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Displaying 1 to 10 of 10 results for morphology

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  • Adam D. Sylvester Lab

    Research in the Adam D. Sylvester Lab primarily focuses on the way in which humans and primates move through the environment, with the aim of reconstructing the locomotor repertoire of extinct hominins and other primates. We use a quantitative approach that involves the statistical analysis of three-dimensional biological shapes, specifically musculoskeletal structures, and then link the anatomy to function and function to locomotor behavior.

    Research Areas: anatomy, biomechanics, locomotion, evolution, skeletal morphology

  • Alex Kolodkin Laboratory

    Research in the Alex Kolodkin Laboratory is focused on understanding how neuronal connectivity is established during development. Our work investigates the function of extrinsic guidance cues and their receptors on axonal guidance, dendritic morphology and synapse formation and function. We have investigated how neural circuits are formed and maintained through the action of guidance cues that include semaphorin proteins, their classical plexin and neuropilin receptors, and also novel receptors. We employ a cross-phylogenetic approach, using both invertebrate and vertebrate model systems, to understand how guidance cues regulate neuronal pathfinding, morphology and synaptogenesis. We also seek to understand how these signals are transduced to cytosolic effectors. Though broad in scope, our interrogation of the roles played by semaphorin guidance cues provides insight into the regulation of neural circuit assembly and function. Our current work includes a relatively new interest in ...understanding the origins of laminar organization in the central nervous system. view more

    Research Areas: central nervous system, neural circuits, neurodevelopment, neuronal connectivity, laminar organization

    Lab Website

    Principal Investigator

    Alex Kolodkin, Ph.D.

    Department

    Neuroscience

  • Biophotonics Imaging Technologies (BIT) Laboratory

    Research in the Biophotonics Imaging Technologies (BIT) Laboratory focuses on developing optical imaging and nano-biophotonics technology to reduce the random sampling errors in clinical diagnosis, improve early disease detection and guidance of biopsy and interventions, and improve targeted therapy and monitoring treatment outcomes. The imaging technologies feature nondestructiveness, unique functional and molecular specificity, and multi-scale resolution (from organ, to architectural morphology, cellular, subcellular and molecular level). The nano-biophotonics technologies emphasize heavily on biocompatibility, multi-function integration and fast track clinical translation. These imaging and nano-biophotonics technologies can also be potentially powerful tools for basic research such as for drug screening, nondestructive assessment of engineered biomaterials in vitro and in vivo, and for studying brain functions on awake animals under normal or controlled social conditions.

    Research Areas: drug screening, imaging, brain, nano-biophotonics

    Lab Website

    Principal Investigator

    Xingde Li, Ph.D.

    Department

    Biomedical Engineering

  • Christopher B. Ruff Lab

    Research in the Christopher B. Ruff Lab focuses on biomechanics and primate locomotion, skeletal growth and development, osteoporosis, skeletal remodeling and the evolution of the hominoid postcranium. We primarily explore how variation in skeletal morphology is related to mechanical forces applied during life. Our studies have shown that the skeleton adapts to its mechanical environment, both developmentally and through evolutionary time, by altering its structural organization.

    Research Areas: anatomy, osteoporosis, biomechanics, locomotion, evolution, skeletal morphology

  • Inoue Lab

    Complexity in signaling networks is often derived from co-opting one set of molecules for multiple operations. Understanding how cells achieve such sophisticated processing using a finite set of molecules within a confined space--what we call the "signaling paradox"--is critical to biology and engineering as well as the emerging field of synthetic biology.

    In the Inoue Lab, we have recently developed a series of chemical-molecular tools that allow for inducible, quick-onset and specific perturbation of various signaling molecules. Using this novel technique in conjunction with fluorescence imaging, microfabricated devices, quantitative analysis and computational modeling, we are dissecting intricate signaling networks.

    In particular, we investigate positive-feedback mechanisms underlying the initiation of neutrophil chemotaxis (known as symmetry breaking), as well as spatio-temporally compartmentalized signaling of Ras and membrane lipids such as phosphoinositides. In parallel,... we also try to understand how cell morphology affects biochemical pathways inside cells. Ultimately, we will generate completely orthogonal machinery in cells to achieve existing, as well as novel, cellular functions. Our synthetic, multidisciplinary approach will elucidate the signaling paradox created by nature. view less

    Research Areas: biochemistry, cell biology, chemotaxis, cancer, signaling paradox, signaling networks, molecular biology, synthetic biology

    Lab Website

    Principal Investigator

    Takanari Inoue, Ph.D.

