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2004 - Phoenix
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Angela Schulz
Title:
PhD
Email:
Phone:
Work +1-49 341-3550-853, Fax +1-49 341-3550-855
Organization:
University of Leipzig
Division:
Dept. Molecular Biochemistry, Medical Faculty
Address:
Deutscher Platz 6
04103 Leipzig,
Germany
7 Articles
7 Articles
Aminoglycoside-Mediated Rescue of a Disease-Causing Nonsense Mutation in the V2 Vasopressin Receptor Gene In Vitro and In Vivo
Aminoglycoside Pretreatment Partially Restores the Function of Truncated V2 Vasopressin Receptors Found in Patients with Nephrogenic Diabetes Insipidus
Generation and Phenotype of Mice Harboring a Nonsense Mutation in the V2 Vasopressin Receptor Gene
Functional Characterization of the Molecular Defects Causing Nephrogenic Diabetes Insipidus in Eight Families
Structural Implication for Receptor Oligomerization from Functional Reconstitution Studies of Mutant V2 Vasopressin Receptors
Compound Deletion of the rhoGAP C1 and V2 Vasopressin Receptor Genes in a Patient with Nephrogenic Diabetes Insipidus
V2 Vasopressin Receptor Dysfunction in Nephrogenic Diabetes Insipidus Caused By Different Molecular Mechanisms
8 Conference Proceedings
8 Conference Proceedings
Supplementation of Receptor Fragments: An approach to Functionally Rescue Mutant V2 Vasopressin Receptors
V2 vasopressin receptor dysfunction in patients with nephrogenic diabetes insipidus is caused by different molecular mechanisms
Structure of V2 vasopressin receptor oligomers: evidence for contact dimer formation
V2 vasopressin receptor function studied in mice and yeast
Analysis of molecular mechanisms causing V2 vasopressin receptor dysfunction in four patients with X-linked nephrogenic diabetes insipidus
Functional rescue of truncated V2-Vasopressin-receptors by aminoglycoside-induced misreading of nonsense-mutations
V2 vasopressin receptor-deficient mouse model: Pathophysiological changes and therapeutical implications
Structural evolution of the V2 vasopressin receptor in mammals
7 Articles
7 Articles