First name,Last name,Preferred title,Overview,Position,Department,Individual
Zhilong,Yang,Associate Professor,"The overarching research goal of the Yang laboratory is to understand the mechanisms governing viral replication, with the rationale that the discoveries will expand the knowledge of both viruses and their hosts, and facilitate the development of novel strategies to combat viral and non-viral diseases. A parallel goal of Yang lab is to provide a highly supportive environment to train the next generations of scientists. The ongoing research focuses on how viruses interact with two cellular housekeeping processes: protein synthesis and metabolism using vaccinia virus as the research model. Vaccinia virus is the prototype poxvirus. Poxviruses significantly impact public health, with many presently causing morbidity and mortality in humans and many economically important animals, including deadly zoonotic pathogens (e.g., monkeypox virus). In addition, despite the eradication of smallpox, one of the most (if not the most) devastating diseases in human history, smallpox resurgence remains a serious biothreat. Poxviruses are also widely developed as veterinary and human vaccine vectors and as cancer treatment agents. Poxviruses provide numerous precious tools to understand many aspects of cell biology and dissect complex life processes, as their large DNA genomes encode hundreds of genes that engage many key nodes of cellular life. Yang's research integrates biochemical, molecular, and omics approaches. Taking advantage of their in-depth knowledge of the poxvirus replication and virus-host interactions, the Yang lab also develops vaccinia virus-based utilities and anti-virals.",Associate Professor,Veterinary Pathobiology,https://scholars.library.tamu.edu/vivo/display/n02daa01b
Yi,Xu,Associate Professor,"Our current research activities focus on understanding the pathogenic mechanism of Streptococcus gallolyticus subsp. gallolyticus (Sgg). Sgg is a gram-positive opportunistic pathogen that causes life-threatening bacteremia and infective endocarditis (IE). It is also strongly associated with colorectal cancer (CRC). My lab was the first to demonstrate that Sgg actively promotes the development of colon tumors, elevating a long-stranding clinical association to a functional causal role of Sgg in tumor development. Despite its medical importance, the pathogenic mechanism of Sgg remains poorly understood. Our recent studies have demonstrated that a type VII secretion system of Sgg plays a key role in pathogenesis. Currently we are interested in understanding the mechanism underlying following key steps in Sgg pathogenesis: 1) colonization of the intestinal epithelium, 2) modulation of intestinal homeostasis in normal and tumor-bearing colons, and 3) dissemination from the gastrointestinal tract to the circulatory system.
Keywords: bacterial pathogenesis, infectious diseases, virulence, colorectal cancer, microbiome, microbiota, type VII secretion system, gastrointestinal tract",Associate Professor,Institute of Biosciences and Technology,https://scholars.library.tamu.edu/vivo/display/n0c22439a
Kayla,Bayless,Associate Professor,"My laboratory conducts research in two areas of molecular and cellular medicine: the mechanism through which primary human endothelial cells invade into 3D matrices, and communication between invading endothelial cells and their surrounding 3D collagen matrix.",Associate Professor,Cell Biology and Genetics,https://scholars.library.tamu.edu/vivo/display/n1dd3799c
Louisbruno,Ruest,Associate Professor,,Associate Professor,Biomedical Sciences,https://scholars.library.tamu.edu/vivo/display/n4ba9bf37
Arthur,Laganowsky,Associate Professor,"A long-term research goal of our group is to determine the molecular basis behind protein-lipid interactions and how these interactions can modulate the structure and function of membrane proteins, including their interactions with signaling molecules. What determines the selectivity of membrane proteins towards lipids, and the coupling between lipid binding events and function remains a key knowledge gap in the field; one that if addressed will significantly advance our understanding of how lipids participate in both normal and pathophysiological processes of membrane proteins. Therefore, there is a critical need to expand our fundamental knowledge in this emerging field by applying and developing innovative approaches to elucidate how lipids modulate the structure function of membrane proteins. To this end, we are studying a number of ion channels, receptors and other types of membrane proteins.",Associate Professor,Chemistry,https://scholars.library.tamu.edu/vivo/display/n542411e4
Mahua,Choudhury,Associate Professor,"Epigenetics, diabetes, obesity, pregnancy, preeclampsia, biomarker",Associate Professor,Nutrition,https://scholars.library.tamu.edu/vivo/display/n55b81876
M,Benson,Associate Professor,,Associate Professor,Biomedical Sciences,https://scholars.library.tamu.edu/vivo/display/n58e9bd13
Narendra,Kumar,Associate Professor,"1. Obesity associated metabolic syndrome (MetS) is both a US and a worldwide epidemic and a major burden to healthcare system. Chronic low-grade inflammation (CLGI) is a well-established characteristic of the obese-human condition and though, the gastrointestinal (GI) mucosa is the first tissue that interacts with dietary components and luminal microbiota both of which are known to regulate obesity, the research on the role of GI-mucosa in obesity associated MetS is lacking. Findings from my lab support a key role of Janus kinase 3 (Jak3), a non-receptor tyrosine kinase, in intestinal and systemic CLGI associated obesity and diabetes in both an animal-model and in humans. Our publications, and unpublished data indicate that Jak3 regulates; colonic and systemic CLGI, and multiple symptoms of metabolic syndrome. Our goal is to determine the associated underlying mechanisms. Our current focus is on tissue-specific roles of Jak3 and associated signaling complexes in CLGI-onset as a precursor for; (a) obesity and diabetes, (b) Obesity and Alzheimer's disease, and (c) inflammatory bowel disease.
