8 research outputs found

    Towards Inferring Neural Circuits from Calcium Population Imaging

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    <p>Vogelstein JT,Packer AM, Mishchenko Y, Yuste R, Paninski L. Towards Inferring Neural Circuits from Calcium Population Imaging. COSYNE, 2010</p

    Towards Confirming Neural Circuit Inference from Population Calcium Imaging. NIPS Workshop on Connectivity Inference in Neuroimaging

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    <p>Vogelstein JT, Mishchenko Y, Packer AM, Machado TA, Yuste R, Paninski L. Towards Confirming Neural Circuit Inference from Population Calcium Imaging. NIPS Workshop on Connectivity Inference in Neuroimaging, 2009</p

    Towards Confirming Cosyne 2010

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    <p>Vogelstein JT, Mishchenko Y, Packer AM, Machado TA, Yuste R, Paninski L. Towards Confirming Neural Circuit Inference from Population Calcium Imaging. COSYNE, 2010</p

    From the neuron doctrine to neural networks

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    Mechanisms of radiotherapy-associated cognitive disability in patients with brain tumours

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    Standard treatment of primary and metastatic brain tumours includes high-dose megavoltage-range radiation to the cranial vault. About half of patients survive \u3e6 months, and many attain long-term control or cure. However, 50-90% of survivors exhibit disabling cognitive dysfunction. The radiation-associated cognitive syndrome is poorly understood and has no effective prevention or long-term treatment. Attention has primarily focused on mechanisms of disability that appear at 6 months to 1 year after radiotherapy. However, recent studies show that CNS alterations and dysfunction develop much earlier following radiation exposure. This finding has prompted the hypothesis that subtle early forms of radiation-induced CNS damage could drive chronic pathophysiological processes that lead to permanent cognitive decline. This Review presents evidence of acute radiation-triggered CNS inflammation, injury to neuronal lineages, accessory cells and their progenitors, and loss of supporting structure integrity. Moreover, injury-related processes initiated soon after irradiation could synergistically alter the signalling microenvironment in progenitor cell niches in the brain and the hippocampus, which is a structure critical to memory and cognition. Progenitor cell niche degradation could cause progressive neuronal loss and cognitive disability. The concluding discussion addresses future directions and potential early treatments that might reverse degenerative processes before they can cause permanent cognitive disability

    The Role of Dynamic Columns in Explaining Gamma-band Synchronization and NMDA Receptors in Cognitive Functions

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