kidneys
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:
- kidneys
-
A pair of vertebrate organs situated in the body cavity near the spinal column that excrete waste products of metabolism, in man are bean-shaped organs about 4-1/2 inches long lying behind the peritoneum in a mass of fatty tissue, and consist chiefly of nephrons by which urine is secreted, collected, and discharged into a main cavity whence it is conveyed by the ureter to the bladder.
Used in 31 Article abstracts
Used in 31 Article abstracts
- A Compartmental Model Predicts that Dietary Potassium Affects Lithium Dynamics in Rats
- Altered Expression of COX-1, COX-2, and mPGES in Rats with Nephrogenic and Central Diabetes Insipidus
- Aquaporin Expression in Normal Human Kidney and in Renal Disease
- Concentrating Defect in Experimental Nephrotic Syndrome: Altered Expression of Aquaporins and Thick Ascending Limb Na+ Transporters
- Development and Characterization of a Mouse Cell Line Expressing the Human V2 Vasopressin Receptor Gene
- Development of Lithium-Induced Nephrogenic Diabetes Insipidus is Dissociated from Adenylyl Cyclase Activity
- Downregulation of AQP1, -2, and -3 After Ureteral Obstruction is Associated With a Long-Term Urine-Concentrating Defect
- Downregulation of Aquaporin-2 Parallels Changes in Renal Water Excretion in Unilateral Ureteral Obstruction
- Downregulation of Renal Aquaporins in Response to Unilateral Ureteral Obstruction
- Effect of an Acute Oral Ibuprofen Intake on Urinary Aquaporin-2 Excretion in Healthy Humans
- Expression of Vasopressin V1a and V2 Receptor Messenger Ribonucleic Acid in the Liver and Kidney of Embryonic, Developing, and Adult Rats
- Impaired Aquaporin and Urea Transporter Expression in Rats with Adriamycin-Induced Nephrotic Syndrome
- Membrane Traffic After Inhibition of Endocytosis in Renal Proximal Tubules
- Methyl-β-Cyclodextrin Induces Vasopressin-Independent Apical Accumulation of Aquaporin-2 in the Isolated, Perfused Rat Kidney
- Metoprine-induced Thirst and Diuresis in Wistar Rats
- Neonatal Mortality in an Aquaporin-2 Knock-in Mouse Model of Recessive Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus. An Unusual Presentation of Recurrent Rectal Cancer
- 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).
- Oxytocin Induces Apical and Basolateral Redistribution of Aquaporin-2 in Rat Kidney
- Role of Inner Medullary Collecting Duct NaCl Transport in Urinary Concentration
- Severe Lactic Acidosis and Renal Involvement in a Patient with Relapsed Burkitt's Lymphoma
- The Perinatal Expression of Aquaporin-2 and Aquaporin-3 in Developing Kidney
- The Property of a Novel V2 Receptor Mutant in a Patient with Nephrogenic Diabetes Insipidus
- Transient Nephrogenic Diabetes Insipidus Accompanied by Possible Psychogenic Polydipsia
- Transport Defects of Rabbit Inner Medullary Collecting Duct Cells in Obstructive Nephropathy
- Treating lithium-induced nephrogenic diabetes insipidus with a COX-2 inhibitor improves polyuria via upregulation of AQP2 and NKCC2.
