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1. Full Text Allosteric enhancers, allosteric agonists and ago-allosteric modulators: where do they bind and how do they act?
by Schwartz, Thue W and Holst, Birgitte
Trends in Pharmacological Sciences, ISSN 0165-6147, 2007, Volume 28, Issue 8, pp. 366 - 373
Many small-molecule agonists also display allosteric properties. Such ago-allosteric modulators act as co-agonists, providing additive efficacy – instead of... 
Advanced Basic Science | MOLECULAR-MECHANISM | ADENOSINE RECEPTORS | ACTIVATION | 7TM RECEPTORS | STRUCTURAL REQUIREMENTS | TRANSMEMBRANE DOMAINS | PHARMACOLOGY & PHARMACY | NK1 RECEPTOR | G-PROTEIN | GABA(B) RECEPTOR | MUSCARINIC ACETYLCHOLINE-RECEPTORS | Pharmaceutical Preparations - metabolism | Models, Biological | Receptors, GABA - chemistry | gamma-Aminobutyric Acid - metabolism | Allosteric Regulation | Humans | Pharmaceutical Preparations - chemistry | Receptors, GABA - metabolism | gamma-Aminobutyric Acid - chemistry | Protein Binding | Ligands | Binding Sites | Allosteric proteins | Chemical properties | Agonists (Biochemistry)
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2. Full Text Exosomal Proteins as Diagnostic Biomarkers in Lung Cancer
by Sandfeld-Paulsen, Birgitte and Jakobsen, Kristine Raaby and Bæk, Rikke and Folkersen, Birgitte Holst and Rasmussen, Torben Riis and Meldgaard, Peter and Varming, Kim and Jørgensen, Malene Møller and Sorensen, Boe Sandahl
Journal of Thoracic Oncology, ISSN 1556-0864, 10/2016, Volume 11, Issue 10, pp. 1701 - 1710
Exosomes have been suggested as promising biomarkers in NSCLC because they contain proteins from their originating cells and are readily available in plasma.... 
Diagnostic | EV array | Exosomes | Lung cancer | Prospective Studies | Humans | Middle Aged | Lung Neoplasms - pathology | Male | Proteins - genetics | Aged, 80 and over | Biomarkers, Tumor - metabolism | Adult | Female | Aged | Lung Neoplasms - diagnosis | Cohort Studies
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3. Full Text Modulation of the Constitutive Activity of the Ghrelin Receptor by Use of Pharmacological Tools and Mutagenesis
by Mokrosiński, Jacek and Holst, Birgitte
2010, ISBN 9780123812988, Volume 484, Issue C
Ghrelin and its receptor are important regulators of metabolic functions, including appetite, energy expenditure, fat accumulation, and growth hormone (GH)... 
Animals | Enzyme-Linked Immunosorbent Assay | Mutagenesis | Receptors, Ghrelin - agonists | Humans | Receptors, Ghrelin - metabolism | Structure-Activity Relationship | Mutation | Inositol Phosphates - metabolism | Receptors, Ghrelin - chemistry | Receptors, Ghrelin - genetics
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4. Full Text Gene Expression of the EGF System—a Prognostic Model in Non–Small Cell Lung Cancer Patients Without Activating EGFR Mutations
by Sandfeld-Paulsen, Birgitte and Folkersen, Birgitte Holst and Rasmussen, Torben Riis and Meldgaard, Peter and Sorensen, Boe S
Translational Oncology, ISSN 1936-5233, 2016, Volume 9, Issue 4, pp. 306 - 312
Abstract OBJECTIVES: Contradicting results have been demonstrated for the expression of the epidermal growth factor receptor ( EGFR ) as a prognostic marker in... 
