A. Heding

发表

Bioluminescence Resonance Energy Transfer as a Screening Assay: Focus on Partial and Inverse Agonism

C. Elling, L. Elster, A. Heding, 2007, Journal of biomolecular screening.

NOVEL METHOD FOR THE STUDY OF RECEPTOR Ca2+ SIGNALLING EXEMPLIFIED BY THE NK1 RECEPTOR

T. Schwartz, C. Elling, A. Heding, 2002, Journal of receptor and signal transduction research.

β-Arrestin-Based Bret2 Screening Assay for the “Non”-β-Arrestin Binding CB1 Receptor

M. Vrecl, D. L. Almholt, L. Elster, 2009, Journal of biomolecular screening.

Beta-Arrestin2 as a Competitor for GRK2 Interaction with the GLP-1 Receptor upon Receptor Activation

C. Elling, Rasmus Jorgensen, A. Heding, 2011, Pharmacology.

GLP-1 Induces Barrier Protective Expression in Brunner's Glands and Regulates Colonic Inflammation

R. Søkilde, F. Pociot, L. Folkersen, 2016, Inflammatory bowel diseases.

Characterization of G-Protein Coupled Receptor Kinase Interaction with the Neurokinin-1 Receptor Using Bioluminescence Resonance Energy Transfer

T. Schwartz, C. Elling, Rasmus Jorgensen, 2008, Molecular Pharmacology.

Amino acid residues 721-729 are required for full factor VIII activity.

E. Persson, A. Heding, J. Thomsen, 1995, European journal of biochemistry.

Evidence for a role of caveolin-1 in neurokinin-1 receptor plasma-membrane localization, efficient signaling, and interaction with β-arrestin 2

M. Vrecl, M. Sentjurc, A. Heding, 2007, Cell and Tissue Research.

Development of a BRET2 Screening Assay Using β-Arrestin 2 Mutants

Rasmus Jorgensen, M. Vrecl, A. Heding, 2004 .

Arrestin 2 Mutants β Development of a BRET2 Screening Assay Using

Rasmus Jorgensen, M. Vrecl, A. Heding, 2013 .

Use of the BRET 7TM receptor/β-arrestin assay in drug discovery and screening

A. Heding, 2004 .

The Rat Gonadotropin-Releasing Hormone Receptor Internalizes via a β-Arrestin-Independent, but Dynamin-Dependent, Pathway: Addition of a Carboxyl-Terminal Tail Confers β-Arrestin Dependency.

M. Vrecl, A. Hanyaloglu, P. L. Taylor, 2000, Endocrinology.

Cooperative binding of insulin-like Peptide 3 to a dimeric relaxin family peptide receptor 2.

J. Wade, J. Nøhr, M. Vrecl, 2008, Endocrinology.

Lack of a C-terminal Tail in the Mammalian Gonadotropin-releasing Hormone Receptor Confers Resistance to Agonist-dependent Phosphorylation and Rapid Desensitization*

M. Vrecl, K. Eidne, M. Blomenröhr, 1999, The Journal of Biological Chemistry.

Biosensor Measurement of the Binding of Insulin-like Growth Factors I and II and Their Analogues to the Insulin-like Growth Factor-binding Protein-3*

R. Gill, P. De Meyts, A. Heding, 1996, The Journal of Biological Chemistry.

Negative cooperativity in H2 relaxin binding to a dimeric relaxin family peptide receptor 1

J. Wade, J. Nøhr, M. Vrecl, 2008, Molecular and Cellular Endocrinology.

Pivotal role for the cytoplasmic carboxyl-terminal tail of a nonmammalian gonadotropin-releasing hormone receptor in cell surface expression, ligand binding, and receptor phosphorylation and internalization.

R. Leurs, K. Eidne, M. Blomenröhr, 1999, Molecular pharmacology.

Internalization kinetics of the gonadotropin-releasing hormone (GnRH) receptor.

M. Vrecl, A. Hanyaloglu, P. L. Taylor, 2000, Pflugers Archiv : European journal of physiology.

Gonadotropin-releasing Hormone Receptors with Intracellular Carboxyl-terminal Tails Undergo Acute Desensitization of Total Inositol Phosphate Production and Exhibit Accelerated Internalization Kinetics*

M. Vrecl, P. L. Taylor, K. Eidne, 1998, The Journal of Biological Chemistry.

Dimerization of ADAR2 is mediated by the double-stranded RNA binding domain.

F. Nielsen, Rasmus Jorgensen, H. Poulsen, 2006, RNA.

The effect of a high-MUFA, low-glycaemic index diet and a low-fat diet on appetite and glucose metabolism during a 6-month weight maintenance period

A. Astrup, J. Holst, B. Sloth, 2008, British Journal of Nutrition.

Nonpeptide and peptide growth hormone secretagogues act both as ghrelin receptor agonist and as positive or negative allosteric modulators of ghrelin signaling.

T. Schwartz, B. Holst, A. Bach, 2005, Molecular Endocrinology.

The rat gonadotropin-releasing hormone receptor internalizes via a beta-arrestin-independent, but dynamin-dependent, pathway: addition of a carboxyl-terminal tail confers beta-arrestin dependency.

M. Vrecl, A. Hanyaloglu, P. L. Taylor, 2000, Endocrinology.

Dimerization and Negative Cooperativity in the Relaxin Family Peptide Receptors

J. Wade, J. Nøhr, M. Vrecl, 2009, Annals of the New York Academy of Sciences.

Development of a BRET2 screening assay using beta-arrestin 2 mutants.

Rasmus Jorgensen, M. Vrecl, A. Heding, 2004, Journal of biomolecular screening.

Opsin Oligomerization in a Heterologous Cell System

C. Elling, L. Drinovec, M. Vrecl, 2006, Journal of receptor and signal transduction research.

GLP-1 Induces Barrier Protective Expression in Brunner's Glands and Regulates Colonic Inflammation

F. Pociot, L. Folkersen, M. Jackerott, 2016, Inflammatory bowel diseases.