associated
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:
- associated
Used in 115 Article abstracts
Used in 115 Article abstracts
- 1-Desamino-8-D-Arginine Vasopressin (DDAVP) in Patients with Congenital Nephrogenic Diabetes Insipidus
- A historical cohort study of kidney damage in long-term lithium patients: continued surveillance needed.
- AQP3, p-AQP2, and AQP2 Expression is Reduced in Polyuric Rats With Hypercalcemia: Prevention by cAMP-PDE Inhibitors
- AVPR2 Variants and V2 Vasopressin Receptor Function in Nephrogenic Diabetes Insipidus
- 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 COX-1, COX-2, and mPGES in Rats with Nephrogenic and Central Diabetes Insipidus
- Altered Expression of Major Renal Na Transporters in Rats with Unilateral Ureteral Obstruction
- 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 Decreases Adenylyl Cyclase Activity and Aquaporin-2 Expression in Rat Kidney
- Amphotericin B-Induced Partial Nephrogenic Diabetes Insipidus in a Child
- Angiotensin II AT1 Receptor Blockade Decreases Vasopressin-Induced Water Reabsorption and AQP2 Levels in NaCl-Restricted Rats
- Apical Extracellular Calcium/Polyvalent Cation-sensing Receptor Regulates Vasopressin-elicited Water Permeability in Rat Kidney Inner Medullary Collecting Duct
- Apparent Loss-of-Function Mutant GPCRs Revealed as Constitutively Desensitized Receptors
- Aquaporin-2 Trafficking is Regulated by PDZ-domain Containing Protein SPA-1
- Aquaporins in the Kidney: From Molecules to Medicine
- Association of Calnexin With Wild Type and Mutant AVPR2 that Cause Nephrogenic Diabetes Insipidus
- Bilateral Ureteral Obstruction Downregulates Expression of Vasopressin-Sensitive AQP-2 Water Channel in Rat Kidney
- Biochemical Basis of Partial Nephrogenic Diabetes Insipidus Phenotypes
- Bladder Function Impairment in Aquaporin-2 Defective Nephrogenic Diabetes Insipidus
- Bradykinin Signaling Counteracts cAMP-elicited aquaporin 2 translocation in renal cells
- Changes of Rat Kidney AQP2 and Na,K-ATPase mRNA Expression in Lithium-Induced Nephrogenic Diabetes Insipidus
- Clinical Utility of Direct Mutation Testing for Congenital Nephrogenic Diabetes Insipidus in Families
- Concentrating Defect in Experimental Nephrotic Syndrome: Altered Expression of Aquaporins and Thick Ascending Limb Na+ Transporters
- Congestive Heart Failure in Rats is Associated with Increased Expression and Targeting of Aquaporin-2 Water Channel in Collecting Duct
- Constitutive Arrestin-Mediated Desensitization of a Human Vasopressin Receptor Mutant Associated with Nephrogenic Diabetes Insipidus
- Dehydration Reverses Vasopressin Antagonist-Induced Diuresis and Aquaporin-2 Downregulation in Rats
- Diabetes Insipidus in Children: Pathophysiology, Diagnosis and Management
- Do Aquaporins Have a Role in Nocturnal Enuresis?
