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University of California, Los Angeles | Los Angeles, California | United States | about 2 months ago
California, Los Angeles to investigate corneal stem cells and corneal diseases with an emphasis on translational application and therapeutic development. The Cornea Biology Laboratory, under the direction
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therapeutic interventions. The core program is to translate AD genetics and functional genomics into human brain cells both in vitro 2D and 3D models using human induced pluripotent stem cells (hiPSCs
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within the Stanford University School of Medicine's Department of Radiation Oncology. The laboratory applies in vitro and in vivo experimental techniques to study normal and malignant stem cells in
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become: effector cells, regulatory cells, or long-lived stem-like TCF1⁺ cells that sustain immunity. How DCs direct these outcomes is still poorly understood. Our lab studies human DC biology and
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postdocs always work collaboratively together in teams towards common goals to ensure that no one is left to work alone on a project. Our labs are located in the Center for stem cell medicine ( https
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interested in studying the role of cell-biomaterial interactions that 1) mediate differentiation of induced pluripotent stem cells into cardiovascular lineages, and 2) biomaterials that mediate
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treatment of some leukaemias, but current therapies remain expensive, complex to manufacture and tailored to individual patients. Differentiation of human pluripotent stem cells (PSCs) offers a promising
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post-mortem brain samples and stem cell derived brain cells from patients with Parkinson’s Disease in order to identify lipid changes associated with the disease pathology. Information on the
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Yale School of Medicine - Department of Genetics | New Haven, Connecticut | United States | 19 days ago
, uterus/embryo), mammary gland, brain, bone marrow, skin or tumours. No prior lung experience is required. We study how stem cells change identity after injury and how this plasticity can lead to
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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