Molecular biology techniques in endocrinology

Clinical Endocrinology

Volumn 45, Issue 2, 1996, Pages 125-133

  Davis, Julian R E ^a  

^a UNIVERSITY OF MANCHESTER   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID SEQUENCE; ENDOCRINOLOGY; HUMAN; MOLECULAR BIOLOGY; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; REVIEW; TRANSGENIC ANIMAL;

EID: 0029799805     PISSN: 03000664     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2265.1996.d01-1560.x     Document Type: Review

References (9)

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3. Collingwood, T.N., Adams, M., Tone, Y. & Chatterjee, V.K.K. (1994) Spectrum of transcriptional, dimerization, and dominant negative properties of twenty different mutant thyroid hormone 3-receptors in thyroid hormone resistance syndrome. Molecular Endocrinology, 8, 1262-1277.
4. Jones, B.K., Monks, B.R., Liebhaber, S.A. & Cooke, N.E. (1995) The human growth hormone gene is regulated by a multi-competent locus control region. Molecular and Cell Biology, 15, 7010-7021.
5. Lifton, R.P. & Dluhy, R.G. (1993) The molecular basis of a hereditary form of hypertension. glucocorticoid-remediable aldosteronism. Trends in Endocrinology and Metabolism, 4, 57-61.
6. Lyons, J., Landis, C.A., Harsh, G., Vallar, L., Grünewald, K., Feichtinger, H., Duh, Q.-Y., Clark, O.H., Kawasaki, E., Bourne, H.R., McCormick, F. (1990) Two G protein oncogenes in human endocrine tumours. Science, 249, 655-659.
7. Miller, W.L. (1994) Genetics, diagnosis, and management of 21-hydroxylase deficiency. Journal of Clinical Endocrinology and Metabolism, 78, 241-248.
8. Phillips, J.A. III, Hjelle, B.L., Seeburg, P.H. & Zachmann, M. (1981) Molecular basis for familial isolated growth hormone deficiency. Proceedings of the National Academy of Sciences, USA, 78, 6372-6375.
9. Stewart, T.A. (1993) Models of human endocrine disorders in transgenic rodents. Trends in Endocrinology and Melabolism, 4, 136-141.