nephrogenic diabetes insipidus
The definitions used in this glossary of terminology either have been provided by the authors of the articles, or have been extracted wholly or in part, or paraphrased from the following sources: The American Medical Association Encyclopedia of Medicine, Charles B. Clayman, MD, Medical Editor, Random House, New York, 1989; Biotechnology from A to Z, 2d Edition, William Bains, Oxford University Press, New York, New York, 2002; A Dictionary of Genetics, 6th Edition, Robert C. King and William D. Stansfield, Oxford University Press, New York, New York, 2002; Dorland's Illustrated Medical Dictionary, 29th and 30th Editions, W. B. Saunders Company, Philadelphia, 2000, 2003; Genes VII, Benjamin Lewin, Oxford University Press, New York, New York, 2000; The Gale Encyclopedia of Genetic Disorders, Volumes I and II, Stacey L. Blachford, Ed., Thomson Learning, New York, New York, 2002; The Merriam-Webster Dictionary, Merriam-Webster, Inc., Springfield, Massachusetts, 1997; Molecular Biology of the Cell, 3rd Edition, Bruce Alberts, et al., Garland Publishing, 1994; The Random House Dictionary of the English Language, Unabridged Edition, 1966; Webster's Ninth New Collegiate Dictionary, 1991.
DEFINITION:
- nephrogenic diabetes insipidus
-
A syndrome of polyuria and hyposthenuria caused by the failure of the renal tubules to reabsorb water in response to antidiuretic hormone, without disturbance in the renal filtration and solute excretion rates; the condition does not respond to exogenous vasopressin. It may be inherited as a rare X-linked trait or be acquired as a result of drug therapy or systemic disease.
Used in 211 Article abstracts
Used in 211 Article abstracts
- A Case of Nephrogenic Diabetes Insipidus Caused by Obstructive Uropathy Due to Prostate Cancer
- A Case of a Novel Mutant Vasopressin Receptor-Dependent Nephrogenic Diabetes Insipidus With Bilateral Non-Obstructive Hydronephrosis in a Middle Aged Man
- A Compartmental Model Predicts that Dietary Potassium Affects Lithium Dynamics in Rats
- A Family Case of Nephrogenic Diabetes Insipidus
- A Low Affinity Vasopressin V2-Receptor in Inherited Nephrogenic Diabetes Insipidus
- A Mouse Model to Test the in vivo Efficacy of Chemical Chaperones
- A Novel Mechanism in Recessive Nephrogenic Diabetes Insipidus: Wild-Type Aquaporin-2 Rescues the Apical Membrane Expression of Intracellularly Retained AQP2-P262L
- A Novel Polymorphism in the Coding Region of the Vasopressin Type 2 Receptor Gene
- A novel splicing mutation in the V2 vasopressin receptor.
- ADH Resistance of LLC-pk1 Cells Caused by Overexpression of cAMP-Phosphodiesterase Type-IV
- ARC Syndrome: An Expanding Range of Phenotypes
- ARDS Following Acute Lithium Carbonate Intoxication
- Acquired Nephrogenic Diabetes Insipidus Secondary to Distal Renal Tubular Acidosis and Nephrocalcinosis Associated with Sjogren's Syndrome
- Aldose Reductase-Deficient Mice Develop Nephrogenic Diabetes Insipidus
- Altered Expression of Renal AQPs and Na+ Transporters in Rats with Lithium-Induced NDI
- Amelioration of Polyuria in Nephrogenic Diabetes Insipidus Due to Aquaporin-2 Deficiency
- Amphotericin B-Induced Partial Nephrogenic Diabetes Insipidus in a Child
- Amphotericin B-induced Nephrogenic Diabetes Insipidus in a Case of Cryptococcemia
- An Impaired Routing of Wild-type Aquaporin-2 after Tetramerization with an Aquaporin-2 Mutant Explains Dominant Nephrogenic Diabetes Insipidus
- An X-linked NDI Mutation Reveals a Requirement for Cell Surface V2R Expression
- Antidiuretic Action of Oxytocin is Associated with Increased Urinary Excretion of Aquaporin-2
- Antidiuretic Effect of Hydrochlorothiazide in Lithium-Induced Nephrogenic Diabetes Insipidus Is Associated with Upregulation of Aquaporin-2, Na-Cl Co-transporter, and Epithelial Sodium Channel
- Apparent Loss-of-Function Mutant GPCRs Revealed as Constitutively Desensitized Receptors
- Aquaporin Expression in Normal Human Kidney and in Renal Disease
- Aquaporin Molecular Biology and Clinical Abnormalities of the Water Transport Channels
- Aquaporin-2 Water Channel Mutations Causing Nephrogenic Diabetes Insipidus
- Aquaporins and The Surgeon: Cautionary Tales
- Aquaporins: Roles in Renal Function and Peritoneal Dialysis
- Association of Calnexin With Wild Type and Mutant AVPR2 that Cause Nephrogenic Diabetes Insipidus
- Binding-, Intracellular Transport-, and Biosynthesis-Defective Mutants of Vasopressin Type 2 Receptor in Patients with X-Linked Nephrogenic Diabetes Insipidus
- Biochemical Basis of Partial Nephrogenic Diabetes Insipidus Phenotypes
- Bladder Function Impairment in Aquaporin-2 Defective Nephrogenic Diabetes Insipidus
- C112R, W323S, N317K Mutations in the Vasopressin V2 Receptor Gene in Patients With Nephrogenic Diabetes Insipidus
- Causes of Reversible Nephrogenic Diabetes Insipidus: A Systematic Review
- Cellular Mechanism of Lithium-Induced Nephrogenic Diabetes Insipidus in Rats
- Cerebral Defects and Nephrogenic Diabetes Insipidus with the ARC Syndrome: Additional Findings or a New Syndrome (ARCC-NDI)?
- Chlorpropamide Upregulates Antidiuretic Hormone Receptors and Unmasks Constitutive Receptor Signaling
- Clinical Phenotype of Nephrogenic Diabetes Insipidus in Females Heterozygous for a Vasopressin Type 2 Receptor Mutation
- Cloning and Characterization of a Vasopressin V2 Receptor and Possible Link to Nephrogenic Diabetes Insipidus
- Colocalization of the Gene for Nephrogenic Diabetes Insipidus (DIR) and the Vasopressin Type 2 Receptor Gene (AVPR2) in the Xq28 Region
- Comparative Mapping on the Mouse and Human X Chromosomes of a Human cDNA Clone Encoding the Vasopressin Renal-Type Receptor (AVP2R)
- Correlation between Magnetic Resonance Imaging of Posterior Pituitary and Neurohypophyseal Function in Children with Diabetes Insipidus
- Cryptococcal Pyelonephritis in a Dog
- Defective processing and trafficking of water channels in nephrogenic diabetes insipidus.
