Eder MM, Carter-Edwards L, Hurd TC, Rumala BB, Wallerstein N. A Logic Model for Community Engagement Within the Clinical and Translational Science Awards Consortium: Can We Measure What We Model? Acad Med. 2013 Jun 7.
Cornejo A, Ivatury S, Crane CN, Myers JG, Wang HT. Analysis of Free Flap Complications and Utilization of Intensive Care Unit Monitoring. J Reconstr Microsurg. 2013 May 9. [Epub ahead of print].
Lam D, Harris D, Qin Z. Inflammatory Mediator Profiling Reveals Immune Properties of Chemotactic Gradients and Macrophage Mediator Production Inhibition during Thioglycollate Elicited Peritoneal Inflammation. Mediators Inflamm. 2013;2013:931562. doi: 10.1155/2013/931562.
BS, 1981, University of Rhode Island, Kingston, RI
MS, 1991, Albany Medical College, Albany, NY
PhD, 1992, Albany Medical College, Albany, NY
1992-1994, Post-Doctoral Fellow in Immunology, Gamble Institute for Medical Research, Cincinnati OH
1994-1997, Post-Doctoral Fellow in Immunology/Microbiology, Temple University School of Medicine, Philadelphia, PA
Research: Dr. Schwacha's laboratory focuses on the role of the innate immune system in the host's response to traumatic injury, with particular emphasis on the response to burn injury. Major burn injury induces an immunopathogenic response with the release of a wide range of pro-inflammatory mediators by macrophages and other cells that contribute to the development of numerous complications including; immune dysfunction, SIRS, sepsis, delayed wound healing and multiple organ failure. Dr. Schwacha's laboratory has shown that post-burn immunosuppression is induced by macrophage-mediated processes. Other findings indicate a central role for gamma-delta T-cells in the post-burn immunoinflammatory responses including the regulation of macrophage hyperactivity, neutrophil-mediated organ injury, and wound healing. This T-cell subset is uniquely positioned in the immune/inflammatory axis to influence tissue repair, inflammation, anti-microbial activity and overall immune status post-injury. Current studies are directed at improving our understanding of gamma-delta T-cells in post-burn immunoinflammatory processes in both experimental and clinical settings. Other areas of major interest are the impact of opiate analgesics on post-injury immune responses and the relationship(s) between insulin resistance post-injury immune function.
MD, Xian Medical University, Shaanxi, China, 1994
PhD, Dermatology and Venereology, Peking Union Medical College & Chinese Academy of Medical Sciences, Peking, China, 2000
MS, Dermatology and Venereology, Xian Medical University, Shaanxi,China, 1997
Research: Dr. Qin received a Master's and MD from Xian Medical University with a specialization in dermatology, and his PhD from the Chinese Academy of Medical Sciences at Peking Union Medical College, with both his Masters and PhD in microbial infections, inflammation and host-pathogen interactions that led to 7 publications. He was a postdoctoral fellow for one year at the National Institute of Infectious Diseases in Atlanta, and a second 3-year postdoctoral fellowship at Emory University. He worked with Drs. Tohru Fukai and David Harrison on reactive oxygen species at Emory Cardiology. Before joining to UTHSCSA Division of Vascular Surgery, Dr. Qin also worked at the University of Cincinnati Division of Cardiovascular Disease for four years as a Research Instructor.
The driving force of Dr. Qin's project is due to advances in techniques and science, it is time to revisit the vascular function of copper, an essential nutrient in human. First, the sensitivity and application of metallomic techniques have greatly improved. Dr. Qin is utilizing a highly novel approach that combines cutting-edge X-ray fluorescence spectrometric (XRF) imaging with inductively coupled plasma-mass spectrometry (ICP-MS) to detect copper concentrations and localization in the blood vessel wall. Application of XRF imaging to biological samples in 2004 represented one of most exciting advances in metallomics. Dr. Barry Lai at the Argonne National Laboratory collaborates with Dr. Qin to apply this technique in vascular study. In addition, the emerging flow injection technique along with improved sample extraction methodology has produced a more powerful ICP-MS. The technique has been optimized and applied in Dr. Qin project in vascular tissues and cells via a close collaboration with Dr. Joseph Caruso in the Department of Chemistry at the University of Cincinnati. Moreover, they established a novel concept, vascular metallomics, to bridge the gap between vascular biology and metallomics. Second, copper trafficking theory has been recently established and validated in several laboratories. This theory convincingly defines a group of proteins in the regulation of uptake, distribution, sequestration and export of copper. Among these proteins, ATP7A has attracted significant attention since the identification of its function as a copper egress pump and the discovery of mutations of ATP7A leading to human Menkes disease. Dr. Qin's approach is to study the physiopathology of the interaction between cardiovascular homeostasis and copper metabolism in vascular biology via dissecting the function of ATP7A.
