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Fig. 5 | Molecular and Cellular Pediatrics

Fig. 5

From: Severe changes in colon epithelium in the Mecp2-null mouse model of Rett syndrome

Fig. 5

Intestinal deletion of Mecp2 does not replicate Mecp2-null intestinal phenotype. a A group of 14 Mecp2-null animals (solid line) was compared with a group of 11 Mecp2 Δ3–4/y conditional knock-out mice (dashed line). Kolmogorov–Smirnov test demonstrated a better survival rate for the conditional knock-out animals over the Mecp2-null mice, P < 0.0005. Determinations of b colon length and c surface–crypt axis length showed no differences among groups (n = 5 for wild-type, n = 9 for Mecp2 Δ3–4/y, n = 4 for Mecp2 flox/y, and n = 6 for Vil-Cre)

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