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de Vries A, Engels F, Henricks PA, Leusink-Muis T, McGregor GP, Braun A, et al. Airway hyper-responsiveness in allergic asthma in guinea-pigs is mediated by nerve growth factor via the induction of substance P: a potential role for trkA. Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology. 2006;36:1192-200. Abstract
de Vries A, Hazlewood L, Fitch PM, Seckl JR, Foster P, Howie SE. High-fat feeding redirects cytokine responses and decreases allergic airway eosinophilia. Clin Exp Allergy. 2009;39(5):731-9. Abstract
de Vries A, Holmes MC, Heijnis A, Seier JV, Heerden J, Louw J, et al. Prenatal dexamethasone exposure induces changes in nonhuman primate offspring cardiometabolic and hypothalamic-pituitary-adrenal axis function. The Journal of clinical investigation. 2007;117:1058-67. Abstract
de Vries A, Hazlewood L, Fitch PM, Seckl JR, Foster P, Howie SE. High-fat feeding redirects cytokine responses and decreases allergic airway eosinophilia. Clin Exp Allergy. 2009;39(5):731-9. Abstract
Voight BF, Peloso GM, Orho-Melander M, Frikke-Schmidt R, Barbalic M, Jensen MK, et al. Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study. Lancet. 2012. Abstract
Voight BF, Scott LJ, Steinthorsdottir V, Morris AP, Dina C, Welch RP, et al. Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat Genet. 2010;42(7):579-89. Abstract
Voice MW, Seckl JR, Chapman KE. The sequence of 5' flanking DNA from the mouse 11 beta-hydroxysteroid dehydrogenase type 1 gene and analysis of putative transcription factor binding sites. Gene. 1996;181(1-2):233-5. Abstract
Voice MW, Seckl JR, Edwards CR, Chapman KE. 11 beta-hydroxysteroid dehydrogenase type 1 expression in 2S FAZA hepatoma cells is hormonally regulated: a model system for the study of hepatic glucocorticoid metabolism. Biochem J. 1996;317 ( Pt 2):621-5. Abstract
Vitart V, Rudan I, Hayward C, Gray NK, Floyd J, Palmer CN, et al. SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout. Nat Genet. 2008;40(4):437-42. Abstract
Vitart V, Bencić G, Hayward C, Skunca Herman J, Huffman J, Campbell S, et al. New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8. Hum Mol Genet. 2010;19(21):4304-11. Abstract
Venkatasubramanian S, Newby DE, Lang NN. Urocortins in heart failure. Biochem Pharmacol. 2010;80(3):289-96. Abstract
Véniant M, Gray GA, Heudes D, Ménard J, Clozel JP. Structural changes and cyclic GMP content of the aorta after calcium antagonism or angiotensin converting enzyme inhibition in renovascular hypertensive rats. J Hypertens. 1995;13(7):731-7. Abstract
Véniant M, Ménard J, Bruneval P, Morley S, Gonzales MF, Mullins J. Vascular damage without hypertension in transgenic rats expressing prorenin exclusively in the liver. The Journal of clinical investigation. 1996;98:1966-70. Abstract
Véniant M, Whitworth CE, Ménard J, Sharp MG, Gonzales MF, Bruneval P, et al. Developmental studies demonstrate age-dependent elevation of renin activity in TGR(mRen2)27 rats. American journal of hypertension. 1995;8:1167-76. Abstract
Venetucci LA, Trafford AW, Díaz ME, O'Neill SC, Eisner DA. Reducing ryanodine receptor open probability as a means to abolish spontaneous Ca2+ release and increase Ca2+ transient amplitude in adult ventricular myocytes. Circ Res. 2006;98(10):1299-305. 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
Velders FP, Kuningas M, Kumari M, Dekker MJ, Uitterlinden AG, Kirschbaum C, et al. Genetics of cortisol secretion and depressive symptoms: A candidate gene and genome wide association approach. Psychoneuroendocrinology. 2011. Abstract
Vass S, Cotterill S, Valdeolmillos AM, Barbero JL, Lin E, Warren WD, et al. Depletion of Drad21/Scc1 in Drosophila cells leads to instability of the cohesin complex and disruption of mitotic progression. Curr Biol. 2003;13(3):208-18. Abstract
Vanourková Z, Kramer HJ, Husková Z, Vanecková I, Opocenský M, Chábová VC, et al. AT1 receptor blockade is superior to conventional triple therapy in protecting against end-organ damage in Cyp1a1-Ren-2 transgenic rats with inducible hypertension. J Hypertens. 2006;24(12):2465-72. Abstract
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
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
Valdeolmillos AM, Viera A, Page J, Prieto I, Santos JL, Parra MT, et al. Sequential loading of cohesin subunits during the first meiotic prophase of grasshoppers. PLoS Genet. 2007;3(2):e28. Abstract
Valdeolmillos A, Rufas JS, Suja JA, Vass S, Heck MM, Martínez-A C, et al. Drosophila cohesins DSA1 and Drad21 persist and colocalize along the centromeric heterochromatin during mitosis. Biol Cell. 2004;96(6):457-62. Abstract