- Defects of G Protein-Coupled Signal Transduction in Human Disease
- Derivatives of Somatic Cell Hybrids Which Carry the Human Gene Locus for Nephrogenic Diabetes Insipidus (NDI) Express Functional Vasopressin Renal V2-type Receptors
- Desmopressin and Indomethacin Therapy for Nephrogenic Diabetes Insipidus in Patients Receiving Lithium Carbonate
- Desmopressin for Nocturnal Enuresis in Nephrogenic Diabetes Insipidus
- Detection of aquaporin-2 in the plasma membranes of oocytes: a novel isolation method with improved yield and purity.
- Development of Lithium-Induced Nephrogenic Diabetes Insipidus is Dissociated from Adenylyl Cyclase Activity
- Diabetes Insipidus (Robertson)
- Diabetes Insipidus [Bell]
- Diabetes Insipidus in Children: Pathophysiology, Diagnosis and Management
- Diabetes Insipidus in Uricase-Deficient Mice: A Model for Evaluating Therapy with Poly(Ethylene Glycol)-Modified Uricase
- Diffusion in the Endoplasmic Reticulum of an Aquaporin-2 Mutant Causing Human Nephrogenic Diabetes Insipidus
- Disease-Causing V2 Vasopressin Receptors are Retained in Different Compartments of the Early Secretory Pathway
- Disordered Water Channel Expression and Distribution in Acquired Nephrogenic Diabetes Insipidus
- Diversity of Nephrogenic Diabetes Insipidus Mutations and Importance of Early Recognition and Treatment
- Do Aquaporins Have a Role in Nocturnal Enuresis?
- Early Onset Bilateral Calcifications and Epilepsy
- Effect of DDAVP on Nocturnal Enuresis in a Patient with Nephrogenic Diabetes Insipidus
- Effect of Hydrochlorothiazide and Indomethacin Treatment on Renal Function in Nephrogenic Diabetes Insipidus
- Effects of Arginine Vasopressin and 1-Desamino-8-D Arginine Vasopressin on Forearm Vasculature of Healthy Subjects and Patients with a V2 Receptor Defect
- Efficacy of COX-2 Inhibitors in a Case of Congenital Nephrogenic Diabetes Insipidus
- Emergency Treatment of Lithium-Induced Diabetes Insipidus with Nonsteroidal Anti-Inflammatory Drugs
- Evaluation and Management of Diabetes Insipidus
- Evidence for Intact V1-vasopressin Receptors in Congenital Nephrogenic Diabetes Insipidus
- Evidence for Stabilization of Aquaporin-2 Folding Mutants by N-linked Glycosylation in the Endoplasmic Reticulum
- Expression Studies of Two Vasopressin V2 Receptor Gene Mutations, R202C and 804insG, in Nephrogenic Diabetes Insipidus
- Familial Juvenile Gouty Nephropathy: Exclusion of 16p12 from the Candidate Locus
- Familial Nephrogenic Diabetes Insipidus: Report of Two Families
- Foscarnet Alters Antidiuretic Hormone-Mediated Transport
- Functional Analysis of Aquaporin-2 Mutants Associated with Nephrogenic Diabetes Insipidus by Yeast Expression
- Functional Rescue of the Constitutively Internalized V2 Vasopressin Receptor Mutant R137H by the Pharmacological Chaperone Action of SR49059
- Glycosylation is Important for Cell Surface Expression of the Water Channel Aquaporin-2, But is Not Essential for Tetramerization in the Endoplasmic Reticulum
- Hemifacial Spasm in Albright's Hereditary Osteodystrophy with Pseudopseudohypoparathyroidism and Nephrogenic Diabetes Insipidus--Case Report
- Hemodynamic and Coagulation Responses to 1-desamino[8-D-arginine] Vasopressin in Patients with Congenital Nephrogenic Diabetes Insipidus
- Hereditary Nephrogenic Diabetes Insipidus and Bilateral Nonobstructive Hydronephrosis
- Heterogeneous AVPR2 Gene Mutations in Congenital Nephrogenic Diabetes Insipidus
- Hyperosmolar Nonketotic Coma Precipitated by Lithium-induced Nephrogenic Diabetes Insipidus
- Hyperuricemia as a Clue for Central Diabetes Insipidus (Lack of V1 Effect) in the Differential Diagnosis of Polydipsia
- Hypokalemic Nephropathy and Nephrogenic Diabetes Insipidus Due to Excessive Consumption of a Soft Drink
- Impaired Solute Accumulation in Inner Medulla of Clcnk1-/- Mice Kidney
- Impairment of AVP Regulation in 17alpha-Hydroxylase Deficiency, a Unique Form of Adrenal Insufficiency
- Importance of Aquaporin-2 Expression Levels in Genotype -Phenotype Studies in Nephrogenic Diabetes Insipidus
- Importance of the Mercury-Sensitive Cysteine on Function and Routing of AQP1 and AQP2 in Oocytes
- In Vitro Micro-Autoradiography of Atrial Natriuretic Peptide in Biopsy Specimens from Patients with Renal Diseases
- Inborn Errors of Signal Transduction: Mutations in G Proteins and G Protein-coupled Receptors as a Cause of Disease
- Indomethacin Treatment in Amphotericin B Induced Nephrogenic Diabetes Insipidus
- Inherited Diseases of the Kidney
- Intracranial Calcification in Siblings with Nephrogenic Diabetes Insipidus: CT and MRI
- Intracranial Calcifications Associated with Nephrogenic Diabetes Insipidus
- Investigation of Folding and Degradation of In Vitro Synthesized Mutant Proteins in Microsomes
- Kidney Damage in Long-Term Lithium Patients: A Cross-Sectional Study of Patients with 15 Years or More on Lithium
- Large-Scale Purification of Functional Recombinant Human Aquaporin-2
- Lithium Nephrotoxicity
- Lithium Nephrotoxicity: A Progressive Combined Glomerular and Tubulointerstitial Nephropathy
- Lithium Revisited
- Lithium-induced Down regulation of Aquaporin-2 Water Channel Expression in Rat Kidney Medulla
- Lithium-induced Nephrogenic Diabetes Insipidus
- Lithiumogenic Disorders of the Thyroid and Parathyroid Glands as Surgical Disease
- Maternal Lithium Therapy and Polyhydramnios
- Mechanism of Lithium-Induced Polyuria in the Rat
- Mesalazine Associated Nephrogenic Diabetes Insipidus Presenting as Weight Loss
- Mild Nephrogenic Diabetes Insipidus Caused by Foxa1 Deficiency
