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October 01, 2009
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Date:09SaturdayApril 2011Cultural Events
Entertainment-"Short and to the Point"
More information Time 21:00 - 21:00Title Short and famous comic skitsLocation Michael Sela AuditoriumContact -
Date:10SundayApril 2011Lecture
The Molecular Basis of Vertebrate Touch
More information Time 11:00 - 11:00Location Arthur and Rochelle Belfer Building for Biomedical ResearchLecturer Prof. Gary Lewin
The Benoziyo Center for Neurological Diseases Lecture Max Delbrück Center for Molecular Medicine BerlinOrganizer Department of Biomolecular SciencesContact -
Date:10SundayApril 2011Lecture
The Molecular Basis of Vertebrate Touch
More information Time 11:00 - 11:00Location Arthur and Rochelle Belfer Building for Biomedical ResearchLecturer Prof. Gary Lewin
MDC, BerlinOrganizer Nella and Leon Benoziyo Center for Neurological DiseasesContact -
Date:10SundayApril 2011Lecture
Spectral Invariance in Atmospheric Radiation: What was missed by van de Hulst?
More information Time 11:00 - 11:00Location Sussman Family Building for Environmental SciencesLecturer Dr. Warren Wiscombe
NASA/Goddard Space Flight Center Maryland, USAOrganizer Department of Earth and Planetary SciencesContact Abstract Show full text abstract about In the highly spectrally variable world of atmospheric radia...» In the highly spectrally variable world of atmospheric radiation, some simple algebraic combinations of single scattering albedo, reflected and/or transmitted radiation spectra depend little on wavelength. As an example, under some rather general conditions, the ratio of the radiation leaving clouds to single scattering albedo is a linear function of the same radiation. In the talk we will identify these spectrally-invariant combinations and discuss the physics (and some mathematics) behind them. Using the results of SBDART simulations, we will test the extent to which the assumptions behind spectral invariance are valid for cloudy atmospheres. Finally, the applications of spectral invariance for climate and remote sensing problems will be briefly crystal-balled.
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Date:10SundayApril 2011Lecture
Journal club - A discussion on selected articles
More information Time 12:30 - 14:00Location Dannie N. Heineman LaboratoryLecturer Prof. Avishay Gal-Yam Organizer Nella and Leon Benoziyo Center for AstrophysicsContact -
Date:10SundayApril 2011Lecture
Journal club - A discussion on selected articles
More information Time 12:30 - 14:00Location Dannie N. Heineman LaboratoryLecturer Prof. Avishay Gal-Yam Organizer Nella and Leon Benoziyo Center for AstrophysicsContact -
Date:10SundayApril 2011Lecture
Lost in Translation-the mysteries of the tRNA pool
More information Time 13:00 - 13:00Location Arthur and Rochelle Belfer Building for Biomedical ResearchLecturer Zohar Bloom
Tzachi Pilpel's group, Dept. of Molecular Genetics, WISOrganizer Department of Molecular GeneticsContact -
Date:10SundayApril 2011Lecture
A dynamical phase transition in a model for evolution with migration
More information Time 14:15 - 14:15Location Edna and K.B. Weissman Building of Physical SciencesLecturer Bartlomiej Waclaw
Edinburgh UniversityOrganizer Department of Physics of Complex SystemsContact Abstract Show full text abstract about Biological dispersal---the movement of organisms between hab...» Biological dispersal---the movement of organisms between habitats---is a
ubiquitous phenomenon with important and wide-ranging consequences. In the
natural environment, organisms expand their ranges, colonise new habitats,
and can undergo speciation if they become spatially isolated. Therefore,
dispersal plays a key role in determining spatial and temporal patterns of
genetic diversity. It has been pointed out recently, that migration from a
favourable habitat to an unfavourable one can explain the genetics of some
pathogenic microbes and viruses. However, despite its importance, a general
understanding of how migration affects mutation-selection balance in
microbial systems is lacking. In particular, one would like to know how
migration changes the proportions of different genotypes in the evolving
population. Here I will discuss a simple model for evolution of asexual
organisms in two different habitats, with different fitness landscapes,
coupled through one-way migration. The key finding is a dynamical phase
transition at a critical value of the migration rate. The time to reach
steady state diverges at this critical migration rate. Above the transition,
the population is dominated by immigrants from the primary habitat. Below
the transition, the genetic composition of the population is highly
non-trivial, with multiple coexisting quasi-species which are not native to
either habitat. Using results from localization theory, I will show that the
critical migration rate may be very small --- demonstrating that
evolutionary outcomes can be very sensitive to even a small amount of
migration.
