case
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:
- case
Used in 42 Article abstracts
Used in 42 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
- ADH Resistance of LLC-pk1 Cells Caused by Overexpression of cAMP-Phosphodiesterase Type-IV
- AQP3, p-AQP2, and AQP2 Expression is Reduced in Polyuric Rats With Hypercalcemia: Prevention by cAMP-PDE Inhibitors
- ARDS Following Acute Lithium Carbonate Intoxication
- Amphotericin B-Induced Partial Nephrogenic Diabetes Insipidus in a Child
- An Impaired Routing of Wild-type Aquaporin-2 after Tetramerization with an Aquaporin-2 Mutant Explains Dominant Nephrogenic Diabetes Insipidus
- Aquaporins: Roles in Renal Function and Peritoneal Dialysis
- Bladder Function Impairment in Aquaporin-2 Defective Nephrogenic Diabetes Insipidus
- Clinical Characteristics of Eight Patients with Congenital Nephrogenic Diabetes Insipidus
- Clinical Presentation and Follow-Up of 30 Patients with Congenital Nephrogenic Diabetes Insipidus
- Clinical Utility of Direct Mutation Testing for Congenital Nephrogenic Diabetes Insipidus in Families
- Congenital Nephrogenic Diabetes Insipidus in an Adult
- Effect of DDAVP on Nocturnal Enuresis in a Patient with Nephrogenic Diabetes Insipidus
- Emergency Treatment of Lithium-Induced Diabetes Insipidus with Nonsteroidal Anti-Inflammatory Drugs
- Heterodimerization of V1a and V2 Vasopressin Receptors Determines the Interaction with Beta-Arrestin and their Trafficking Patterns
- In Vitro Micro-Autoradiography of Atrial Natriuretic Peptide in Biopsy Specimens from Patients with Renal Diseases
- Indomethacin Treatment in Amphotericin B Induced Nephrogenic Diabetes Insipidus
- Lithium-Induced Nephrogenic Diabetes Insipidus Treated with Indomethacin
- Lithium-induced Nephrogenic Diabetes Insipidus
- Maternal Lithium Therapy and Polyhydramnios
- 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 Presenting After Head Trauma
- 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 persisting 57 months after cessation of lithium carbonate therapy: report of a case and review of the literature.
- 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).
- Persistent Nephrogenic Diabetes Insipidus Following Lithium Therapy
- Polyuria in Childhood
- Possible Liposomal Amphotericin B-Induced Nephrogenic Diabetes Insipidus
- Posterior Lobe of the Pituitary in Diabetes Insipidus: Dynamic MR Imaging
- Reconstitution of a Regulated Transepithelial Water Pathway in Cells Transfected with AQP2 and an AQP1/AQP2 Hybrid Containing the AQP2-C Terminus
- The valve bladder syndrome: 20 years later.
- 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
- Two Novel Types of Contiguous Gene Deletion of the AVPR2 and ARHGAP4 Genes in Unrelated Japanese Kindreds with Nephrogenic Diabetes Insipidus
- Very Severe Self-Poisoning Lithium Carbonate Intoxication Causing a Myocardial Infarction
- [Idiopathic Retroperitoneal Fibrosis Disclosed by Nephrogenic Diabetes Insipidus] (French)
- [Two Cases of Hypercalcemic Nephropathy Associated with Primary Hyperparathyroidism] (Japanese)
Used in 17 Article bodies
Used in 17 Article bodies
- A Congenital Renal Tubular Defect
- Hyperosmolar Coma and Lithium-induced Diabetes Insipidus
- 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
- 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
- Nephrogenic Diabetes Insipidus: Transmitted by Females and Appearing During Infancy in Males
- Notes on Some Cases of Diabetes Insipidus with Marked Family and Hereditary Tendencies
- 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 95 Article translations
Used in 95 Article translations
- A Low-Affinity Vasopressin V2-Receptor Gene in a Kindred with X-Linked Nephrogenic Diabetes Insipidus
- A Novel Deletion Mutation in the Arginine Vasopressin Receptor 2 Gene and Skewed X Chromosome Inactivation in a Female Patient with Congenital Nephrogenic Diabetes Insipidus
- A Serine Cluster Prevents Recycling of the V2 Vasopressin Receptor
- Amphotericin B-Induced Partial Nephrogenic Diabetes Insipidus in a Child
- An Aquaporin-2 Water Channel Mutant Which Causes Autosomal Dominant Nephrogenic Diabetes Insipidus is Retained in the Golgi Complex
- 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
- 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
- Aquaporin-2, a Vasopressin-sensitive Water Channel, and Nephrogenic Diabetes Insipidus
- Aquaporins: From Physiology to Nephrogenic Diabetes Insipidus
- Bidirectional Regulation of AQP2 Trafficking and Recycling: Involvement of AQP2-S256 Phosphorylation
- Bilateral Ureteral Obstruction Downregulates Expression of Vasopressin-Sensitive AQP-2 Water Channel in Rat Kidney
- Clinical Utility of Direct Mutation Testing for Congenital Nephrogenic Diabetes Insipidus in Families
- Congenital Nephrogenic Diabetes Insipidus in an Adult
- Detection of Skewed X-Inactivation in Two Female Carriers of Vasopressin Type 2 Receptor Gene Mutation
- Diabetes Insipidus (Robertson)
- Diabetes Insipidus [Bell]
- Differential Diagnosis and Pathophysiology of Diabetes Insipidus
- Do Aquaporins Have a Role in Nocturnal Enuresis?