- V2R Structure and Diabetes Insipidus
- Vasopressin Receptor Mutations and Nephrogenic Diabetes Insipidus
- Water Transport in the Kidney and Nephrogenic Diabetes Insipidus
- Xanthopterin-Induced Renal Dysfunction: A Reversible Model of Crystal Nephropathy
- [Expression of Aquaporin in Rats' Endolymphatic Sac and Kidney and the Effect of Anti-Diuretic Hormone on the Expression of Aquaporin]
Used in 10 Article bodies
Used in 10 Article bodies
- A Congenital Renal Tubular Defect
- Hereditary Vasopressin Resistance in Man and Mouse
- 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: Transmitted by Females and Appearing During Infancy in Males
- Notes on Some Cases of Diabetes Insipidus with Marked Family and Hereditary Tendencies
- Proposed Cause of Marked Vasopressin Resistance in a Female with an X-Linked Recessive V2 Receptor Abnormality
- Role of Aquaporin-2 Water Channels in Urinary Concentration and Dilution Defects
Used in 166 Article translations
Used in 166 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 Fully Active Nonglycosylated V2 Vasopressin Receptor
- A Low-Affinity Vasopressin V2-Receptor Gene in a Kindred with X-Linked Nephrogenic Diabetes Insipidus
- A Variant of Nephrogenic Diabetes Insipidus: V2 Receptor Abnormality Restricted to the Kidney
- Aldose Reductase-Deficient Mice Develop Nephrogenic Diabetes Insipidus
- Amphotericin B Decreases Adenylyl Cyclase Activity and Aquaporin-2 Expression in Rat Kidney
- 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
- Angiotensin II AT1 Receptor Blockade Decreases Vasopressin-Induced Water Reabsorption and AQP2 Levels in NaCl-Restricted Rats
- Angiotensin II Upregulates the Expression of Vasopressin V2 mRNA in the Inner Medullary Collecting Duct of the Rat
- Aquaporin-2 Water Channel Mutations and Nephrogenic Diabetes Insipidus: New Variations on a Theme
- Aquaporins: From Physiology to Nephrogenic Diabetes Insipidus
- Autosomal Recessive Nephrogenic Diabetes Insipidus Caused by an Aquaporin-2 Mutation
- Bilateral Ureteral Obstruction Downregulates Expression of Vasopressin-Sensitive AQP-2 Water Channel in Rat Kidney
- Biochemical Basis of Partial Nephrogenic Diabetes Insipidus Phenotypes
- Biology and Genetics of Inherited Renal Tubular Disorders (editorial)
- Brief Report: A Molecular Defect in the Vasopressin V2-Receptor Gene Causing Nephrogenic Diabetes Insipidus
- Brief Report: A Mutation in the Vasopressin V2-Receptor Gene in a Kindred with X-Linked Nephrogenic Diabetes Insipidus
- Calcineurin-NFATc Signaling Pathway Regulates AQP2 Expression in Response to Calcium Signals and Osmotic Stress
- Cellular Distribution of the Aquaporins: A Family of Water Channel Proteins
- Cellular Mechanism of Lithium-Induced Nephrogenic Diabetes Insipidus in Rats
- 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
- Cloning, Characterization, and Chromosomal Mapping of Human Aquaporin of Collecting Duct
- Concentrating Defect in Experimental Nephrotic Syndrome: Altered Expression of Aquaporins and Thick Ascending Limb Na+ Transporters
- Congenital Nephrogenic Diabetes Insipidus in an Adult
- Correlation between Magnetic Resonance Imaging of Posterior Pituitary and Neurohypophyseal Function in Children with Diabetes Insipidus
- Current Understanding of the Cellular Biology and Molecular Structure of the Antidiuretic Hormone-stimulated Water Transport Pathway
- Defects of G Protein-Coupled Signal Transduction in Human Disease
- Dehydration Reverses Vasopressin Antagonist-Induced Diuresis and Aquaporin-2 Downregulation in Rats
- Desmopressin and Indomethacin Therapy for Nephrogenic Diabetes Insipidus in Patients Receiving Lithium Carbonate
- Desmopressin for Nocturnal Enuresis in Nephrogenic Diabetes Insipidus
- Development and Characterization of a Mouse Cell Line Expressing the Human V2 Vasopressin Receptor Gene
- Development of Lithium-Induced Nephrogenic Diabetes Insipidus is Dissociated from Adenylyl Cyclase Activity
- Diabetes Insipidus (Hendy, Bichet)
- Diabetes Insipidus (Robertson)
- Diabetes Insipidus [Bell]
- Differential Diagnosis and Pathophysiology of Diabetes Insipidus
- Differential Diagnosis of Polyuria
- Disordered Water Channel Expression and Distribution in Acquired Nephrogenic Diabetes Insipidus
- Do Aquaporins Have a Role in Nocturnal Enuresis?
