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Postdoctoral Research Associate: Drug Development Targeting Neuroinflammation in Alzheimer's Disease
Alzheimer's Disease Hiring Department: Department of Biochemistry and Molecular Genetics Location: Chicago, IL USA Requisition ID: 1035736 Posting Close Date: 7/18/2025 Salary: Salary will follow NIH
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to join our dynamic research team investigating post-transcriptional and epigenetic mechanisms that control cell fate, stem cell plasticity, and cancer progression. Research Focus We employ cutting
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A postdoctoral associate position is available to study the molecular and circuit basis of sleep. We use sophisticated genetic approaches in Drosophila and mice to study the genes and circuitry
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, the applicant will have the opportunity to be involved in ongoing projects, e.g. development of novel strategies for anti amyloid-beta immunotherapy. The applicant will employ a range of molecular cloning and
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Pharmaceutical Sciences, Pharmacology, Biology, Molecular Biology, Biochemistry, Immunology, Bioengineering, Chemistry, Data Science or related fields. Post-doctorate experience preferred. Proven track record in
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research positions. We are seeking exceptionally motivated and talented individuals to join our dynamic team, dedicated to pioneering research at the intersection of HIV infection, drug abuse, mitochondrial
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there is no consistent evidence yet of increased cancer incidence [2]. It is therefore crucial to better understand the molecular responses to low dose IR (LDR) in order to improve the assessment of cancer
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own research and administrative activities, and contribute to wider project planning. The post-holder must have a first degree in Biochemistry, Molecular Biology or related biomedical sciences with
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, interdisciplinary environment. The Sen Lab focuses on the development of new treatment paradigms for clinically relevant molecular subsets of lung cancer, the leading cause of cancer mortality. The Sen Lab takes
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increased risk of cardiovascular complications. Using molecular and genetic techniques in transgenic murine models, MPN patient-derived induced pluripotent stem cell lines, and primary patient samples, we