- 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 Mechanisms and Drug Development in Aquaporin Water Channel Diseases: Molecular Mechanism of Water Channel Aquaporin-2 Trafficking
- Molecular Pathogenesis of Nephrogenic Diabetes Insipidus
- Molecular and Cellular Defects in Nephrogenic Diabetes Insipidus
- Mutations in the Founder of the MIP Gene Family Underlie Cataract Development in the Mouse
- Mutations in the Vasopressin Type 2 Receptor Gene (AVPR2) Associated with Nephrogenic Diabetes Insipidus
- Mutations in the Vasopressin V2 Receptor Gene in Families with Nephrogenic Diabetes Insipidus and Functional Expression of the Q-2 Mutant
- Mutations in the Vasopressin V2 Receptor and Aquaporin-2 Genes in 12 Families with Congenital Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus (Bichet - November 1998)
- Nephrogenic Diabetes Insipidus Associated with Bilateral Ureteral Obstruction
- Nephrogenic Diabetes Insipidus Associated with Hemochromatosis
- Nephrogenic Diabetes Insipidus Due to Hydronephrosis in a Patient with a Solitary Kidney
- Nephrogenic Diabetes Insipidus Induced by Lobenzarit Disodium Treatment in Patients with Rheumatoid Arthritis
- Nephrogenic Diabetes Insipidus Secondary to Lithium Therapy in the Postoperative Patient: A Case Report
- Nephrogenic Diabetes Insipidus and Renal Tubular Acidosis Secondary to Foscarnet Therapy
- Nephrogenic Diabetes Insipidus and Tethered Cord Syndrome with a Lipoma of the Cauda Equina
- Nephrogenic Diabetes Insipidus in Mice Lacking All Nitric Oxide Synthase Isoforms
- Nephrogenic Diabetes Insipidus in Mice Lacking Aquaporin-3 Water Channels
- Nephrogenic Diabetes Insipidus in Sibling Colts
- Nephrogenic Diabetes Insipidus--Prodromal Phase of Multiple Myeloma
- Nephrogenic Diabetes Insipidus: An X Chromosome-Linked Dominant Inheritance Pattern with a Vasopressin Type 2 Receptor Gene that is Structurally Normal
- Nephrogenic Diabetes Insipidus: Clinical Symptoms, Pathogenesis, Genetics and Treatment
- Nephrogenic Diabetes Insipidus: Close Linkage with Markers from the Distal Long Arm of the Human X Chromosome
- Nephrogenic diabetes insipidus persisting 57 months after cessation of lithium carbonate therapy: report of a case and review of the literature.
- Nephrogenic diabetes insipidus.
- New Mutations in the AQP2 Gene in Nephrogenic Diabetes Insipidus Resulting in Functional but Misrouted Water Channels
- Normal Fibrinolytic Responses to 1-Desamino-8-D-Arginine Vasopressin in Patients with Nephrogenic Diabetes Insipidus Caused by Mutations in the Aquaporin 2 Gene
- Novel Down-Regulatory Mechanism of the Surface Expression of Vasopressin V2 Receptor by an Alternative Splice Receptor Variant
- Novel Mutations in Aquaporin-2 Gene in Female Siblings with Nephrogenic Diabetes Insipidus: Evidence of Disrupted Water Channel Function
- Novel Vasopressin Type 2 (AVPR2) Gene Mutations in Brazilian Nephrogenic Diabetes Insipidus Patients
- Overt Nephrogenic Diabetes Insipidus in Mice Lacking the CLC-K1 Chloride Channel
- Pathogenesis and Treatment of Autosomal-Dominant Nephrogenic Diabetes Insipidus Caused by an Aquaporin 2 Mutation
- Pathogenesis of Nephrogenic Diabetes Insipidus by Aquaporin-2 C-Terminus Mutations
- Pathophysiology of the Aquaporin Water Channels
- Patients with Autosomal Nephrogenic Diabetes Insipidus Homozygous for Mutations in the Aquaporin 2 Water-Channel Gene
- Pemetrexed-Induced Acute Renal Failure, Nephrogenic Diabetes Insipidus, and Renal Tubular Acidosis in a Patient with Non-Small Cell Lung Cancer
- Persistent Nephrogenic Diabetes Insipidus Following Lithium Therapy
- Pharmacochaperones Post-Translationally Enhance Cell Surface Expression by Increasing Conformational Stability of Wild-Type and Mutant Vasopressin V2 Receptors
- Pharmacological Chaperones Rescue Cell-Surface Expression and Function of Misfolded V2 Vasopressin Receptor Mutants
- Pharmacological Chaperones in Nephrogenic Diabetes Insipidus: Possibilities for Clinical Application
- Pharmacological Chaperones: Potential Treatment for Conformational Diseases
- Physiological Importance of Aquaporin Water Channels
- Physiological relevance of aquaporins: luxury or necessity?
- Physiology and Pathophysiology of Renal Aquaporins
- Polyuria in Childhood
- Possible Liposomal Amphotericin B-Induced Nephrogenic Diabetes Insipidus
- Primary Hyperparathyroidism and Coexisting Nephrogenic Diabetes Insipidus: Rapid Postoperative Correction
- Reconstitution of Mutant V2 Vasopressin Receptors by Adenovirus-mediated Gene Transfer
- Relief of Nocturnal Enuresis by Desmopressin is Kidney and Vasopressin Type 2 Receptor Independent
- Renal Function On and Off Lithium in Patients Treated with Lithium for 15 Years or More. A Controlled, Prospective Lithium-Withdrawal Study
- Renal Resistance to Vasopressin in Poorly Controlled Type 1 Diabetes Mellitus
- Requirement of Human Renal Water Channel Aquaporin-2 for Vasopressin-Dependent Concentration of Urine
- Rescue of Vasopressin V2 Receptor Mutants by Chemical Chaperones: Specificity and Mechanism
- Rescue of a Nephrogenic Diabetes Insipidus-Causing Vasopressin V2 Receptor Mutant by Cell-Penetrating Peptides
- Reverse Pharmacological Effect of Loop Diuretics and Altered rBSC1 Expression in Rats with Lithium Nephropathy
- Risk Factors for Ifosfamide Nephrotoxicity in Children
- Role of Sodium Depletion in Acute Antidiuretic Effect of Bendroflumethiazide in Rats with Nephrogenic Diabetes Insipidus
- Routing of the aquaporin-2 water channel in health and disease.
