Current Lecture Season
Dr. Maquat is the J. Lowell Orbison Endowed Chair and Professor of Biochemistry and Biophysics in the School of Medicine and Dentistry, Director of the Center for RNA Biology, and Chair of Graduate Women in Science at the University of Rochester, Rochester, NY. After obtaining her Ph.D. in Biochemistry from the University of Wisconsin-Madison and undertaking post-doctoral work at the McArdle Laboratory for Cancer Research, she joined Roswell Park Cancer Institute before moving to the University of Rochester.
Dr. Nelson is president of the Social Science Research Council and professor of sociology at Columbia University. An award-winning scholar of science, medicine, and social inequality, her recent books include The Social Life of DNA: Race, Reparations, and Reconciliation after the Genome, Genetics and the Unsettled Past: The Collision of DNA, Race, and History, and Body and Soul: The Black Panther Party and the Fight Against Medical Discrimination. Dr.
Dr. Hubbell uses biomaterials and protein engineering approaches to investigate topics in regenerative medicine and immunotherapeutics. In regenerative medicine, he focuses on biomaterial matrices that mimic the extracellular matrix and on growth factor - extracellular matrix interactions, working in a variety of animal models of regenerative medicine.
Dr. Rubin will discuss the current state of circuit neuroscience in the fly, using examples from his lab’s work on learning and memory, sleep and aggression. Within the next five years, those of us working with Drosophila can expect to have comprehensive datasets, including a complete connectome, and powerful tools with which to study the fly’s brain and behavior.
Research in the Ghedin Lab meets at the interface of microbiology, genomics, and systems biology. Projects touch on the extent of intra- and inter-host microparasite (viruses and bacteria) diversity within the context of transmission and virulence, and parse the relationship between microbial ecology in the respiratory tract and disease progression.
Cancer and aging are intricately intertwined. Organisms with dividing cells are at a substantial risk for developing cancer. Evolution “solved” the cancer problem by selecting for tumor suppressive mechanisms, which protect these organisms for cancer – at least for the reproductively active portion of the life span. Beyond that portion of the life span, these mechanisms can drive pathologies associated with aging, including, ironically, cancer. For her lecture, Dr.
Dr. Fischer is interested in understanding how genetic errors cause vulnerability to microorganisms, autoimmunity, inflammation and allergy, with the dual goal to decipher in vivo immunity in humans and to correct its defects.
Noncoding RNAs play critical roles in the metabolism of all cells. The Wolin laboratory studies how noncoding RNAs function, how cells recognize and degrade defective noncoding RNAs, and how failure to degrade these RNAs affects cell function and contributes to human disease. Their studies revealed new mechanisms by which defective RNAs are targeted for degradation and new classes of noncoding RNAs. Most recently, their work has contributed to a novel theory for how the autoimmune disease systemic lupus erythematosus may be triggered in genetically susceptible individuals.
Dr. Walsh's clinical research has focused on pharmacological issues in opioid and cocaine dependence. She has conducted studies on pharmacodynamic and pharmacokinetic characteristics of opioid treatment agents, including buprenorphine, methadone and LAAM and has evaluated potential pharmacotherapies for efficacy and safety in the treatment of cocaine dependence.
The Bakaletz laboratory’s research focus is attempting to understand the pathogenic mechanisms operational in the highly prevalent pediatric disease, otitis media (OM) (or middle ear infection). Specifically, we are interested in elucidating how upper respiratory tract viruses predispose the middle ear to invasion by any of the three predominant bacterial pathogens of OM (nontypeable Haemophilus influenzae, Moraxella catarrhalis and Streptococcus pneumoniae).
The page was last updated on Wednesday, June 11, 2014 - 4:07pm