Structural bases of vasopressin/oxytocin receptor function

[1] ALA Y, 1998, IN PRESS J AM SOC NE

[2] Barberis C, 1996, CRIT REV NEUROBIOL, V10, P119

[3] X-LINKED NEPHROGENIC DIABETES-INSIPIDUS MUTATIONS IN NORTH-AMERICA AND THE HOPEWELL HYPOTHESIS [J]. JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (03) : 1262 - 1268

[4] AN EXTRACELLULAR CONGENITAL NEPHROGENIC DIABETES-INSIPIDUS MUTATION OF THE VASOPRESSIN RECEPTOR REDUCES CELL-SURFACE EXPRESSION, AFFINITY FOR LIGAND, AND COUPLING TO THE G(S)/ADENYLYL CYCLASE SYSTEM [J]. MOLECULAR ENDOCRINOLOGY, 1994, 8 (07) : 886 - 894

[5] MOLECULAR-CLONING OF THE RECEPTOR FOR HUMAN ANTIDIURETIC-HORMONE [J]. NATURE, 1992, 357 (6376) : 333 - 335

[6] THE CLONED VASOPRESSIN V1A RECEPTOR STIMULATES PHOSPHOLIPASE A(2), PHOSPHOLIPASE-C, AND PHOSPHOLIPASE-D THROUGH ACTIVATION OF RECEPTOR-OPERATED CALCIUM CHANNELS [J]. NEUROPEPTIDES, 1994, 27 (01) : 63 - 74

[7] Efficient photoaffinity labeling of the rat V-1a vasopressin receptor using a linear azidopeptidic antagonist [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 247 (03): : 906 - 913

[8] A NEW SERIES OF PHOTOACTIVATABLE AND IODINATABLE LINEAR VASOPRESSIN ANTAGONISTS [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (12) : 1841 - 1849

[9] TYR115 IS THE KEY RESIDUE FOR DETERMINING AGONIST SELECTIVITY IN THE V1A VASOPRESSIN RECEPTOR [J]. EMBO JOURNAL, 1995, 14 (10) : 2176 - 2182

[10] Two aromatic residues regulate the response of the human oxytocin receptor to the partial agonist arginine vasopressin [J]. FEBS LETTERS, 1996, 397 (2-3) : 201 - 206

[1] ALA Y, 1998, IN PRESS J AM SOC NE

[2] Barberis C, 1996, CRIT REV NEUROBIOL, V10, P119

[3] X-LINKED NEPHROGENIC DIABETES-INSIPIDUS MUTATIONS IN NORTH-AMERICA AND THE HOPEWELL HYPOTHESIS [J]. JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (03) : 1262 - 1268

[4] AN EXTRACELLULAR CONGENITAL NEPHROGENIC DIABETES-INSIPIDUS MUTATION OF THE VASOPRESSIN RECEPTOR REDUCES CELL-SURFACE EXPRESSION, AFFINITY FOR LIGAND, AND COUPLING TO THE G(S)/ADENYLYL CYCLASE SYSTEM [J]. MOLECULAR ENDOCRINOLOGY, 1994, 8 (07) : 886 - 894

[5] MOLECULAR-CLONING OF THE RECEPTOR FOR HUMAN ANTIDIURETIC-HORMONE [J]. NATURE, 1992, 357 (6376) : 333 - 335

[6] THE CLONED VASOPRESSIN V1A RECEPTOR STIMULATES PHOSPHOLIPASE A(2), PHOSPHOLIPASE-C, AND PHOSPHOLIPASE-D THROUGH ACTIVATION OF RECEPTOR-OPERATED CALCIUM CHANNELS [J]. NEUROPEPTIDES, 1994, 27 (01) : 63 - 74

[7] Efficient photoaffinity labeling of the rat V-1a vasopressin receptor using a linear azidopeptidic antagonist [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 247 (03): : 906 - 913

[8] A NEW SERIES OF PHOTOACTIVATABLE AND IODINATABLE LINEAR VASOPRESSIN ANTAGONISTS [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (12) : 1841 - 1849

[9] TYR115 IS THE KEY RESIDUE FOR DETERMINING AGONIST SELECTIVITY IN THE V1A VASOPRESSIN RECEPTOR [J]. EMBO JOURNAL, 1995, 14 (10) : 2176 - 2182

[10] Two aromatic residues regulate the response of the human oxytocin receptor to the partial agonist arginine vasopressin [J]. FEBS LETTERS, 1996, 397 (2-3) : 201 - 206