- Effect of DDAVP on Nocturnal Enuresis in a Patient with Nephrogenic Diabetes Insipidus
- Effect of an Acute Oral Ibuprofen Intake on Urinary Aquaporin-2 Excretion in Healthy Humans
- Effects of Arginine Vasopressin and 1-Desamino-8-D Arginine Vasopressin on Forearm Vasculature of Healthy Subjects and Patients with a V2 Receptor Defect
- Evaluation and Management of Diabetes Insipidus
- Evidence for Intact V1-vasopressin Receptors in Congenital Nephrogenic Diabetes Insipidus
- Evidence that the Antidiuretic Substance in the Plasma of Children with Nephrogenic Diabetes Insipidus is Antidiuretic Hormone
- Familial Nephrogenic Diabetes Insipidus: Report of Two Families
- Fibrinolytic Responses to 1-desamino-8-D-arginine-vasopressin in Patients with Congenital Nephrogenic Diabetes Insipidus
- From Vasopressin Receptor to Water Channel: Intracellular Traffic, Constraint and By-pass
- Functional Characterization of Five V2 Vasopressin Receptor Gene Mutations
- Functional Rescue of Mutant V2 Vasopressin Receptors Causing Nephrogenic Diabetes Insipidus by a Co-Expressed Receptor Polypeptide
- G-Protein-Coupled Receptors in Endocrine Disease
- G-Protein-Coupled Receptors: Molecular Mechanisms Involved in Receptor Activation and Selectivity of G-Protein Recognition
- GS-Activating Receptors: Modes of Transmembrane Signalling and Genetic Defects
- Genetic Restoration of Aldose Reductase to the Collecting Tubules Restores Maturation of the Urine Concentrating Mechanism
- Hemodynamic and Coagulation Responses to 1-desamino[8-D-arginine] Vasopressin in Patients with Congenital Nephrogenic Diabetes Insipidus
- Hereditary Nephrogenic Diabetes Insipidus
- Hereditary Nephrogenic Diabetes Insipidus and Bilateral Nonobstructive Hydronephrosis
- Hereditary Vasopressin Resistance in Man and Mouse
- 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
- 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
- Hyponatremia and Hypernatremia
- Identification and Characterization of Aquaporin-2 Water Channel Mutations Causing Nephrogenic Diabetes Insipidus with Partial Vasopressin Response
- 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
- In Vitro Micro-Autoradiography of Atrial Natriuretic Peptide in Biopsy Specimens from Patients with Renal Diseases
- Increased Renal Responsiveness to Vasopressin and Enhanced V2 Receptor Signaling in RGS2-/- Mice
- Index of Suspicion. Case 2. Nephrogenic Diabetes Insipidus
- Indomethacin Enhances Shuttling of Aquaporin-2 Despite Decreased Abundance in Rat Kidney
- Indomethacin Treatment in Amphotericin B Induced Nephrogenic Diabetes Insipidus
- Inheritance of Mutations in the V2 Receptor Gene in Thirteen Families with Nephrogenic Diabetes Insipidus
- Kidney Damage in Long-Term Lithium Patients: A Cross-Sectional Study of Patients with 15 Years or More on Lithium
- Kinetic Model of Water and Urea Permeability Regulation by Vasopressin in Collecting Duct
- Kinetics of Urea and Water Permeability Activation by Vasopressin in Rat Terminal IMCD
- 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 Nephrogenic Diabetes Insipidus
- Long-Term Regulation of Urinary Concentrating Capacity
- Maturation of Receptor Proteins in Eukaryotic Expression Systems
- Mechanism of Lithium-Induced Polyuria in the Rat
- Mechanism of Vasopressin Action in the Renal Collecting Duct
- Mechanisms of Impaired Urinary Concentrating Ability in Adult Rats Treated Neonatally with Enalapril
- Methyl-β-Cyclodextrin Induces Vasopressin-Independent Apical Accumulation of Aquaporin-2 in the Isolated, Perfused Rat Kidney
- Molecular Analysis of X-Linked Nephrogenic Diabetes Insipidus
- Molecular Biology of Diabetes Insipidus
- Molecular Cloning of the Receptor for Human Antidiuretic Hormone
- Molecular and Cellular Defects in Nephrogenic Diabetes Insipidus
- Mutations and Diseases of G Protein Coupled Receptors
