Differential cellular handling of defective arginine vasopressin (AVP) prohormones in cells expressing mutations of the AVP gene associated with autosomal dominant and recessive familial neurohypophyseal diabetes insipidus.

Christensen, Jane H; Siggaard, Charlotte; Corydon, Thomas J; Robertson, Gary L; Gregersen, Niels; Bolund, Lars; Rittig, Søren

Christensen, Jane H; Siggaard, Charlotte; Corydon, Thomas J; Robertson, Gary L; Gregersen, Niels; Bolund, Lars; Rittig, Søren.

Affiliation

Christensen JH; Department of Pediatrics, Aarhus University Hospital, Skejby Sygehus, Brendstrupgaardsvej, DK-8200 Aarhus N, Denmark.

J Clin Endocrinol Metab ; 89(9): 4521-31, 2004 Sep.

Article in En | MEDLINE | ID: mdl-15356057

Subject(s)

Arginine Vasopressin/genetics; Diabetes Insipidus, Neurogenic/genetics; Mutation; Vasopressins/metabolism; Arginine Vasopressin/biosynthesis; Cells, Cultured; Humans; Microscopy, Confocal; Neurophysins/immunology; Precipitin Tests

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Collection: 01-internacional Database: MEDLINE Main subject: Arginine Vasopressin / Vasopressins / Diabetes Insipidus, Neurogenic / Mutation Type of study: Risk_factors_studies Limits: Humans Language: En Journal: J Clin Endocrinol Metab Year: 2004 Document type: Article Affiliation country: Denmark Country of publication: United States

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