Futers TS - Search Results

1

The association of complement C3 genotype with coronary artery disease, markers of the metabolic syndrome and C3 plasma levels.

Ajjan RA, Grant PJ, Futers TS, Brown JM, Carter AM. Ajjan RA, et al. Among authors: futers ts. Thromb Haemost. 2006 Feb;95(2):393-4. Thromb Haemost. 2006. PMID: 16493504 No abstract available.

2

Complement C3 and C-reactive protein levels in patients with stable coronary artery disease.

Ajjan R, Grant PJ, Futers TS, Brown JM, Cymbalista CM, Boothby M, Carter AM. Ajjan R, et al. Among authors: futers ts. Thromb Haemost. 2005 Nov;94(5):1048-53. doi: 10.1160/TH05-06-0384. Thromb Haemost. 2005. PMID: 16363249

3

Prevalence of three common polymorphisms in the A-subunit gene of factor XIII in patients with coronary artery disease.

Kohler HP, Futers TS, Grant PJ. Kohler HP, et al. Among authors: futers ts. Thromb Haemost. 1999 Apr;81(4):511-5. Thromb Haemost. 1999. PMID: 10235430

4

FXII (46C-->T) polymorphism and in vivo generation of FXII activity--gene frequencies and relationship in patients with coronary artery disease.

Kohler HP, Futers TS, Grant PJ. Kohler HP, et al. Among authors: futers ts. Thromb Haemost. 1999 May;81(5):745-7. Thromb Haemost. 1999. PMID: 10365748

5

Identification of novel polymorphisms within the protein Z gene, haplotype distribution and linkage analysis.

Rice GI, Futers TS, Grant PJ. Rice GI, et al. Among authors: futers ts. Thromb Haemost. 2001 Jun;85(6):1123-4. Thromb Haemost. 2001. PMID: 11434699 No abstract available.

6

Human endothelial cell-derived nuclear proteins that recognise polymorphic DNA elements in the von Willebrand factor gene promoter include YY1.

Costa M, Grant PJ, Rice GI, Futers TS, Medcalf RL. Costa M, et al. Among authors: futers ts. Thromb Haemost. 2001 Aug;86(2):672-9. Thromb Haemost. 2001. PMID: 11522021

7

Joint linkage and association of six single-nucleotide polymorphisms in the factor XIII-A subunit gene point to V34L as the main functional locus.

de Lange M, Andrew T, Snieder H, Ge D, Futers TS, Standeven K, Spector TD, Grant PJ, Ariëns RA. de Lange M, et al. Among authors: futers ts. Arterioscler Thromb Vasc Biol. 2006 Aug;26(8):1914-9. doi: 10.1161/01.ATV.0000231538.60223.92. Epub 2006 Jun 8. Arterioscler Thromb Vasc Biol. 2006. PMID: 16763156

8

RAGE polymorphisms and the heritability of insulin resistance: the Leeds family study.

Sullivan CM, Futers TS, Barrett JH, Hudson BI, Freeman MS, Grant PJ. Sullivan CM, et al. Among authors: futers ts. Diab Vasc Dis Res. 2005 Feb;2(1):42-4. doi: 10.3132/dvdr.2005.005. Diab Vasc Dis Res. 2005. PMID: 16305072 Free article.

9

The Human hydroxyacylglutathione hydrolase (HAGH) gene encodes both cytosolic and mitochondrial forms of glyoxalase II.

Cordell PA, Futers TS, Grant PJ, Pease RJ. Cordell PA, et al. Among authors: futers ts. J Biol Chem. 2004 Jul 2;279(27):28653-61. doi: 10.1074/jbc.M403470200. Epub 2004 Apr 26. J Biol Chem. 2004. PMID: 15117945 Free article.

10

Effects of novel polymorphisms in the RAGE gene on transcriptional regulation and their association with diabetic retinopathy.

Hudson BI, Stickland MH, Futers TS, Grant PJ. Hudson BI, et al. Among authors: futers ts. Diabetes. 2001 Jun;50(6):1505-11. doi: 10.2337/diabetes.50.6.1505. Diabetes. 2001. PMID: 11375354

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