- Effect of DDAVP on Nocturnal Enuresis in a Patient with Nephrogenic Diabetes Insipidus
- Endosomes from Kidney Collecting Tubule Cells Contain the Vasopressin-sensitive Water Channel
- Expression Studies of Two Vasopressin V2 Receptor Gene Mutations, R202C and 804insG, in Nephrogenic Diabetes Insipidus
- Fate of Antidiuretic Hormone Water Channel Proteins after Retrieval from Apical Membrane
- Functional Rescue of the Constitutively Internalized V2 Vasopressin Receptor Mutant R137H by the Pharmacological Chaperone Action of SR49059
- Functional Study of Two V2 Vasopressin Mutant Receptors Related to NDI: P322S and P322H
- GS-Activating Receptors: Modes of Transmembrane Signalling and Genetic Defects
- Genetic Renal Diseases in Children
- Hemifacial Spasm in Albright's Hereditary Osteodystrophy with Pseudopseudohypoparathyroidism and Nephrogenic Diabetes Insipidus--Case Report
- 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
- Hyponatremia and Hypernatremia
- 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
- Index of Suspicion. Case 2. Nephrogenic Diabetes Insipidus
- Indomethacin Treatment in Amphotericin B Induced Nephrogenic Diabetes Insipidus
- Indomethacin in the Treatment of Lithium-Induced Nephrogenic Diabetes Insipidus
- Inheritance of Mutations in the V2 Receptor Gene in Thirteen Families with Nephrogenic Diabetes Insipidus
- Inherited Diseases of the Kidney
- Intracranial Calcifications Associated with Nephrogenic Diabetes Insipidus
- Lithium-Induced Nephrogenic Diabetes Insipidus Treated with Indomethacin
- Lithium-Induced Nephrogenic Diabetes Insipidus Treated with Intravenous Ketorolac
- Maturation of Receptor Proteins in Eukaryotic Expression Systems
- Mesalazine Associated Nephrogenic Diabetes Insipidus Presenting as Weight Loss
- Methotrexate-Induced Nephrogenic Diabetes Insipidus: First Case Report
- Molecular Biology of Diabetes Insipidus
- Molecular Genetic Study of Congenital Nephrogenic Diabetes Insipidus and Rescue of Mutant Vasopressin V2 Receptor by Chemical Chaperones
- Molecular and Cellular Defects in Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus Caused By Mutation of Tyr205: A Key Residue of V2 Vasopressin Receptor Function
- 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, Thiazide Treatment and Renal Cell Carcinoma
- Nephrogenic Diabetes Insipidus--Prodromal Phase of Multiple Myeloma
- Nephrogenic Diabetes Insipidus. A V2 Vasopressin Receptor Unable to Stimulate Adenylyl Cyclase
- Nephrogenic Diabetes Insipidus: A Cause of Severe Nonobstructive Urinary Tract Dilatation
- Nephrogenic Diabetes Insipidus: Causes Revealed
- Nephrogenic Diabetes Insipidus: Transmitted by Females and Appearing During Infancy in Males
- 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
- 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
- Pharmacological Chaperones: Potential Treatment for Conformational Diseases
- Phenotypes Developed in Secretin Receptor-Null Mice Indicated a Role for Secretin in Regulating Renal Water Reabsorption
- Phosphorylation of the V2 Vasopressin Receptor
- Physiology and Pathophysiology of the Aquaporin-2 Water Channel
- Possible Liposomal Amphotericin B-Induced Nephrogenic Diabetes Insipidus
- Posterior Lobe of the Pituitary in Diabetes Insipidus: Dynamic MR Imaging
- Prolongation of Antidiuretic Response to Desmopressin Acetate by Iontophoretic Transdermal Delivery in Rats
- Proposed Cause of Marked Vasopressin Resistance in a Female with an X-Linked Recessive V2 Receptor Abnormality
- Reconstitution of Mutant V2 Vasopressin Receptors by Adenovirus-mediated Gene Transfer
- Reconstitution of a Regulated Transepithelial Water Pathway in Cells Transfected with AQP2 and an AQP1/AQP2 Hybrid Containing the AQP2-C Terminus
- Recurrent Dehydration in a Young Girl
- Rescue of Vasopressin V2 Receptor Mutants by Chemical Chaperones: Specificity and Mechanism
- Risk Factors for Ifosfamide Nephrotoxicity in Children
- Role of Aquaporins in Water Balance Disorders