Paula K. Shireman, MD
Professor, Vascular Surgery and
Vice Dean for Research, Dielmann Chair in Surgery, UT School of Medicine San Antonio
2004 - MS, Clinical Investigation, University of Texas Health Science Center at San Antonio
1990 - MD, Indiana University School of Medicine, Indianapolis, IN
1986 - BS, Purdue University, West Lafayette, IN
1999 - Post Doctoral Fellowship, Vascular Surgery, Loyola University Medical Center, Maywood, IL
1998 - Post Doctoral Fellowship, Peripheral Vascular Surgery Research Fellow, Loyola University Medical Center, Maywood, IL
1997 - Residency, General Surgery, Northwestern University Medical Center, Chicago, IL
1995 - Post Doctoral Fellowship, Vascular Surgery Research Fellow, Northwestern University Chicago, IL
Research: Our lab studies the inflammatory-mediated mechanisms of angiogenesis and skeletal muscle regeneration. We are particularly interested in how hematopoietic stem cells, myogenic stem cells and inflammatory cells interact to form muscle after injury. A better understanding of muscle regeneration will be useful in tissue regeneration strategies for limb salvage.
Univ. of Massachusetts, Amherst, Massachusetts, PhD, Microbiology, 1968
Univ. of Massachusetts, Amherst, Massachusetts, MS, Microbiology, 1965
Tufts University, Medford, Massachusetts, BS, Biology-Chemistry, 1963
Research: Dr. Baseman's laboratory examines the molecular pathogenesis of microbial-mediated human disease, emphasizing the virulence potential of bacteria and the host response to bacterial infection. We study several pathogenic Mycoplasma species using a variety of experimental approaches. Mycoplasmas are biologically unique prokaryotes that are associated with common acute and chronic infections of the respiratory and genitourinary tracts, with dissemination to distant tissue sites. More about Dr. Baseman's research.
Georgtown University, DDS
Uniformed Services University of the Health Sciences, PhD
Research: Dr. Hargreaves' primary research interests are in the pharmacology of pain and inflammation. A major focus is on pharmacological regulation of unmyelinated "C" fiber nociceptors, as well as their plasticity in response to inflammation or nerve injury. Investigations are in progress evaluating the effects of cannabinoids, opioids, adrenergics, NPY, sex steroids and other drugs on regulating the activity of these fibers. In addition, his lab is working to identify major classes of inflammatory mediators and associated receptor/signal transduction systems which mediate activation, sensitization and phenotypic plasticity of these primary afferent fibers in response to tissue inflammation. Responses are measured using isolated superfused tissue, primary trigeminal cultures, microdialysis probes implanted in situ, RIA, EIA, real time PCR, Affymetrex analyses, IHC, ISH, confocal microscopy, behavior, etc.
Institute of Cancer Research of the University of London, England, PhD, Cell Biology
University of California, San Diego, School of Medicine Postdoctoral Studies, Biochemistry
University of Oxford, Oxford, England, BA, Animal Physiology
Research: Multipotent stem cells are now known to be present in almost every tissue of the human body. Fat is a particularly abundant and useful source of these cells. They have the potential to become bone, cartilage, muscle, blood vessels and nerves. Therefore, in theory they present an unprecedented opportunity for new methods of therapeutic repair of tissue injuries.
In this lab we use human stem cells implanted into a new type of profoundly immunodeficient mouse model, which is superior to others for accepting normal human cells as transplants. Using novel methods of bioluminescence and fluorescence imaging, including the use of innovative surgical techniques like skin windows, we are studying how to control the fate of stem cells, which is the key to being able to use them on a large scale in regenerative medicine.
MS, Mathematics, Wayne State University, Detroit, Michigan, 1968
PhD, Mathematical Statistics, Wayne State University, Detroit, Michigan, 1973(br>
Research: Dr. Michalek has 30 years experience in the analysis and reporting of clinical and epidemiological studies and 20 years experience as a consultant to the pharmaceutical industry. He has published papers in statistical methodology, clinical trials, and epidemiology, and his current interests include methods to analyze survival and count data in cross-over studies.
Brad H. Pollock, PhD, MPH
Professor and Chairman, Department of Epidemiology and Biostatistics
Associate Director, Prevention and Control, San Antonio Cancer Institute
Website: Department of Epidemiology & Biostatistics
Phone: 210-567-0836 | Fax: 210-567-0921
UCLA School of Public Health, Los Angeles, CA, PhD
UCLA School of Public Health, Los Angeles, CA, MPH
Research: Dr. Pollock's research focus is in the area of cancer epidemiology and prevention research. He has been a national leader in the field of childhood cancer epidemiology and cancer control research, and is the principal investigator of the national Children’s Oncology Group Community Clinical Oncology Program Research Base Grant from the National Cancer Institute. He has extensive experience conducting large populationbased epidemiologic investigations as well as cancer prevention and control intervention trials. Dr. Pollock has also served as a biostatistician for over 50 multi-institutional clinical trials and served on a number of NCI study sections. Dr. Pollock established the Center for Epidemiology and Biostatistics at UTHSCSA and led the growth of this unit into a full academic department within the School of Medicine. He works closely with researchers from the all over the Health Science Center and has provided critical core resources for several of the large research entities at UTHSCSA.