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the recently published work of Spateo for spatiotemporal modeling of whole mouse embryos with 3D single cell spatial genomics: Qiu et al., Cell (https://doi.org/10.1016/j.cell.2024.10.011 (link is external
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-specific mechanisms underlying vascular diseases, ultimately to inform new treatment and prevention strategies. Other opportunities include use of animal model of disease to dissect the mechanism
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. Develop and apply ab initio computations, molecular dynamics simulations, and machine learning models. Collaborate with other researchers within the group and external partners. Present research findings
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learning to derive principled models of cortical computation. Our newly refurbished primate facility, state‑of‑the‑art Neuropixels rigs, and high‑performance computing cluster offer an unmatched playground
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, and traumatic brain injury patients. Building on a long history of transplanting hiPSC-derived cells to promote neural repair in pre-clinical models, this newly funded research program aims to develop
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thymic tissues to develop a robust in vitro and in vivo developmental model of thymic development. This model can now be applied to differentiating iPSCs into regenerative thymic tissues for clinical
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include, but are not limited to, using the latest computational learning-driven approaches, including computational social science, foundation models and multimodal machine learning, to enhance
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human samples collected by our clinical colleagues from patients, mouse models, primary explants, and organoid cultures. Our group collaborates with multiple departments at Stanford and beyond
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individuals who have a Ph.D. or are nearing completion of their Ph.D. with experience in cell biology, structural biology, protein biochemistry, or neurobiology to join a highly interactive, international and
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to investigate the pathogenesis and treatment of optic neuropathies, which includes studies using multimodal assessments including measurements of visual function and structure. We will use noninvasive