renal
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:
- renal
-
Pertaining to the kidney.
Used in 113 Article abstracts
Used in 113 Article abstracts
- A Mouse Model to Test the in vivo Efficacy of Chemical Chaperones
- A New Series of Photoactivatable and Iodinatable Linear Vasopressin Antagonists
- A Novel Polymorphism in the Coding Region of the Vasopressin Type 2 Receptor Gene
- 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
- Acquired Nephrogenic Diabetes Insipidus Secondary to Distal Renal Tubular Acidosis and Nephrocalcinosis Associated with Sjogren's Syndrome
- Aggravation of Subclinical Diabetes Insipidus During Pregnancy
- 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
- Amiloride restores renal medullary osmolytes in lithium-induced nephrogenic diabetes insipidus
- Angiotensin II AT1 Receptor Blockade Decreases Vasopressin-Induced Water Reabsorption and AQP2 Levels in NaCl-Restricted Rats
- 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
- Aquaporin Expression in Normal Human Kidney and in Renal Disease
- Aquaporin-2 Trafficking is Regulated by PDZ-domain Containing Protein SPA-1
- Aquaporin-2: COOH Terminus is Necessary But Not Sufficient for Routing to the Apical Membrane
- Aquaporins: Roles in Renal Function and Peritoneal Dialysis
- Bilateral Ureteral Obstruction Downregulates Expression of Vasopressin-Sensitive AQP-2 Water Channel in Rat Kidney
- Bradykinin Signaling Counteracts cAMP-elicited aquaporin 2 translocation in renal cells
- CHIP28 Water Channels are Localized in Constitutively Water-Permeable Segments of the Nephron
- Calcineurin-NFATc Signaling Pathway Regulates AQP2 Expression in Response to Calcium Signals and Osmotic Stress
- Calcium and Cyclic Adenosine Monophosphate as Second Messengers for Vasopressin in the Rat Inner Medullary Collecting Duct
- Characterization of SR 121463A, A Highly Potent and Selective, Orally Active Vasopressin V2 Receptor Antagonist
- Clinical Phenotype of Nephrogenic Diabetes Insipidus in Females Heterozygous for a Vasopressin Type 2 Receptor Mutation
- Comparative Mapping on the Mouse and Human X Chromosomes of a Human cDNA Clone Encoding the Vasopressin Renal-Type Receptor (AVP2R)
- Concentration of Solutes in the Renal Inner Medulla: Interstitial Hyaluronan as a Mechano-Osmotic Transducer
- Congenital Nephrogenic Diabetes Insipidus in an Adult
- Cross Talk Between Stimulatory and Inhibitory Guanosine 5'-Triphosphate Binding Proteins: Role in Activation and Desensitization of the Adenylate Cyclase Response to Vasopressin
- Cyclooxygenase-2 Inhibitor Preserves Medullary Aquaporin-2 Expression and Prevents Polyuria After Ureteral Obstruction
- Derivatives of Somatic Cell Hybrids Which Carry the Human Gene Locus for Nephrogenic Diabetes Insipidus (NDI) Express Functional Vasopressin Renal V2-type Receptors
- Development of Lithium-Induced Nephrogenic Diabetes Insipidus is Dissociated from Adenylyl Cyclase Activity
- Development of Urinary Concentrating Capacity: Role of Aquaporin-2
- Diabetes Insipidus (Robertson)
- Diabetes Insipidus in Uricase-Deficient Mice: A Model for Evaluating Therapy with Poly(Ethylene Glycol)-Modified Uricase
- Discovery of Aquaporins: a Breakthrough in Research on Renal Water Transport
- Dissociation Between Urine Osmolality and Urinary Excretion of Aquaporin-2 in Healthy Volunteers
- Downregulation of AQP1, -2, and -3 After Ureteral Obstruction is Associated With a Long-Term Urine-Concentrating Defect
- Downregulation of Renal Aquaporins in Response to Unilateral Ureteral Obstruction
- Downregulation of Renal Vasopressin V2 Receptor and Aquaporin-2 Expression Parallels Age-Associated Defects in Urine Concentration
- Dynein and dynactin colocalize with AQP2 water channels in intracellular vesicles from kidney collecting duct
- Effect of Water Deprivation and Hypertonic Saline Infusion on Urinary AQP2 Excretion in Healthy Humans
- Effective Water Clearance and Tonicity Balance: The Excretion of Water Revisited
- Effects of Dietary Fat, NaCl, and Fructose on Renal Sodium and Water Transporter Abundances and Systemic Blood Pressure
- Evidence for a Role of Protein Kinase C-a in Urine Concentration
- Expression of Renal Aquaporins 1, 2, and 3 in a Rat Model of Cisplatin-Induced Polyuria
- Functional Studies of Twelve Mutant V2 Vasopressin Receptors Related to Nephrogenic Diabetes Insipidus: Molecular Basis of a Mild Clinical Phenotype
- Generation and Phenotype of Mice Harboring a Nonsense Mutation in the V2 Vasopressin Receptor Gene
- Genetic Renal Diseases in Children