Oncology | SURVIVAL | GROWTH-FACTOR RECEPTOR | OVEREXPRESSION | GEFITINIB | EPIREGULIN | ONCOLOGY | ADENOCARCINOMA
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5. Full Text Effects of PYY1–36 and PYY3–36 on appetite, energy intake, energy expenditure, glucose and fat metabolism in obese and lean subjects
by Birgitte Sloth and Jens Juul Holst and Anne Flint and Nikolaj Ture Gregersen and Arne Astrup
American Journal of Physiology - Endocrinology And Metabolism, ISSN 0193-1849, 04/2007, Volume 292, Issue 4, pp. 1062 - 1068
Peptide YY (PYY)3–36 has been shown to produce dramatic reductions in energy intake (EI), but no human data exist regarding energy expenditure (EE), glucose... 
Peptide YY | Insulin sensitivity | Arcuate nucleus | Neuropeptide Y receptors | Free fatty acids | INHIBITS FOOD-INTAKE | YY3-36 | PHYSIOLOGY | PEPTIDE YY PYY | HEALTHY-SUBJECTS | RECEPTOR | free fatty acids | SERUM | GUT HORMONE | RELEASE | insulin sensitivity | arcuate nucleus | PLASMA | neuropeptide Y receptors | ENDOCRINOLOGY & METABOLISM | peptide YY | Peptide YY - pharmacology | Peptide Fragments | Lipolysis - drug effects | Humans | Appetite - drug effects | Male | Obesity - physiopathology | Energy Intake - drug effects | Insulin - blood | Obesity - metabolism | Cross-Over Studies | Dose-Response Relationship, Drug | Fatty Acids, Nonesterified - metabolism | Heart Rate - drug effects | Osmolar Concentration | Peptide YY - administration & dosage | Postprandial Period | Glucose - metabolism | Adult | Fatty Acids, Nonesterified - blood | Thermogenesis - drug effects | Blood Glucose - metabolism | Energy Metabolism - drug effects
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6. Full Text Functional and genetic epidemiological characterisation of the FFAR4 (GPR120) p.R270H variant in the Danish population
by Vestmar, Marie A and Andersson, Ehm A and Christensen, Charlotte R and Hauge, Maria and Glümer, Charlotte and Linneberg, Allan and Witte, Daniel R and Jørgensen, Marit E and Christensen, Cramer and Brandslund, Ivan and Lauritzen, Torsten and Pedersen, Oluf and Holst, Birgitte and Grarup, Niels and Schwartz, Thue W and Hansen, Torben
Journal of Medical Genetics, ISSN 0022-2593, 09/2016, Volume 53, Issue 9, pp. 616 - 623
Backgroundp.R270H (rs116454156) in the long chain fatty acid 7TM receptor FFAR4 (GPR120) which results in impaired Gαq (Gq) coupled signalling, has been... 
Obesity | CELLS | FASTING PLASMA-GLUCOSE | HOMEOSTASIS | Molecular genetics | COUPLED RECEPTOR REPERTOIRE | POTENT | GPR120 | INSULIN-RESISTANCE | PHARMACOLOGY | GENETICS & HEREDITY | FFAR4 | Genetics | COHORT | SECRETION | AGONIST | Biomarkers - metabolism | Cell Line | Lipids - genetics | Humans | Liver - metabolism | Middle Aged | Glucose Tolerance Test - methods | Glucose - genetics | Male | Signal Transduction - genetics | Obesity - genetics | Case-Control Studies | beta-Arrestins - genetics | HEK293 Cells | Inflammation - genetics | Adult | Blood Glucose - genetics | Female | Ligands | Genetic Variation - genetics | Receptors, G-Protein-Coupled - genetics | Gene expression | Phenotype | Research
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7. Full Text Goblet cell carcinoids: Characteristics of a Danish cohort of 83 patients
by Olsen, Ingrid Holst and Holt, Nanna and Langer, Seppo W and Hasselby, Jane P and Grønbæk, Henning and Hillingsø, Jens and Mahmoud, Masti and Ladekarl, Morten and Iversen, Lene H and Kjær, Andreas and Federspiel, Birgitte H and Knigge, Ulrich
PLoS ONE, ISSN 1932-6203, 02/2015, Volume 10, Issue 2, p. e0117627
Background Appendiceal goblet cell carcinoids (GCCs) exhibit neuroendocrine and adenocarcinoma features. Patients and Methods Analysis of demography,... 
