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Field
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is supported by NIH funding and sits within a rich collaborative network at Yale, including the Yale Cancer Center, the Yale Stem Cell Center, the Wu Tsai Institute, and computational collaborators in
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has studied B cell fate, function and dysfunction after allogeneic stem cell transplantation (SCT). Our studies also aim to identify potential anti-tumor B cell activity in patients who have undergone
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Yale School of Medicine - Department of Genetics | New Haven, Connecticut | United States | about 2 months ago
. The position is supported by NIH funding and sits within a rich collaborative network at Yale, including the Yale Cancer Center, the Yale Stem Cell Center, the Wu Tsai Institute, and computational collaborators
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research program in immune metabolism, hematopoietic stem cell transplantation, and next-generation cellular immunotherapies. Our group combines cutting-edge basic immunology with investigator-initiated
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. or equivalent doctorate (e.g. Sc.D., M.D., D.V.M.) Preferred Qualifications:. A PhD or MD/PhD (or equivalent) in biological sciences Strong research background in cell biology, molecular biology, mouse models
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Skills/Qualifications WHAT WE NEED • PhD in Cell Biology, Developmental Biology, Stem Cell Biology or a related discipline. • Strong hands-on expertise in human hematopoietic and pluripotent stem cell
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microscopy, HSC transplantation and assays of multiple organs. Required skills: PhD in hematology, hematopoietic stem cell biology, aging biology or a related field At least one first-author publication in a
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targeted by T cells mediating Graft-versus-Host Disease (GvHD) and Graft-versus-Leukaemia (GvL) following stem cell transplantation (SCT) as a treatment for blood cancers. In this role you will carry out
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, or MD/PhD. in Immunology, Hematology, Stem Cell Biology, Molecular Biology, Genetics, or a related field. Demonstrated research productivity and the ability to conduct independent scientific research
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chromatin regulatory mechanisms are also essential. Experience with mouse embryonic stem cells, inducible protein degradation systems, high-resolution chromosome conformation capture approaches such as Micro