- Genetic Restoration of Aldose Reductase to the Collecting Tubules Restores Maturation of the Urine Concentrating Mechanism
- Hyperuricemia as a Clue for Central Diabetes Insipidus (Lack of V1 Effect) in the Differential Diagnosis of Polydipsia
- Identification of a Multiprotein "Motor" Complex Binding to Water Channel Aquaporin-2
- Identification of a Novel A-kinase Anchoring Protein 18 Isoform and Evidence for its Role in the Vasopressin-induced Aquaporin-2 Shuttle in Renal Principal Cells
- Impaired Aquaporin and Urea Transporter Expression in Rats with Adriamycin-Induced Nephrotic Syndrome
- Impaired Solute Accumulation in Inner Medulla of Clcnk1-/- Mice Kidney
- 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
- Inheritance of Mutations in the V2 Receptor Gene in Thirteen Families with Nephrogenic Diabetes Insipidus
- Inherited Diseases of the Kidney
- 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
- Long-term Regulation of Aquaporins in the Kidney
- Mechanisms of Impaired Urinary Concentrating Ability in Adult Rats Treated Neonatally with Enalapril
- Membrane Traffic After Inhibition of Endocytosis in Renal Proximal Tubules
- Metoprine-induced Thirst and Diuresis in Wistar Rats
- Mild Nephrogenic Diabetes Insipidus Caused by Foxa1 Deficiency
- Molecular Cloning of the Receptor for Human Antidiuretic Hormone
- Molecular Mechanisms and Drug Development in Aquaporin Water Channel Diseases: Molecular Mechanism of Water Channel Aquaporin-2 Trafficking
- Molecular Physiology of Urinary Concentrating Mechanism: Regulation of Aquaporin Water Channels by Vasopressin
- Mutations in the Vasopressin Type 2 Receptor Gene (AVPR2) Associated with Nephrogenic Diabetes Insipidus
- N-ethylmaleimide (NEM) Causes Aquaporin-2 Trafficking in the Renal Inner Medullary Collecting Duct by Direct Activation of Protein Kinase A
- Nature and Recurrence of AVPR2 Mutations in X-Linked Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus Associated with Hemochromatosis
- Nephrogenic Diabetes Insipidus Presenting After Head Trauma
- Nephrogenic Diabetes Insipidus in Mice Lacking All Nitric Oxide Synthase Isoforms
- 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
- 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
- Persistent Nephrogenic Diabetes Insipidus Following Lithium Therapy
- Phenotypes Developed in Secretin Receptor-Null Mice Indicated a Role for Secretin in Regulating Renal Water Reabsorption
- Platelet Vasopressin Receptors in Patients With Congenital Nephrogenic Diabetes Insipidus
- Quantitation of Aquaporin-2 Abundance in Microdissected Collecting Ducts: Axial Distribution and Control by AVP
- Rat Kidney Papilla Contains Abundant Synaptobrevin Protein that Participates in the Fusion of Antidiuretic Hormone-regulated Water Channel-containing Endosomes In Vitro
- Recent Insights into the Coordinate Regulation of Body Water and Divalent Mineral Ion Metabolism
- Regional Time-Dependent Changes in Vasopressin V2 Receptor Expression in the Rat Kidney During Water Restriction
- Relief of Nocturnal Enuresis by Desmopressin is Kidney and Vasopressin Type 2 Receptor Independent
- Renal Expression of Sodium Transporters and Aquaporin-2 in Hypothyroid Rats
- Renal Haemodynamics, Sodium and Water Reabsorption During Continuous Intravenous Infusion of Recombinant Interleukin-2
- Reversed Polarized Delivery of an Aquaporin-2 Mutant Causes Dominant Nephrogenic Diabetes Insipidus
- Rho Inhibits cAMP-Induced Translocation of Aquaporin-2 into the Apical Membrane of Renal Cells
- Role of Renal Aquaporins in Escape from Vasopressin-induced Antidiuresis in Rat
- Role of the Ca2+-Sensing Receptor in Divalent Mineral Ion Homeostasis
- Routing of the aquaporin-2 water channel in health and disease.
- Segment Specific ENaC Downregulation in Kidney of Rats with Lithium-Induced NDI
- Short-Chain Ubiquitination Mediates the Regulated Endocytosis of the Aquaporin-2 Water Channel
- Structure and Function of Kidney Water Channels
- Tenofovir-related Fanconi Syndrome with Nephrogenic Diabetes Insipidus in a Patient with Acquired Immunodeficiency Syndrome: The Role of Lopinavir-Ritonavir-Didanosine
- The Aquaporin Family of Water Channel Proteins in Clinical Medicine
- The Role of Putative Phosphorylation Sites in the Targeting and Shuttling of the Aquaporin-2 Water Channel
- Therapeutic Potential of Vasopressin Receptor Antagonists
- Treating lithium-induced nephrogenic diabetes insipidus with a COX-2 inhibitor improves polyuria via upregulation of AQP2 and NKCC2.
