Signal transduction, Beta-Arrestins, Cell biology, G protein-coupled receptor kinase and Protein kinase A are his primary areas of study. His Signal transduction research integrates issues from Receptor, Internalization and Neuroscience. His work in Beta-Arrestins addresses subjects such as Heterotrimeric G protein, which are connected to disciplines such as RHOA and Gq alpha subunit.
The G protein-coupled receptor kinase study combines topics in areas such as Arrestin, Molecular biology and 5-HT5A receptor. His research investigates the connection between Molecular biology and topics such as Beta adrenergic receptor kinase that intersect with issues in MAPK/ERK pathway. The various areas that Eric Reiter examines in his Protein kinase A study include Angiotensin II and Pertussis toxin.
His primary areas of investigation include Cell biology, Receptor, Internal medicine, Endocrinology and G protein-coupled receptor. Signal transduction, Arrestin, G protein and Heterotrimeric G protein are the primary areas of interest in his Cell biology study. Eric Reiter has included themes like Molecular biology and Protein phosphorylation, Protein kinase A in his Signal transduction study.
His studies deal with areas such as Mutant and Northern blot as well as Internal medicine. His research in G protein-coupled receptor is mostly concerned with G protein-coupled receptor kinase. His G protein-coupled receptor kinase study combines topics in areas such as 5-HT5A receptor and Beta adrenergic receptor kinase.
His main research concerns Cell biology, Receptor, Follicle-stimulating hormone receptor, Internal medicine and Endocrinology. His Signal transduction, G protein and G protein-coupled receptor study are his primary interests in Cell biology. His studies in Signal transduction integrate themes in fields like Autocrine signalling, Paracrine signalling and Protein kinase A.
His study in G protein-coupled receptor is interdisciplinary in nature, drawing from both Biophysics, Regulation of gene expression, Internalization and Gene regulatory network. Eric Reiter combines subjects such as Gene expression and Cellular differentiation with his study of Receptor. His work carried out in the field of Internal medicine brings together such families of science as Mutant and Protein kinase A signaling.
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β-Arrestin-dependent, G Protein-independent ERK1/2 Activation by the β2 Adrenergic Receptor
Sudha K. Shenoy;Matthew T. Drake;Christopher D. Nelson;Daniel A. Houtz.
Journal of Biological Chemistry (2006)
GRKs and β-arrestins: roles in receptor silencing, trafficking and signaling
Eric Reiter;Robert J. Lefkowitz;Robert J. Lefkowitz.
Trends in Endocrinology and Metabolism (2006)
Molecular Mechanism of β-Arrestin-Biased Agonism at Seven-Transmembrane Receptors
Eric Reiter;Seungkirl Ahn;Arun K. Shukla;Robert J. Lefkowitz.
Annual Review of Pharmacology and Toxicology (2012)
Distinct β-arrestin- and G protein-dependent pathways for parathyroid hormone receptor-stimulated ERK1/2 activation
Diane Gesty-Palmer;Minyong Chen;Eric Reiter;Seungkirl Ahn.
Journal of Biological Chemistry (2006)
Functional antagonism of different G protein-coupled receptor kinases for β-arrestin-mediated angiotensin II receptor signaling
Jihee Kim;Seungkirl Ahn;Xiu Rong Ren;Erin J. Whalen.
Proceedings of the National Academy of Sciences of the United States of America (2005)
Different G protein-coupled receptor kinases govern G protein and β-arrestin-mediated signaling of V2 vasopressin receptor
Xiu-Rong Ren;Eric Reiter;Seungkirl Ahn;Jihee Kim.
Proceedings of the National Academy of Sciences of the United States of America (2005)
β-Arrestin 1 and Gαq/11 Coordinately Activate RhoA and Stress Fiber Formation following Receptor Stimulation
William G. Barnes;Eric Reiter;Eric Reiter;Jonathan D. Violin;Xiu-Rong Ren.
Journal of Biological Chemistry (2005)
The ERK-dependent signalling is stage-specifically modulated by FSH, during primary Sertoli cell maturation.
Pascale Crépieux;Sébastien Marion;Nadine Martinat;Véronique Fafeur.
Oncogene (2001)
A Phosphorylation Cluster of Five Serine and Threonine Residues in the C-Terminus of the Follicle-Stimulating Hormone Receptor Is Important for Desensitization But Not for β-Arrestin-Mediated ERK Activation
Elodie Kara;Pascale Crépieux;Christophe Gauthier;Nadine Martinat.
Molecular Endocrinology (2006)
β-Arrestin 2-dependent angiotensin II type 1A receptor-mediated pathway of chemotaxis
Dacia L. Hunton;William G. Barnes;Jihee Kim;Xiu-Rong Ren.
Molecular Pharmacology (2005)
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