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2004 - Phoenix
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Carel van Os
Title:
PhD
Email:
Phone:
Work +131243613654, Fax +131243540525
Organization:
University of Nijmegen
Division:
Institute of Cellular Signalling
Department:
Dept. of Cell Physiology
Address:
P.O. Box 9101
NL-6500 HB Nijmegen,
Netherlands
25 Articles
25 Articles
Aquaporin 2 Mutations in Nephrogenic Diabetes Insipidus
A Novel Mechanism in Recessive Nephrogenic Diabetes Insipidus: Wild-Type Aquaporin-2 Rescues the Apical Membrane Expression of Intracellularly Retained AQP2-P262L
Reversed Polarized Delivery of an Aquaporin-2 Mutant Causes Dominant Nephrogenic Diabetes Insipidus
Cell-Biologic and Functional Analyses of Five New Aquaporin-2 Missense Mutations that Cause Recessive Nephrogenic Diabetes Insipidus
Heteroligomerization of an Aquaporin-2 Mutant with Wild-Type Aquaporin-2 and Their Misrouting to Late Endosomes/Lysosomes Explains Dominant Nephrogenic Diabetes Insipidus
Defective processing and trafficking of water channels in nephrogenic diabetes insipidus.
Dissociation Between Urine Osmolality and Urinary Excretion of Aquaporin-2 in Healthy Volunteers
Physiological relevance of aquaporins: luxury or necessity?
An Impaired Routing of Wild-type Aquaporin-2 after Tetramerization with an Aquaporin-2 Mutant Explains Dominant Nephrogenic Diabetes Insipidus
Aquaporin-2 Water Channel Mutations Causing Nephrogenic Diabetes Insipidus
An Aquaporin-2 Water Channel Mutant Which Causes Autosomal Dominant Nephrogenic Diabetes Insipidus is Retained in the Golgi Complex
Role of Aquaporins in Renal Water Handling: Physiology and Pathophysiology
Aquaporin-2 transfection of Madin-Darby canine kidney cells reconstitutes vasopressin-regulated transcellular osmotic water transport.
Importance of the Mercury-Sensitive Cysteine on Function and Routing of AQP1 and AQP2 in Oocytes
Aquaporins and Ion Conductance
New Mutations in the AQP2 Gene in Nephrogenic Diabetes Insipidus Resulting in Functional but Misrouted Water Channels
Physiology and Pathophysiology of Aquaporins
Molecular and Cellular Defects in Nephrogenic Diabetes Insipidus
Urinary Content of Aquaporin 1 and 2 in Nephrogenic Diabetes Insipidus
Aquaporins: From Physiology to Nephrogenic Diabetes Insipidus
The Clinical Importance of the Urinary Excretion of Aquaporin-2
Water Channels Encoded by Mutant Aquaporin-2 Genes in Nephrogenic Diabetes Insipidus are Impaired in Their Cellular Routing
Patients with Autosomal Nephrogenic Diabetes Insipidus Homozygous for Mutations in the Aquaporin 2 Water-Channel Gene
Requirement of Human Renal Water Channel Aquaporin-2 for Vasopressin-Dependent Concentration of Urine
Assignment of the Human Gene for the Water Channel of Renal Collecting Duct Aquaporin 2 (AQP2) to Chromosome 12 Region q12-->q13
6 Conference Proceedings
6 Conference Proceedings
Determination of the functionality of AQP2 missense mutants in recessive NDI
An impaired routing of wild type aquaporin-2 after tetramerization with an aquaporin-2 mutant explains dominant nephrogenic diabetes insipidus
Consequences of tetramerization and expression levels of Aquaporin-2 in phenotype-genotype correlation studies in autosomal NDI
The stoichiometry of phosphorylated and non-phosphorylated monomers in an aquaporin-2 tetramer determines its subcellular localization
Molecular mechanisms underlying dominant Nephrogenic Diabetes Insipidus caused by mutations in the AQP2 gene
Cell biological and functional analysis of five new Aquaporin-2 gene missense mutations in recessive Nephrogenic Diabetes Insipidus
25 Articles
25 Articles