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Publications by Kyuzi KAMOI
Novel Mutant Vasopressin-Neurophysin II Gene Associated With Familial Neurohypophyseal Diabetes Insipidus
Endocrine Journal
Endocrinology
Metabolism
Diabetes
Gitelman's Syndrome First Diagnosed as Bartter's Syndrome.
Internal Medicine
Internal Medicine
Medicine
Related publications
Familial Neurohypophyseal Diabetes Insipidus (Nhdi) Due to a Mutation in the Vasopressin-Neurophysine Ii (Vp-NPH Ii) Gene
Pediatric Research
Child Health
Pediatrics
Perinatology
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
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
Mutant Vasopressin Precursors That Cause Autosomal Dominant Neurohypophyseal Diabetes Insipidus Retain Dimerization and Impair the Secretion of Wild-Type Proteins
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Continuous Vasopressin Replacement in Diabetes Insipidus.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
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
Rescue of a Nephrogenic Diabetes Insipidus-Causing Vasopressin V2Receptor Mutant by Cell-Penetrating Peptides
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Neurophysin Biosynthesis in Normal Rats and in Rats With Hereditary Diabetes Insipidus.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
