Inglis GC - Search Results

1

Variation at the beta-1 adrenoceptor gene locus affects left ventricular mass in renal failure.

Stanton T, Inglis GC, Padmanabhan S, Dominiczak AF, Jardine AG, Connell JM. Stanton T, et al. Among authors: inglis gc. J Nephrol. 2002 Sep-Oct;15(5):512-8. J Nephrol. 2002. PMID: 12455717

2

The genetic determination of left ventricular mass in healthy adults.

Swan L, Birnie DH, Padmanabhan S, Inglis G, Connell JM, Hillis WS. Swan L, et al. Eur Heart J. 2003 Mar;24(6):577-82. doi: 10.1016/s0195-668x(02)00524-9. Eur Heart J. 2003. PMID: 12643891

3

The Y chromosome effect on blood pressure in two European populations.

Charchar FJ, Tomaszewski M, Padmanabhan S, Lacka B, Upton MN, Inglis GC, Anderson NH, McConnachie A, Zukowska-Szczechowska E, Grzeszczak W, Connell JM, Watt GC, Dominiczak AF. Charchar FJ, et al. Among authors: inglis gc. Hypertension. 2002 Feb;39(2 Pt 2):353-6. doi: 10.1161/hy0202.103413. Hypertension. 2002. PMID: 11882572

4

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

5

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.

6

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.

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

Rapid diagnosis of glucocorticoid suppressible hyperaldosteronism in infants and adolescents.

Jamieson A, Inglis GC, Campbell M, Fraser R, Connell JM. Jamieson A, et al. Among authors: inglis gc. Arch Dis Child. 1994 Jul;71(1):40-3. doi: 10.1136/adc.71.1.40. Arch Dis Child. 1994. PMID: 7915100 Free PMC article.

9

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

10

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

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