2. Inflammatory bowel disease (IBD) that includes Crohn's disease and Ulcerative colitis is a chronic inflammatory condition of gastrointestinal tract. Annual death from these diseases are over 70,000.00, and the incidences of new cases have been rising over the years. Because the repairs of intestinal mucosa (Restitution) are compromised during IBD, the research focus of our lab is to dissect the roles of intestinal epithelial, intestinal immune cells and gut microbiota in mucosal restitution. Our lab was pioneered the functions of Jak3 in intestinal epithelial mucosa. We show that IL-2 (a cytokine produced during intestinal inflammation) promotes mucosal wound repair through Jak3 complexed with villin, ShcA, and ?-catenin. Studies are underway to define the tissue-specific Jak3-mediated signaling pathways that regulate CLGI as a precursor for the onset of IBD.",Associate Professor and Director of Graduate Studies||Associate Professor,Pharmaceutical Sciences||Pharmaceutical Sciences,https://scholars.library.tamu.edu/vivo/display/n5bcfc45e
Yanan,Tian,Associate Professor,Transcriptional control of the Ah receptor-regulated gene expression. Interaction between the Ah receptor and NF-kB signal transduction pathways. lncRNAs and their role in regulation of gene expression,Associate Professor,Veterinary Physiology and Pharmacology,https://scholars.library.tamu.edu/vivo/display/n7f54d80b
Gregg,Wells,Associate Professor,"The general theme of the research in my laboratory is the role of protein structure in disease, particularly in neurological disease. One area of study is the structure and function of the superfamily of neurotransmitter-gated ion channels that includes nicotinic acetylcholine, serotonin 5HT3, glycine, and GABAA receptors. Members of this superfamily are involved in drug addiction and alcoholism, neurodegenerative diseases such as Alzheimer disease and Parkinson disease, genetic forms of epilepsy, and neuropsychiatric disorders such as schizophrenia and depression. We are developing new approaches to elucidating the molecular structures of these ion channels from animals and bacteria. Cyclic nucleotide gated channels (CNGCs) are a second area of study. We are interpreting their electrophysiological properties in terms of structure and thermodynamics. Hearing is a third area of study. We are using computational models of calcium and potassium ion channels and mechanotransduction to explain electrophysiological function of cochlear hair cells. Fourth, analysis of genomes and tissue-specific transcriptomes of electrogenic animals (e.g., electric fish) is expected reveal new aspects of lifecycles of ion channels. Explaining neurological diseases in terms of protein structure is a theme linking our neuroscience research with neuropathology, my medical specialty.",Associate Professor,Cell Biology and Genetics,https://scholars.library.tamu.edu/vivo/display/nb25f91ff
Xiaofang,Wang,Associate Professor,"My research interests are focused on the signaling regulation of bone and tooth development. Currently, my lab is focused on two kinases on the secretory pathway that are critical for bone and tooth development, Fam20B and Fam20C. I am also interested in mapping the pathogenic genes for bone and tooth diseases in mutant mice/humans. We characterize the gene function using multidisciplinary methods, including genetically engineered animal models, tissue/organ culture/transplantation, Single Cell RNA-Seq, ISH, IHC, and proteomic approaches.
Key words: bone, cartilage, tooth, dentin, enamel, chondrocytes, transgenic, genetics, signaling, FAM20C, FAM20B, kinase, mineralization, FGF23",Associate Professor,Biomedical Sciences,https://scholars.library.tamu.edu/vivo/display/nb47c8381
Zhilei,Chen,Associate Professor,"The Chen Medicinal Protein Lab aims to accelerate the discovery, development and clinical translation of protein therapeutics through innovative protein engineering research. We believe that better medicine enables a higher quality of living, and protein engineers are charged to create the better medicine for today and tomorrow. We are particularly interested in the creation and engineering of affordable protein therapeutics to prevent and treat infectious diseases and cancer.",Associate Professor,Microbial Pathogenesis and Immunology,https://scholars.library.tamu.edu/vivo/display/nc9a6c3ae
Yongbo,Lu,Associate Professor,,Associate Professor,Biomedical Sciences,https://scholars.library.tamu.edu/vivo/display/ncce6bd83
Paul,Brandt,Associate Professor,"Understanding how the target cells ""interpret"" hormonal signals is the primary focus of our laboratory.Most of our research centers on regulation of steroid hormone-transduced signals. One area of study is the calcium-dependent regulation of glucocorticoid and androgen receptor-mediated transcription. A second major area of interest concerns glucocorticoid and steroid sex hormone regulation of nitric oxide (NO) production. Other areas of interest in our laboratory are: development of androgen-independence in prostate cancer; stress responses in PMCA1(-) cell lines; and the involvement of NO in dry eye syndrome.",Associate Dean for Academic Technology and Curriculum Innovation||Associate Professor,Neuroscience and Experimental Therapeutics||School of Medicine,https://scholars.library.tamu.edu/vivo/display/nd24a6df6
Yun,Huang,Associate Professor,"Dr. Huang is currently an Assistant Professor at the Center for Epigenetics and Disease Prevention, Institute of Biosciences & Technology, Texas A&M University. Her long-term goal is to elucidate the molecular basis of epigenetic changes in the human genome and to develop novel therapies by targeting aberrant DNA methylation and demethylation associated with human diseases, including cancer, immunoinflammatory and cardiovascular diseases.
