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stress affects specific cell types in the nervous system and the gut, using human pluripotent stem cell (hPSC)-derived models of the enteric nervous system. Our work sits at the intersection of stem cell
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molecular structures during normal and leukemic stem cell differentiation. Integrated in the translational research environment at the Center for Hematology and Regenerative Medicine at the Karolinska
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University of California, Los Angeles | Los Angeles, California | United States | about 18 hours ago
Skip to main content Recruit Home Open Recruitments UCLA Broad Stem Cell Research Center Tenure Track Assistant to Associate Professor (JPF11124) UCLA Broad Stem Cell Research Center Tenure Track
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Fully Funded PhD Position: Decoding Chromosome 1 Risk in AMD Using Stem Cell–Derived Retinal Models Host: Newcastle University (UNEW), UK Consortium: MSCA Innovative Training Network Pandora Start date
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it compares with the aneuploidy seen in cancer. This position generates the core experimental data for that work: maintaining human trophoblast stem cell, organoid, and cancer cell line cultures
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microphysiological systems (MPS), are rapidly emerging as transformative and strategic technologies with the potential to redefine the future of health and life sciences. By integrating stem cell biology, patient
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laboratory (http://www.garglab.org ) uses approaches from genomics, molecular biology, systems biology, and data science to understand cellular heterogeneity. We want to understand how cell systems with
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encephalitis, and related neurological disorders. The project combines human induced pluripotent stem cell (hiPSC) technology, brain organoids, genome engineering, advanced imaging, systems immunology, and high
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secondments (lab exchanges). The doctoral candidate will utilize cutting-edge techniques: Cell and tissue culture (human primary and stem cell-derived retinal models) Molecular biology and biochemistry
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Albert Einstein College of Medicine (Bronx, NY) | New York City, New York | United States | 3 days ago
investigating how environmental exposures and inflammation drive hematopoietic stem cell dysfunction, clonal hematopoiesis, and the development of blood and prostate cancers. Our research bridges basic