- Downregulation of AQP1, -2, and -3 After Ureteral Obstruction is Associated With a Long-Term Urine-Concentrating Defect
- Downregulation of Aquaporin-2 and -3 in Aging Kidney is Independent of V2 Vasopressin Receptor
- Downregulation of Renal Aquaporins in Response to Unilateral Ureteral Obstruction
- Dynein and dynactin colocalize with AQP2 water channels in intracellular vesicles from kidney collecting duct
- Early Onset Bilateral Calcifications and Epilepsy
- Escape from Vasopressin-Induced Antidiuresis: Role of Vasopressin Resistance of the Collecting Duct
- Evidence for Dual Signaling Pathways for V2 Vasopressin Receptor in Rat Inner Medullary Collecting Duct
- Expression Studies of Two Vasopressin V2 Receptor Gene Mutations, R202C and 804insG, in Nephrogenic Diabetes Insipidus
- Expression of Renal Aquaporins 1, 2, and 3 in a Rat Model of Cisplatin-Induced Polyuria
- Foscarnet Alters Antidiuretic Hormone-Mediated Transport
- Fourfold Reduction of Water Permeability in Inner Medullary Collecting Duct of Aquaporin-4 Knockout Mice
- Functional Characterization of the Molecular Defects Causing Nephrogenic Diabetes Insipidus in Eight Families
- Genetics of Vasopressin Receptors
- Heterodimerization of V1a and V2 Vasopressin Receptors Determines the Interaction with Beta-Arrestin and their Trafficking Patterns
- Hypokalemia-Induced Downregulation of Aquaporin-2 Water Channel Expression in Rat Kidney Medulla and Cortex
- Hyponatremia and Hypernatremia
- Identification of Mutations in the Arginine Vasopressin Receptor 2 Gene Causing Nephrogenic Diabetes Insipidus in Chinese Patients
- Identification of a Multiprotein "Motor" Complex Binding to Water Channel Aquaporin-2
- Impaired Aquaporin and Urea Transporter Expression in Rats with Adriamycin-Induced Nephrotic Syndrome
- Impaired Urinary Concentration After Vasopressin and its Gradual Correction in Hypothalamic Diabetes Insipidus
- Impairment of AVP Regulation in 17alpha-Hydroxylase Deficiency, a Unique Form of Adrenal Insufficiency
- Intrafamilial Phenotype Variability in Nephrogenic Diabetes Insipidus
- Kidney Damage in Long-Term Lithium Patients: A Cross-Sectional Study of Patients with 15 Years or More on Lithium
- Lithium Nephrotoxicity
- Lithium Nephrotoxicity: A Progressive Combined Glomerular and Tubulointerstitial Nephropathy
- Lithium-Induced Nephrogenic Diabetes Insipidus Treated with Indomethacin
- Lithium-induced Nephrogenic Diabetes Insipidus
- Lithiumogenic Disorders of the Thyroid and Parathyroid Glands as Surgical Disease
- Long-Term Regulation of Collecting Duct Water Permeability: Freeze-Fracture Analysis of Isolated Perfused Tubules
- Loss of Calcineurin Aα Results in Altered Trafficking of AQP2 and in Nephrogenic Diabetes Insipidus
- MAL Decreases the Internalization of the Aquaporin-2 Water Channel
- Mechanism of Antidiuresis Caused by Bendroflumethiazide in Conscious Rats with Diabetes Insipidus
- Modulation of Plasma and Platelet Vasopressin by Cardiac Function in Patients with Heart Failure
- Molecular Analyses of the Vasopressin Type 2 Receptor and Aquaporin-2 Genes in Brazilian Kindreds with Nephrogenic Diabetes Insipidus
- 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 in Mice Lacking All Nitric Oxide Synthase Isoforms
- Neurogenic Disorders of Osmoregulation
- Nonmuscle Myosin II and Myosin Light Chain Kinase are Downstream Targets for Vasopressin Signaling in the Renal Collecting Duct
- Novel Vasopressin Type 2 (AVPR2) Gene Mutations in Brazilian Nephrogenic Diabetes Insipidus Patients
- Pathophysiology of Aquaporin-2 in Water Balance Disorders
- Pathophysiology of Renal Fluid Retention
- Pemetrexed-Induced Acute Renal Failure, Nephrogenic Diabetes Insipidus, and Renal Tubular Acidosis in a Patient with Non-Small Cell Lung Cancer
- Polyuria and Polydipsia. Problems Associated with Patient Evaluation
- Possible Liposomal Amphotericin B-Induced Nephrogenic Diabetes Insipidus
- Rat Kidney Papilla Contains Abundant Synaptobrevin Protein that Participates in the Fusion of Antidiuretic Hormone-regulated Water Channel-containing Endosomes In Vitro
- Rat Renal Arcade Segment Expresses Vasopressin-regulated Water Channel and Vasopressin V2 Receptor
- Redistribution of Aquaporin-2 Water Channels Induced by Vasopressin in Rat Kidney Inner Medullary Collecting Duct
- Regulation of Membrane Permeability by Vasopressin; Activation of the Water Permeability Pathway in Toad Urinary Bladder by N-Ethyl-Maleimide
- Renal Expression of Sodium Transporters and Aquaporin-2 in Hypothyroid Rats
- Renal Resistance to Vasopressin in Poorly Controlled Type 1 Diabetes Mellitus
- 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
- Rho Inhibits cAMP-Induced Translocation of Aquaporin-2 into the Apical Membrane of Renal Cells
- Risk Factors for Ifosfamide Nephrotoxicity in Children
- Role of Aquaporins in Water Balance Disorders
- Role of Renal Aquaporins in Escape from Vasopressin-induced Antidiuresis in Rat
- Role of Sodium Depletion in Acute Antidiuretic Effect of Bendroflumethiazide in Rats with Nephrogenic Diabetes Insipidus
- Segment Specific ENaC Downregulation in Kidney of Rats with Lithium-Induced NDI
- Ser-256 Phosphorylation Dynamics of Aquaporin 2 During Maturation From the Endoplasmic Reticulum to the Vesicular Compartment in Renal Cells
- 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 Aquaporins. A Family of Water Channel Proteins
- 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
- 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 Nephrogenic Diabetes Insipidus with Hydrochlorothiazide and Amiloride
- Upregulation of Collecting Duct Aquaporin-2 by Metabolic Acidosis: Role of Vasopressin
- Vasopressin Activates Collecting Duct Urea Transporters and Water Channels by Distinct Physical Processes
- Vasopressin Receptor Mutations Causing Nephrogenic Diabetes Insipidus
- 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 Permeability and Fluidity of Renal Basolateral Membranes
- Water Transport in the Kidney and Nephrogenic Diabetes Insipidus
- Xanthopterin-Induced Renal Dysfunction: A Reversible Model of Crystal Nephropathy
- [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)
- [Pathological Aspects of Water Transport in the Collecting Ducts] (French)
- [Simultaneous Familial Occurrence of Distal Renal Tubular Acidosis, Polycystic Kidney and Nephrogenic Diabetes Insipidus] (Hungarian)
- [Two Cases of Hypercalcemic Nephropathy Associated with Primary Hyperparathyroidism] (Japanese)
- cDNA Array Identification of Genes Regulated in Rat Renal Medulla in Response to Vasopressin Infusion
Used in 19 Article bodies
Used in 19 Article bodies
- A Congenital Renal Tubular Defect
- 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
- Hereditary Vasopressin Resistance in Man and Mouse
- 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
- Molecular Analysis of X-Linked Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus Secondary to Lithium Therapy in the Postoperative Patient: A Case Report
- 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
- 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
- Role of Vasopressin in Abnormal Water Excretion in Cirrhotic Patients
Used in 94 Article translations
Used in 94 Article translations
- 1-Desamino-8-D-Arginine Vasopressin (DDAVP) in Patients with Congenital Nephrogenic Diabetes Insipidus
- A Compartmental Model Predicts that Dietary Potassium Affects Lithium Dynamics in Rats
- A Heterotrimeric G Protein of the Gi Family is Required for cAMP-triggered Trafficking of Aquaporin 2 in Kidney Epithelial Cells
- 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
- 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
- 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
- Aquaporins: From Physiology to Nephrogenic Diabetes Insipidus
- Association of Calnexin With Wild Type and Mutant AVPR2 that Cause Nephrogenic Diabetes Insipidus
- Bilateral Ureteral Obstruction Downregulates Expression of Vasopressin-Sensitive AQP-2 Water Channel in Rat Kidney
- Binding-, Intracellular Transport-, and Biosynthesis-Defective Mutants of Vasopressin Type 2 Receptor in Patients with X-Linked Nephrogenic Diabetes Insipidus
- Causes of Reversible Nephrogenic Diabetes Insipidus: A Systematic Review
- Changes of Rat Kidney AQP2 and Na,K-ATPase mRNA Expression in Lithium-Induced Nephrogenic Diabetes Insipidus
- Cognitive and Psychosocial Functioning of Patients with Congenital Nephrogenic Diabetes Insipidus
- Congenital Nephrogenic Diabetes Insipidus
- Congestive Heart Failure in Rats is Associated with Increased Expression and Targeting of Aquaporin-2 Water Channel in Collecting Duct
- Correlation between Magnetic Resonance Imaging of Posterior Pituitary and Neurohypophyseal Function in Children with Diabetes Insipidus