- Ser-256 Phosphorylation Dynamics of Aquaporin 2 During Maturation From the Endoplasmic Reticulum to the Vesicular Compartment in Renal Cells
- Severely Impaired Urine-Concentrating Ability in Mice Lacking the CLC-K1 Chloride Channel
- Stimulation of AQP2 Membrane Insertion in Renal Epithelial Cells In Vitro and In Vivo by the cGMP Phosphodiesterase Inhibitor Sildenafil Citrate (Viagra)
- Tenofovir-Related Nephrotoxicity in Human Immunodeficiency Virus-Infected Patients: Three Cases of Renal Failure, Fanconi Syndrome, and Nephrogenic Diabetes Insipidus
- The Apical Compartment: Trafficking Pathways, Regulators and Scaffolding Proteins
- The C-Terminal Tail of Aquaporin-2 Determines Apical Trafficking
- The Effect of Eight V2 Vasopressin Receptor Mutations on Stimulation of Adenylyl Cyclase and Binding to Vasopressin
- The Management of Diabetes Insipidus in Adults
- The Molecular Basis of Nephrogenic Diabetes Insipidus
- The Property of a Novel V2 Receptor Mutant in a Patient with Nephrogenic Diabetes Insipidus
- The V2 vasopressin receptor mutations and fluid homeostasis.
- The valve bladder syndrome: 20 years later.
- Therapeutic Potential of Vasopressin Receptor Antagonists
- Transient Central Diabetes Insipidus in the Setting of Underlying Chronic Nephrogenic Diabetes Insipidus Associated with Lithium Use
- Transient Nephrogenic Diabetes Insipidus Accompanied by Possible Psychogenic Polydipsia
- Traumatic Rupture of the Urinary Tract in a Patient Presenting Nephrogenic Diabetes Insipidus Associated with Hydronephrosis and Chronic Renal Failure: Case Report and Review of the Literature
- Treating lithium-induced nephrogenic diabetes insipidus with a COX-2 inhibitor improves polyuria via upregulation of AQP2 and NKCC2.
- Treatment of Lithium-Induced Diabetes Insipidus with Amiloride
- Treatment of Nephrogenic Diabetes Insipidus with Hydrochlorothiazide and Amiloride
- Two Novel Mutations in the Vasopressin V2 Receptor Gene in Unrelated Japanese Kindreds with Nephrogenic Diabetes Insipidus
- Two Novel Types of Contiguous Gene Deletion of the AVPR2 and ARHGAP4 Genes in Unrelated Japanese Kindreds with Nephrogenic Diabetes Insipidus
- Type 2 Vasopressin Receptor Gene, the Gene Responsible for Nephrogenic Diabetes Insipidus, Maps to Xq28 Close to the LICAM Gene
- Urinary Aquaporin-2 Excretion in Dogs: A Marker for Collecting Duct Responsiveness to Vasopressin
- Urinary Concentrating Defect in Experimental Hemochromatosis
- Urinary Excretion of Aquaporin-2 in Patients with Diabetes Insipidus
- Use of T1-weighted MR Imaging to Differentiate between Primary Polydipsia and Central Diabetes Insipidus
- Vasopressin Receptor Mutations and Nephrogenic Diabetes Insipidus
- Vasopressin Type-2 Receptor and Aquaporin-2 Water Channel Mutants in Nephrogenic Diabetes Insipidus
- Very Severe Self-Poisoning Lithium Carbonate Intoxication Causing a Myocardial Infarction
- Water Channels Encoded by Mutant Aquaporin-2 Genes in Nephrogenic Diabetes Insipidus are Impaired in Their Cellular Routing
- Water Channels and Urea Transporters
- Water Intake and 24-hour Blood Pressure Monitoring in a Patient with Nephrogenic Diabetes Insipidus Caused by a Novel Mutation of the Vasopressin V2R Gene [Letter; Comment]
- Water Transport in the Kidney and Nephrogenic Diabetes Insipidus
- X-linked Nephrogenic Diabetes Insipidus: from the Ship Hopewell to RFLP Studies
- [Abnormal Serum Uric Acid Level in Endocrine Disorders] (Japanese)
- [Clinical Spectrum of Distal Renal Tubular Acidosis and Its Study with Bicarbonate Loading] (Hungarian)
- [Congenital Diabetes Insipidus. Recent Advances in Molecular Genetics] (French)
- [Diseases Caused by Disorders of Membrane Transport: an Overview] (Japanese)
- [Idiopathic Retroperitoneal Fibrosis Disclosed by Nephrogenic Diabetes Insipidus] (French)
- [Molecular biological studies on patients with nephrogenic diabetes insipidus]. (Hungarian)
- [Nephrogenic Diabetes Insipidus] (Hungarian)
- [Nephrogenic Diabetes Insipidus] (Japanese)
- [Nephropathic Cystinosis: Report of 2 Cases and Review of the Literature] (Portuguese)
- [Pathological Aspects of Water Transport in the Collecting Ducts] (French)
- [Recent Advances in Vasopressin Receptors and Signal Transduction System] (Japanese)
- [Simultaneous Familial Occurrence of Distal Renal Tubular Acidosis, Polycystic Kidney and Nephrogenic Diabetes Insipidus] (Hungarian)
- cDNA and Genomic Cloning of Mouse Aquaporin-2: Functional Analysis of an Orthologous Mutant Causing Nephrogenic Diabetes Insipidus
Used in 22 Article bodies
Used in 22 Article bodies
- A Novel Polymorphism in the Coding Region of the Vasopressin Type 2 Receptor Gene
- Analysis of Vasopressin Receptor Type II (V2R) Gene in Three Japanese Pedigrees with Congenital Nephrogenic Diabetes Insipidus: Identification of a Family with Complete Deletion of the V2R Gene
- Evidence that the Antidiuretic Substance in the Plasma of Children with Nephrogenic Diabetes Insipidus is Antidiuretic Hormone
- Hereditary Vasopressin Resistance in Man and Mouse
- Hyperosmolar Coma and Lithium-induced Diabetes Insipidus
- Importance of the Mercury-Sensitive Cysteine on Function and Routing of AQP1 and AQP2 in Oocytes
- Inborn Errors of Signal Transduction: Mutations in G Proteins and G Protein-coupled Receptors as a Cause of Disease
