Article
Developmental defects and rescue from glucose intolerance of a catalytically-inactive novel Ship2 mutant mouse.
Cellular signalling - 1 Nov 2012
Dubois Eléonore, Jacoby Monique, Blockmans Marianne, Pernot Eileen, Schiffmann Serge N, Foukas Lazaros C, Henquin Jean-Claude, Vanhaesebroeck Bart, Erneux Christophe, Schurmans Stéphane
Abstract excerpt
The function of the phosphoinositide 5-phosphatase Ship2 was investigated in a new mouse model expressing a germline catalytically-inactive Ship2(∆/∆) mutant protein. Ship2(∆/∆) mice were viable with defects in somatic growth and in development of muscle, adipose tissue and female genital tract. Lipid metabolism and insulin secretion were also affected in these mice, but glucose tolerance, insulin sensitivity and...
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