NEUROENDOCRINE NEOPLASMS | DIAGNOSIS | MANAGEMENT | MARKER | SURVIVIN | BEHAVIOR | MULTIDISCIPLINARY SCIENCES | GUIDELINES | APPENDIX | TUMORS | CHEMOTHERAPY | Prognosis | Humans | Middle Aged | Postoperative Period | Carcinoid Tumor - diagnostic imaging | Carcinoid Tumor - epidemiology | Male | Carcinoid Tumor - pathology | Carcinoid Tumor - therapy | Radionuclide Imaging | Survival Analysis | Denmark - epidemiology | Adult | Female | Aged | Receptors, Somatostatin - metabolism | Retrospective Studies | Neoplasm Staging | Cohort Studies | Databases, Factual | Cancer survivors | Reports | Care and treatment | Carcinoid | Adenocarcinoma | Health sciences | Nuclear medicine | Demography | p53 Protein | Oncology | Metastasis | Males | Medical diagnosis | Small intestine | Data bases | Ovarian cancer | Surgery | Hepatology | Classification | Gastroenterology | Physiology | Medical research | Synaptophysin | Lymphatic system | Serotonin | Committees | Regression analysis | Patients | Survival | Pathology | Hospitals | Females | Endocrinology | Tumors
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8. Full Text Acute disruption of glucagon secretion or action does not improve glucose tolerance in an insulin-deficient mouse model of diabetes
by Steenberg, Vivi R and Steenberg, Vivi R and Jensen, Signe M and Jensen, Signe M and Pedersen, Jens and Pedersen, Jens and Madsen, Andreas N and Madsen, Andreas N and Windeløv, Johanne A and Windeløv, Johanne A and Holst, Birgitte and Holst, Birgitte and Quistorff, Bjørn and Quistorff, Bjørn and Poulsen, Steen S and Poulsen, Steen S and Holst, Jens J and Holst, Jens J
Diabetologia, ISSN 0012-186X, 2/2016, Volume 59, Issue 2, pp. 363 - 370
Normal glucose metabolism depends on pancreatic secretion of insulin and glucagon. The bihormonal hypothesis states that while lack of insulin leads to glucose... 
Medicine & Public Health | Human Physiology | Glucagon | Glucose homeostasis | Type 1 diabetes | Metabolic Diseases | Internal Medicine | Streptozotocin | Endocrine pancreas | GLP-1 | BLOOD-GLUCOSE | HUMANS | RATS | RECEPTOR | ANTIBODY | ENDOGENOUS GLUCAGON | PEPTIDE-1 | ENDOCRINOLOGY & METABOLISM | MICE | IMMUNONEUTRALIZATION | Receptors, Glucagon - antagonists & inhibitors | Streptozocin | Diabetes Mellitus, Experimental - genetics | Male | Glucagon - antagonists & inhibitors | Glucose Intolerance - blood | Glucose Intolerance - drug therapy | Glucagon-Secreting Cells - drug effects | Insulin-Secreting Cells - metabolism | Diabetes Mellitus, Experimental - chemically induced | Diabetes Mellitus, Experimental - metabolism | Receptors, Glucagon - genetics | Glucose Intolerance - genetics | Glucose Tolerance Test | Glucagon-Like Peptide 1 - metabolism | Glucagon-Secreting Cells - pathology | Mice, Inbred C57BL | Glucagon - physiology | Mice, Knockout | Blood Glucose - drug effects | Insulin - metabolism | Animals | Insulin-Secreting Cells - drug effects | Diabetes Mellitus, Experimental - pathology | Insulin - deficiency | Diphtheria Toxin | Mice | Glucagon - secretion | Insulin-Secreting Cells - pathology | Blood Glucose - metabolism | Glucose metabolism | Hyperglycemia | Analysis | Genetic engineering | Glucose | Glucose tolerance tests | Insulin | Dextrose
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9. Full Text Ghrelin receptor mutations - Too little height and too much hunger
by Holst, Birgitte and Schwartz, Thue W
Journal of Clinical Investigation, ISSN 0021-9738, 03/2006, Volume 116, Issue 3, pp. 637 - 641
The ghrelin receptor is known from in vitro studies to signal in the absence of the hormone ghrelin at almost 50% of its maximal capacity. But, as for many... 
