Mechanisms of Hypertension: The Expanding Role of Aldosterone

gan FREEL, E. MARIE, CONNELL, JOHN M.C.
Cyhoeddwyd 2004

Partial end organ resistance to thyroid hormone in congenital hypothyroidism

gan Connell, John M. C., McLaren, E. H.
Cyhoeddwyd 1981

Stroke affecting young men after alcoholic binges

gan Stott, David James, Ball, Stephen G, Connell, John M C, McInnes, Gordon T
Cyhoeddwyd 1985

ACTH and Polymorphisms at Steroidogenic Loci as Determinants of Aldosterone Secretion and Blood Pressure

gan MacKenzie, Scott M., Freel, E. Marie, Connell, John M., Fraser, Robert, Davies, Eleanor
Cyhoeddwyd yn Int J Mol Sci (2017)

Cardiac tissue engineering and regeneration using cell-based therapy

gan Alrefai, Mohammad T, Murali, Divya, Paul, Arghya, Ridwan, Khalid M, Connell, John M, Shum-Tim, Dominique
Cyhoeddwyd yn Stem Cells Cloning (2015)

How reproducible is bilateral forearm plethysmography?

gan Petrie, John R, Ueda, Shinichiro, Morris, Andrew D, Murray, Lilian S, Elliott, Henry L, Connell, John M C
Cyhoeddwyd 1998

Insulin rapidly stimulates l-arginine transport in human aortic endothelial cells via Akt

gan Kohlhaas, Christine F., Morrow, Valerie A., Jhakra, Neelam, Patil, Vrushali, Connell, John M.C., Petrie, John R., Salt, Ian P.
Cyhoeddwyd 2011

Effects of ACTH, dexamethasone, and adrenalectomy on 11β-hydroxylase (CYP11B1) and aldosterone synthase (CYP11B2) gene expression in the rat central nervous system

gan Ye, Ping, Kenyon, Christopher J, MacKenzie, Scott M, Nichol, Katherine, Seckl, Jonathan R, Fraser, Robert, Connell, John M C, Davies, Eleanor
Cyhoeddwyd 2008

Regulation of Corticosteroidogenic Genes by MicroRNAs

gan Robertson, Stacy, Diver, Louise A., Alvarez-Madrazo, Samantha, Livie, Craig, Ejaz, Ayesha, Fraser, Robert, Connell, John M., MacKenzie, Scott M., Davies, Eleanor
Cyhoeddwyd yn Int J Endocrinol (2017)

Genotype at the P554L Variant of the Hexose-6 Phosphate Dehydrogenase Gene Is Associated with Carotid Intima-Medial Thickness

gan Rahman, Thahira J., Walker, Elizabeth A., Mayosi, Bongani M., Hall, Darroch H., Avery, Peter J., Connell, John M. C., Watkins, Hugh, Stewart, Paul M., Keavney, Bernard
Cyhoeddwyd 2011

Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency

gan Lavery, Gareth G., Walker, Elizabeth A., Tiganescu, Ana, Ride, Jon P., Shackleton, Cedric H. L., Tomlinson, Jeremy W., Connell, John M. C., Ray, David W., Biason-Lauber, Anna, Malunowicz, Ewa M., Arlt, Wiebke, Stewart, Paul M.
Cyhoeddwyd 2008

Health Status of Adults with Congenital Adrenal Hyperplasia: A Cohort Study of 203 Patients

gan Arlt, Wiebke, Willis, Debbie S., Wild, Sarah H., Krone, Nils, Doherty, Emma J., Hahner, Stefanie, Han, Thang S., Carroll, Paul V., Conway, Gerry S., Rees, D. Aled, Stimson, Roland H., Walker, Brian R., Connell, John M. C., Ross, Richard J.
Cyhoeddwyd 2010

Genetic association analysis of inositol polyphosphate phosphatase‐like 1 (INPPL1, SHIP2) variants with essential hypertension

gan Marçano, Ana Carolina Braga, Burke, Beverley, Gungadoo, Johannie, Wallace, Chris, Kaisaki, Pamela J, Woon, Peng Y, Farrall, Martin, Clayton, David, Brown, Morris, Dominiczak, Anna, Connell, John M, Webster, John, Lathrop, Mark, Caulfield, Mark, Samani, Nilesh, Gauguier, Dominique, Munroe, Patricia B
Cyhoeddwyd 2007

Functionally-Competent Cardiac Stem Cells Can Be Isolated from Endomyocardial Biopsies of Patients with Advanced Cardiomyopathies

gan D'Amario, Domenico, Fiorini, Claudia, Campbell, Patricia M., Goichberg, Polina, Sanada, Fumihiro, Zheng, Hanqiao, Hosoda, Toru, Rota, Marcello, Connell, John M., Gallegos, Robert P., Welt, Frederick G., Givertz, Michael M., Mitchell, Richard N., Leri, Annarosa, Kajstura, Jan, Pfeffer, Marc A., Anversa, Piero
Cyhoeddwyd 2011

