CFTR is a tumor suppressor gene in murine and human intestinal cancer [microarray]
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ABSTRACT: Analysis of the cystic fibrosis gene Cftr in the colon and small intestine of Cftr-deficient murine model. The hypothesis was loss of Cftr altered expression of genes important in intestinal homeostasis and oncogenic signaling pathways. The results identified potential roles of Cftr in up- or down-regulating major gene clusters that belong to groups of immune response, ion channel, intestinal stem cell and other growth regulators.
ORGANISM(S): Mus musculus
PROVIDER: GSE75996 | GEO | 2015/12/15
SECONDARY ACCESSION(S): PRJNA305920
REPOSITORIES: GEO
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