- Role of Inner Medullary Collecting Duct NaCl Transport in Urinary Concentration
- The Management of Diabetes Insipidus in Adults
- The Molecular Basis of Nephrogenic Diabetes Insipidus
- 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
- Treatment of Congenital Nephrogenic Diabetes Insipidus by Hydrochlorothiazide and Cyclooxygenase-2 Inhibitor
- Two Novel Mutations in the Aquaporin-2 and the Vasopressin V2 Receptor Genes in Patients with Congenital Nephrogenic Diabetes Insipidus
- Two Novel Mutations in the Vasopressin V2 Receptor Gene in Unrelated Japanese Kindreds with Nephrogenic Diabetes Insipidus
- Vasopressin Receptors in Health and Disease
- Water Channels Encoded by Mutant Aquaporin-2 Genes in Nephrogenic Diabetes Insipidus are Impaired in Their Cellular Routing
- cDNA and Genomic Cloning of Mouse Aquaporin-2: Functional Analysis of an Orthologous Mutant Causing Nephrogenic Diabetes Insipidus
Used in 6 Faq answers
Used in 6 Faq answers
- What causes NDI?
- How can a girl have NDI? I thought only boys had it.
- How do I know if I am a carrier of the NDI gene? Do I need genetic screening, and if so, how do I get that?
- How is NDI treated?
- How would I know if I carry a defective gene that could result in NDI if passed onto my children?
- Should females with NDI be medicated differently than males?
Used in 11 Proceeding abstracts
Used in 11 Proceeding abstracts
- An impaired routing of wild type aquaporin-2 after tetramerization with an aquaporin-2 mutant explains dominant nephrogenic diabetes insipidus
- Characterization of mutant vasopressin V2 receptors with a misfolded AVP binding site
- Clinical analysis of eight Japanese patients with congenital nephrogenic diabetes insipidus
- Complete deletions of the vasopressin type 2 receptor gene in nephrogenic diabetes insipidus
- Differences between ER-retained vasopressin V2 receptor mutants in antagonist-mediated restoration of cell surface expression
- Follow up of NDI patients and presentation of a case report
- Impaired routing of AQP2 to late endosomes/lysosomes following heterotetramerization with AQP2-E258K is likely to explain dominant nephrogenic diabetes insipidus
- Mutations of the vasopressin V2 receptor gene in X-linked Nephrogenic Diabetes Insipidus: functional analysis of receptor mutants and identification of new mutations in Italian families.
- Pitfalls in the Differential Diagnosis of Nephrogenic Diabetes Insipidus.
- Prostaglandins as Stimulants of AQP2 Expression: a Possible Future Treatment for NDI?
- V2 vasopressin receptor dysfunction in patients with nephrogenic diabetes insipidus is caused by different molecular mechanisms
Used in 7 Proceeding translations
Used in 7 Proceeding translations
- An impaired routing of wild type aquaporin-2 after tetramerization with an aquaporin-2 mutant explains dominant nephrogenic diabetes insipidus
- Clinical Data and Cell Biological Aspects of Mutations in Nephrogenic Diabetes Insipidus
- Follow up of NDI patients and presentation of a case report
- Functional rescue of three vasopressin V2 receptor mutants causing nephrogenic diabetes insipidus by a second site suppressor mutation
- Functional studies of twelve mutant V2 vasopressin receptors related to nephrogenic diabetes insipidus: molecular basis of a mild clinical phenotype.
- Pitfalls in the Differential Diagnosis of Nephrogenic Diabetes Insipidus.
- V2 vasopressin receptor dysfunction in patients with nephrogenic diabetes insipidus is caused by different molecular mechanisms
Used in 31 Term definitions
Used in 31 Term definitions
- breast cancer
- case
- case study
- control
- control group
- control rats
- cure
- diagnosis
- end-organ resistance
- genitive
- immunoglobulins
- index case
- kidney cancer
- leg
- median
- oncotic pressure
- parameter
- principle
- proerythroblast
- proerythroblasts
- prognosis
- protocol
- purpura
- renal lithium clearance
- subsumed
- tubular epithelium
- two base deletion
- type
- urinary osmolality
- urine osmolality
- vasopressin-sensitive water channel



