama - National tragedy
    Location
    Michael Sela Auditorium
    Contact
    Cultural Events
  • Date:08ThursdaySeptember 2016

    Life Sciences Open Day

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    Time
    All day
    Location
    The David Lopatie Conference Centre
    Chairperson
    Elior Peles
    Contact
    Conference
  • Date:08ThursdaySeptember 2016

    Observation of quantum Hawking radiation and its entanglement in an analogue black hole

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    Time
    11:15 - 12:30
    Location
    Edna and K.B. Weissman Building of Physical Sciences
    LecturerJeff Steinhauer
    Technion – Israel Institute of Technology
    Organizer
    Faculty of Physics
    Contact
    AbstractShow full text abstract about We observe spontaneous Hawking radiation, stimulated by quan...»
    We observe spontaneous Hawking radiation, stimulated by quantum vacuum fluctuations, emanating from an analogue black hole in an atomic Bose-Einstein condensate. The Hawking radiation is observed via the correlations between the Hawking radiation exiting the black hole and the partner particles falling into the black hole. The quantum nature of the Hawking radiation is observed through entanglement, by comparing the Fourier transform of the corre-lations to a measurement of the population. This comparison shows that the experiment is well within the quantum regime, since the measured Hawking temperature determined from the population distribution is far below the upper limit for quantum entanglement. A broad energy spectrum of entangled Hawking pairs are observed. Maximal entanglement is ob-served for the high energy part of the Hawking spectrum, while the lowest energies are not entangled. Thermal behavior is seen at very low energies where the finite extent of the corre-lation function implies frequency dependence. Thermal behavior is also seen at high energies through the agreement of the correlation spectrum with the appropriate function of the Planck distribution. Further insight is obtained by a preliminary experiment in which the horizon is caused to oscillate at a fixed frequency, which stimulates waves travelling into and out of the black hole. The rate of particle production by the oscillating horizon is consistent with the measured Hawking temperature. Furthermore, the observed ratio of the phase velocities of the Hawking and partner particles are consistent with this preliminary ex-periment, as is the width of the Hawking/partner correlation feature. Additional confirmation of the results is obtained through a numerical simulation, which demonstrates that the Hawk-ing radiation occurs in an approximately stationary background. It also confirms the width of the Hawking/partner correlation feature. The measurement reported here verifies Hawking’s calculation, which is viewed as a milestone in the quest for quantum gravity. The observation of Hawking radiation and its entanglement verifies important elements in the discussion of information loss in a real black hole.

    Colloquia
  • Date:12MondaySeptember 2016

    Dopamine receptors in breast cancer: Overexpression, signaling and Therapeutic targeting

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    Time
    14:00 - 15:00
    Title
    CANCER RESEARCH CLUB
    Location
    Raoul and Graziella de Picciotto Building for Scientific and Technical Support
    LecturerProfessor Nira Ben-Jonathan
    Department of Cancer Biology, University of Cincinnati, Cincinnati, Ohio, USA
    Organizer
    Department of Immunology and Regenerative Biology
    Contact
    Lecture
  • Date:14WednesdaySeptember 2016

    "Studying dynamics of DNA methylation in single cells during development and disease"

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    Time
    11:00 - 11:00
    Location
    Wolfson Building for Biological Research
    LecturerProf. Yonatan Stelzer
    Whitehead Institute of MIT
    Organizer
    Department of Molecular Cell Biology
    Contact
    Lecture
  • Date:14WednesdaySeptember 2016

    Studying dynamics of DNA methylation in single cells during development and disease

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    Time
    11:00 - 12:00
    Location
    Wolfson Building for Biological Research
    LecturerProf. Yonatan Stelzer
    Whitehead Institute of MIT
    Organizer
    Department of Immunology and Regenerative Biology
    Contact
    Lecture
  • Date:14WednesdaySeptember 2016

    Wonder child - children's theater

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    Time
    17:30 - 17:30
    Location
    Michael Sela Auditorium
    Homepage
    Contact
    Cultural Events
  • Date:15ThursdaySeptember 2016

    An evolution-based approach to de novo protein design

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    Time
    11:00 - 12:00
    Location
    Helen and Milton A. Kimmelman Building
    LecturerProf. Pralay Mitra
    Department of Computer Science & Engineering Indian Institute of Technology, Kharagpur
    Organizer
    Department of Chemical and Structural Biology
    Contact
    Lecture
  • Date:18SundaySeptember 201619MondaySeptember 2016

    BioSoft Frontiers: Physics of Soft and Biological Matter

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    Time
    All day
    Location
    The David Lopatie Conference Centre
    Chairperson
    Nir Gov
    Contact
    Conference
  • Date:18SundaySeptember 2016

    Unlocking the Combinatorial Epigenetic Code at a Single-Molecule Level

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    Time
    09:00 - 09:00
    Location
    Arthur and Rochelle Belfer Building for Biomedical Research
    LecturerProf. Efrat Shema
    Massachusetts General Hospital, Harvard Medical School and the Broad Institute of MIT and Harvard
    Organizer
    Department of Molecular Genetics
    Contact
    Lecture
  • Date:18SundaySeptember 2016

