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Rainer Leitgeb, Medical University Vienna Institution: International Centre for Translational Eye Research & the Department of Physical Chemistry of Biological Systems Place:ĭespite the vast clinical acceptance of optical coherence tomography (OCT) in visualizing the structure and vasculature system (angiography) of the retina, the method is still lacking the capability to provide molecular fingerprints of retinal tissue. Multimodal OCT Imaging and Raman Spectroscopy for the Human EyeĢ022, 16:30 CEST Lecturer: Prof. These results allow me to classify the ability of various two-gene regulatory motifs to produce stable gene expression patterns.
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A sub-class of genuinely stationary patterns is then identified, alongside the exact conditions ensuring this stability.
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In particular, the phase transition is observed, between the phase of indeterminate patterning, where region of mixed gene expression is ever-growing, and the phase of travelling gene expression patterns, where two expression domains form and preserve a well-defined contact zone. It is found that its dynamics is governed by the conservation law, which leads to a range of analytical results. The reaction-diffusion equation with the bi-stable production term is employed as a generic model for this problem. spinal cord development, limb formation and many others. In this presentation I will address the problem of gene expression patterns stability in the systems where two diffusible morphogens affect each other’s production and control the growth of their own source regions. This leads to the emergence of gene expression patterns, whose dynamics is still not fully understood. In developmental systems, cells determine their fate by decoding chemical signals, called morphogens. Stability of gene expression patterns in developmental systems with dynamic morphogen sourcesĢ022, 12:00 Lecturer: Maciej Majka, PhD, Theory of Complex Systems Department, Institute of Theoretical Physics, Jagiellonian University Krakow, Poland Institution: Biophysical Chemistry Group (Z31) seminar Place: The event is obligatory to all doctoral students, and of interest, I hope, to the whole IChF community. The lecture will present modern techniques of creating tools for the study of viral proteases. Moreover, in order to detect the active form of the protease, one should use chemical tools called activity-based probes. Given the fact that more and more proteases are actively involved in viral diseases, there is an urgent need to develop new chemical tools that, thanks to the activity of enzymes, can be used for their precise monitoring or the search for drug candidates. Recent studies show that proteases operate in a network that involves the activity of many different proteolytic enzymes at the same time. Proteases are key players in the development of viral diseases. Unfortunately, these drugs can only be used for a limited number of diseases, and many other proteases (around 650 proteases have been described in humans to date) involved in various disorders in humans and other living organisms require further research. An excellent reason for research on proteases are commercially available anti-cancer, anti-diabetic and anti-viral HIV drugs that rely on the inhibition of protease activity. From this point of view, one of the most important groups of enzymes are proteases, the increased or decreased level of which allows for rapid clinical diagnosis using specific markers, and also gives the opportunity for rational, rapid research on drug discovery based on protease activity. Much hope is placed on research into the origin of a disease, usually involving tens or hundreds of biological macromolecules called enzymes. Perfect methods of treatment have still not been found. Marcin Drąg, Division of Chemical Biology and Bioimaging, Wroclaw University of Science and Technology Institution: Dream Chemistry Lecture: Mentors Place:ĭiseases such as cancer, diabetes or viral and bacterial infections are one of the main causes of human mortality, regardless of age and origin. Proteases as medical target in bioimaging and drug developmentĢ022, 13:00 Lecturer: Prof.