Disease: Diabetes insipidus- nephrogenic type 3
- 1-Desamino-8-D-arginine vasopressin (DDAVP) in patients with congenital nephrogenic diabetes insipidus
- A low-affinity vasopressin V2-receptor gene in a kindred with X-linked nephrogenic diabetes insipidus
- A Novel Mutation in the <em>AVPR2</em> Gene Causing Congenital Nephrogenic Diabetes Insipidus
- A Novel Mutation in the AVPR2 Gene Causing Congenital Nephrogenic Diabetes Insipidus
- A novel polymorphism in the coding region of the vasopressin type 2 receptor gene
- A novel SLC12A1 mutation in Bedouin kindred with antenatal Bartter syndrome type I
- A snake toxin as a theranostic agent for the type 2 vasopressin receptor
- Absence of PKC-alpha attenuates lithium-induced nephrogenic diabetes insipidus
- Activation of AQP2 water channels without vasopressin: therapeutic strategies for congenital nephrogenic diabetes insipidus
- ADH resistance of LLC-pk1 cells caused by overexpression of cAMP-phosphodiesterase type-IV
- AKAPs-PKA disruptors increase AQP2 activity independently of vasopressin in a model of nephrogenic diabetes insipidus
- Altered expression of renal acid-base transporters in rats with lithium-induced NDI
- Altered expression of renal AQPs and Na(+) transporters in rats with lithium-induced NDI
- Amiloride modifies the progression of lithium-induced renal interstitial fibrosis
- An AMPK activator as a therapeutic option for congenital nephrogenic diabetes insipidus
- Aquaporin gene delivery to kidney
- Aquaporin-2: new mutations responsible for autosomal-recessive nephrogenic diabetes insipidus-update and epidemiology
- Attenuation of lithium-induced natriuresis and kaliuresis in P2Y₂ receptor knockout mice
- AVPR2 variants and mutations in nephrogenic diabetes insipidus: review and missense mutation significance
- Bardet-Biedl syndrome and cystinuria
- Bladder function impairment in aquaporin-2 defective nephrogenic diabetes insipidus
- Cannabinoid receptor type 1 activation causes a water diuresis by inducing an acute central diabetes insipidus in mice
- Causes of the urinary concentrating defect in mice with nephrogenic diabetes insipidus
- Central pontine myelinolysis secondary to hypokalaemic nephrogenic diabetes insipidus
- Characterization of D150E and G196D aquaporin-2 mutations responsible for nephrogenic diabetes insipidus: importance of a mild phenotype
- Combined renal tubular acidosis and diabetes insipidus in hematological disease
- Comprehensive analysis of clinical and laboratory features of 440 published cases of Sjögren's syndrome and renal tubular acidosis
- Contiguous 22.1-kb deletion embracing AVPR2 and ARHGAP4 genes at novel breakpoints leads to nephrogenic diabetes insipidus in a Chinese pedigree
- Cyclic-3',5'-nucleotide phosphodiesterase isozymes in cell biology and pathophysiology of the kidney
- Derlin-1 and p97/valosin-containing protein mediate the endoplasmic reticulum-associated degradation of human V2 vasopressin receptors
- Detection of aquaporin-2 in the plasma membranes of oocytes: a novel isolation method with improved yield and purity
- Diffusion in the endoplasmic reticulum of an aquaporin-2 mutant causing human nephrogenic diabetes insipidus
- Dissecting the roles of aquaporins in renal pathophysiology using transgenic mice
- Dynamics and energetics of water transport through aquaporin mutants causing nephrogenic diabetes insipidus (NDI): A molecular dynamics study
- Effects of arginine vasopressin and 1-desamino-8-D arginine vasopressin on forearm vasculature of healthy subjects and patients with a V2 receptor defect
- Effects of periodontal therapy on serum C-reactive protein, sE-selectin, and tumor necrosis factor-alpha secretion by peripheral blood-derived macrophages in diabetes. A pilot study
- Epac1 null mice have nephrogenic diabetes insipidus with deficient corticopapillary osmotic gradient and weaker collecting duct tight junctions
- Equine renal tubular disorders
- Erythrocyte water permeability and renal function in double knockout mice lacking aquaporin-1 and aquaporin-3
- Evaluation of cellular plasticity in the collecting duct during recovery from lithium-induced nephrogenic diabetes insipidus
- Familial cases of congenital nephrogenic diabetes insipidus type II: Remarkable increment of urinary adenosine 3',5'-monophosphate in response to antidiuretic hormone
- Familial juvenile gouty nephropathy: exclusion of 16p12 from the candidate locus
- Fanconi's syndrome and nephrogenic diabetes insipidus in an adult treated with ifosfamide
- First report on female monozygotic twins discordant for congenital nephrogenic diabetes insipidus
- Functional and structural analysis of ClC-K chloride channels involved in renal disease
- Genetic ablation of aquaporin-2 in the mouse connecting tubules results in defective renal water handling
- Genetic deletion of the P2Y2 receptor offers significant resistance to development of lithium-induced polyuria accompanied by alterations in PGE2 signaling
- Glycogen synthase kinase 3α regulates urine concentrating mechanism in mice
- GSK3beta mediates renal response to vasopressin by modulating adenylate cyclase activity
- Hereditary nephrogenic diabetes insipidus in Japanese patients: analysis of 78 families and report of 22 new mutations in AVPR2 and AQP2
- Hereditary polyuric disorders: new concepts and differential diagnosis
- Human β3-Adrenoreceptor is Resistant to Agonist-Induced Desensitization in Renal Epithelial Cells
- Identification and characterization of aquaporin-2 water channel mutations causing nephrogenic diabetes insipidus with partial vasopressin response
- Identification, characterization and rescue of a novel vasopressin-2 receptor mutation causing nephrogenic diabetes insipidus
- Importance of Early Genetic Sequencing in Neonates Admitted to NICU with Recurrent Hypernatremia: Results of a Prospective Cohort Study
- Inactivating mutations of G protein-coupled receptors and diseases: structure-function insights and therapeutic implications
- Integrin-linked kinase regulates tubular aquaporin-2 content and intracellular location: a link between the extracellular matrix and water reabsorption
- Interactions between angiotensin II and arginine vasopressin in water homeostasis
- Intracellular activation of vasopressin V2 receptor mutants in nephrogenic diabetes insipidus by nonpeptide agonists
- Lithium in the Kidney: Friend and Foe?
