Adrenomedullary function is severely impaired in 21-hydroxylase- deficient mice

FASEB Journal

Volumn 13, Issue 10, 1999, Pages 1185-1194

  Bornstein, S R ^a   Tajima, T ^a,c   Eisenhofer, G ^b   Haidan, A ^d   Aguilera, G ^a  

^a EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT   (United States)

^b NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

^c HOKKAIDO UNIVERSITY   (Japan)

^d Hokkaido University ^*

Author keywords

21 OH deficiency; Adrenal medulla; Catecholamine synthesis

Indexed keywords

ADRENALIN; CORTICOSTERONE; DOPAMINE; GLUCOCORTICOID; MINERALOCORTICOID; NORADRENALIN; PHENYLETHANOLAMINE N METHYLTRANSFERASE; STEROID 21 MONOOXYGENASE;

ADRENAL CORTEX; ADRENAL MEDULLA DISEASE; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CELL DIFFERENTIATION; CELL MATURATION; CELL MIGRATION; CELL STRUCTURE; CHROMAFFIN CELL; CONGENITAL ADRENAL HYPERPLASIA; CONTROLLED STUDY; CORTICOSTERONE BLOOD LEVEL; GENETIC DISORDER; MORPHOLOGY; MOUSE; NONHUMAN; PRIORITY JOURNAL; STEROID 21 MONOOXYGENASE DEFICIENCY;

ANIMALIA;

EID: 0033063173     PISSN: 08926638     EISSN: None     Source Type: Journal    
DOI: 10.1096/fasebj.13.10.1185     Document Type: Article

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