Dr. Huang's laboratory is focused on elucidating the physiological and pathophysiological functions of TET2 protein and its 5-methylcytosine oxidation products (5hmC, 5fC and 5caC) in cancer and development (Nature Genet 2014; Trends in Genetics 2014).",Associate Professor,Institute of Biosciences and Technology,https://scholars.library.tamu.edu/vivo/display/nd7ed0926
Dekai,Zhang,Associate Professor,"Our laboratory is studying the molecular mechanisms of innate immune recognition by identification and analysis of receptors involved in innate immune recognition and activated signaling pathways. We are particularly interested in the recently identified family of Toll-like receptors, which play a critical role in the mounting of innate immune responses. We wish to understand the mechanisms by which TLRs recognize different pathogen associate molecular patterns (PAMPs), as well as the regulatory mechanisms of TLR signal pathways that lead to NF- k B activation. We are also interested in studying the important links between chronic infection, inflammation and cancer by utilizing biochemical as well as whole animal approaches.",Associate Professor||Associate Professor,Center for Infectious and Inflammatory Diseases||Institute of Biosciences and Technology,https://scholars.library.tamu.edu/vivo/display/ndf8a94d4
Hays,Rye,Associate Professor,"A fundamental principle of biology is the use of chemical energy in the form of ATP to assemble, disassemble and alter macromolecular structure. Specialized control proteins known as molecular chaperones are often responsible for this activity and have been recognized in recent years to be essential for regulating many aspects of cellular biology. Using a variety of biophysical and biochemical techniques, the Rye lab focuses on three fundamental cellular processes that require molecular chaperones: (1) protein folding (2) protein disaggregation and (3) vesicle trafficking. In each of these cases, large quantities ATP are burned, resulting in molecular organization in the case of protein folding, and molecular disassembly and remodeling in the case of protein disaggregation and vesicle trafficking. We are interested in understanding the detailed biophysical mechanisms that underpin these events. Why are these processes so energetically expensive? Are there any similarities in how the energy is used between these very different molecular processes? Are there general principles of energy transduction in biology that can be gleaned by comparing these examples with other molecular machines, such as cytoskeletal motors? Understanding how molecular chaperones control protein and membrane organization will provide key insights into not only basic cell biology, but will also illuminate aspects of many diseases that spring from aberrant protein and membrane dynamics.",Associate Professor,Biochemistry and Biophysics,https://scholars.library.tamu.edu/vivo/display/ne7fb85e1
Carl,Gregory,Associate Professor,"Our lab has been examining the biology of MSCs with a view to developing rapid molecular markers and tests for evaluating/purifying maximally efficacious cultures of MSCs. The group also specializes in bone repair by MSCs. Based on detailed characterization of the molecular mechanism of osteoblast differentiation by MSCs, a novel and effective bone regeneration strategy has been developed. Additionally, we are currently examining the effects of various small molecules and immunological strategies for the safe and effective inhibition of Dkk-1 activity in bone tumors.We have recently established methods to model bone-tumor interactions using bioreactors that simulate microgravity.",Associate Professor,Cell Biology and Genetics,https://scholars.library.tamu.edu/vivo/display/ne92fd9fb
Steven,Maxwell,Associate Professor,"My primary interests include Cancer; Oncogenes; Tumor Suppressor; Genes Programmed Cell Death (apoptosis); Chemoresistance, and Angiogenesis. My laboratory studies mechanisms of evolution of chemoresistance in diffuse large B-cell lymphoma (DLBCL). One current primary objective is to conduct a Phase I study that (1) confirms RTI-79 safety in platinum-resistant/refractory ovarian cancer patients, and (2) demonstrates signals of efficacy in humans (ex: time-to-disease progression and changes in CA125 biomarker). A second objective is to better define the RTI-79 mechanism of action (MOA) by (1) determining how RTI-79 causes a rapid burst in superoxides, and (2) elucidating the basis of Nrf-2 pathway downregulation.",Associate Professor,Cell Biology and Genetics,https://scholars.library.tamu.edu/vivo/display/neb5b702f