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We use cutting-edge techniques to discover cures for kidney disease. We culture mouse embryonic stem cells and perform gene targeting by homologous recombination. Our experience with genome modification allows us to generate unique models to interrogate disease models with precision. Crispr-Cas9 based gene editing offers genome editing with unparalleled specificity and speed. All trainees learn this technology which we apply in cell lines and stem cells. In The Humphreys Lab we are de.