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receptor transactivation, c-fos expression, adenylyl cyclase and cAMP mediated signalling and ERK-1/2 in a variety of cell types ( Prossnitz et al . 2008 ). Intriguingly, only a small fraction of total cellular GPR30 appears to be expressed on the cell
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MAPK by ORA and ORB in H295R cells and we have examined further the precise pathway components using a combination of selective inhibitors of adenylyl cyclase (AC), protein kinase A (PKA), protein kinase C (PKC), MAPK kinase (MEK) and OX1R
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E890 –E896. Böl G-F , Gros C, Hülster A, Bösel A & Pfeuffer T 1997 Phorbol ester-induced sensitisation of adenylyl cyclase type II is related to phosphorylation of threonine 1057. Biochemical and Biophysical Research
Área de Morfología, Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis, Chacabuco 917, 5700 San Luis, Argentina
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Área de Morfología, Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis, Chacabuco 917, 5700 San Luis, Argentina
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Área de Morfología, Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis, Chacabuco 917, 5700 San Luis, Argentina
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Área de Morfología, Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis, Chacabuco 917, 5700 San Luis, Argentina
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Área de Morfología, Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis, Chacabuco 917, 5700 San Luis, Argentina
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be related to the inhibition produced by the NO of the activity of steroid synthesis-limiting enzyme, cytochrome P 450 , of the two isoforms of adenylyl cyclase, the second intracellular messenger ( McVey et al. 1999 ), and/or of the inhibition of
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of SST and cortistatin, an endogenous neuropeptide similar to SST ( Ibáñez-Costa et al . 2017 ), in primate pituitary primary cultures, which is mediated exclusively by SSTR5 through adenylyl cyclase/cAMP/protein kinase A and intracellular Ca 2
Centro de Ciências Biológicas e da Saúde, Department of Cell and Developmental Biology, School of Arts, Natural and Humans Science Center, Department of Anatomy, Division of Endocrinology, School of Physical Education and Sport, AFIP and Pathology, Universidade Presbiteriana Mackenzie, Rua da Consolação, 869 Prédio 16, 1° Andar, 01302-907 São Paulo, Brazil
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Metabolism 9 203 – 209 . doi:10.1016/j.cmet.2008.12.014 . Granneman JG 1992 Effects of agonist exposure on the coupling of β1 and β3 adrenergic receptors to adenylyl cyclase in isolated adipocytes . Journal of Pharmacology and Experimental
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LH/CG-R cDNA ( Rao 1997 , Themmen & Huhtaniemi 2000 ). The main intracellular signalling pathway activated by the LH/CG-R is the adenylyl cyclase pathway, leading to an increase in intracellular cAMP ( Dufau 1998 , Ascoli et al. 2002
University of Technology Dresden, University Clinic III, Dresden, Germany
School of Medicine, Department of Histology and Embryology, Poznan, Poland
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University of Technology Dresden, University Clinic III, Dresden, Germany
School of Medicine, Department of Histology and Embryology, Poznan, Poland
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University of Technology Dresden, University Clinic III, Dresden, Germany
School of Medicine, Department of Histology and Embryology, Poznan, Poland
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University of Technology Dresden, University Clinic III, Dresden, Germany
School of Medicine, Department of Histology and Embryology, Poznan, Poland
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University of Technology Dresden, University Clinic III, Dresden, Germany
School of Medicine, Department of Histology and Embryology, Poznan, Poland
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University of Technology Dresden, University Clinic III, Dresden, Germany
School of Medicine, Department of Histology and Embryology, Poznan, Poland
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of the adrenal gland. Many effects of ACTH are associated with the intracellular increase of cyclic AMP (cAMP). Here we demonstrate that forskolin, an activator of the adenylyl cyclase, increased both CITED2-promotor activity and mRNA levels
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& Gozes 1994 , Duncan et al . 1995 , Shinohara et al . 1995 , Cagampang et al . 1998 , Dardente et al . 2004 ). The VPAC2 receptor is a Gα s -coupled receptor that activates adenylyl cyclase, cAMP, PKA, and CRE-dependent transcription ( Fig. 4A
Department of Endocrinology, Endocrinology Division, Bart's and the London School of Medicine, Queen Mary University of London, London EC1M 6BQ, UK
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). cAMP is generated in the cytoplasm by activation of adenylyl cyclase, but it is inactivated by phosphodiesterases (PDEs). PDEs are a huge family of enzymes that catalyse the hydrolysis of cAMP and cGMP, generating the corresponding nucleotides 5′AMP and