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genomics and single-cell spatial transcriptomics, participate in T cell-targeted therapy development, hone their computational, leadership, communication, and funding acquisition skills, and join the vibrant
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leads that target undrugged proteins or proteins prone to drug resistance. 3. Combining mass spectrometry with genetic perturbations to mechanistically define protein function. 4. Developing automation
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and severe complication following hematopoietic stem cell transplantation. Our group works on developing targeted tools which abrogate impairments in mitochondrial dynamics as therapeutic candidates
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to treat malignant brain cancer glioblastoma. Part of our work centers on targeting EGFRvIII, which is splice variant of EGFR and is highly expressed in these tumors. Recently, we demonstrated a tyrosine
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biochemistry and biophysics directed at the discovery and development of new antibacterial therapeutics targeting difficult-to-treat bacteria. More broadly and coupled to drug discovery, we define the molecular
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responsibilities include: Leading experiments to optimize Cas9/gRNA complex delivery into oocytes of diverse marine phyla, potentially utilizing techniques like microinjection or targeted incubation. Developing and
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School of Medicine. The project will focus on optimization of peptide ligands targeting promising cancer antigens followed by subsequent radiolabeling and pre-clinical validation. The Beinat lab employs
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. This is a two-year position that is targeted at applicants who are preparing for an academic career at a leading research university. The Fellow is expected to start this position in Fall 2025
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developmental challenges. Research in this area is critical for developing targeted therapies and improving patient outcomes. Position Overview: The selected candidate will be responsible for analyzing large
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will primarily rely on perturbation assay via targeted treatments and manipulation of gene expression in cell culture, and patient-derived models. Required Qualifications: The ideal candidate should have