Chapter 21 The molecular biology of human hereditary central diabetes insipidus
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Elsevier
Reference67 articles.
1. Genetic diseases: diagnosis by restriction endonuclease analysis;Antonarakis;J. Pediatr.,1982
2. Hereditary diabetes insipidus: an immunohistochemical study of the hypothalamus and pituitary gland;Bergeron;Acta Neuropathol. (Berl.),1991
3. Familial central diabetes insipidus: vasopressin and nicotine stimulated neurophysin deficiency with subnormal oxytocin and estrogen stimulated neurophysin;Blackett;Am. J. Med. Sci.,1983
4. Nephrogenic diabetes insipidus in North America - The Hopewell hypothesis;Bode;N. Engl. J. Med.,1969
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1. A Missense Mutation Encoding Cys67 → Gly in Neurophysin II Is Associated with Early Onset Autosomal Dominant Neurohypophyseal Diabetes Insipidus;Molecular Genetics and Metabolism;2001-01
2. Long-term gene therapy in the CNS: Reversal of hypothalamic diabetes insipidus in the Brattleboro rat by using an adenovirus expressing arginine vasopressin;Nature Medicine;1997-12
3. Decreased Profilaggrin Expression in Ichthyosis Vulgaris Is a Result of Selectively Impaired Posttranscriptional Control;Journal of Biological Chemistry;1995-01
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