First name,Last name,Preferred title,Overview,Position,Department,Individual
Qian,Wang,Associate Professor,"Dr. Wang's earlier work focused on the comparative morphology of craniofacial skeletons of Mid Pleistocene hominin fossils. During his postdoctoral training, he was involved in a number of studies examining the internal structure of craniofacial bone and suture morphology and how it is related to skeletal growth, function and adaptation. His recent research focuses on the functional morphology and biomechanics of the craniofacial skeleton. He has incorporated a range of methods, including geometric morphometrics (e.g., 3D Euclidean Distance Matrix Analysis and Generalized Procrustes Analysis/GPA), experimental approaches (e.g., in vitro strain measurements and ultrasonic techniques), computer-aided modeling and biomechanical analysis ( e.g., Finite Element Analysis), as well as phenotypic analyses. He has worked intensively on the various primate skeletal collections and has developed protocols for data collection and analyses of museum skeletal collections. In addition, he is a member of a multi-institutional research team made up of anatomists and anthropologists who have specialized in various aspects of functional morphology in order to systematically reassess the reconstruction and biomechanical interpretation of the face of early human types, based on current morphological and phylogenetic evidence and advances in biomechanical methods.",Associate Professor,Biomedical Sciences,https://scholars.library.tamu.edu/vivo/display/n10bc652f
Xiuren,Zhang,Professor,"Our laboratory focuses on systemic analysis of biochemical, molecular and biological functions of AGO family proteins (AGOs-mics) in genetically tractable Arabidopsis and economically important crops (i.e. rice). We'd like to identify the small RNAs, mRNA targets and protein components which associate with these AGOs. We will study protein/RNA and protein/protein interactions in these RISC assembly events. Our goal is to understand how these AGOs are functionally specialized or redundant corresponding to endogenous development cues and external environmental stimuli. Particularly, we'd like to learn how plants reprogram their gene expression through the small RNAs and AGOs to construct a new cellular niche in responses to environmental challenges and biotic stresses.
Another aspect of our research involves host/virus interaction. Plants take advantage of RNA silencing pathways to defend themselves from exogenous nucleic acid invaders (i.e. viruses). As an anti-host defense mechanism, viruses encode suppressors that can block RNA silencing responses. We have recently demonstrated that CMV 2b disables AGO1 cleavage activity to inhibit RNA silencing and to counter host defense. We are now extending our study to suppressors of several other viruses and the molecular mechanisms of their suppression.",Associate Professor,Biochemistry and Biophysics,https://scholars.library.tamu.edu/vivo/display/n220933ad
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
George,Perry,Associate Professor,,Associate Professor,Texas A&M AgriLife Research,https://scholars.library.tamu.edu/vivo/display/nacfdace6
Lin,Zhu,Associate Professor,,Associate Professor,Irma Lerma Rangel School of Pharmacy,https://scholars.library.tamu.edu/vivo/display/nb936a5d7
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
Zachary,Adelman,Professor,,Associate Professor,Entomology,https://scholars.library.tamu.edu/vivo/display/ndc81a8e5
Matt,Pharr,Associate Professor,"My current areas of interest include mechanics of materials for energy storage and conversion, deformation and fracture of soft materials, mechanics of flexible/wearable electronics, coupled electro-chemo-mechanics, and mass transport in materials.",Associate Professor||Faculty Affiliate,Mechanical Engineering||Energy Institute,https://scholars.library.tamu.edu/vivo/display/ne059f41f
Jerome,Menet,Associate Professor,"Most organisms from bacteria to humans exhibit 24-hours rhythms in their biochemistry, physiology and behavior. Best exemplified by the sleep/wake cycle, these rhythms are remarkably widespread and include in humans hormonal (e.g., melatonin, insulin, cortisol), metabolic (e.g., glucose, cholesterol), physiological and behavioral oscillations. In fact, most biological functions are rhythmic and are set to perform optimally at the most appropriate time of the day. For example, the human digestion process performs better during the day when we are supposed to eat.
These circadian rhythms are generated by ""molecular clocks"", which consist of a few ""clock genes"" interacting in feedback loops, and which drive the rhythmic expression of a large number of genes, i.e. ~10% of the transcriptome in any tissues. This wide impact of clock genes in regulating gene expression is underscored by the surprisingly large number of pathologies developed by clock-deficient mice. In addition to being arrhythmic, these mice indeed develop pathologies as diverse as mania-like behaviors, learning and memory defects, depression, drug addiction, insomnia, metabolic diseases, arthropathy, hematopoiesis defects and cancers.
Research in our lab aims at characterizing how circadian clocks and clock genes regulate gene expression to provide insights into how and why clock dysfuntion leads to a wide spectra of pathologies. To this end, we are using a wide-range of molecular and biochemical techniques to investigate the circadian clock function at the genome-wide level (e.g., next-generation sequencing). We are currently extending some of our recent results and focus on 1) how clock genes rhythmically regulate chromatin environment and 2) the mechanisms involved in rhythmic post-transcriptional regulation of gene expression.",Associate Professor,Biology,https://scholars.library.tamu.edu/vivo/display/nf680fb91