development
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:
- development
-
The process of growth and differentiation.
Used in 28 Article abstracts
Used in 28 Article abstracts
- AQP3, p-AQP2, and AQP2 Expression is Reduced in Polyuric Rats With Hypercalcemia: Prevention by cAMP-PDE Inhibitors
- Altered Expression of Renal AQPs and Na+ Transporters in Rats with Lithium-Induced NDI
- 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 in the Kidney: From Molecules to Medicine
- Bilateral Ureteral Obstruction Downregulates Expression of Vasopressin-Sensitive AQP-2 Water Channel in Rat Kidney
- Bladder Function Impairment in Aquaporin-2 Defective Nephrogenic Diabetes Insipidus
- Changes of Rat Kidney AQP2 and Na,K-ATPase mRNA Expression in Lithium-Induced Nephrogenic Diabetes Insipidus
- Characterization of Vasopressin V2 Receptor Mutants in Nephrogenic Diabetes Insipidus in a Polarized Cell Model
- Compound Deletion of the rhoGAP C1 and V2 Vasopressin Receptor Genes in a Patient with 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
- Development of Lithium-Induced Nephrogenic Diabetes Insipidus is Dissociated from Adenylyl Cyclase Activity
- Development of Urinary Concentrating Capacity: Role of Aquaporin-2
- Functional Rescue of Vasopressin V2 Receptor Mutants in MDCK Cells by Pharmacochaperones: Relevance to Therapy of Nephrogenic Diabetes Insipidus
- Generation and Phenotype of Mice Harboring a Nonsense Mutation in the V2 Vasopressin Receptor Gene
- Hypokalemia-Induced Downregulation of Aquaporin-2 Water Channel Expression in Rat Kidney Medulla and Cortex
- Hyponatremia and Hypernatremia
- Lithium Nephrotoxicity
- Lithium-induced Down regulation of Aquaporin-2 Water Channel Expression in Rat Kidney Medulla
- Loss of Calcineurin Aα Results in Altered Trafficking of AQP2 and in Nephrogenic Diabetes Insipidus
- Mutations in the Founder of the MIP Gene Family Underlie Cataract Development in the Mouse
- Possible Liposomal Amphotericin B-Induced Nephrogenic Diabetes Insipidus
- The Molecular Basis of Nephrogenic Diabetes Insipidus
- The V2 vasopressin receptor mutations and fluid homeostasis.
- Therapeutic Potential of Vasopressin Receptor Antagonists
- Urinary Aquaporin-2 Excretion in Dogs: A Marker for Collecting Duct Responsiveness to Vasopressin
- Urinary Excretion of Aquaporin-2 in Humans: A Potential Marker of Collecting Duct Responsiveness to Vasopressin
Used in 14 Article bodies
Used in 14 Article bodies
- A Congenital Renal Tubular Defect
- A Novel Polymorphism in the Coding Region of the Vasopressin Type 2 Receptor Gene
- 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
- Molecular Analysis of X-Linked Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus in a Patient Taking Cidofovir
- 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 39 Article translations
Used in 39 Article translations
- Aminoglycoside Pretreatment Partially Restores the Function of Truncated V2 Vasopressin Receptors Found in Patients with Nephrogenic Diabetes Insipidus
- An X-linked NDI Mutation Reveals a Requirement for Cell Surface V2R Expression
- Biochemical Basis of Partial Nephrogenic Diabetes Insipidus Phenotypes
- Changes of Rat Kidney AQP2 and Na,K-ATPase mRNA Expression in Lithium-Induced Nephrogenic Diabetes Insipidus
- Characterization of Vasopressin V2 Receptor Mutants in Nephrogenic Diabetes Insipidus in a Polarized Cell Model
- Defects of G Protein-Coupled Signal Transduction in Human Disease
- Disordered Water Channel Expression and Distribution in Acquired Nephrogenic Diabetes Insipidus
- Early Onset Bilateral Calcifications and Epilepsy
- Effect of DDAVP on Nocturnal Enuresis in a Patient with Nephrogenic Diabetes Insipidus
- Evidence for Stabilization of Aquaporin-2 Folding Mutants by N-linked Glycosylation in the Endoplasmic Reticulum
- Foscarnet Alters Antidiuretic Hormone-Mediated Transport
- Functional Studies of Twelve Mutant V2 Vasopressin Receptors Related to Nephrogenic Diabetes Insipidus: Molecular Basis of a Mild Clinical Phenotype
- G-Protein-Coupled Receptors in Endocrine Disease
- Hemifacial Spasm in Albright's Hereditary Osteodystrophy with Pseudopseudohypoparathyroidism and Nephrogenic Diabetes Insipidus--Case Report
- Inherited Diseases of the Kidney
- Intracranial Calcification in Nephrogenic Diabetes Insipidus
- Lithium Nephrotoxicity
- Lithium-induced Down regulation of Aquaporin-2 Water Channel Expression in Rat Kidney Medulla
- Mechanisms of Impaired Urinary Concentrating Ability in Adult Rats Treated Neonatally with Enalapril
- Meniere's Disease in Congenital Nephrogenic Diabetes Insipidus: Report of Two Twins
- Molecular Biology of Diabetes Insipidus
- Mutations in the Founder of the MIP Gene Family Underlie Cataract Development in the Mouse
- Nephrogenic Diabetes Insipidus
- Nephrogenic Diabetes Insipidus (Bichet - November 1998)
- 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