- Mechanisms of prolonged lithium therapy-induced nephrogenic diabetes insipidus
- Metformin improves urine concentration in rodents with nephrogenic diabetes insipidus
- Methyl-beta-cyclodextrin induces vasopressin-independent apical accumulation of aquaporin-2 in the isolated, perfused rat kidney
- Misfolded vasopressin V2 receptors caused by extracellular point mutations entail congential nephrogenic diabetes insipidus
- Misfolding of mutant aquaporin-2 water channels in nephrogenic diabetes insipidus
- Molecular analyses of the vasopressin type 2 receptor and aquaporin-2 genes in Brazilian kindreds with nephrogenic diabetes insipidus
- Molecular characterization of an aquaporin-2 mutation causing a severe form of nephrogenic diabetes insipidus
- Multiple electrolyte disturbances as the presenting feature of multiple endocrine neoplasia type 1 (MEN-1)
- Mutations in the vasopressin V2 receptor gene in families with nephrogenic diabetes insipidus and functional expression of the Q-2 mutant
- Neonatal mortality in an aquaporin-2 knock-in mouse model of recessive nephrogenic diabetes insipidus
- Nephrogenic diabetes insipidus in mice lacking aquaporin-3 water channels
- Nephrogenic diabetes insipidus: essential insights into the molecular background and potential therapies for treatment
- Nephrogenic syndrome of inappropriate antidiuresis: a novel disorder in water balance in pediatric patients
- New autosomal recessive mutations in aquaporin-2 causing nephrogenic diabetes insipidus through deficient targeting display normal expression in Xenopus oocytes
- Novel <em>AQP2</em> Mutations and Clinical Characteristics in Seven Chinese Families With Congenital Nephrogenic Diabetes Insipidus
- Novel AQP2 Mutations and Clinical Characteristics in Seven Chinese Families With Congenital Nephrogenic Diabetes Insipidus
- Novel AVPR2 mutation causing partial nephrogenic diabetes insipidus in a Japanese family
- Novel criteria of urine osmolality effectively predict response to tolvaptan in decompensated heart failure patients--association between non-responders and chronic kidney disease
- Novel mutation in the AVPR2 gene in a Danish male with nephrogenic diabetes insipidus caused by ER retention and subsequent lysosomal degradation of the mutant receptor
- Novel vasopressin type 2 (AVPR2) gene mutations in Brazilian nephrogenic diabetes insipidus patients
- Pathogenesis and treatment of autosomal-dominant nephrogenic diabetes insipidus caused by an aquaporin 2 mutation
- Pattern of hereditary renal tubular disorders in Egyptian children
- Peculiarities of uric acid balance disorders in patients with type 2 diabetes and metabolic syndrome
- Pharmacological chaperones in nephrogenic diabetes insipidus: possibilities for clinical application
- Phenotype heterogeneity of congenital adrenal hyperplasia due to genetic mosaicism and concomitant nephrogenic diabetes insipidus in a sibling
- Renal resistance to vasopressin in poorly controlled type 1 diabetes mellitus
- Salt-losing nephrogenic diabetes insipidus caused by fetal exposure to angiotensin receptor blocker
- Segment-specific ENaC downregulation in kidney of rats with lithium-induced NDI
- Sildenafil reduces polyuria in rats with lithium-induced NDI
- Stimulation of AQP2 membrane insertion in renal epithelial cells in vitro and in vivo by the cGMP phosphodiesterase inhibitor sildenafil citrate (Viagra)
- The beta3-AR agonist BRL37344 ameliorates the main symptoms of X-linked nephrogenic diabetes insipidus in the mouse model of the disease
- The evolutionary origin of the vasopressin/V2-type receptor/aquaporin axis and the urine-concentrating mechanism
- Treating lithium-induced nephrogenic diabetes insipidus with a COX-2 inhibitor improves polyuria via upregulation of AQP2 and NKCC2
- Two novel aquaporin-2 mutations responsible for congenital nephrogenic diabetes insipidus in Chinese families
- Two novel mutations in the aquaporin-2 and the vasopressin V2 receptor genes in patients with congenital nephrogenic diabetes insipidus
- Two vasopressin type 2 receptor gene mutations R143P and delta V278 in patients with nephrogenic diabetes insipidus impair ligand binding of the receptor
- Type 2 vasopressin receptor gene, the gene responsible nephrogenic diabetes insipidus, maps to Xq28 close to the LICAM gene
- Urinary adenosine 3',5'-monophosphate (cAMP) response to antidiuretic hormone in diabetes insipidus (DI): comparison between congenital nephrogenic DI type 1 and 2, and vasopressin sensitive DI
- V2 vasopressin receptor (V2R) mutations in partial nephrogenic diabetes insipidus highlight protean agonism of V2R antagonists
- What we need to know about the effect of lithium on the kidney