- Defects of G Protein-Coupled Signal Transduction in Human Disease
- Diabetes Insipidus (Hendy, Bichet)
- Differential Diagnosis of Polyuria
- Disordered Water Channel Expression and Distribution in Acquired Nephrogenic Diabetes Insipidus
- Downregulation of Aquaporin-2 Parallels Changes in Renal Water Excretion in Unilateral Ureteral Obstruction
- Dual Actions of Vasopressin and Oxytocin in Regulation of Water Permeability in Terminal Collecting Duct
- Dynein and dynactin colocalize with AQP2 water channels in intracellular vesicles from kidney collecting duct
- Early Onset Bilateral Calcifications and Epilepsy
- 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
- Functional Analysis of Aquaporin-2 Mutants Associated with Nephrogenic Diabetes Insipidus by Yeast Expression
- Hemifacial Spasm in Albright's Hereditary Osteodystrophy with Pseudopseudohypoparathyroidism and Nephrogenic Diabetes Insipidus--Case Report
- Heterogeneous AVPR2 Gene Mutations in Congenital Nephrogenic Diabetes Insipidus
- Hyperuricemia as a Clue for Central Diabetes Insipidus (Lack of V1 Effect) in the Differential Diagnosis of Polydipsia
- Hyponatremia and Hypernatremia
- Identification of a Multiprotein "Motor" Complex Binding to Water Channel Aquaporin-2
- Ifosfamide-induced Renal Fanconi Syndrome with Associated Nephrogenic Diabetes Insipidus in an Adult Patient
- Impaired Aquaporin and Urea Transporter Expression in Rats with Adriamycin-Induced Nephrotic Syndrome
- 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
- Indomethacin Enhances Shuttling of Aquaporin-2 Despite Decreased Abundance in Rat Kidney
- Intracranial Calcification in Nephrogenic Diabetes Insipidus
- Intrafamilial Phenotype Variability in Nephrogenic Diabetes Insipidus
- Kidney Damage in Long-Term Lithium Patients: A Cross-Sectional Study of Patients with 15 Years or More on Lithium
- Lithium-Induced Nephrogenic Diabetes Insipidus Treated with Indomethacin
- Lithiumogenic Disorders of the Thyroid and Parathyroid Glands as Surgical Disease
- MAL Decreases the Internalization of the Aquaporin-2 Water Channel
- Mechanism of Vasopressin Action in the Renal Collecting Duct
- Meniere's Disease in Congenital Nephrogenic Diabetes Insipidus: Report of Two Twins
- 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 Analysis of X-Linked Nephrogenic Diabetes Insipidus
- Molecular Insights into the Pathogenesis of Inherited Renal Tubular Disorders
- Molecular and Cellular Defects in Nephrogenic Diabetes Insipidus
- Mutations in the Vasopressin V2 Receptor and Aquaporin-2 Genes in 12 Families with Congenital Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus (Bichet - November 1998)
- Nephrogenic Diabetes Insipidus (Bichet)
- Nephrogenic Diabetes Insipidus in Mice Lacking All Nitric Oxide Synthase Isoforms
- 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: Clinical Symptoms, Pathogenesis, Genetics and Treatment
- Pathophysiology of Aquaporin-2 in Water Balance Disorders
- Pathophysiology of the Aquaporin Water Channels
- Pemetrexed-Induced Acute Renal Failure, Nephrogenic Diabetes Insipidus, and Renal Tubular Acidosis in a Patient with Non-Small Cell Lung Cancer
- 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
- Polyuria in Childhood
- Recurrent Dehydration in a Young Girl
- Regulation of Collecting Duct Water Channel Expression by Vasopressin in Brattleboro Rat
- Regulation of Collecting Duct Water Permeability Independent of cAMP-Mediated AVP Response
- Rescue of a Nephrogenic Diabetes Insipidus-Causing Vasopressin V2 Receptor Mutant by Cell-Penetrating Peptides
- Risk Factors for Ifosfamide Nephrotoxicity in Children
- Role of Aquaporin Water Channels in Kidney and Lung
- Role of Aquaporins in Water Balance Disorders
- Role of Sodium Depletion in Acute Antidiuretic Effect of Bendroflumethiazide in Rats with Nephrogenic Diabetes Insipidus
- Severely Impaired Urinary Concentrating Ability in Transgenic Mice Lacking Aquaporin-1 Water Channels
- Severely Impaired Urine-Concentrating Ability in Mice Lacking the CLC-K1 Chloride Channel
- Structure and Chromosomal Localization of the Human Antidiuretic Hormone Receptor Gene
- The Clinical Importance of the Urinary Excretion of Aquaporin-2
- The Molecular Basis of Nephrogenic Diabetes Insipidus
- The Role of Membrane Turnover in the Water Permeability Response to Antidiuretic Hormone
- Three Novel AVPR2 Mutations in Three Japanese Families with X-Linked Nephrogenic Diabetes Insipidus
- Transient Central Diabetes Insipidus in the Setting of Underlying Chronic Nephrogenic Diabetes Insipidus Associated with Lithium Use
- 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 Mutations in the Aquaporin-2 and the Vasopressin V2 Receptor Genes in Patients with Congenital Nephrogenic Diabetes Insipidus
- Type 2 Vasopressin Receptor Gene, the Gene Responsible for Nephrogenic Diabetes Insipidus, Maps to Xq28 Close to the LICAM Gene
- Urea Transporter UT-A1 and Aquaporin-2 Proteins Decrease in Response to Angiotensin II or Norepinephrine-Induced Acute Hypertension
- V2 Vasopressin Receptor Dysfunction in Nephrogenic Diabetes Insipidus Caused By Different Molecular Mechanisms
- Vasopressin Receptors in Health and Disease
- Vasopressin Type-2 Receptor and Aquaporin-2 Water Channel Mutants in Nephrogenic Diabetes Insipidus
- Water Channels
- Water Channels in Cell Membranes
- Water Transport Across Mammalian Cell Membranes
- Xanthopterin-Induced Renal Dysfunction: A Reversible Model of Crystal Nephropathy
Used in 25 Proceeding abstracts
Used in 25 Proceeding abstracts
- Renal medullary gene expression in aquaporin-1 null mice
- 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
- 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
- Candesartan treatment prevents dysregulation of AQP2, BSC-1 and NaPi2 in ureteral obstruction-induced NDI
- Clinical Phenotype and Molecular Characterization of A Mutant V2 Receptor Associated with Partial Congenital Nephrogenic Diabetes Insipidus
- Congenital (present a birth) severe diabetes insipidus. Most patients have nephrogenic diabetes insipidus (NDI), but some patients have autosomal recessive central (neurogenic) diabetes insipidus
- Correction of age-related polyuria by dDAVP: Molecular involvement of aquaporins and urea transporters
- 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
- Effects of Carbenoxolone on Sodium Transporter and Aquaporin-2 Abundance in Kidney
- Expressional alteration of sodium transporter in the thick ascending limb of Henle and urinary concentration
- Growth in males with (well-managed) nephrogenic diabetes insipidus
- Lithium-induced Nephrogenic Diabetes Insipidus: A Cell Culture Model
- Mineralocorticoid receptor mediated ENaC and AQP2 regulation in rats with lithium-induced NDI
- Mutations in the vasopressin V2 receptor and aquaporin-2 genes in twelve families with congenital nephrogenic diabetes insipidus
- Obstructive nephropathy -- a common acquired condition of nephrogenic diabetes insipidus
- Purinergic Control of Medullary Collecting Duct Function: A Novel Vasopressin-independent Regulatory Mechanism
- Recycling of the V2 Vasopressin Receptor
- Regulation of renal aquaporins and sodium transporters in conditions with urinary tract obstruction
- The Ontogeny and Regulation of AQP2 Gene Expression in the Ovine Fetal Kidney
- Toward gene therapy for nephrogenic diabetes insipidus
- Variations in clinical phenotype associated with different mutations of the V2 receptor gene in X-linked recessive congenital nephrogenic DI (xCNDI)
- Vasopressin-V2-receptor dependent and independent regulation of collecting duct aquaporin-2 expression and trafficking
Used in 17 Proceeding translations
Used in 17 Proceeding translations
- 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
- Clinical Data and Cell Biological Aspects of Mutations in Nephrogenic Diabetes Insipidus
- Clinical presentation of the polyuric and hyperprostaglandinuric salt losing tubulopathies (HPS/aBS) and the therapeutic option with COX inhibitors
- Congenital (present a birth) severe diabetes insipidus. Most patients have nephrogenic diabetes insipidus (NDI), but some patients have autosomal recessive central (neurogenic) diabetes insipidus
- 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
- Expressional alteration of sodium transporter in the thick ascending limb of Henle and urinary concentration
- Identification of proteins involved in the vasopressin-induced shuttle of aquaporin-2
- Lithium-induced Nephrogenic Diabetes Insipidus: A Cell Culture Model
- 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
- Mutations in the vasopressin V2 receptor and aquaporin-2 genes in twelve families with congenital 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.