- Mutations in the Vasopressin Type 2 Receptor Gene (AVPR2) Associated 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
- Nephrogenic Diabetes Insipidus (Bichet - November 1998)
- Nephrogenic Diabetes Insipidus Associated with Foscarnet - A Case Report [letter]
- Nephrogenic Diabetes Insipidus Secondary to Lithium Therapy in the Postoperative Patient: A Case Report
- Nephrogenic Diabetes Insipidus in Mice Lacking All Nitric Oxide Synthase Isoforms
- Nephrogenic Diabetes Insipidus in Sibling Colts
- Nephrogenic Diabetes Insipidus in a Lethargic Lithium-Treated Patient
- 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: Causes Revealed
- Nephrogenic Diabetes Insipidus: Clinical Symptoms, Pathogenesis, Genetics and Treatment
- 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
- Novel Mutations in the V2 Vasopressin Receptor Gene of Patients with X-Linked Nephrogenic Diabetes Insipidus
- Pathophysiology of the Aquaporin Water Channels
- Persistent Nephrogenic Diabetes Insipidus Following Lithium Therapy
- Pharmacologic Chaperones as a Potential Treatment for X-linked Nephrogenic Diabetes Insipidus
- 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 and Polydipsia. Problems Associated with Patient Evaluation
- Posterior Lobe of the Pituitary in Diabetes Insipidus: Dynamic MR Imaging
- Primary Hyperparathyroidism and Coexisting Nephrogenic Diabetes Insipidus: Rapid Postoperative Correction
- 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
- Renal Function On and Off Lithium in Patients Treated with Lithium for 15 Years or More. A Controlled, Prospective Lithium-Withdrawal Study
- Requirement of Human Renal Water Channel Aquaporin-2 for Vasopressin-Dependent Concentration of Urine
- Role of Aquaporin Water Channels in Kidney and Lung
- Role of Aquaporin-2 Water Channels in Urinary Concentration and Dilution Defects
- Role of Aquaporins in Water Balance Disorders
- Role of Inner Medullary Collecting Duct NaCl Transport in Urinary Concentration
- Role of cAMP-Phosphodiesterase Isozymes in Pathogenesis of Murine Nephrogenic Diabetes Insipidus
- Severe Lactic Acidosis and Renal Involvement in a Patient with Relapsed Burkitt's Lymphoma
- Severely Impaired Urinary Concentrating Ability in Transgenic Mice Lacking Aquaporin-1 Water Channels
- Short-Chain Ubiquitination Mediates the Regulated Endocytosis of the Aquaporin-2 Water Channel
- Six Novel Mutations in the Vasopressin V2 Receptor Gene Causing Nephrogenic Diabetes Insipidus
- The Aquaporin Family of Water Channel Proteins in Clinical Medicine
- The Management of Diabetes Insipidus in Adults
- The Molecular Basis of Nephrogenic Diabetes Insipidus
- The Perinatal Expression of Aquaporin-2 and Aquaporin-3 in Developing Kidney
- Therapy for Hereditary Nephrogenic Diabetes Insipidus
- Tonicity-Responsive Enhancer Binding Protein is an Essential Regulator of Aquaporin-2 Expression in Renal Collecting Duct Principal Cells
- 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
- Treatment of Nephrogenic Diabetes Insipidus with Hydrochlorothiazide and Amiloride
- 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 Patients with Congenital Nephrogenic Diabetes Insipidus
- Urea Transporter UT-A1 and Aquaporin-2 Proteins Decrease in Response to Angiotensin II or Norepinephrine-Induced Acute Hypertension
- 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 Humans: A Potential Marker of Collecting Duct Responsiveness to Vasopressin
- 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
- V2 Vasopressin Receptor Dysfunction in Nephrogenic Diabetes Insipidus Caused By Different Molecular Mechanisms
- Vasopressin Effects on Urea and H20 Transport in Inner Medullary Collecting Duct Subsegments
- 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 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 9 Faq answers
Used in 9 Faq answers
- What causes NDI?
