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1 Department of Molecular and Cellular Physiology, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
2 Biology Department, University of Puerto Rico-Río Piedras, San Juan, Puerto Rico.
3 Department of Pediatrics, W.F. Maternal & Child Health Hospital, 76 Qingnian Road, Weifang, 261011, People's Republic of China.
4 Department of Internal Medicine, University of Cincinnati, Cincinnati, OH, USA.
5 Department of Molecular and Cellular Physiology, University of Cincinnati College of Medicine, 231 Albert B. Sabin Way, Room 4255 MSB, Cincinnati, OH, 45267-0576, USA. yana.zavros@uc.edu.
1 Department of Molecular and Cellular Physiology, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
2 Biology Department, University of Puerto Rico-Río Piedras, San Juan, Puerto Rico.
3 Department of Pediatrics, W.F. Maternal & Child Health Hospital, 76 Qingnian Road, Weifang, 261011, People's Republic of China.
4 Department of Internal Medicine, University of Cincinnati, Cincinnati, OH, USA.
5 Department of Molecular and Cellular Physiology, University of Cincinnati College of Medicine, 231 Albert B. Sabin Way, Room 4255 MSB, Cincinnati, OH, 45267-0576, USA. yana.zavros@uc.edu.
The culture of organoids has represented a significant advancement in the gastrointestinal research field. Previous research studies have described the oncogenic transformation of human intestinal and mouse gastric organoids. Here we detail the protocol for the oncogenic transformation and orthotopic transplantation of human-derived gastric organoids.
Keywords:
CRISPR/Cas-9; Human fundic gastric organoids; Nucleofection; Organoid orthotopic transplantation.
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