MARIA DOLORES
IVORRA INSA
CATEDRÁTICO/A DE UNIVERSIDAD
MARIA ANTONIA
NOGUERA ROMERO
CATEDRÁTICO/A DE UNIVERSIDAD
Publicacións nas que colabora con MARIA ANTONIA NOGUERA ROMERO (32)
2021
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NT3/TrkC Pathway Modulates the Expression of UCP-1 and Adipocyte Size in Human and Rodent Adipose Tissue
Frontiers in Endocrinology, Vol. 12
2017
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Activation of α1A-adrenoceptors desensitizes the rat aorta response to phenylephrine through a neuronal NOS pathway, a mechanism lost with ageing
British Journal of Pharmacology, Vol. 174, Núm. 13, pp. 2015-2030
2015
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β2-and β1-adrenoceptor expression exhibits a common regulatory pattern with GRK2 and GRK5 in human and animal models of cardiovascular diseases
Journal of Cardiovascular Pharmacology, Vol. 66, Núm. 5, pp. 478-486
2014
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Action of an extract from the seeds of Fraxinus excelsior L. on metabolic disorders in hypertensive and obese animal models
Food and Function, Vol. 5, Núm. 4, pp. 786-796
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Changes in adrenoceptors and G-protein-coupled receptor kinase 2 in L-NAME-induced hypertension compared to spontaneous hypertension in rats
Journal of Vascular Research, Vol. 51, Núm. 3, pp. 209-220
2013
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Different β-adrenoceptor subtypes coupling to cAMP or NO/cGMP pathways: Implications in the relaxant response of rat conductance and resistance vessels
British Journal of Pharmacology, Vol. 169, Núm. 2, pp. 413-425
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α1D-Adrenoceptors are responsible for the high sensitivity and the slow time-course of noradrenaline-mediated contraction in conductance arteries
Pharmacology Research and Perspectives, Vol. 1, Núm. 1
2005
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8-NH2-boldine, an antagonist of α1A and α1B adrenoceptors without affinity for the α1D subtype: Structural requirements for aporphines at α1- adrenoceptor subtypes
Planta Medica, Vol. 71, Núm. 10, pp. 897-903
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Acute and chronic captopril, but not prazosin or nifedipine, normalize alterations in adrenergic intracellular Ca2+ handling observed in the mesenteric arterial tree of spontaneously hypertensive rats
Journal of Pharmacology and Experimental Therapeutics, Vol. 313, Núm. 1, pp. 359-367
2004
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Vascular activity of (-)-anonaine, (-)-roemerine and (-)-pukateine, three natural 6a(R)-1,2-methylenedioxyaporphines with different affinities for α1-adrenoceptor subtypes
Planta Medica, Vol. 70, Núm. 7, pp. 603-609
2003
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Cytosolic Ca2+ and phosphoinositide hydrolysis linked to constitutively active α1D-adrenoceptors in vascular smooth muscle
Journal of Pharmacology and Experimental Therapeutics, Vol. 305, Núm. 3, pp. 1006-1014
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Functional characterization of α1-adrenoceptor subtypes in vascular tissues using different experimental approaches: A comparative study
British Journal of Pharmacology, Vol. 138, Núm. 2, pp. 359-368
2002
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Modulatory role of a constitutively active population of α1d-adrenoceptors in conductance arteries
American Journal of Physiology - Heart and Circulatory Physiology, Vol. 282, Núm. 2 51-2
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Pathological role of a constitutively active population of α1d-adrenoceptors in arteries of spontaneously hypertensive rats
British Journal of Pharmacology, Vol. 135, Núm. 1, pp. 206-216
2001
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Role of cyclic nucleotide phosphodiesterase isoenzymes in contractile responses of denuded rat aorta related to various Ca2+ sources
Naunyn-Schmiedeberg's Archives of Pharmacology, Vol. 363, Núm. 6, pp. 612-619
2000
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Functional evidence of a constitutively active population of α(1D)-adrenoceptors in rat aorta
Journal of Pharmacology and Experimental Therapeutics, Vol. 295, Núm. 2, pp. 810-817
1999
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Effect of divalent cations on KCl- and noradrenaline-induced contractile responses in rat aorta after nifedipine treatment
General Pharmacology, Vol. 33, Núm. 1, pp. 43-50
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Halogenated derivatives of boldine with high selectivity for α(1A)- adrenoceptors in rat cerebral cortex
Life Sciences, Vol. 64, Núm. 14, pp. 1205-1214
1998
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Characterization of two different Ca2+ entry pathways dependent on depletion of internal Ca2+ pools in rat aorta
Naunyn-Schmiedeberg's Archives of Pharmacology, Vol. 357, Núm. 2, pp. 92-99
1997
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Capacitative Ca2+ entry associated with α1-adrenoceptors in rat aorta
Naunyn-Schmiedeberg's Archives of Pharmacology, Vol. 356, Núm. 1, pp. 83-89