- Index of Suspicion. Case 2. Nephrogenic Diabetes Insipidus
- Intracranial Calcification in Nephrogenic Diabetes Insipidus
- Lithium-Induced Nephrogenic Diabetes Insipidus Treated with Indomethacin
- Molecular Analysis of X-Linked Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus Following High Dose Epirubicin Chemotherapy for Metastatic Soft Tissue Sarcoma [Letter]
- Nephrogenic Diabetes Insipidus Secondary to Lithium Therapy in the Postoperative Patient: A Case Report
- Nephrogenic Diabetes Insipidus in North America. The Hopewell Hypothesis
- Nephrogenic Diabetes Insipidus in a Patient Taking Cidofovir
- Nephrogenic Diabetes Insipidus--Prodromal Phase of Multiple Myeloma
- Nephrogenic Diabetes Insipidus: A Cause of Severe Nonobstructive Urinary Tract Dilatation
- Persistent Nephrogenic Diabetes Insipidus Following Lithium Therapy
- Proposed Cause of Marked Vasopressin Resistance in a Female with an X-Linked Recessive V2 Receptor Abnormality
- Risk Factors for Ifosfamide Nephrotoxicity in Children
- Role of Aquaporin-2 Water Channels in Urinary Concentration and Dilution Defects
Used in 152 Article translations
Used in 152 Article translations
- A Compartmental Model Predicts that Dietary Potassium Affects Lithium Dynamics in Rats
- A Congenital Renal Tubular Defect
- A Family Case of Nephrogenic Diabetes Insipidus
- A Low Affinity Vasopressin V2-Receptor in Inherited Nephrogenic Diabetes Insipidus
- ADH Resistance of LLC-pk1 Cells Caused by Overexpression of cAMP-Phosphodiesterase Type-IV
- ARDS Following Acute Lithium Carbonate Intoxication
- Aldose Reductase-Deficient Mice Develop Nephrogenic Diabetes Insipidus
- Amelioration of Polyuria in Nephrogenic Diabetes Insipidus Due to Aquaporin-2 Deficiency
- Amiloride-Hydrochlorothiazide Versus Indomethacin-Hydrochlorothiazide in the Treatment of Nephrogenic Diabetes Insipidus
- Aminoglycoside Pretreatment Partially Restores the Function of Truncated V2 Vasopressin Receptors Found in Patients with Nephrogenic Diabetes Insipidus
- Amphotericin B-Induced Nephrogenic Diabetes Insipidus: Resolution with Its Liposomal Counterpart [Letter]
- Amphotericin B-Induced Partial Nephrogenic Diabetes Insipidus in a Child
- An Extracellular Congenital Nephrogenic Diabetes Insipidus Mutation of the Vasopressin Receptor Reduces Cell Surface Expression, Affinity for Ligand, and Coupling to the Gs/adenylyl Cyclase System
- An X-linked NDI Mutation Reveals a Requirement for Cell Surface V2R Expression
- Aquaporin-2, a Vasopressin-sensitive Water Channel, and Nephrogenic Diabetes Insipidus
- Aquaporins: From Physiology to Nephrogenic Diabetes Insipidus
- Assignment of the Human Gene for the Water Channel of Renal Collecting Duct Aquaporin 2 (AQP2) to Chromosome 12 Region q12-->q13
- Autosomal Recessive Nephrogenic Diabetes Insipidus Caused by an Aquaporin-2 Mutation
- Binding-, Intracellular Transport-, and Biosynthesis-Defective Mutants of Vasopressin Type 2 Receptor in Patients with X-Linked Nephrogenic Diabetes Insipidus
- Biochemical Basis of Partial Nephrogenic Diabetes Insipidus Phenotypes
- Cellular Mechanism of Lithium-Induced Nephrogenic Diabetes Insipidus in Rats
- Cerebral Defects and Nephrogenic Diabetes Insipidus with the ARC Syndrome: Additional Findings or a New Syndrome (ARCC-NDI)?
- Cloning of the Human Type-2 Vasopressin Receptor Gene
- Cloning, Characterization, and Chromosomal Mapping of Human Aquaporin of Collecting Duct
- Cognitive and Psychosocial Functioning of Patients with Congenital Nephrogenic Diabetes Insipidus
- Colocalization of the Gene for Nephrogenic Diabetes Insipidus (DIR) and the Vasopressin Type 2 Receptor Gene (AVPR2) in the Xq28 Region
- Comparative Mapping on the Mouse and Human X Chromosomes of a Human cDNA Clone Encoding the Vasopressin Renal-Type Receptor (AVP2R)
- Concentrating Defect in Experimental Nephrotic Syndrome: Altered Expression of Aquaporins and Thick Ascending Limb Na+ Transporters
- Congenital Nephrogenic Diabetes Insipidus in an Adult
- Defective Aquaporin-2 Trafficking in Nephrogenic Diabetes Insipidus and Correction by Chemical Chaperones
- Defects of G Protein-Coupled Signal Transduction in Human Disease
- Diabetes Insipidus (Hendy, Bichet)
- Discovery of Aquaporins: a Breakthrough in Research on Renal Water Transport
- Disordered Water Channel Expression and Distribution in Acquired Nephrogenic Diabetes Insipidus
- Do Aquaporins Have a Role in Nocturnal Enuresis?
- Early Onset Bilateral Calcifications and Epilepsy
- Effect of Hydrochlorothiazide and Indomethacin Treatment on Renal Function in Nephrogenic Diabetes Insipidus
- Effects of Arginine Vasopressin and 1-Desamino-8-D Arginine Vasopressin on Forearm Vasculature of Healthy Subjects and Patients with a V2 Receptor Defect
- Epinephrine and dDAVP Administration in Patients with Congenital Nephrogenic Diabetes Insipidus. Evidence for a pre-cyclic AMP V2 Receptor Defective Mechanism
- Evidence that the Antidiuretic Substance in the Plasma of Children with Nephrogenic Diabetes Insipidus is Antidiuretic Hormone
- Expression Studies of Two Vasopressin V2 Receptor Gene Mutations, R202C and 804insG, in Nephrogenic Diabetes Insipidus
- Foscarnet Alters Antidiuretic Hormone-Mediated Transport
- Functional Analysis of Aquaporin-2 Mutants Associated with Nephrogenic Diabetes Insipidus by Yeast Expression
