Species-specific differences in the expression of the HNF1A, HNF1B and HNF4A genes. by Harries, L, Brown, J, Gloyn, A

Update of mutations in the genes encoding the pancreatic beta-cell K(ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulin... by Flanagan, SE, Clauin, S, Bellanné-Chantelot, C, de Lonlay, P, Harries, L, Gloyn, A, Ellard, S

Extracellular calreticulin is present in the joints of patients with rheumatoid arthritis and inhibits FasL (CD95L)-mediated apoptosis of T cells. by Tarr, J, Winyard, P, Ryan, B, Harries, L, Haigh, R, Viner, N, Eggleton, P

Origin of de novo KCNJ11 mutations and risk of neonatal diabetes for subsequent siblings. by Edghill, E, Gloyn, A, Goriely, A, Harries, L, Flanagan, SE, Rankin, J, Hattersley, A, Ellard, S

Permanent neonatal diabetes due to paternal germline mosaicism for an activating mutation of the KCNJ11 Gene encoding the Kir6.2 subunit of the beta-cell potassium adenosine tripho... by Gloyn, A, Cummings, E, Edghill, E, Harries, L, Scott, R, Costa, T, Temple, I, Hattersley, A, Ellard, S

Mosaic paternal uniparental isodisomy and an ABCC8 gene mutation in a patient with permanent neonatal diabetes and hemihypertrophy. by Shield, J, Flanagan, SE, Mackay, D, Harries, L, Proks, P, Girard, C, Ashcroft, F, Temple, I, Ellard, S

Changes in apoptotic gene expression in lymphocytes from rheumatoid arthritis and systemic lupus erythematosus patients compared with healthy lymphocytes. by Eggleton, P, Harries, L, Alberigo, G, Wordsworth, P, Viner, N, Haigh, R, Donnelly, S, Jones, H, Chikanza, I, O'Conner, T, Thomson, A, Winyard, P

Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects. by Ellard, S, Flanagan, SE, Girard, C, Patch, A, Harries, L, Parrish, A, Edghill, E, Mackay, D, Proks, P, Shimomura, K, Haberland, H, Carson, D, Shield, J, Hattersley, A, Ashcroft, F

Glycosylation is an androgen-regulated process essential for prostate cancer cell viability. by Munkley, J, Vodak, D, Livermore, K, James, K, Wilson, B, Knight, B, Mccullagh, P, Mcgrath, J, Crundwell, M, Harries, L, Leung, H, Robson, C, Mills, I, Rajan, P, Elliott, D

A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. by Frayling, T, Timpson, N, Weedon, M, Zeggini, E, Freathy, R, Lindgren, C, Perry, JR, Elliott, K, Lango, H, Rayner, N, Shields, B, Harries, L, Barrett, J, Ellard, S, Groves, C, Knight, B, Patch, A, Ness, A, Ebrahim, S, Lawlor, D, Ring, S, Ben-Shlomo, Y, Jarvelin, MR, Sovio, U, Bennett, A

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. by Zeggini, E, Weedon, M, Lindgren, C, Frayling, T, Elliott, K, