Publications

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2012
Coutinho AE, Gray M, Brownstein DG, Salter DM, Sawatzky DA, Clay S, et al. 11β-Hydroxysteroid dehydrogenase type 1, but not type 2, deficiency worsens acute inflammation and experimental arthritis in mice. Endocrinology. 2012;153(1):234-40. Abstract
2011
Jamieson PM, Cleasby ME, Kuperman Y, Morton NM, Kelly PA, Brownstein DG, et al. Urocortin 3 transgenic mice exhibit a metabolically favourable phenotype resisting obesity and hyperglycaemia on a high-fat diet. Diabetologia. 2011. Abstract
Veloso GF, Ohad DG, Francis AJ, Vaughan JM, Brownstein DG, Culshaw GJ, et al. Expression of urocortin peptides in canine myocardium and plasma. Vet J. 2011;188(3):318-24. Abstract
Deuchar GA, McLean D, Hadoke PW, Brownstein DG, Webb DJ, Mullins JJ, et al. 11β-hydroxysteroid dehydrogenase type 2 deficiency accelerates atherogenesis and causes proinflammatory changes in the endothelium in apoe-/- mice. Endocrinology. 2011;152(1):236-46. Abstract
2010
Van Agtmael T, Bailey MA, Schlötzer-Schrehardt U, Craigie E, Jackson IJ, Brownstein DG, et al. 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. Abstract
2009
Mullins LJ, Peter A, Wrobel N, McNeilly JR, McNeilly AS, Al-Dujaili EA, et al. Cyp11b1 null mouse, a model of congenital adrenal hyperplasia. The Journal of biological chemistry. 2009;284:3925-34. Abstract
Semprini S, Friedrichsen S, Harper CV, McNeilly JR, Adamson AD, Spiller DG, et al. 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. Abstract
2008
Michailidou Z, Carter RN, Marshall E, Sutherland HG, Brownstein DG, Owen E, et al. 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. Abstract
Patek CE, Brownstein DG, Fleming S, Wroe C, Rose L, Webb A, et al. Effects on kidney disease, fertility and development in mice inheriting a protein-truncating Denys-Drash syndrome allele (Wt1tmT396). Transgenic research. 2008;17:459-75. Abstract
Bailey MA, Paterson JM, Hadoke PW, Wrobel N, Bellamy CO, Brownstein DG, et al. 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. Abstract
2007
Newbery HJ, Loh DH, O’Donoghue JE, Tomlinson VA, Chau Y-, Boyd JA, et al. Translation elongation factor eEF1A2 is essential for post-weaning survival in mice. The Journal of biological chemistry. 2007;282:28951-9. Abstract
2005
Van Agtmael T, Schlötzer-Schrehardt U, McKie L, Brownstein DG, Lee AW, Cross SH, et al. Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy. Human molecular genetics. 2005;14:3161-8. Abstract
2004
Pall GS, Wallis J, Axton R, Brownstein DG, Gautier P, Buerger K, et al. A novel transmembrane MSP-containing protein that plays a role in right ventricle development. Genomics. 2004;84(6):1051-9. Abstract