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Publication : Intestinal secretory defects and dwarfism in mice lacking cGMP-dependent protein kinase II.

First Author  Pfeifer A Year  1996
Journal  Science Volume  274
Issue  5295 Pages  2082-6
PubMed ID  8953039 Mgi Jnum  J:37306
Mgi Id  MGI:84708 Doi  10.1126/science.274.5295.2082
Citation  Pfeifer A, et al. (1996) Intestinal secretory defects and dwarfism in mice lacking cGMP-dependent protein kinase II. Science 274(5295):2082-6
abstractText  Cyclic guanosine 3',5'-monophosphate (cGMP)-dependent protein kinases (cGKs) mediate cellular signaling induced by nitric oxide and cGMP. Mice deficient in the type II cGK were resistant to Escherichia coli STa, an enterotoxin that stimulates cGMP accumulation and intestinal fluid secretion. The cGKII-deficient mice also developed dwarfism that was caused by a severe defect in endochondral ossification at the growth plates. These results indicate that cGKII plays a central role in diverse physiological processes.
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