    Department

    Cell Biology

  • Jonathan M.G. Perry Lab

    Research in the Jonathan M.G. Perry Lab focuses on the connection between skull formation and diet, and how properties of food influence skull morphology over evolutionary time. We also investigate how skull features can be used to determine the diets of extinct mammals. We’re especially interested in whether changes in diet prompted changes to the skull that characterize the first primates.

    Research Areas: anatomy, biomechanics, evolution, diets, skeletal morphology

  • Keri Martinowich Laboratory

    Neural plasticity allows for physiological changes in the brain during both development and in adulthood. The Keri Martinowich Laboratory studies how specific forms of plasticity contribute to regulation of circuits that mediate complex brain function and behavior in order to define how deficits in these processes lead to psychiatric and neurodevelopmental disorders. Current projects focus on brain-derived neurotrophic factor (BDNF), a member of the neurotrophin family implicated in survival, maturation and differentiation of numerous cell types, synaptogenesis and regulation of dendritic morphology. BDNF is a key regulator of synaptic plasticity both in the developing and adult brain. These studies aim to contribute to the long-term goal of understanding how neural plasticity contributes to the function of circuits mediating complex brain function and behavior.

    Research Areas: brain-derived neurotrophic factor (BDNF), neurodevelopment, brain, neural plasticity, mental illness

  • Sesaki Lab

    The Sesaki Lab is interested in the molecular mechanisms and physiological roles of mitochondrial fusion. Mitochondria are highly dynamic and control their morphology by a balance of fusion and fission. The regulation of membrane fusion and fission generates a striking diversity of mitochondrial shapes, ranging from numerous small spheres in hepatocytes to long branched tubules in myotubes. In addition to shape and number, mitochondrial fusion is critical for normal organelle function.

    Research Areas: brain, mitochondrial fusion, mitochondria, molecular biology

    Lab Website

    Principal Investigator

    Hiromi Sesaki, Ph.D.

    Department

    Cell Biology

  • The Nauen Lab

    Epilepsy affects 1-3% of the population and can have a profound impact on general health, employment and quality of life. Medial temporal lobe epilepsy (MTLE) develops in some patients following head injury or repeated febrile seizures. Those affected may first suffer spontaneous seizures many years after the initial insult, indicating that the neural circuit undergoes a slow pathologic remodeling over the interim. There are currently no methods of preventing the development of MTLE. It is our goal to better understand the process in order to slow, halt, and ultimately reverse it.

    Our laboratory draws on electrophysiology, molecular biology, and morphology to study the contribution of dysregulated neurogenesis and newborn neuron connectivity to the development of MTLE. We build on basic research in stem cell biology, hippocampal development, and synaptic plasticity. We work closely with colleagues in the Institute for Cell Engineering, Neurology, Neurosurgery, Biomedical Engineering..., and Radiology. As physician neuropathologists our grounding is in tissue alterations underlying human neurologic disease; using human iPSC-derived neurons and surgical specimens we focus on the pathophysiological processes as they occur in patients.

    By understanding changes in cell populations and morphologies that affect the circuit, and identifying pathologic alterations in gene expression that lead to the cell-level abnormalities, we hope to find treatment targets that can prevent the remodeling and break the feedback loop of abnormal activity > circuit change > abnormal activity.
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    Research Areas: Medial temporal lobe epilepsy

    Lab Website

    Principal Investigator

    David Nauen, M.D., Ph.D.

    Department

    Pathology

  • Zhou Lab

    In the Zhou Lab, the overall goal of our research is to understand the molecular mechanisms underlying development of the mammalian nervous system. Specifically, we are interested in understanding how neurons generate their complex morphology and form proper circuitries during development and how neurons regenerate to restore connections after brain or spinal cord injuries.

    Research Areas: orthopaedics, morphology, brain, spinal cord, neuroscience, nervous system

    Lab Website

    Principal Investigator

    Feng-Quan Zhou, Ph.D.

    Department

    Orthopaedic Surgery

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