MEDICINE, RESEARCH & EXPERIMENTAL | OBESITY | HORMONE | HUMANS | CONSTITUTIVE ACTIVITY | IDENTIFICATION | WEIGHT | Puberty - metabolism | Humans | Obesity - physiopathology | Signal Transduction - genetics | Obesity - genetics | Body Height - genetics | Syndrome | Obesity - metabolism | Puberty - genetics | Peptide Hormones - metabolism | Receptors, G-Protein-Coupled - deficiency | Ghrelin | Amino Acid Substitution - genetics | Receptors, G-Protein-Coupled - genetics | Hunger - physiology | Receptors, G-Protein-Coupled - physiology | Receptors, Ghrelin
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10. Full Text Common Structural Basis for Constitutive Activity of the Ghrelin Receptor Family
by Birgitte Holst and Nicholas D. Holliday and Anders Bach and Christian E. Elling and Helen M. Cox and Thue W. Schwartz
Journal of Biological Chemistry, ISSN 0021-9258, 12/2004, Volume 279, Issue 51, pp. 53806 - 53817
Three members of the ghrelin receptor family were characterized in parallel: the ghrelin receptor, the neurotensin receptor 2 and the orphan receptor GPR39. In... 
NEURITE RETRACTION | SIGNALING PATHWAYS | INVERSE AGONISM | GROWTH-HORMONE SECRETAGOGUE | CANNABINOID CB1 RECEPTORS | BIOCHEMISTRY & MOLECULAR BIOLOGY | SERUM RESPONSE FACTOR | PROTEIN-COUPLED RECEPTORS | LIGAND-BINDING SITES | DEPENDENT GENE-EXPRESSION | ENDOCYTOSIS | Receptors, Gastrointestinal Hormone - chemistry | Receptors, Neurotensin - metabolism | Humans | Molecular Sequence Data | Type C Phospholipases - metabolism | Receptors, Neuropeptide - metabolism | Phylogeny | Receptors, Gastrointestinal Hormone - metabolism | GTP-Binding Protein alpha Subunits, G12-G13 - metabolism | MAP Kinase Signaling System | Dose-Response Relationship, Drug | Transfection | DNA Mutational Analysis | Transcription, Genetic | Inositol Phosphates - metabolism | Cyclic AMP - metabolism | Receptors, G-Protein-Coupled - physiology | Receptors, Ghrelin | Protein Structure, Tertiary | Amino Acid Sequence | Cell Line | Enzyme-Linked Immunosorbent Assay | Protein Structure, Secondary | Signal Transduction | Phosphatidylinositols - chemistry | Models, Molecular | Animals | Microscopy | Ligands | Protein Conformation | COS Cells | DNA, Complementary - metabolism | Receptors, G-Protein-Coupled - chemistry | Receptors, Neuropeptide - chemistry
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11. Full Text A Conserved Aromatic Lock for the Tryptophan Rotameric Switch in TM-VI of Seven-transmembrane Receptors
by Birgitte Holst and Rie Nygaard and Louise Valentin-Hansen and Anders Bach and Maja S. Engelstoft and Pia S. Petersen and Thomas M. Frimurer and Thue W. Schwartz
Journal of Biological Chemistry, ISSN 0021-9258, 02/2010, Volume 285, Issue 6, pp. 3973 - 3985
The conserved tryptophan in position 13 of TM-VI (Trp-VI:13 or Trp-6.48) of the CW X P motif located at the bottom of the main ligand-binding pocket in TM-VI... 
