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Publications by Takashi Daitsu
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
Related publications
P291 Nephrogenic Diabetes Insipidus in a Female Infant
V2 Vasopressin Receptor Mutation Y205c Causing Nephrogenic Diabetes Insipidus Retains Partial Function in Vitro. † 885
Pediatric Research
Child Health
Pediatrics
Perinatology
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
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
Thirst Perception and Arginine Vasopressin Production in a Kindred With an Activating Mutation of the Type 2 Vasopressin Receptor: The Pathophysiology of Nephrogenic Syndrome of Inappropriate Antidiuresis
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Three Novel AVPR2 Mutations in Three Japanese Families With X-Linked Nephrogenic Diabetes Insipidus
Pediatric Research
Child Health
Pediatrics
Perinatology
Rescue of a Nephrogenic Diabetes Insipidus-Causing Vasopressin V2Receptor Mutant by Cell-Penetrating Peptides
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Novel Mutant Vasopressin-Neurophysin II Gene Associated With Familial Neurohypophyseal Diabetes Insipidus
Endocrine Journal
Endocrinology
Metabolism
Diabetes
Familial Neurohypophyseal Diabetes Insipidus (Nhdi) Due to a Mutation in the Vasopressin-Neurophysine Ii (Vp-NPH Ii) Gene
Pediatric Research
Child Health
Pediatrics
Perinatology
