Channer K - Search Results

1

Insertion/deletion polymorphism in the angiotensin-converting enzyme gene and risk of and prognosis after myocardial infarction.

Samani NJ, O'Toole L, Martin D, Rai H, Fletcher S, Lodwick D, Thompson JR, Morice AH, Channer K, Woods KL. Samani NJ, et al. Among authors: channer k. J Am Coll Cardiol. 1996 Aug;28(2):338-44. doi: 10.1016/0735-1097(96)00139-8. J Am Coll Cardiol. 1996. PMID: 8800107 Free article.

2

A meta-analysis of the association of the deletion allele of the angiotensin-converting enzyme gene with myocardial infarction.

Samani NJ, Thompson JR, O'Toole L, Channer K, Woods KL. Samani NJ, et al. Among authors: channer k. Circulation. 1996 Aug 15;94(4):708-12. doi: 10.1161/01.cir.94.4.708. Circulation. 1996. PMID: 8772692

3

Distribution of tissue plasminogen activator insertion/deletion polymorphism in myocardial infarction and control subjects.

Steeds R, Adams M, Smith P, Channer K, Samani NJ. Steeds R, et al. Among authors: channer k. Thromb Haemost. 1998 May;79(5):980-4. Thromb Haemost. 1998. PMID: 9609233

4

Effect of the insertion/deletion polymorphism of the angiotensin-converting enzyme gene on response to angiotensin-converting enzyme inhibitors in patients with heart failure.

O'Toole L, Stewart M, Padfield P, Channer K. O'Toole L, et al. Among authors: channer k. J Cardiovasc Pharmacol. 1998 Dec;32(6):988-94. doi: 10.1097/00005344-199812000-00017. J Cardiovasc Pharmacol. 1998. PMID: 9869506 Clinical Trial.

5

Analysis of promoter region polymorphism in the aldosterone synthase gene (CYP11B2) as a risk factor for myocardial infarction.

Patel S, Steeds R, Channer K, Samani NJ. Patel S, et al. Among authors: channer k. Am J Hypertens. 2000 Feb;13(2):134-9. doi: 10.1016/s0895-7061(99)00176-4. Am J Hypertens. 2000. PMID: 10701812

6

Human vascular reactivity and polymorphisms of the angiotensin-converting enzyme and the angiotensin type 1 receptor genes.

Steeds RP, Toole LO, Channer KS, Morice AH. Steeds RP, et al. Among authors: channer ks. J Vasc Res. 1999 Nov-Dec;36(6):445-55; discussion 535-8. doi: 10.1159/000025687. J Vasc Res. 1999. PMID: 10629420

7

Analysis of the postulated interaction between the angiotensin II sub-type 1 receptor gene A1166C polymorphism and the insertion/deletion polymorphism of the angiotensin converting enzyme gene on risk of myocardial infarction.

Steeds RP, Wardle A, Smith PD, Martin D, Channer KS, Samani NJ. Steeds RP, et al. Among authors: channer ks. Atherosclerosis. 2001 Jan;154(1):123-8. doi: 10.1016/s0021-9150(00)00438-x. Atherosclerosis. 2001. PMID: 11137090

8

Genotypes and haplotypes predisposing to myocardial infarction: a multilocus case-control study.

Tobin MD, Braund PS, Burton PR, Thompson JR, Steeds R, Channer K, Cheng S, Lindpaintner K, Samani NJ. Tobin MD, et al. Among authors: channer k. Eur Heart J. 2004 Mar;25(6):459-67. doi: 10.1016/j.ehj.2003.11.014. Eur Heart J. 2004. PMID: 15039125

9

LGALS2 functional variant rs7291467 is not associated with susceptibility to myocardial infarction in Caucasians.

Mangino M, Braund P, Singh R, Steeds R, Thompson JR, Channer K, Samani NJ. Mangino M, et al. Among authors: channer k. Atherosclerosis. 2007 Sep;194(1):112-5. doi: 10.1016/j.atherosclerosis.2006.10.004. Epub 2006 Nov 13. Atherosclerosis. 2007. PMID: 17098239

10

The prothrombin 20210A allele and its association with myocardial infarction.

Croft SA, Daly ME, Steeds RP, Channer KS, Samani NJ, Hampton KK. Croft SA, et al. Among authors: channer ks. Thromb Haemost. 1999 Jun;81(6):861-4. Thromb Haemost. 1999. PMID: 10404757

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