- Functional Rescue of Mutant V2 Vasopressin Receptors Causing Nephrogenic Diabetes Insipidus by a Co-Expressed Receptor Polypeptide
- G-Protein-Coupled Receptors: Molecular Mechanisms Involved in Receptor Activation and Selectivity of G-Protein Recognition
- Genetic Renal Diseases in Children
- Heat Shock Protein 70 Interacts with Aquaporin-2 (AQP2) and Regulates Its Trafficking
- Hemifacial Spasm in Albright's Hereditary Osteodystrophy with Pseudopseudohypoparathyroidism and Nephrogenic Diabetes Insipidus--Case Report
- Heterogeneous AVPR2 Gene Mutations in Congenital Nephrogenic Diabetes Insipidus
- High Activity of Low-Michaelis-Menten Constant 3',5'-Cyclic Adenosine Monophosphate-Phosphodiesterase Isozymes in Renal Inner Medulla of Mice With Hereditary Nephrogenic Diabetes Insipidus
- Homer Smith: His Contribution to the Practice of Nephrology
- Ifosfamide-induced Renal Fanconi Syndrome with Associated Nephrogenic Diabetes Insipidus in an Adult Patient
- In Vitro Micro-Autoradiography of Atrial Natriuretic Peptide in Biopsy Specimens from Patients with Renal Diseases
- Inborn Errors of Signal Transduction: Mutations in G Proteins and G Protein-coupled Receptors as a Cause of Disease
- Indomethacin Treatment in Amphotericin B Induced Nephrogenic Diabetes Insipidus
- Indomethacin in the Treatment of Lithium-Induced Nephrogenic Diabetes Insipidus
- Induction of Intramembranous Particle Clusters in Mice with Nephrogenic Diabetes Insipidus
- Inherited Diseases of the Kidney
- Intracranial Calcifications Associated with Nephrogenic Diabetes Insipidus
- Kidney Damage in Long-Term Lithium Patients: A Cross-Sectional Study of Patients with 15 Years or More on Lithium
- Linkage of X-linked Nephrogenic Diabetes Insipidus with DXS52, a Polymorphic DNA Marker
- Lithium Nephrotoxicity
- Lithium-Induced Diabetes Insipidus in a Surgical Patient: Report of a Case and Review of the Literature
- Lithium-Induced Nephrogenic Diabetes Insipidus Treated with Indomethacin
- Lithium-Induced Nephrogenic Diabetes Insipidus Treated with Intravenous Ketorolac
- Lithium-induced Down regulation of Aquaporin-2 Water Channel Expression in Rat Kidney Medulla
- Lithium-induced Nephrogenic Diabetes Insipidus
- Lithiumogenic Disorders of the Thyroid and Parathyroid Glands as Surgical Disease
- Maternal Lithium Therapy and Polyhydramnios
- Mechanism of Antidiuresis Caused by Bendroflumethiazide in Conscious Rats with Diabetes Insipidus
- Mechanism of Lithium-Induced Polyuria in the Rat
- Meniere's Disease in Congenital Nephrogenic Diabetes Insipidus: Report of Two Twins
- Mesalazine Associated Nephrogenic Diabetes Insipidus Presenting as Weight Loss
- Mild Nephrogenic Diabetes Insipidus Caused by Foxa1 Deficiency
- Molecular Analysis of X-Linked Nephrogenic Diabetes Insipidus
- Molecular Genetic Study of Congenital Nephrogenic Diabetes Insipidus and Rescue of Mutant Vasopressin V2 Receptor by Chemical Chaperones
- Molecular Insights into the Pathogenesis of Inherited Renal Tubular Disorders
- Molecular and Cellular Biology of Vasopressin and Oxytocin Receptors and Action in the Kidney
- Mutations in the V2 Vasopressin Receptor Gene are Associated with X-linked Nephrogenic Diabetes Insipidus
- Mutations in the Vasopressin V2 Receptor Gene in Families with Nephrogenic Diabetes Insipidus and Functional Expression of the Q-2 Mutant
- Mutations in the Vasopressin V2 Receptor Gene in Two Families with Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus (Bichet - November 1998)
- Nephrogenic Diabetes Insipidus Associated with Bilateral Ureteral Obstruction
- Nephrogenic Diabetes Insipidus Associated with Foscarnet - A Case Report [letter]
- Nephrogenic Diabetes Insipidus Following High Dose Epirubicin Chemotherapy for Metastatic Soft Tissue Sarcoma [Letter]
- Nephrogenic Diabetes Insipidus Induced by Lobenzarit Disodium Treatment in Patients with Rheumatoid Arthritis
- Nephrogenic Diabetes Insipidus Secondary to Lithium Therapy in the Postoperative Patient: A Case Report
- Nephrogenic Diabetes Insipidus and Renal Tubular Acidosis Secondary to Foscarnet Therapy
- Nephrogenic Diabetes Insipidus and Tethered Cord Syndrome with a Lipoma of the Cauda Equina
- Nephrogenic Diabetes Insipidus in North America. The Hopewell Hypothesis
- Nephrogenic Diabetes Insipidus in Sibling Colts
- Nephrogenic Diabetes Insipidus in a Patient Taking Cidofovir
- Nephrogenic Diabetes Insipidus--Prodromal Phase of Multiple Myeloma
- Nephrogenic Diabetes Insipidus. An Unusual Presentation of Recurrent Rectal Cancer
- Nephrogenic Diabetes Insipidus: A Cause of Severe Nonobstructive Urinary Tract Dilatation
- Nephrogenic Diabetes Insipidus: Causes Revealed
- Nephrogenic Diabetes Insipidus: Clinical Symptoms, Pathogenesis, Genetics and Treatment
- Nephrogenic Diabetes Insipidus: Transmitted by Females and Appearing During Infancy in Males
- New Mutations in the AQP2 Gene in Nephrogenic Diabetes Insipidus Resulting in Functional but Misrouted Water Channels
- Normal Fibrinolytic Responses to 1-Desamino-8-D-Arginine Vasopressin in Patients with Nephrogenic Diabetes Insipidus Caused by Mutations in the Aquaporin 2 Gene
- Normal Hemodynamic and Coagulation Responses to 1-Diamino-8-D-Arginine Vasopressin in a Case of Lithium-Induced Nephrogenic Diabetes Insipidus. Results of Treatment by a Prostaglandin Synthesis Inhibitor (Indomethacin).
