Inglis GC - Search Results

1

An influence of variation in the aldosterone synthase gene (CYP11B2) on corticosteroid responses to ACTH in normal human subjects.

Davies E, Holloway CD, Ingram MC, Friel EC, Inglis GC, Swan L, Hillis WS, Fraser R, Connell JM. Davies E, et al. Among authors: inglis gc. Clin Endocrinol (Oxf). 2001 Jun;54(6):813-7. doi: 10.1046/j.1365-2265.2001.01264.x. Clin Endocrinol (Oxf). 2001. PMID: 11422117 Clinical Trial.

2

Altered 11 beta-hydroxylase activity in glucocorticoid-suppressible hyperaldosteronism.

Jamieson A, Ingram MC, Inglis GC, Davies E, Fraser R, Connell JM. Jamieson A, et al. Among authors: inglis gc. J Clin Endocrinol Metab. 1996 Jun;81(6):2298-302. doi: 10.1210/jcem.81.6.8964867. J Clin Endocrinol Metab. 1996. PMID: 8964867

3

Aldosterone excretion rate and blood pressure in essential hypertension are related to polymorphic differences in the aldosterone synthase gene CYP11B2.

Davies E, Holloway CD, Ingram MC, Inglis GC, Friel EC, Morrison C, Anderson NH, Fraser R, Connell JM. Davies E, et al. Among authors: inglis gc. Hypertension. 1999 Feb;33(2):703-7. doi: 10.1161/01.hyp.33.2.703. Hypertension. 1999. PMID: 10024332

4

Familial pattern of corticosteroids and their metabolism in adult human subjects--the Scottish Adult Twin Study.

Inglis GC, Ingram MC, Holloway CD, Swan L, Birnie D, Hillis WS, Davies E, Fraser R, Connell JM. Inglis GC, et al. J Clin Endocrinol Metab. 1999 Nov;84(11):4132-7. doi: 10.1210/jcem.84.11.6146. J Clin Endocrinol Metab. 1999. PMID: 10566661

5

Polymorphic differences from normal in the aldosterone synthase gene (CYP11B2) in patients with primary hyperaldosteronism and adrenal tumour (Conn's syndrome).

Inglis GC, Plouin PF, Friel EC, Davies E, Fraser R, Connell JM. Inglis GC, et al. Clin Endocrinol (Oxf). 2001 Jun;54(6):725-30. doi: 10.1046/j.1365-2265.2001.01287.x. Clin Endocrinol (Oxf). 2001. PMID: 11422106

6

Glucocorticoid-suppressible hyperaldosteronism: effects of crossover site and parental origin of chimaeric gene on phenotypic expression.

Jamieson A, Slutsker L, Inglis GC, Fraser R, White PC, Connell JM. Jamieson A, et al. Among authors: inglis gc. Clin Sci (Lond). 1995 May;88(5):563-70. doi: 10.1042/cs0880563. Clin Sci (Lond). 1995. PMID: 7614815

7

Microsatellite polymorphism analysis allows the individual assignment of the rat 11 beta-hydroxylase gene (Cyp11b1) and the rat aldosterone synthase gene (Cyp11b2) to chromosome 7 using rat x mouse somatic cell hybrids and identifies differences between and within various rat strains.

Inglis GC, Kenyon CJ, Szpirer C, Klinga-Levan K, Sutcliffe RG, Connell JM. Inglis GC, et al. J Mol Endocrinol. 1995 Jun;14(3):303-11. doi: 10.1677/jme.0.0140303. J Mol Endocrinol. 1995. PMID: 7669222

8

Atrial natriuretic hormone: a paracrine or endocrine role within the human placenta?

Inglis GC, Kingdom JC, Nelson DM, Lindop GB, Whittle MJ, Connell JM. Inglis GC, et al. J Clin Endocrinol Metab. 1993 Apr;76(4):1014-8. doi: 10.1210/jcem.76.4.8473375. J Clin Endocrinol Metab. 1993. PMID: 8473375

9

Rapid diagnosis and identification of cross-over sites in patients with glucocorticoid remediable aldosteronism.

MacConnachie AA, Kelly KF, McNamara A, Loughlin S, Gates LJ, Inglis GC, Jamieson A, Connell JM, Haites NE. MacConnachie AA, et al. Among authors: inglis gc. J Clin Endocrinol Metab. 1998 Dec;83(12):4328-31. doi: 10.1210/jcem.83.12.5309. J Clin Endocrinol Metab. 1998. PMID: 9851772

10

Dexamethasone-suppressible hyperaldosteronism: clinical, biochemical and genetic relations.

Connell JM, Inglis GC, Fraser R, Jamieson A. Connell JM, et al. Among authors: inglis gc. J Hum Hypertens. 1995 Jun;9(6):505-9. J Hum Hypertens. 1995. PMID: 7473536 Review.

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