메뉴 건너뛰기




Volumn 48, Issue 2, 1998, Pages 129-134

Human ACTH hypersensitivity syndrome associated with abnormalities of the ACTH receptor gene

Author keywords

[No Author keywords available]

Indexed keywords

CORTICOTROPIN; CORTICOTROPIN RECEPTOR; TRIAMCINOLONE ACETONIDE;

EID: 0031936126     PISSN: 03000664     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2265.1998.00397.x     Document Type: Article
Times cited : (23)

References (11)
  • 1
    • 0027396787 scopus 로고
    • Familial glucocorticoid deficiency associated with point mutation in the adrenocorticotropin receptor
    • Clark, A.J.L., McLoughlin, L. & Grossman, A. (1993) Familial glucocorticoid deficiency associated with point mutation in the adrenocorticotropin receptor. Lancet. 341, 461-462.
    • (1993) Lancet , vol.341 , pp. 461-462
    • Clark, A.J.L.1    McLoughlin, L.2    Grossman, A.3
  • 2
    • 0028129676 scopus 로고
    • Molecular insights into inherited ACTH resistance syndromes
    • Clark, A.J.L. & Weber, A. (1994) Molecular insights into inherited ACTH resistance syndromes. Trends in Endocrinology and Metabolism, 5, 209-214.
    • (1994) Trends in Endocrinology and Metabolism , vol.5 , pp. 209-214
    • Clark, A.J.L.1    Weber, A.2
  • 5
    • 0026076322 scopus 로고
    • Adrenal androgen secretion in postadolescent acne: Increased adrenocortical function without hypersensitivity to adrenocorticotiopin
    • Laue, L., Peck, G.L., Loriaux, D.L., Gallucci, W. & Chrousos, G.P. (1991) Adrenal androgen secretion in postadolescent acne: increased adrenocortical function without hypersensitivity to adrenocorticotiopin. Journal of Clinical Endocrinology and Metabolism, 73, 380-384.
    • (1991) Journal of Clinical Endocrinology and Metabolism , vol.73 , pp. 380-384
    • Laue, L.1    Peck, G.L.2    Loriaux, D.L.3    Gallucci, W.4    Chrousos, G.P.5
  • 6
    • 0026800892 scopus 로고
    • The cloning of a family of genes that encode the melanocortin receptors
    • Mountjoy, K.G., Robbins, L.S., Mortrud, M.T. & Cone, R.D. (1992) The cloning of a family of genes that encode the melanocortin receptors. Science, 257, 1248-1251.
    • (1992) Science , vol.257 , pp. 1248-1251
    • Mountjoy, K.G.1    Robbins, L.S.2    Mortrud, M.T.3    Cone, R.D.4
  • 7
    • 0027413475 scopus 로고
    • Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function
    • Robbins, L.S., Nadeau, J.H., Johnson, K.R., Kelly, M.A., Roselli-Rehfuss, L., Baack, E., Mountjoy, K.G. & Cone, R.D. (1993) Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function. Cell, 72, 827-834.
    • (1993) Cell , vol.72 , pp. 827-834
    • Robbins, L.S.1    Nadeau, J.H.2    Johnson, K.R.3    Kelly, M.A.4    Roselli-Rehfuss, L.5    Baack, E.6    Mountjoy, K.G.7    Cone, R.D.8
  • 8
    • 0027423948 scopus 로고
    • Hereditary isolated glucocorticoid deficiency is associated with abnormalities of the adrenocorticotropin receptor gene
    • Tsigos, C., Arai, K., Hung, W. & Chrousos, G.P. (1993) Hereditary isolated glucocorticoid deficiency is associated with abnormalities of the adrenocorticotropin receptor gene. Journal of Clinical Investigation. 92, 2458-2461.
    • (1993) Journal of Clinical Investigation. , vol.92 , pp. 2458-2461
    • Tsigos, C.1    Arai, K.2    Hung, W.3    Chrousos, G.P.4
  • 9
    • 0029029505 scopus 로고
    • A novel mutation of the adrenocorticotropin receptor (ACTH-R) gene in a family with the syndrome of isolated glucocorticoid deficiency, but no ACTH-R abnormalities in two families with the triple A syndrome
    • Tsigos, C., Arai, K., Latronico, A.C., Digeorge, A.M., Rapaport, R. & Chrousos, G.P. (1995) A novel mutation of the adrenocorticotropin receptor (ACTH-R) gene in a family with the syndrome of isolated glucocorticoid deficiency, but no ACTH-R abnormalities in two families with the triple A syndrome. Journal of Clinical Endocrinology and Metabolism. 80, 2186-2189.
    • (1995) Journal of Clinical Endocrinology and Metabolism. , vol.80 , pp. 2186-2189
    • Tsigos, C.1    Arai, K.2    Latronico, A.C.3    Digeorge, A.M.4    Rapaport, R.5    Chrousos, G.P.6
  • 10
    • 0027500950 scopus 로고
    • Functional characterization of the cloned human ACTH receptor: Impaired responsiveness of a mutant receptor in familial glucocorticoid deficiency
    • Weber, A., Kapas, S., Hinson, J., Grant, D.B., Grossman, A. & Clark, A.J.L. (1993) Functional characterization of the cloned human ACTH receptor: impaired responsiveness of a mutant receptor in familial glucocorticoid deficiency. Biochemical Biophysical Research Communication. 197, 172-178.
    • (1993) Biochemical Biophysical Research Communication , vol.197 , pp. 172-178
    • Weber, A.1    Kapas, S.2    Hinson, J.3    Grant, D.B.4    Grossman, A.5    Clark, A.J.L.6
  • 11
    • 0025817113 scopus 로고
    • ACTH-induced inhibition of the action of angiotensin II in bovine zona glomerulosa cells - A modulatory effect of cyclic AMP on the angiotensin II receptor
    • Yoshida, A., Nishikawa, T., Tamura, Y. & Yoshida, S. (1991) ACTH-induced inhibition of the action of angiotensin II in bovine zona glomerulosa cells - a modulatory effect of cyclic AMP on the angiotensin II receptor. Journal of Biological Chemistry, 266, 4288-4294.
    • (1991) Journal of Biological Chemistry , vol.266 , pp. 4288-4294
    • Yoshida, A.1    Nishikawa, T.2    Tamura, Y.3    Yoshida, S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.