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Date:11MondayApril 2011Conference
Graduate Students in Control
More information Time All dayTitle GSC 2011Location Wolfson Building for Biological ResearchChairperson Zvi ArtsteinOrganizer The Y. Leon Benoziyo Institute for Molecular MedicineHomepage Contact -
Date:11MondayApril 2011Lecture
Brain Sciences Open Day
More information Time 09:30 - 14:00Location Gerhard M.J. Schmidt Lecture HallOrganizer Department of Brain SciencesContact -
Date:11MondayApril 2011Colloquia
“Regulation of proteasome activity by ubiquitin chain editing”
More information Time 11:00 - 11:00Location Dolfi and Lola Ebner AuditoriumLecturer Prof. Daniel Finley
Department of Cell Biology Harvard Medical School, Boston, USAContact -
Date:11MondayApril 2011Lecture
Towards a Conjecture of Kostant
More information Time 11:00 - 11:00Location Ziskind Bldg.Lecturer Prof. Anthony Joseph
Organizer Faculty of Mathematics and Computer Science -
Date:11MondayApril 2011Lecture
Elucidating the molecular mechanism of tumor dormancy using polymer therapeutics
More information Time 14:00 - 14:00Location Max and Lillian Candiotty BuildingLecturer Dr. Ronit Satchi Fainaru
Dept. Physiology and Pharmacology Sackler School of Medicine Tel Aviv UniversityOrganizer Department of Immunology and Regenerative BiologyContact -
Date:11MondayApril 2011Lecture
The Price of Anarchy: Out-of-Equilibrium Guarantees, Intrinsic Robustness, and Beyond
More information Time 14:30 - 14:30Location Ziskind Bldg.Lecturer Tim Roughgarden
Stanford UniversityOrganizer Faculty of Mathematics and Computer Science -
Date:11MondayApril 2011Lecture
Meetings at the Frontiers of Science
More information Time 19:15 - 19:15Organizer Science for All UnitHomepage Contact -
Date:12TuesdayApril 2011Lecture
Forming stem cell units: how to coordinate niches and stem cells
More information Time 10:00 - 10:00Location Wolfson Building for Biological ResearchLecturer Dr. Lilach Gilboa Organizer Department of Biomolecular SciencesContact -
Date:12TuesdayApril 2011Lecture
" GLUON SCATTERING FROM WEAK TO STRONG COUPLING IN N=4 SUPER-YANG-MILLS THEORY”
More information Time 10:30 - 11:30Location Neve ShalomLecturer Prof. Lance Dixon
SLACOrganizer Department of Particle Physics and AstrophysicsContact -
Date:12TuesdayApril 2011Lecture
Open Source Drug Discovery
More information Time 11:00 - 12:30Location Arthur and Rochelle Belfer Building for Biomedical ResearchLecturer Prof. SamirK. Brahmachari
Institute of Genomics & Integrative Biology (IGIB), Delhi Council of Scientific & Industrial Research (CSIR), IndiaHomepage Contact Abstract Show full text abstract about Just as the original open source software was propelled by s...» Just as the original open source software was propelled by software developers motivated to contribute to large collaborative projects, proponents of Open Source Drug Discovery (OSDD) believe that the global need for new low-cost drugs, particularly for treating neglected tropical diseases, will make this model effective. Because drug research is so complex, different OSDD initiatives are applying different strategies. For example, under Brahmachari’s direction, India launched an OSDD program in 2008, aimed to have a web-enabled interactive open source platform listing the current design challenges for developing drugs to treat diseases such as tuberculosis, malaria, and HIV. Research teams from CSIR and other government, university and industry participants contribute to the posted drug design challenges. This may include new algorithm or information about a new drug target. As first steps, the CSIR’s OSDD initiative has launched an open source website hosting information about Mycobacterium tuberculosis, including gene sequences, expression, function, activity, and the response to drugs of all M. tuberculosis proteins as well as host-pathogen interactions
(http://mtbsysborg.igib.res.in). As the next step, CSIR will initiates an open source program for malaria, with global participation. (see S. Singh, Cell 113:201-3 (2008)
Professor Brahmachariis Secretary to the Department of Scientific and Industrial Research (DSIR), Ministry of Science and Technology, Government of India and Director General of Council of Scientific and Industrial Research (CSIR), India.
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Date:12TuesdayApril 2011Lecture
Open Source Drug Discovery
More information Time 11:00 - 12:30Location Arthur and Rochelle Belfer Building for Biomedical ResearchLecturer Prof. SamirK. Brahmachari
Institute of Genomics & Integrative Biology (IGIB), Delhi Council of Scientific & Industrial Research (CSIR), IndiaHomepage Contact Abstract Show full text abstract about Just as the original open source software was propelled by s...» Just as the original open source software was propelled by software developers motivated to contribute to large collaborative projects, proponents of Open Source Drug Discovery (OSDD) believe that the global need for new low-cost drugs, particularly for treating neglected tropical diseases, will make this model effective. Because drug research is so complex, different OSDD initiatives are applying different strategies. For example, under Brahmachari’s direction, India launched an OSDD program in 2008, aimed to have a web-enabled interactive open source platform listing the current design challenges for developing drugs to treat diseases such as tuberculosis, malaria, and HIV. Research teams from CSIR and other government, university and industry participants contribute to the posted drug design challenges. This may include new algorithm or information about a new drug target. As first steps, the CSIR’s OSDD initiative has launched an open source website hosting information about Mycobacterium tuberculosis, including gene sequences, expression, function, activity, and the response to drugs of all M. tuberculosis proteins as well as host-pathogen interactions
(http://mtbsysborg.igib.res.in). As the next step, CSIR will initiates an open source program for malaria, with global participation. (see S. Singh, Cell 113:201-3 (2008)
Professor Brahmachariis Secretary to the Department of Scientific and Industrial Research (DSIR), Ministry of Science and Technology, Government of India and Director General of Council of Scientific and Industrial Research (CSIR), India.
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Date:12TuesdayApril 2011Lecture
"Bacterial type III effectors and plant resistance signaling in the tomato-Xanthomonas interaction"
More information Time 11:15 - 12:30Location Ullmann Building of Life SciencesLecturer Dr. Guido Sessa
Dept. of Molecular Biology and Ecology of Plants, Tel-Aviv UniversityOrganizer Department of Plant and Environmental SciencesContact