- Two Novel Mutations in the Vasopressin V2 Receptor Gene in Unrelated Japanese Kindreds with Nephrogenic Diabetes Insipidus
- Urinary Concentrating Defect in Experimental Hemochromatosis
- Urinary Excretion of Aquaporin-2 in Humans: A Potential Marker of Collecting Duct Responsiveness to Vasopressin
- Vasopressin Receptor Mutations Causing Nephrogenic Diabetes Insipidus
- Vasopressin and Oxytocin Receptors
- Water Channel Aquaporin-2 Directly Binds to Actin
- Water Disturbances in Cardiac Failure
- X-linked Nephrogenic Diabetes Insipidus: from the Ship Hopewell to RFLP Studies
- Xanthopterin-Induced Renal Dysfunction: A Reversible Model of Crystal Nephropathy
- [Abnormal Serum Uric Acid Level in Endocrine Disorders] (Japanese)
- [Non-Lithiasic Hereditary Tubulopathies] (Article in French)
- [Pathological Aspects of Water Transport in the Collecting Ducts] (French)
Used in 17 Article bodies
Used in 17 Article bodies
- 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
- Index of Suspicion. Case 2. 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 in North America. The Hopewell Hypothesis
- 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
- Persistent Nephrogenic Diabetes Insipidus Following Lithium Therapy
- 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 27 Proceeding abstracts
Used in 27 Proceeding abstracts
- Renal medullary gene expression in aquaporin-1 null mice
- Antidiuretic Effect of Hydrochlorothiazide in Lithium-Induced Nephrogenic Diabetes Insipidus Is Associated with Upregulation of Aquaporin-2, Na-Cl Cotransporter and Epithelial Sodium Channel
- Bartter syndrome with sensorineural deafness: molecular genetics
- 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
- Clinical presentation of the polyuric and hyperprostaglandinuric salt losing tubulopathies (HPS/aBS) and the therapeutic option with COX inhibitors
- 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
- Functional studies of twelve mutant V2 vasopressin receptors related to nephrogenic diabetes insipidus: molecular basis of a mild clinical phenotype.
- Growth in males with (well-managed) nephrogenic diabetes insipidus
- High proportion of ROMK processing defects underlying hyperprostaglandin E syndrome/antenatal Bartter syndrome
- Identification of proteins involved in the vasopressin-induced shuttle of aquaporin-2
- Lack of AVP-induced phosphorylation of the Aquaporin-2 mutants AQP2-R254L and AQP2-R254Q explains dominant Nephrogenic Diabetes Insipidus
- Long- and Short-Term Regulation of AQP2 Expression and Function
- 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
- New insights in water channel physiology revealed by transgenic mouse models
- Production and purification of Aquaporin-2 and Vasopressin 2 Receptor: towards elucidation of the structure
- Purinergic Control of Medullary Collecting Duct Function: A Novel Vasopressin-independent Regulatory Mechanism
- 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
- The Ontogeny and Regulation of AQP2 Gene Expression in the Ovine Fetal Kidney
- Toward gene therapy for nephrogenic diabetes insipidus
- V2 Vasopressin Receptors in NDI: Where did they go?
- V2 vasopressin receptor function studied in mice and yeast
- V2 vasopressin receptor-deficient mouse model: Pathophysiological changes and therapeutical implications
- Wild-type aquaporin-2 rescues a novel aquaporin-2 mutant in recessive Nephrogenic Diabetes Insipidus to the apical plasma membrane
Used in 36 Term definitions
Used in 36 Term definitions
- LLC
- LLC-AQP2
- LLC-PK1
- Liddle's syndrome
- NDI Abstract of Article: 510
- X-linked NDI
- X-linked congenital nephrogenic diabetes insipidus
- X-linked nephrogenic diabetes insipidus
- arteriolae rectae renis
- atrial natriuretic peptide
- capsular epithelium
- chronic lymphocytic leukemia
- collecting ducts
- countercurrent
- diabetes insipidus
- glomerular epithelium
- heart failure
- horseshoe kidney
- hypokalemia
- hypophosphatasia
- hypothalamo-neurohypophysial-renal
- intercalated cells
- kidney cancer
- nephrogenic diabetes insipidus
- nervus vagus
- parathyroid hormone
- pentetic acid
- prostaglandin E2
- reflux
- reflux nephropathy
- renal calyx
- renal cell carcinoma
- renin-angiotensin system
- splenorenal shunt
- urinary tract
- water load test



