Influence of Ni nanoparticle on the morphology and growth of interfacial intermetallic compounds between Sn–3.8Ag–0.7Cu lead-free solder and copper substrate by Tay, S.L., Haseeb, A.S. Md. Abdul, Johan, M.R., Munroe, P.R., Quadir, M.Z.

Chromosome 2p shows genome wide significant linkage to anti-hypertensive medication response in the British genetics hypertension (BRIGHT) study by Padmanabhan, S, Munroe, P, Brown, M, Clayton, D, Farrall, M, Webster, J, Lathrop, M, Caulfield, M, Dominiczak, A, Connell, J

The benefit and impact of on-line tools for microscopy and microanalysis training and education in core facilities by Shapter, J., Muhling, J., Soon, L., Ringer, S.P., Grinan, E., Frost, C., Cribb, B., Apperley, M., Munroe, P.R., White, Timothy John

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Haplotypes of the beta-2 adrenergic receptor associate with high diastolic blood pressure in the Caerphilly prospective study. by Binder, A, Garcia, E, Wallace, C, Gbenga, K, Ben-Shlomo, Y, Yarnell, J, Brown, P, Caulfield, M, Skrabal, F, Kotanko, P, Munroe, P

Chromosome 2p shows genome wide significant linkage to of anti-hypertensive medication response in the British genetics of hypertension (BRIGHT) study. by Padmanabhan, S, Wallace, C, Munroe, P, Brown, M, Samani, N, Clayton, D, Farrall, M, Webster, J, Lathrop, M, Caulfield, M, Dominiczak, A, Connell, J

Chromosome 2p shows significant linkage to antihypertensive response in the British Genetics of Hypertension Study. by Padmanabhan, S, Wallace, C, Munroe, P, Dobson, R, Brown, M, Samani, N, Clayton, D, Farrall, M, Webster, J, Lathrop, M, Caulfield, M, Dominiczak, A, Connell, J

Novel associations of the Wnk1 gene with risk for essential hypertension and electrolyte homeostasis by Newhouse, S, Wallace, C, Hoti, M, Dobson, R, Farrall, M, Brown, M, Samani, N, Dominiczak, A, Connell, J, Webster, J, Lathrop, M, Caulfield, M, Munroe, P

Urinary albumin excretion in hypertensive siblings in the British Genetics of Hypertension study by Padmanabhan, S, Menni, C, Delles, C, Munroe, P, Brown, M, Samani, N, Farrall, M, Dobson, R, Webster, J, Lathrop, M, Caulfield, M, Connell, J, Dominiczak, A

WNK1 - functional analyses of variants associated with blood pressure and essential hypertension by Hoti, M, Newhouse, S, Clayton, D, Samani, N, Dominiczak, A, Brown, M, Webster, J, Lathrop, M, Farrall, M, Connell, J, Hodgkinson, C, Ye, S, Caulfield, M, Munroe, P

WNK1-functional analyses of variants associated with blood pressure and essential hypertension by Hoti, M, Newhouse, S, Clayton, D, Samani, N, Dominiczak, A, Brown, M, Webster, J, Lathrop, M, Farrall, M, Connell, J, Hodgkinson, C, Ye, S, Caulfield, M, Munroe, P

Novel loci discovery for blood pressure and heart rate using the Exome chip by Warren, H, Surendran, P, Manning, A, van den Berg, M, van der Harst, P, Verweij, N, Eijgelsheim, M, Stricker, B, Lindgren, C, Howson, J, Munroe, P

Validation of Association of Hypertension at the CYP11B1/B2 Locus in Caucasians. by Alvarez-Madrazo, S, Padmanabhan, S, Friel, E, MacKenzie, S, Brown, M, Caulfield, M, Munroe, P, Farrall, M, Webster, J, Samani, N, Dominiczak, A, Melander, O, Davies, E, Connell, J

Familial atherosclerotic disease and hypertension localised to chromosome 7p in the British genetics of hypertension study by Padmanabhan, S, Hastie, C, Wallace, C, Munroe, P, Dobson, R, Brown, M, Samani, N, Clayton, D, Farrall, M, Webster, J, Lathrop, M, Caulfield, M, Connell, J, Dominiczalk, A

Genomewide linkage analysis for loci affecting electrocardiographic LV mass by Padmanabhan, S, Wallace, C, McBride, M, Munroe, P, Dobson, R, Brown, M, Samani, N, Clayton, D, Farrall, M, Webster, J, Lathrop, M, Caulfield, M, Dominiczak, A, Connell, J

Variants of the human mu type glutathione-s-transferase (GSTM) gene family are associated with hypertension by Delles, C, Marcano, A, Munroe, P, Padmanabhan, S, McClure, J, Brain, N, Brown, M, Samani, N, Clayton, D, Farrall, M, Webster, J, Connell, J, Caulfield, M, Dominiczak, A

Phenotypic consequences of variation across the aldosterone synthase and 11-beta hydroxylase locus in a hypertensive cohort: data from the MRC BRIGHT Study. by Freel, E, Ingram, M, Friel, E, Fraser, R, Brown, M, Samani, N, Caulfield, M, Munroe, P, Farrall, M, Webster, J, Clayton, D, Dominiczak, A, Davies, E, Connell, J

Association between variants of the human GSTM gene family and hypertension by Delles, C, Braga-Marcano, A, Munroe, P, Padmanabhan, S, McClure, J, Brain, N, Brown, M, Samani, N, Clayton, D, Farrall, M, Webster, J, Connell, J, Caulfield, M, Dominiczak, A

Variants and haplotypes of the angiotensinogen gene are associated with hypertension in the Caerphilly Prospective Study by Xue, M, Wallace, C, Dobson, R, Garcia, E, Kazeem, G, Gardener, G, Needham, E, Mattu, R, Ben-Shlomo, Y, Yarnell, J, Sweetnam, P, Farrall, M, Caulfield, M, Munroe, P

Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study. by Newhouse, S, Wallace, C, Dobson, R, Mein, C, Pembroke, J, Farrall, M, Clayton, D, Brown, M, Samani, N, Dominiczak, A, Connell, J, Webster, J, Lathrop, G, Caulfield, M, Munroe, P

A new tool for checks of data precision within the MRC British genetics of hypertension study by Caulfield, M, Papp, J, Pembroke, J, Munroe, P, Farrall, M, Dominiczak, A, Clayton, D, Ratcliffe, P, Lathrop, M, Webster, J, Keaveney, B, Benjamin, N, Brown, M, Samani, N, Connell, J