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Theralase Technologies Inc. V.TLT

Alternate Symbol(s):  V.TLT.WT | TLTFF

Theralase Technologies Inc. is a Canada-based clinical-stage pharmaceutical company. The Company is engaged in the research and development of light activated compounds and their associated drug formulations. The Company operates through two divisions: Anti-Cancer Therapy (ACT) and Cool Laser Therapy (CLT). The Anti-Cancer Therapy division develops patented, and patent pending drugs, called Photo Dynamic Compounds (PDCs) and activates them with patent pending laser technology to destroy specifically targeted cancers, bacteria and viruses. The CLT division is responsible for the Company’s medical laser business. The Cool Laser Therapy division designs, develops, manufactures and markets super-pulsed laser technology indicated for the healing of chronic knee pain. The technology has been used off-label for healing numerous nerve, muscle and joint conditions. The Company develops products both internally and using the assistance of specialist external resources.


TSXV:TLT - Post by User

Post by Eoganachton Aug 21, 2020 1:50pm
381 Views
Post# 31439393

Professor Coombs SomaScan Webinar

Professor Coombs SomaScan WebinarWHAT CAN PROTEOMICS TEACH US ABOUT INFECTIOUS DISEASE? | WEBINAR
 
Dr. Kevin Coombs has authored six different publications (2 pending) describing the use of the SomaScan Assay to investigate human cellular protein alterations in tissue culture in response to infection by Zika virus and various strains of influenza. In this webinar, Dr. Coombs will summarize the major findings produced from these studies and comment on how the SomaScan Assay could be used to further study infectious disease, including the current COVID-19 pandemic, in the immediate future.
 
ABSTRACT
 
Dr. Coomb’s group has used the SomaScan assay to screen >1300 host proteins in Zika virus-infected cells, both globally and specifically in the central nervous system. Significant findings include the identification of nearly 300 astrocyte proteins that were significantly dysregulated by Zika infections, pointing to pathways that may be involved in neurological complications resulting from Zika, such as microcephaly and Guillain-Barr syndrome.
 
Dr. Coombs’ work in influenza has included extensive proteomic scanning of H5N1, H1N1, and H7N9 in various cell types including induced-pluripotent stem cells. Significant findings include the observation that low-pathogenicity strains induce less profound changes to the global proteome. For instance, avian strains stimulate significant downregulation of key proteins, including those involved in antimicrobial response. Seasonal strains do not elicit the same response. Further, Dr. Coombs’ team found that viral infection in stem cells can reduce pluripotency, activate autophagy, and lead to abnormal differentiation.
 
Key highlights include:
 
- using proteomics to identify biological processes associated with infection
- measuring proteomic changes in response to antimicrobials
- comparing and contrasting cellular response to Zika and influenza 
- exploring how the SomaScan Assay could be used to study COVID-19



KEVIN COOMBS PH.D.
PROFESSOR OF MEDICAL MICROBIOLOGY WITH CROSS-APPOINTMENTS IN PHYSIOLOGY, PATHOPHYSIOLOGY, AND MICROBIOLOGY
THE UNIVERSITY OF MANITOBA
 
Dr. Kevin Coombs is a Professor in the Department of Medical Microbiology with cross-appointments in Physiology and Pathophysiology and in Microbiology. He serves on several Cell Biology, Molecular Biology, and Virology Editorial Boards and is currently Chair of the CIHR Virology & Viral Pathogenesis Committee.
 
Dr. Coombs received his B.A.s in Biology and English from the State University of New York in Geneseo and his M.A. and Ph.D. from the University of Texas in Austin. His post-doctoral training in molecular and structural virology was done in the labs of Drs. Bernie Fields and Steve Harrison at Harvard.
 
His research interests include delineation of the protein and nucleic acid interactions in nucleoprotein complexes, using a variety of RNA viruses as models. His lab studies how these interactions change as a result of, and in turn, are modulated by, conformational transitions that occur during macromolecular assembly and disassembly, how these processes can be attenuated by anti-viral compounds, and how these processes in virus infections contribute to pathogenesis in the host.
 
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