- Novel Mutations in the V2 Vasopressin Receptor Gene of Patients with X-Linked Nephrogenic Diabetes Insipidus
- Pathophysiology of Aquaporin-2 in Water Balance Disorders
- Pathophysiology of the Aquaporin Water Channels
- Pharmacological Chaperones in Nephrogenic Diabetes Insipidus: Possibilities for Clinical Application
- Pharmacological Chaperones: Potential Treatment for Conformational Diseases
- Phenotypes Developed in Secretin Receptor-Null Mice Indicated a Role for Secretin in Regulating Renal Water Reabsorption
- Physiology and Pathophysiology of Aquaporins
- Physiology and Pathophysiology of the Aquaporin-2 Water Channel
- Polarized Expression of the Vasopressin V2 Receptor in Madin-Darby Canine Kidney Cells
- Posterior Lobe of the Pituitary in Diabetes Insipidus: Dynamic MR Imaging
- Primary Hyperparathyroidism and Coexisting Nephrogenic Diabetes Insipidus: Rapid Postoperative Correction
- Reconstitution of Mutant V2 Vasopressin Receptors by Adenovirus-mediated Gene Transfer
- Recurrent Dehydration in a Young Girl
- Relief of Nocturnal Enuresis by Desmopressin is Kidney and Vasopressin Type 2 Receptor Independent
- Renal Function On and Off Lithium in Patients Treated with Lithium for 15 Years or More. A Controlled, Prospective Lithium-Withdrawal Study
- Renal Histology in a Patient with Nephrogenic Diabetes Insipidus
- Requirement of Human Renal Water Channel Aquaporin-2 for Vasopressin-Dependent Concentration of Urine
- Risk Factors for Ifosfamide Nephrotoxicity in Children
- Role of Aquaporin Water Channels in Kidney and Lung
- Role of Aquaporin-2 Water Channels in Urinary Concentration and Dilution Defects
- Severely Impaired Urine-Concentrating Ability in Mice Lacking the CLC-K1 Chloride Channel
- The Aquaporin Family of Molecular Water Channels
- The Aquaporin Family of Water Channel Proteins in Clinical Medicine
- The Aquaporin Family of Water Channels in Kidney: an Update on Physiology and Pathophysiology of Aquaporin-2
- The Cellular Action of Antidiuretic Hormone
- The Clinical Importance of the Urinary Excretion of Aquaporin-2
- The Effect of Eight V2 Vasopressin Receptor Mutations on Stimulation of Adenylyl Cyclase and Binding to Vasopressin
- The Hydrophobic Amino Acid Residues in the Membrane-Proximal C Tail of the G Protein-Coupled Vasopressin V2 Receptor are Necessary for Transport-Competent Receptor Folding
- The Molecular Basis of Nephrogenic Diabetes Insipidus
- Therapeutic Potential of Vasopressin Receptor Antagonists
- Transient Nephrogenic Diabetes Insipidus in a Neonate
- Treatment of Nephrogenic Diabetes Insipidus with Hydrochlorothiazide and Amiloride
- Two Novel Mutations in the Vasopressin V2 Receptor Gene in Unrelated Japanese Kindreds with 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 for Nephrogenic Diabetes Insipidus, Maps to Xq28 Close to the LICAM Gene
- Urinary Arginine Vasopressin (AVP) Measurement in Children: Water Deprivation Test Incorporating Urinary AVP
- Urinary Concentrating Defect in Experimental Hemochromatosis
- Urinary Content of Aquaporin 1 and 2 in Nephrogenic Diabetes Insipidus
- Urinary Excretion of Aquaporin-2 in Patients with Diabetes Insipidus
- Vasopressin Receptors in Health and Disease
- Vasopressin Type-2 Receptor and Aquaporin-2 Water Channel Mutants in Nephrogenic Diabetes Insipidus
- Vasopressin V2 Receptor Mutants that Cause X-linked Nephrogenic Diabetes Insipidus: Analysis of Expression, Processing, and Function
- Vasopressin and Oxytocin Receptors
- Very Severe Self-Poisoning Lithium Carbonate Intoxication Causing a Myocardial Infarction
- Water Channels Encoded by Mutant Aquaporin-2 Genes in Nephrogenic Diabetes Insipidus are Impaired in Their Cellular Routing
- Water Channels and Urea Transporters
- Water Channels in Health and Disease
- Water Transport Across Mammalian Cell Membranes
- X-linked Nephrogenic Diabetes Insipidus: from the Ship Hopewell to RFLP Studies
- Xanthopterin-Induced Renal Dysfunction: A Reversible Model of Crystal Nephropathy
Used in 14 Faq answers
Used in 14 Faq answers
- How can I contact other people who are dealing with NDI?
- My doctor is not familiar with NDI. What should I do?
- At the hospital when my grandson was diagnosed with NDI, the nurses told his mother they could not cut his fingernails or toenails, and I thought this was just for diabetes mellitis patients. Now we are wondering if we should keep a close watch on his fee
- Could you explain, in layman's terms, what happens genetically when a father, daughter, and male child of the daughter all have DI?
- How can I help other families with NDI?
- How can a girl have NDI? I thought only boys had it.
- How is NDI treated?
- Is it possible to control the symptoms of NDI without medication--through diet and fluid intake alone?
- Is there any danger to the patient if use of any of the medications is discontinued suddenly as opposed to weaning a patient off the medication?
- Is there any way I can contribute to the search for treatment and a cure for NDI?
- Maxide is a brand-name diuretic to treat high-blood pressure. In my case, however, this diuretic causes my system to require less water intake and therefore less fluid output. Have you heard of this reverse-effect on persons with diabetes insipidus?
- What are potential new future treatments?
- What can I do to help support research for better treatment and a cure for NDI?
- Will NDI ever go away?
Used in 53 Proceeding abstracts
Used in 53 Proceeding abstracts
- Rescue of the Cell Surface Expression of Vasopressin V2 Receptor Mutants in Nephrogenic Diabetes Insipidus
- A Novel dominant mutation of the aquaporin-2 gene resulting in partial nephrogenic diabetes insipidus
- A defect in AQP2 phosphorylation at Ser256 in the Golgi apparatus might explain the molecular basis of the dominant form of NDI caused by the mutation E258K-AQP2
- A patient's perspective
- A pharmacological chaperone acting at the V2-vasopressin receptor offers a treatment for Nephrogenic Diabetes Insipidus
- A proposal for the building and maintenance of an AVPR2 molecular model database
- Action Mechanism of Pharmacological Chaperones Acting on the V2 Vasopressin Receptor in the Treatment of Nephrogenic Diabetes Insipidus
- Altered expression pattern of solute transporters in inner medulla of AQP1 (-/-) and CLC-nK1 (-/-) mice
- Amelioration of Polyuria in Nephrogenic Diabetes Insipidus due to Aquaporin-2 Deficiency
- An impaired routing of wild type aquaporin-2 after tetramerization with an aquaporin-2 mutant explains dominant nephrogenic diabetes insipidus
- Analysis of naturally occurring and in vitro mutations of the V2 receptor gene interfering with proper splicing
- Antidiuretic Effect of Hydrochlorothiazide in Lithium-Induced Nephrogenic Diabetes Insipidus Is Associated with Upregulation of Aquaporin-2, Na-Cl Cotransporter and Epithelial Sodium Channel
- Aquaporin 2-containing Apical Membrane Endosomes (AQP-2 Endosomes) Possess a Multiprotein Signaling Complex
- Calcineurin A-alpha knockout is a new model of nephrogenic diabetes insipidus
- Candesartan treatment prevents dysregulation of AQP2, BSC-1 and NaPi2 in ureteral obstruction-induced NDI
- Clinical Data and Cell Biological Aspects of Mutations in Nephrogenic Diabetes Insipidus
- Collecting Duct Specific Gene Regulation: Creation And Use of Transgenic Mouse Models
- Complete deletions of the vasopressin type 2 receptor gene in nephrogenic diabetes insipidus
- Contribution of chloride channels in urine concentrating ability
- Decreased Aquaporin-2 Water Channel Expression in Acquired Nephrogenic Diabetes Insipidus
- Differences between ER-retained vasopressin V2 receptor mutants in antagonist-mediated restoration of cell surface expression
- Diversity of Nephrogenic Diabetes Insipidus Mutations and Importance of Early Recognition and Treatment
- Downregulation of renal aquaporins and sodium transporters in rats with bilateral ureteral obstruction (BUO) is prevented by a-MSH treatment
- Dysregulation of genes in rats with lithium-induced NDI
- Follow up of NDI patients and presentation of a case report
- Functional rescue of truncated V2-Vasopressin-receptors by aminoglycoside-induced misreading of nonsense-mutations
- Lack of AVP-induced phosphorylation of the Aquaporin-2 mutants AQP2-R254L and AQP2-R254Q explains dominant Nephrogenic Diabetes Insipidus
- Lithium-induced Nephrogenic Diabetes Insipidus: A Cell Culture Model
- Long- and Short-Term Regulation of AQP2 Expression and Function
- Long-term regulation of aquaporin-2: a possible therapeutic approach to NDI?