- Pharmacologic Chaperones as a Potential Treatment for X-linked Nephrogenic Diabetes Insipidus
- Pharmacological Chaperones in Nephrogenic Diabetes Insipidus: Possibilities for Clinical Application
- Prevention of Intracranial Calcifications and Brain Damage Associated with Nephrogenic Diabetes Insipidus [Letter; Comment]
- Rescue of Vasopressin V2 Receptor Mutants by Chemical Chaperones: Specificity and Mechanism
- Sequence-Specific "Gene Signatures" can be Obtained by PCR with Single Specific Primers at Low Stringency
- Structure and Chromosomal Localization of the Human Antidiuretic Hormone Receptor Gene
- The Molecular Basis of Nephrogenic Diabetes Insipidus
- The Perinatal Expression of Aquaporin-2 and Aquaporin-3 in Developing Kidney
- Transient Nephrogenic Diabetes Insipidus Accompanied by Possible Psychogenic Polydipsia
- Treatment of Nephrogenic Diabetes Insipidus with Hydrochlorothiazide and Amiloride
- V2 Vasopressin Receptor Dysfunction in Nephrogenic Diabetes Insipidus Caused By Different Molecular Mechanisms
- Vasopressin Type-2 Receptor and Aquaporin-2 Water Channel Mutants in Nephrogenic Diabetes Insipidus
Used in 21 Proceeding abstracts
Used in 21 Proceeding abstracts
- Action Mechanism of Pharmacological Chaperones Acting on the V2 Vasopressin Receptor in the Treatment of Nephrogenic Diabetes Insipidus
- 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 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
- Candesartan treatment prevents dysregulation of AQP2, BSC-1 and NaPi2 in ureteral obstruction-induced NDI
- Collecting Duct Specific Gene Regulation: Creation And Use of Transgenic Mouse Models
- Decrease in urine volume and increase in urine osmolality after SR49059 administration in five adult male patients with X-linked nephrogenic diabetes insipidus
- Determination of the functionality of AQP2 missense mutants in recessive NDI
- 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
- Functional investigations of the vasopressin regulated antidiuretic machinery in single inner medullary collecting duct (IMCD) cells
- Gene Mutation Analysis of NDI patients in Japan
- 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
- Long-range transcriptional regulation of the AVPR2 gene
- N-linked glycosylation is essential for transport of the Aquaporin-2 water channel to the plasma membrane in MDCK cells
- Nutritional Concerns for Persons with NDI
- Obstructive nephropathy -- a common acquired condition of nephrogenic diabetes insipidus
- Phenotype of aquaporin knockout mice, and AQP2 misprocessing in NDI
- Proteomic Studies of Vasopressin Action in the Collecting Duct
- The Low Sodium Diet for Nephrogenic Diabetes Insipidus
- 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
- 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
- Collecting Duct Specific Gene Regulation: Creation And Use of Transgenic Mouse Models
- Modulation of vasopressin-dependent AQP2 expression in cultured mpkCCDc14 collecting duct principal cells by aldosterone, insulin, and hypertonicity
- 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.
- Novel Roles of Aquaporin Water Channels Revealed by Phenotype Analysis of Knockout Mice
- Pharmacological chaperones functionally rescue misfolded mutant V2 vasopressin receptors that cause nephrogenic diabetes insipidus
- V2 vasopressin receptor dysfunction in patients with nephrogenic diabetes insipidus is caused by different molecular mechanisms
Used in 95 Term definitions
Used in 95 Term definitions
- Apicomplexa
- alcohol dependence
- analogous
- anaphylaxis
- anaplastic
- anthropology
- antineoplastic
- antiseptic
- aplasia
- atopy
- blast
- bone marrow hypoplasia
- cleft
- compression
- constrict
- contraction
- convergence
- coronary thrombosis
- culminating
- developmental
- down-regulates
- downregulation
- dysmorphism
- dysplasia
- embryo
- embryology
- embryonic disc
- environment
- epigenesis
- erythrocyte burst-forming cell
- erythrocyte colony-forming cell
- erythrocytic series
- evolution
- evolutionarily
- evolutionary
- failure to thrive
- fertilization
- fertilize
- fetal
- fixation
- gamete
- gene amplification
- genetic
- gestation
- gonadal dysgenesis
- growth retardation
- hematopoiesis
- histogenesis
- horizon
- hyperuricemia
- hypogonadism
- hypoplasia
- hypothalamus
- immunologic tolerance
- incubated
- incubation
- innidiation
- insidious
- leukemia
- luteinizing hormone
- malaria
- maturity
- mental retardation
- milestone
- moderate mental retardation
- mole
- mononucleosis
- myelocytes
- neurodevelopmental
- notochord
- ontogeny
- orthodontic appliance
- ovarian follicle
- pathogenesis
- pediatrics
- peptic ulceration
- physique
- polymorphic
- primary
- proerythrocyte
- profound mental retardation
- progesterone
- programmed cell death
- pseudounipolar neuron
- ray
- restraining
- retardation
- scrofuloderma
- severe mental retardation
- sexual reproduction
- sperm
- thymus
- umbilical vesicle
- vascularization
- yolk sac



