Heterologous expression of human vasopressin-neurophysin precursors in a pituitary cell line: Defective transport of a mutant protein from patients with familial diabetes insipidus

DNA and Cell Biology

Volumn 15, Issue 11, 1996, Pages 929-935

  Olias, Gisela ^a  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

NEUROPHYSIN; VASOPRESSIN;

ARTICLE; CELL LINE; DIABETES INSIPIDUS; ENDOPLASMIC RETICULUM; HORMONE SYNTHESIS; HUMAN; HUMAN CELL; HYPOPHYSIS CELL; POINT MUTATION; PRIORITY JOURNAL; PROTEIN CONFORMATION; PROTEIN PROCESSING; PROTEIN TRANSPORT; REGULATORY MECHANISM;

EID: 0029801679     PISSN: 10445498     EISSN: None     Source Type: Journal    
DOI: 10.1089/dna.1996.15.929     Document Type: Article

References (9)

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3. BENSON, M.D. (1989). Familial amyloidotic polyneuropathy. Trends Genet. 12, 88-92.
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7. QUINN, D., ORCI, L., RAVAZZOLA, M., and MOORE, H.-P. (1991). Intracellular transport and sorting of mutant human proinsulins that fail to form hexamers. J. Cell Biol. 113, 987-996.
8. REPASKE, D.R., and BROWNING, J.E. (1994). A de novo mutation in the coding sequence for neurophysin-II (Pro24 →Leu) is associated with onset and transmission of autosomal dominant neurohypophyseal diabetes insipidus. J. Clin. Endocrinol. Metab. 79, 421-427.
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