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experience with mammalian cell culture, protein expression (E. coli, yeast, and mammalian cells) and purification, and/or Drosophila genetics, including dissection, immunostaining, and confocal microscopy
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Be You. At Duke, we celebrate individuality and the unique perspectives that each member of our community brings. As the Postdoctoral Associate, you will join a collaborative and innovative research
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glioblastoma models, cerebral organoids and single-cell epigenomics to understand how epigenetic heterogeneity drives treatment resistance and recurrence. The post holder will lead the experimental programme
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cell division counting in mice and humans to investigate the differentiation of individual stem and progenitor cells. In the longer term, our results will improve understanding of healthy hematopoieisis
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pathways that regulate hematopoiesis. Our current research focuses are: 1) Study of epigenetic modulation in hematopoietic stem cell differentiation using genome wide and single cell RNA seq analysis; 2
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Infrastructure? No Offer Description The characteristic feature of several B-cell lymphomas are translocations involving the immunoglobulin heavy chain (IGH) locus and oncogenes such as MYC, BCL2, BCL6, CCND1. As
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, the Post Doctoral Associate promotes institutional recognition through literal contributions to the scientific community. CORE JOB FUNCTIONS 1. Conducts research on specific areas of study as assigned. 2
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development. Research Areas Research projects may include: Vaccine-induced CD8⁺ and CD4⁺ T-cell immunity Innate immune regulation of adaptive responses Immune correlates of protection against malaria
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. The project focuses on developing and applying single-cell multi-omics approaches to uncover regulators acting upstream of known epigenetic writers and erasers during embryonic development. Expected start date
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fundamental biological processes, including cell–cell communication, pathogen recognition, and receptor-mediated signaling. Emerging evidence suggests that these newly identified surface molecules form