Skip to main content
. Author manuscript; available in PMC: 2011 Sep 1.
Published in final edited form as: Gastroenterology. 2010 Jun 4;139(3):942–952. doi: 10.1053/j.gastro.2010.05.083

Figure 6. ICC stem cells are hyperplastic in KitK641E mice but unaffected by hypomorphic Kit (W/Wv) and Kitl (Sl/Sld) mutations or imatinib treatment.

Figure 6

(A) 14–16-day-old KitK641E mice. (B) Adult W/Wv mice. (C) Adult Sl/Sld mice. +/+: age- and strain-matched, wild-type controls. Box plots show median and interquartile range; n=3–4/group. The frequency of ICC and ICC progenitors was higher in juvenile wild-type littermates of the KitK641E mice than in the adult wild-type controls for the hypomorphic mutants. (D) Effects of 28-day in vivo imatinib treatment on ICC and precursors in adult KitK641E/+ mice lacking the neomycin resistance cassette (n=3/group).

HHS Vulnerability Disclosure