- Can a person recover from Lithium-induced NDI?
- Could you explain, in layman's terms, what happens genetically when a father, daughter, and male child of the daughter all have DI?
- How does someone get NDI from taking Lithium?
- How is NDI diagnosed?
- How is NDI treated?
- Is NDI life-threatening, and what symptoms should be watched for?
- What is the importance of maintaining a low salt/low protein diet?
- Will NDI ever go away?
Used in 5 Proceeding abstracts
Used in 5 Proceeding abstracts
- Collecting Duct Specific Gene Regulation: Creation And Use of Transgenic Mouse Models
- Functional rescue of truncated V2-Vasopressin-receptors by aminoglycoside-induced misreading of nonsense-mutations
- Obstructive nephropathy -- a common acquired condition of nephrogenic diabetes insipidus
- Pitfalls in the Differential Diagnosis of Nephrogenic Diabetes Insipidus.
- Regulation and distribution of phosphorylated aquaporin-2 (AQP2) in rat kidney collecting duct principal cells
Used in 15 Proceeding translations
Used in 15 Proceeding translations
- Biochemical Characterization of Partial Nephrogenic Diabetes Insipidus (NDI) Phenotypes
- Candesartan treatment prevents dysregulation of AQP2, BSC-1 and NaPi2 in ureteral obstruction-induced NDI
- Clinical presentation of the polyuric and hyperprostaglandinuric salt losing tubulopathies (HPS/aBS) and the therapeutic option with COX inhibitors
- Decreased Aquaporin-2 Water Channel Expression in Acquired Nephrogenic 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
- Identification of proteins involved in the vasopressin-induced shuttle of aquaporin-2
- 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
- Nephrogenic Diabetes Insipidus in mice lacking aquaporin-3 water channels
- Pitfalls in the Differential Diagnosis of Nephrogenic Diabetes Insipidus.
- 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
- Urinary Aquaporin-2 in Diagnosis of Disorders of Water Metabolism
- Vasopressin-Independent Regulation of Aquaporin-2 Protein
Used in 46 Term definitions
Used in 46 Term definitions
- AQP2 protein
- CNDI
- LLC
- LLC-AQP2
- LLC-PK1
- Wilms' tumor
- adrenal
- amniotic fluid
- aquaporin 2
- aquaporin-1
- aquaporin-2
- aquaporin-2s
- aquaporin2
- blastomycosis
- carbon tetrachloride
- congenital NDI
- congenital nephrogenic diabetes insipidus
- cyclooxygenase-2 (COX-2)
- glomerular filtration rate
- horseshoe kidney
- humoralism
- kidney cancer
- kidney disorders
- kidney function tests
- nephropathy
- nephrosis
- obstructive nephropathy
- polycystic disease of the kidneys
- reabsorption
- renal biopsy
- renal clearance
- renal insufficiency
- renal lithium clearance
- renal tubular
- systemic lupus erythematosus
- threshold
- tubule
- type 1 diabetes mellitus
- urinary bladder
- urinary concentrating ability
- urinary output
- urinary tract
- urine
- urine output
- urine volume
- vasopressin-regulated water channels