- Obstructive nephropathy -- a common acquired condition of nephrogenic diabetes insipidus
- Recycling of the V2 Vasopressin Receptor
- The Medical Geneticist's Perspective on NDI Research
- Toward gene therapy for nephrogenic diabetes insipidus
Used in 131 Term definitions
Used in 131 Term definitions
- Bartter's syndrome
- Fanconi syndrome
- Fanconi's syndrome
- Golgi
- Golgi Complex
- MALDI-TOF
- MALDI-TOF mass spectrometry
- Mycobacterium avium-intracellulare
- NADPH oxidase
- REM sleep
- T lymphocytes
- Turner's syndrome
- X-linked gene
- absorptive cell
- academic
- acute promyelocytic leukemia
- affiliation
- agitation
- alcohol dependence
- amyloidosis
- antigenic shift
- aplastic anemia
- atonic neurogenic bladder
- autonomic plexuses
- basement membrane
- cancer
- chorioallantois
- chromosome
- chronic granulocytic leukemia
- club
- collagen fibrils
- collagenoblasts
- complicated
- condensation
- confabulation
- conjunctivitis
- coronary thrombosis
- correlation
- couple
- cowpox
- cyanocobalamin
- cytochrome c oxidase
- dentistry
- depressed
- digestive system
- down-regulates
- downregulation
- dysthymia
- electric field
- electromagnetic field
- emotion
- epididymo-orchitis
- factor VII
- fasciculus
- food poisoning
- fraternity
- gadopentetate dimeglumine
- gamma ray
- gangrene
- gene
- genes
- gentian violet
- gouty nephropathy
- gustatory
- histone
- humoralism
- hydrocephalus
- hypersensitivity reaction
- hypersensitivity reactions
- hyperviscosity syndrome
- hypokalemic alkalosis
- hypoparathyroidism
- hypostatic
- immunocytic amyloidosis
- immunopathology
- individual
- lichen myxedematosus
- light chain nephropathy
- limbic system
- linkage
- linkage analysis
- loop diuretics
- low-renin hypertension
- lymphoblastic leukemia
- lymphoid system
- lymphoproliferative disorders
- malaria
- mathematical expectation
- meningism
- mental deficiency
- mental retardation
- microcephaly
- multiple myeloma
- mumps
- myelomanephropathy
- myxedema
- nucleus subcuneiformis
- organizing pneumonia
- orthopedics
- pancreatitis
- polycystic disease of the kidneys
- pre-eclampsia
- primary amyloidosis
- primary syphilis
- prokaryote
- pseudohypoparathyroidism
- psychomotor agitation
- pulmonary embolism
- purpura
- regulatory gene
- risk factors
- roentgen
- sacroiliac
- senility
- septic shock
- sex chromosomes
- software
- streptococcus and Streptococcus
- streptozocin
- syndrome of inappropriate antidiuretic hormone secretion
- thalamus
- thirst
- thirsting
- thrombocytopenic purpura
- thrombophlebitis
- thymus
- underfilling theory
- vaccinia
- vasovagal attack
- von Willebrand's disease
- zinc