TACHYKININ NK1 RECEPTOR | RHODOPSIN STRUCTURE | GHRELIN RECEPTOR | TOGGLE SWITCHES | PROTEIN-COUPLED RECEPTOR | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | METAL-ION SITE | METARHODOPSIN-I | HELIX MOVEMENT | BETA-ADRENERGIC RECEPTOR | Receptors, G-Protein-Coupled - metabolism | Allosteric Regulation | Humans | Cercopithecus aethiops | Molecular Sequence Data | Tryptophan - chemistry | Receptors, G-Protein-Coupled - agonists | Rhodopsin - metabolism | Receptors, Ghrelin - genetics | Tryptophan - metabolism | Rhodopsin - agonists | Phenylalanine - chemistry | Receptors, Ghrelin - metabolism | Binding Sites | Rhodopsin - chemistry | Amino Acid Sequence | Phenylalanine - metabolism | Receptors, Adrenergic, beta-2 - genetics | Tryptophan - genetics | Models, Molecular | Molecular Dynamics Simulation | Receptors, Adrenergic, beta-2 - metabolism | Animals | Phenylalanine - genetics | Receptors, G-Protein-Coupled - antagonists & inhibitors | Retinaldehyde - pharmacology | Protein Binding | Protein Conformation | Receptors, G-Protein-Coupled - genetics | Mutation | COS Cells | Proteins | Receptors | Mechanisms of Signal Transduction | Signal Transduction | G Proteins | Adenylate Cyclase | Membrane | Coupled Receptors (GPCR) | Inositol Phosphates | Hormones | Peptide | G-proteins
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12. Full Text High-dose anakinra as treatment for macrophage activation syndrome caused by refractory Kawasaki disease in an infant
by Lind-Holst, Marie and Hartling, Ulla Birgitte and Christensen, Anne Estmann
BMJ Case Reports, ISSN 1757-790X, 08/2019, Volume 12, Issue 8, p. e229708
We report a 12-week-old boy presenting with incomplete refractory Kawasaki disease (KD) complicated with macrophage activation syndrome (MAS). The infant... 
Proteins | Case studies | Kawasaki disease | Cytokines | Laboratories | Coronary vessels | Rheumatology | Rheumatic diseases | Arthritis | Veins & arteries | Children & youth
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13. Full Text Insulin-Like Growth Factor Bioactivity, Stanniocalcin-2, Pregnancy-Associated Plasma Protein-A, and IGF-Binding Protein-4 in Pleural Fluid and Serum From Patients With Pulmonary Disease
by Espelund, Ulrick Skipper and Bjerre, Mette and Hjortebjerg, Rikke and Rasmussen, Torben Riis and Lundby, Anders and Hoeflich, Andreas and Folkersen, Birgitte Holst and Oxvig, Claus and Frystyk, Jan
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 09/2017, Volume 102, Issue 9, pp. 3526 - 3534
CONTEXT:Members of the insulin-like growth factor (IGF) system are primarily produced in the liver and secreted into the circulation, but they are also... 
