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Publications by Carolyn A. Ecelbarger
Generation and Phenotype of Mice Harboring a Nonsense Mutation in the V2 Vasopressin Receptor Gene
Journal of Clinical Investigation
Medicine
Reduced Expression of Insulin Receptors in the Kidneys of Insulin-Resistant Rats
Journal of the American Society of Nephrology : JASN
Medicine
Nephrology
Related publications
Loop-Tail Phenotype in Heterozygous Mice and Neural Tube Defects in Homozygous Mice Result From a Nonsense Mutation in the Vangl2 Gene
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
The Vasopressin V2 Receptor Antagonists: The Vaptans
Global Journal of Endocrinological Metabolism
A Serine Cluster Prevents Recycling of the V2 Vasopressin Receptor
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
A Nonsense Mutation in a Cinnamyl Alcohol Dehydrogenase Gene Is Responsible for the Sorghum Brown Midrib6 Phenotype
Plant Physiology
Plant Science
Genetics
Physiology
V2 Vasopressin Receptor Mutation Y205c Causing Nephrogenic Diabetes Insipidus Retains Partial Function in Vitro. † 885
Pediatric Research
Child Health
Pediatrics
Perinatology
Membrane Targeting and Determination of Transmembrane Topology of the Human Vasopressin V2 Receptor
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Identification of a Nonsense Mutation in the PAX9 Gene in Molar Oligodontia
European Journal of Human Genetics
Genetics
Pharmacological Profile of VP-343, a Novel Selective Vasopressin V2 Receptor Antagonist, in Rats.
Biological and Pharmaceutical Bulletin
Medicine
Pharmacology
Pharmaceutical Science
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