- Mineralocorticoid receptor mediated ENaC and AQP2 regulation in rats with lithium-induced NDI
- Mono-ubiquitination and missorting to lysosomes of the Aquaporin-2 water channel mutant AQP2-E258K explains dominant Nephrogenic Diabetes Insipidus
- N-linked glycosylation is essential for transport of the Aquaporin-2 water channel to the plasma membrane in MDCK cells
- Nephrogenic Diabetes Insipidus Mutation Database
- Nephrogenic Diabetes Insipidus in mice lacking aquaporin-3 water channels
- Obstructive nephropathy -- a common acquired condition of nephrogenic diabetes insipidus
- Pharmacological Chaperones Functionally Rescue Misfolded V2-Vasopressin Receptor Mutants that Cause Nephrogenic Diabetes Insipidus: Potential Clinical Implications
- Pharmacological chaperones functionally rescue misfolded mutant V2 vasopressin receptors that cause nephrogenic diabetes insipidus
- Prostaglandins as Stimulants of AQP2 Expression: a Possible Future Treatment for NDI?
- Quality control of nephrogenic diabetes insipidus-causing vasopressin V2 receptor mutants in the ER and in the ER/Golgi intermediate compartment
- Regulation of renal aquaporins and sodium transporters in conditions with urinary tract obstruction
- Routing and function of mutant AQP2 water channels in nephrogenic diabetes insipidus
- Structure of V2 vasopressin receptor oligomers: evidence for contact dimer formation
- The Low Sodium Diet for Nephrogenic Diabetes Insipidus
- The Medical Geneticist's Perspective on NDI Research
- The Ontogeny and Regulation of AQP2 Gene Expression in the Ovine Fetal Kidney
- The last fifty years; a retrospective on NDI
- Thirteen Large Deletions/Rearrangements of the AVPR2 Gene Causing X-linked Nephrogenic Diabetes Insipidus
- Toward a mouse model of human non-X-linked NDI
- Two new Aquaporin-2 mutations responsible for Congenital Nephrogenic Diabetes Insipidus
- V2 vasopressin receptor mutants responsible for nephrogenic diabetes insipidus associate with the molecular chaperones calnexin and Hsp70
- V2 vasopressin receptor-deficient mouse model: Pathophysiological changes and therapeutical implications
- Vasopressin-Independent Regulation of Aquaporin-2 Protein
Used in 25 Proceeding translations
Used in 25 Proceeding translations
- Amelioration of Polyuria in Nephrogenic Diabetes Insipidus due to Aquaporin-2 Deficiency
- Aquaporin 2-containing Apical Membrane Endosomes (AQP-2 Endosomes) Possess a Multiprotein Signaling Complex
- Aquaporin-2 Expression in Primary Cultures of Rat Inner Medullary Collecting Duct Cells - A New In-Vitro Model System Facilitating the Study of the Vasopressin-Regulated Antidiuretic Machinery at the Cellular Level
- Biochemical Characterization of Partial Nephrogenic Diabetes Insipidus (NDI) Phenotypes
- Chemical Chaperones as a Novel Therapeutic Strategy for NDI
- Clinical Data and Cell Biological Aspects of Mutations in Nephrogenic Diabetes Insipidus
- Complete deletions of the vasopressin type 2 receptor gene in nephrogenic diabetes insipidus
- Follow up of NDI patients and presentation of a case report
- Functional investigations of the vasopressin regulated antidiuretic machinery in single inner medullary collecting duct (IMCD) cells
- Identification of proteins involved in the vasopressin-induced shuttle of aquaporin-2
- Identification of sequence determinants that direct different intracellular folding pathways for kidney aquaporins
- Long-term regulation of aquaporin-2: a possible therapeutic approach to NDI?
- Nephrogenic Diabetes Insipidus Patients in Japan
- Nephrogenic Diabetes Insipidus in a Palestine Sibship
- Nephrogenic Diabetes Insipidus in mice lacking aquaporin-3 water channels
- Nephrogenic diabetes insipidus in Italian families
- Nutritional Concerns for Persons with NDI
- Progress in the function and structure of aquaporin-1 and aquaporin-2
- Routing and function of mutant AQP2 water channels in nephrogenic diabetes insipidus
- Targeting of the V2 Vasopressin Receptor Gene in Mice
- The Medical Geneticist's Perspective on NDI Research
- The Ontogeny and Regulation of AQP2 Gene Expression in the Ovine Fetal Kidney
- V2 vasopressin receptor dysfunction in patients with nephrogenic diabetes insipidus is caused by different molecular mechanisms
- V2 vasopressin receptor mutants responsible for nephrogenic diabetes insipidus associate with the molecular chaperones calnexin and Hsp70
- Vasopressin-Independent Regulation of Aquaporin-2 Protein
Used in 32 Term definitions
Used in 32 Term definitions
- AD-NDI
- AQP2 protein
- AR-NDI
- CNDI
- NDI
- NDI Abstract of Article: 510
- NDI Abstract of Article: 538
- NDI Abstract of Article: 539
- acquired NDI
- acquired nephrogenic diabetes insipidus
- aquaporin 2
- aquaporin-2
- aquaporin-2s
- aquaporin2
- autosomal NDI
- autosomal nephrogenic diabetes insipidus
- autosomal recessive nephrogenic diabetes insipidus
- congenital nephrogenic diabetes insipidus
- dominant NDI
- end-organ resistance
- hereditary nephrogenic diabetes insipidus
- hypertonic dehydration
- kidney collecting duct cells
- kidney disorders
- lithium-induced NDI
- nephrogenic DI
- nephrogenic vasopressin-resistant diabetes
- recessive NDI
- synthetic AVP
- vasopressin
- vasopressin-resistant diabetes
- vasopressin-resistant diabetes insipidus