SYSTEM | VITRO | PROTEOLYTIC ACTIVITY | ASCITES | IGFBP-3 | ENDOCRINOLOGY & METABOLISM | PAPP-A | I BIOACTIVITY | CLEAVAGE | CARCINOMA | AXIS | Biomarkers - metabolism | Severity of Illness Index | Prognosis | Humans | Pleural Effusion - metabolism | Glycoproteins - metabolism | Male | Glycoproteins - blood | Insulin-Like Growth Factor Binding Protein 4 - blood | Pregnancy | Analysis of Variance | Lung Diseases - blood | Sensitivity and Specificity | Insulin-Like Growth Factor Binding Protein 4 - metabolism | Aged, 80 and over | Female | Aged | Lung Diseases - pathology | Pregnancy-Associated Plasma Protein-A - metabolism | Insulin-Like Growth Factor I - metabolism | Cohort Studies | Phosphorylation | Correlation | Insulin-like growth factor I | Liver | Lung cancer | Proteinase | Interleukin | Immunoblotting | Insulin-like growth factors | Tissues | Blood | Interleukin 6 | Proteins | Etiology | Protein folding | Compartments | Binding | Stanniocalcin | Lung diseases | Insulin | Patients | Biological activity | Pleural fluid | Immunoassays
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14. Full Text l-Arginine improves multiple physiological parameters in mice exposed to diet-induced metabolic disturbances
by Clemmensen, Christoffer and Clemmensen, Christoffer and Madsen, Andreas N and Madsen, Andreas N and Smajilovic, Sanela and Smajilovic, Sanela and Holst, Birgitte and Holst, Birgitte and Bräuner-Osborne, Hans and Bräuner-Osborne, Hans
Amino Acids, ISSN 0939-4451, 9/2012, Volume 43, Issue 3, pp. 1265 - 1275
l-Arginine (l-Arg) is a conditionally essential amino acid and a natural constituent of dietary proteins. Studies in obese rats and type 2 diabetic humans have... 
Biochemistry, general | Obesity | Insulin sensitivity | Neurobiology | Amino acids | Life Sciences | Low protein | Analytical Chemistry | Life Sciences, general | Diet | Proteomics | Biochemical Engineering | Diabetes | l -Arginine | L-Arginine | LOW-PROTEIN DIETS | FOOD-INTAKE | BIOCHEMISTRY & MOLECULAR BIOLOGY | WEIGHT-LOSS | INDUCED THERMOGENESIS | ENERGY-BALANCE | SKELETAL-MUSCLE | TYPE-2 DIABETIC-PATIENTS | INDUCED OBESITY | ADIPOSE-TISSUE | Gene Expression - drug effects | Homeostasis | Motor Activity - drug effects | Male | Hyperphagia - chemically induced | Insulin - blood | Arginine - administration & dosage | Hypoglycemic Agents - administration & dosage | Diet, Protein-Restricted - adverse effects | Adipose Tissue, White - pathology | Adiposity - drug effects | Mice, Inbred C57BL | Insulin Resistance | Blood Glucose | Energy Intake - drug effects | Mitochondria - drug effects | Genes, Mitochondrial | Animals | Oxygen Consumption - drug effects | Arginine - adverse effects | Glucose - metabolism | Mice | Dietary Supplements | Hypoglycemic Agents - adverse effects | Adipose Tissue, White - drug effects | Energy Metabolism - drug effects | Diets | Expenditures | Mathematical models | Glucose | Arrays | Insulin
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15. Full Text Effects of gastric bypass surgery on glucose absorption and metabolism during a mixed meal in glucose-tolerant individuals
by Jacobsen, Siv H and Bojsen-Møller, Kirstine N and Dirksen, Carsten and Jørgensen, Nils B and Clausen, Trine R and Wulff, Birgitte S and Kristiansen, Viggo B and Worm, Dorte and Hansen, Dorte L and Holst, Jens J and van Hall, Gerrit and Madsbad, Sten
Diabetologia, ISSN 0012-186X, 10/2013, Volume 56, Issue 10, pp. 2250 - 2254
Roux-en-Y gastric bypass surgery (RYGB) improves glucose tolerance in patients with type 2 diabetes, but also changes the glucose profile in response to a meal... 
Gastrointestinal hormone response | Obesity | Human Physiology | Insulin sensitivity | Metabolic Diseases | Gastric bypass | Postprandial absorption | Internal Medicine | Glucagon-like peptide-1 | Rate of appearance | Glucose kinetics | Medicine & Public Health | Endogenous glucose production | Rate of disappearance | ENDOCRINOLOGY & METABOLISM | BETA-CELL FUNCTION | Body Mass Index | Gastric Bypass | Humans | Glucose - metabolism | Female | Male | Absorptiometry, Photon | Physiological aspects | Glucose metabolism | Glucose | Surgery | Analysis | Dextrose
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