COMMON POLYMORPHISMS AT THE CYP17A1 LOCUS ASSOCIATE WITH STEROID PHENOTYPE: SUPPORT FOR BLOOD PRESSURE GWAS SIGNALS AT THIS LOCUS

gan Diver, Louise A., MacKenzie, Scott M., Fraser, Robert, McManus, Frances, Freel, E. Marie, Alvarez-Madrazo, Samantha, McClure, John D., Friel, Elaine C., Hanley, Neil A., Dominiczak, Anna F., Caulfield, Mark J., Munroe, Patricia B., Connell, John M., Davies, Eleanor
Cyhoeddwyd yn Hypertension (2016)

Linkage Analysis Using Co-Phenotypes in the BRIGHT Study Reveals Novel Potential Susceptibility Loci for Hypertension

gan Wallace, Chris, Xue, Ming-Zhan, Newhouse, Stephen J., Marçano, Ana Carolina B., Onipinla, Abiodun K., Burke, Beverley, Gungadoo, Johannie, Dobson, Richard J., Brown, Morris, Connell, John M., Dominiczak, Anna, Lathrop, G. Mark, Webster, John, Farrall, Martin, Mein, Charles, Samani, Nilesh J., Caulfield, Mark J., Clayton, David G., Munroe, Patricia B.
Cyhoeddwyd 2006

Genome-wide Association Study Identifies Genes for Biomarkers of Cardiovascular Disease: Serum Urate and Dyslipidemia

gan Wallace, Chris, Newhouse, Stephen J., Braund, Peter, Zhang, Feng, Tobin, Martin, Falchi, Mario, Ahmadi, Kourosh, Dobson, Richard J., Marçano, Ana Carolina B., Hajat, Cother, Burton, Paul, Deloukas, Panagiotis, Brown, Morris, Connell, John M., Dominiczak, Anna, Lathrop, G. Mark, Webster, John, Farrall, Martin, Spector, Tim, Samani, Nilesh J., Caulfield, Mark J., Munroe, Patricia B.
Cyhoeddwyd 2008

Polymorphisms in the WNK1 Gene Are Associated with Blood Pressure Variation and Urinary Potassium Excretion

gan Newhouse, Stephen, Farrall, Martin, Wallace, Chris, Hoti, Mimoza, Burke, Beverley, Howard, Philip, Onipinla, Abiodun, Lee, Kate, Shaw-Hawkins, Sue, Dobson, Richard, Brown, Morris, Samani, Nilesh J., Dominiczak, Anna F., Connell, John M., Lathrop, G. Mark, Kooner, Jaspal, Chambers, John, Elliott, Paul, Clarke, Robert, Collins, Rory, Laan, Maris, Org, Elin, Juhanson, Peeter, Veldre, Gudrun, Viigimaa, Margus, Eyheramendy, Susana, Cappuccio, Francesco P., Ji, Chen, Iacone, Roberto, Strazzullo, Pasquale, Kumari, Meena, Marmot, Michael, Brunner, Eric, Caulfield, Mark, Munroe, Patricia B.
Cyhoeddwyd 2009

SLC2A9 Is a High-Capacity Urate Transporter in Humans

gan Caulfield, Mark J, Munroe, Patricia B, O'Neill, Deb, Witkowska, Kate, Charchar, Fadi J, Doblado, Manuel, Evans, Sarah, Eyheramendy, Susana, Onipinla, Abiodun, Howard, Philip, Shaw-Hawkins, Sue, Dobson, Richard J, Wallace, Chris, Newhouse, Stephen J, Brown, Morris, Connell, John M, Dominiczak, Anna, Farrall, Martin, Lathrop, G. Mark, Samani, Nilesh J, Kumari, Meena, Marmot, Michael, Brunner, Eric, Chambers, John, Elliott, Paul, Kooner, Jaspal, Laan, Maris, Org, Elin, Veldre, Gudrun, Viigimaa, Margus, Cappuccio, Francesco P, Ji, Chen, Iacone, Roberto, Strazzullo, Pasquale, Moley, Kelle H, Cheeseman, Chris
Cyhoeddwyd 2008

Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype–phenotype correlations, codon bias and dominant-negative...

gan Hannan, Fadil M., Howles, Sarah A., Rogers, Angela, Cranston, Treena, Gorvin, Caroline M., Babinsky, Valerie N., Reed, Anita A., Thakker, Clare E., Bockenhauer, Detlef, Brown, Rosalind S., Connell, John M., Cook, Jacqueline, Darzy, Ken, Ehtisham, Sarah, Graham, Una, Hulse, Tony, Hunter, Steven J., Izatt, Louise, Kumar, Dhavendra, McKenna, Malachi J., McKnight, John A., Morrison, Patrick J., Mughal, M. Zulf, O'Halloran, Domhnall, Pearce, Simon H., Porteous, Mary E., Rahman, Mushtaqur, Richardson, Tristan, Robinson, Robert, Scheers, Isabelle, Siddique, Haroon, van't Hoff, William G., Wang, Timothy, Whyte, Michael P., Nesbit, M. Andrew, Thakker, Rajesh V.
Cyhoeddwyd yn Hum Mol Genet (2015)