Vascular smooth muscle cells from small human omental arteries express P2X1 and P2X4 receptor subunits
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O. Khan | O. Povstyan | M. Harhun | T. Khong | G. Vasilikostas | M. Reddy | Claire M. Nichols | A. Wan | A. Albert | D. Gordienko
[1] O. Povstyan,et al. Characterization of transcriptional and posttranscriptional properties of native and cultured phenotypically modulated vascular smooth muscle cells , 2013, Cell and Tissue Research.
[2] M. Harhun,et al. Resident phenotypically modulated vascular smooth muscle cells in healthy human arteries , 2012, Journal of cellular and molecular medicine.
[3] L. Ren,et al. P2X1 receptor-mediated pressor responses in the anesthetized mouse , 2012 .
[4] V. Ralevic. P2X receptors in the cardiovascular system , 2012 .
[5] D. Gordienko,et al. Ca2+ entry following P2X receptor activation induces IP3 receptor‐mediated Ca2+ release in myocytes from small renal arteries , 2011, British journal of pharmacology.
[6] D. Gordienko,et al. Purinoreceptor‐mediated current in myocytes from renal resistance arteries , 2010, British journal of pharmacology.
[7] E. Inscho,et al. P2X(1) receptor blockade inhibits whole kidney autoregulation of renal blood flow in vivo. , 2010, American journal of physiology. Renal physiology.
[8] R. Marée,et al. P2X1 Ion Channels Promote Neutrophil Chemotaxis through Rho Kinase Activation , 2009 .
[9] T. Bolton,et al. Interstitial cells from rat middle cerebral artery belong to smooth muscle cell type , 2008, Journal of cellular and molecular medicine.
[10] J. Brock,et al. ATP is the predominant sympathetic neurotransmitter in rat mesenteric arteries at high pressure , 2007, The Journal of physiology.
[11] V. Ralevic,et al. Raised tone reveals purinergic-mediated responses to sympathetic nerve stimulation in the rat perfused mesenteric vascular bed. , 2007, European journal of pharmacology.
[12] T. Bolton,et al. Role of intracellular stores in the regulation of rhythmical [Ca2+]i changes in interstitial cells of Cajal from rabbit portal vein. , 2006, Cell calcium.
[13] G. Burnstock,et al. P2X1 receptors are closely associated with connexin 43 in human ventricular myocardium. , 2005, International journal of cardiology.
[14] A. Nicke,et al. Biochemical and functional evidence for heteromeric assembly of P2X1 and P2X4 subunits , 2005, Journal of neurochemistry.
[15] G. Schmalzing,et al. NF449, a novel picomolar potency antagonist at human P2X1 receptors. , 2003, European journal of pharmacology.
[16] D. Erlinge,et al. Potent P2Y6 receptor mediated contractions in human cerebral arteries , 2003, BMC pharmacology.
[17] E. Schwiebert,et al. Sustained Calcium Entry through P2X Nucleotide Receptor Channels in Human Airway Epithelial Cells* , 2003, The Journal of Biological Chemistry.
[18] R. North. Molecular physiology of P2X receptors. , 2002, Physiological reviews.
[19] G. Schmalzing,et al. NF449: a subnanomolar potency antagonist at recombinant rat P2X1 receptors , 2001, Naunyn-Schmiedeberg's Archives of Pharmacology.
[20] G. Schmalzing,et al. The suramin analogue NF279 is a novel and potent antagonist selective for the P2X1 receptor , 2000, Neuropharmacology.
[21] T. Egan,et al. Hetero-oligomeric Assembly of P2X Receptor Subunits , 1999, The Journal of Biological Chemistry.
[22] GervaiseLoirand,et al. P2X7 Receptor Activation–Induced Contraction and Lysis in Human Saphenous Vein Smooth Muscle , 1998 .
[23] G Burnstock,et al. Pharmacological and histochemical evidence for P2X receptors in human umbilical vessels. , 1998, European journal of pharmacology.
[24] G. Dubyak,et al. The P2X1 receptor, an adenosine triphosphate-gated cation channel, is expressed in human platelets but not in human blood leukocytes. , 1998, Blood.
[25] J. Firth,et al. Pressure-induced myogenic responses in human isolated cerebral resistance arteries. , 1996, Stroke.
[26] W. Stühmer,et al. P2X4: an ATP-activated ionotropic receptor cloned from rat brain. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[27] R. Evans,et al. Vasoconstriction of guinea‐pig submucosal arterioles following sympathetic nerve stimulation is mediated by the release of ATP , 1992, British journal of pharmacology.
[28] G. Burnstock. Noradrenaline and ATP as cotransmitters in sympathetic nerves , 1990, Neurochemistry International.
[29] G. Burnstock. Local mechanisms of blood flow control by perivascular nerves and endothelium. , 1990, Journal of hypertension. Supplement : official journal of the International Society of Hypertension.
[30] M. Mulvany,et al. Structure and function of small arteries. , 1990, Physiological reviews.
[31] A. Somlyo. Excitation-contraction coupling and the ultrastructure of smooth muscle. , 1985, Circulation research.
[32] O. Povstyan,et al. Identification of functional P2X receptors in rat middle cerebral arteries. , 2013 .
[33] Geoffrey Burnstock,et al. Purinergic signalling , 2012, Acta physiologica.
[34] A. Nicke,et al. Monomeric and dimeric byproducts are the principal functional elements of higher order P2X1 concatamers. , 2003, Molecular pharmacology.
[35] J. Huidobro-Toro,et al. Pharmacological identification of P2X1, P2X4 and P2X7 nucleotide receptors in the smooth muscles of human umbilical cord and chorionic blood vessels. , 2003, Placenta.
[36] G. Burnstock. Purinergic nerves. , 1972, Pharmacological reviews.