    The contribution of ventromedial prefrontal cortex to memory and decision making

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    Time
    12:30 - 12:30
    Location
    Nella and Leon Benoziyo Building for Brain Research
    LecturerProf. Asaf Gilboa
    Rotman Research Institute at Baycrest Health Sciences and Dept of Psychology, University of Toronto
    Organizer
    Department of Brain Sciences
    Contact
    Lecture
  • Date:19MondaySeptember 2016

    G-INCPM - Special Seminar - Prof. Mag. Dr. Andreas J. Kungl, Institute of Pharmaceutical Chemistry, Karl-Franzens Univ. of Graz, Austria

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    Time
    11:00 - 12:30
    Title
    "Therapeutically targeting glycosaminoglycans by chemokine decoys: evidence from in vitro, in vivo and phase 1 clinical data"
    Location
    Edna and K.B. Weissman Building of Physical Sciences
    LecturerProf. Mag. Dr. Andreas J. Kungl
    Institute of Pharmaceutical Chemistry, Karl-Franzens Univ. of Graz, Austria
    Organizer
    Department of Biomolecular Sciences
    Contact
    AbstractShow full text abstract about Glycosaminoglycans (GAGs) are linear, highly charged/sulfate...»
    Glycosaminoglycans (GAGs) are linear, highly charged/sulfated polysaccharides which were shown by us and others, applying pull-down proteomics, to be involved in binding and structurally activating a multitude of proteins. Specifically endothelial GAGs such as heparan sulphate (HS) play an important role in chemokine presentation to chemokine GPC receptors on leukocytes and transportation across the endothelial barrier. As such, the chemokine-GAG interaction interface is involved in a plethora of diseases like acute/chronic inflammation and tumorigenesis. We have engineered several chemokines with respect to their GAG binding and GPC receptor activity so that they become dominant-negative decoys thereby antagonising the biological activity of their wild type counterparts with excellent dose-response profiles in vitro and in vivo. Recent data from CXCL8, CXCL12, and CCL2 chemokine mutants in inflammatory and oncology models will be presented.
    Lecture
  • Date:19MondaySeptember 2016

    Building Better Biofilms: Chemical Interactions and Structure-Function Relationships in Bacterial Communities

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    Time
    15:00 - 15:00
    Location
    Ullmann Building of Life Sciences
    LecturerProf. Allon I. Hochbaum
    Department of Chemical Engineering and Materials Science, Department of Chemistry, University of California, Irvine, USA
    Organizer
    Department of Plant and Environmental Sciences
    Contact
    AbstractShow full text abstract about Microbial communities are ubiquitous – found in natural and ...»
    Microbial communities are ubiquitous – found in natural and anthropogenic environments – and regulate processes spanning vast scales and ecological niches from the human microbiome to biogeochemical cycles. Surface-associated bacterial communities, called biofilms, are smart materials: they are self-organizing, self-renewing, respond to environmental stimuli, and perform complex functions. Therefore, biofilms represent an ideal system in which to study structure-function relationships in bacterial communities. Chemical gradients, such as of oxygen, nutrients, and signaling molecules, determine critical processes within biofilms. Biofilm morphology, species segregation and organization affect these gradients and thus community function. In this talk, I will describe our efforts to parse and manipulate the interactions governing community development in multispecies bacterial biofilms of Escherichia coli and Pseudomonas aeruginosa. These species have an antagonistic relationship in coculture, and we have identified some of the chemical and biophysical driving forces of these interactions, including a new biofilm dispersal signaling pathway. Furthermore, using microfabricated growth substrates, we are able to modulated the competitive signaling interactions within these coculture biofilms. Structured substrates alter biofilm morphology and deterministically switch a biological signaling pathway between E. coli and P. aeruginosa via manipulation of metabolite exchange rates. In this way, physical cues are transduced to chemical stimuli which control biofilm outcomes and community properties, including antibiotic susceptibility and probiotic resistance to pathogens. With these and other studies of biophysical mechanisms of bacterial signal transduction, we are developing design principles for engineering the structure and properties of multi-species bacterial biofilms.
    Lecture
  • Date:20TuesdaySeptember 201621WednesdaySeptember 2016

    Imaging the Immune System II

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    Time
    All day
    Location
    The David Lopatie Conference Centre
    Chairperson
    Ronen Alon
    Contact
    Conference
  • Date:20TuesdaySeptember 2016

    Unlocking the Combinatorial Epigenetic Code at a Single-Molecule Level

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    Time
    11:00 - 12:00
    Location
    Raoul and Graziella de Picciotto Building for Scientific and Technical Support
    LecturerProf. Efrat Shema
    Massachusetts General Hospital, Harvard Medical School and the Broad Institute of MIT and Harvard
    Organizer
    Department of Immunology and Regenerative Biology
    Contact
    Lecture

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