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Previous Job Job Title Rsch Pro 3-Genetics/Cell Bio Next Job Apply for Job Job ID 376486 Location Twin Cities Job Family Research Full/Part Time Full-Time Regular/Temporary Regular Job Code 8353GC
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expertise in cell and molecular biology, assay development, and therapeutic screening. The successful candidate will be responsible for driving ASO therapeutic development projects, including candidate design
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cell culture and biological assays Additional Information Benefits What can you expect from us? 232 vacation hours per year, based on a 38-hour workweek (1.0 FTE). You can also work more or fewer hours
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Previous Job Job Title Research Professional - Genetics/Cell Bio Next Job Apply for Job Job ID 376477 Location Twin Cities Job Family Research Full/Part Time Full-Time Regular/Temporary Regular Job
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at the finest scale to create impact on a global scale. For more information on the Lee laboratory: https://www.lsi.umich.edu/science/our-labs/t-lee-lab Job Summary The Tzumin Lee laboratory at the Life Sciences
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position in the field of Gene regulation and Single cell genomics. The position is hosted by the School of Medicine at the Faculty of Health Sciences and located on the Kuopio Campus. The position will be
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Application Deadline: Applications accepted all year round Details Cardiovascular diseases such as atherosclerosis and aortic aneurysms develop when communication between cells in the blood vessel wall becomes
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PhD candidate for the project "Modulation of inflammatory Dendritic cell subsets in atherosclerosis"
project “Modulation of inflammatory Dendritic cell subsets in atherosclerosis” Atherosclerosis is a chronic inflammatory disease where atherosclerotic plaques develop in the larger arteries. Atherosclerosis
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their website at https://www.naritalab.com/ Our laboratory investigates the biology of preneoplastic cell states, with particular interest in how changes in cell functional identity and plasticity are controlled
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seeking a postdoctoral fellow to study the cell fate decision mechanisms in hematopoietic stem and multipotent progenitor cells using primary mouse and human bone marrow cells and patient samples. We study