VasopressinsArginine VasopressinReceptors, VasopressinPoint MutationMutation, MissenseDeamino Arginine VasopressinMutationFrameshift MutationOxytocinRats, BrattleboroLypressinGerm-Line MutationNeurophysinsRenal AgentsDiabetes InsipidusPedigreePituitary Gland, PosteriorVasotocinMutation RateAntidiuretic AgentsAquaporin 2Supraoptic NucleusBase SequenceExonsMolecular Sequence DataHeterozygoteAmino Acid SubstitutionPituitary Hormones, PosteriorKidney Tubules, CollectingAmino Acid SequencePolymerase Chain ReactionDNA Mutational AnalysisWater DeprivationAllelesDiuresisMutagenesis, Site-DirectedWater-Electrolyte BalancePolymorphism, Single-Stranded ConformationalOsmolar ConcentrationReceptors, OxytocinAquaporin 6HomozygoteGenotypeMutagenesisHyponatremiaCodon, NonsenseSequence Analysis, DNACell LineDiabetes Insipidus, NephrogenicInappropriate ADH SyndromeKidney MedullaKidney Concentrating AbilityGenes, RecessiveKidneySequence DeletionGenes, DominantDNA PrimersProtein Structure, TertiaryRats, Inbred StrainsGenetic TestingModels, MolecularPhenotypeBinding SitesParaventricular Hypothalamic NucleusThirstVasoconstrictor AgentsEscherichia coliSuppression, GeneticRNA, MessengerSequence Homology, Amino AcidAquaporinsChromosome MappingPolyuriaSaline Solution, HypertonicCodonBlood PressureHypothalamusReceptors, AngiotensinSodiumKineticsDNA-Binding ProteinsProtein BindingCalciumCloning, MolecularGenetic Complementation TestTranscription FactorsDehydrationDNAGene DeletionSyndromeCorticotropin-Releasing HormoneUrineTransfectionFounder EffectMembrane ProteinsBenzazepinesGenes, p53Sequence AlignmentRats, Sprague-DawleyGenetic Linkage