Filters: Author is Brownstein, D G [Clear All Filters]
Glucocorticoid receptor is required for foetal heart maturation. Hum Mol Genet. 2013;22(16):3269-82.
Mast cells express 11β-hydroxysteroid dehydrogenase type 1: a role in restraining mast cell degranulation. PLoS ONE. 2013;8(1):e54640.
11β-Hydroxysteroid dehydrogenase type 1, but not type 2, deficiency worsens acute inflammation and experimental arthritis in mice. Endocrinology. 2012;153(1):234-40.
Expression of urocortin peptides in canine myocardium and plasma. Vet J. 2011;188(3):318-24.
Col4a1 mutation in mice causes defects in vascular function and low blood pressure associated with reduced red blood cell volume. Human molecular genetics. 2010;19:1119-28.
Cyp11b1 null mouse, a model of congenital adrenal hyperplasia. The Journal of biological chemistry. 2009;284:3925-34.
Real-time visualization of human prolactin alternate promoter usage in vivo using a double-transgenic rat model. Molecular endocrinology (Baltimore, Md.). 2009;23:529-38.
Glucocorticoid receptor haploinsufficiency causes hypertension and attenuates hypothalamic-pituitary-adrenal axis and blood pressure adaptions to high-fat diet. The FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 2008;22:3896-907.
Effects on kidney disease, fertility and development in mice inheriting a protein-truncating Denys-Drash syndrome allele (Wt1tmT396). Transgenic research. 2008;17:459-75.
A switch in the mechanism of hypertension in the syndrome of apparent mineralocorticoid excess. Journal of the American Society of Nephrology : JASN. 2008;19:47-58.
Translation elongation factor eEF1A2 is essential for post-weaning survival in mice. The Journal of biological chemistry. 2007;282:28951-9.
Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy. Human molecular genetics. 2005;14:3161-8.