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modifiers. We study maternal obesity — a rapidly rising but modifiable CHD risk factor — and its convergence with non-canonical WNT/Planar Cell Polarity signaling. Using a clinically relevant high-fat-diet
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scattering theory, heavy-ion collisions and the properties of hot QCD matter, hadronic probes of beyond-the-Standard-Model physics, and formal developments in lattice QCD. IU Physics Department also maintains
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experimental systems – from ecosystems to microbiology and developmental biology, from evolution to cell biology, from molecular biology to systems biology, bioinformatics, and genomics. It is always an exciting
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experimental systems — from ecosystems to microbiology and developmental biology, from evolution to cell biology, from molecular biology to systems biology, bioinformatics, and genomics. It is always an exciting
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translate these discoveries into precision medicine. We develop computational and statistical methods while integrating human genetics, single-cell and multi-omics, large-scale biobank resources, and
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studies the mechanisms by which chronic viral infections suppress antiviral immunity and drive T cell exhaustion to facilitate viral persistence. We also have a major interest in how chronic viral
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fellow to join the 3D Stem Cell Biology Research Lab (https://www.hashinolab.com ) and study normal and pathological development of the human inner ear using stem cell-derived organoids as a model system
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the processes that take place in the bacterial cell envelope with emphasis into oxidative protein folding. The overarching goal for this position is to make timely progress on our NIH and CFF grants (https
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the genetic and developmental basis of pediatric heart disease. We analyze genetic variation in samples from patients with congenital heart defects and utilize mouse, Xenopus and cell-based models to assess
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research environment and opportunities for career advancement, and has a strong publication record in mouse genetics, electrophysiology and molecular biology. We routinely employ mouse models of sickle cell