Development of a Personalized Intestinal Fibrosis Model Using Human Intestinal Organoids Derived From Induced Pluripotent Stem Cells.

Interestingly, although changes in E-cadherin and Snai1 did not reach statistical significance and Twist2 was below the limit of detection, we did observe a significant increase in Twist1, Snai2, vimentin, and N-cadherin ( Figure 5B ).

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