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Publications by Robert S Wildin
V2 Vasopressin Receptor Mutation Y205c Causing Nephrogenic Diabetes Insipidus Retains Partial Function in Vitro. † 885
Pediatric Research
Child Health
Pediatrics
Perinatology
Related publications
Analysis of the V2 Vasopressin Receptor (V2R) Mutations Causing Partial Nephrogenic Diabetes Insipidus Highlights a Sustainable Signaling by a Non-Peptide V2R Agonist
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Rescue of a Nephrogenic Diabetes Insipidus-Causing Vasopressin V2Receptor Mutant by Cell-Penetrating Peptides
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
A Novel Deletion Mutation of the Arginine Vasopressin Receptor 2 Gene in a Japanese Infant With Nephrogenic Diabetes Insipidus
Clinical Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Constitutive Arrestin-Mediated Desensitization of a Human Vasopressin Receptor Mutant Associated With Nephrogenic Diabetes Insipidus
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Vasopressin Function in Familial Cranial Diabetes Insipidus.
Postgraduate Medical Journal
Medicine
Constitutive Arrestin-Mediated Desensitization of a Human Vasopressin Receptor Mutant Associated With Nephrogenic Diabetes Insipidus
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Physiopathology and Diagnosis of Nephrogenic Diabetes Insipidus
Annales d'Endocrinologie
Medicine
Endocrinology
Metabolism
Diabetes
P291 Nephrogenic Diabetes Insipidus in a Female Infant
Continuous Vasopressin Replacement in Diabetes Insipidus.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
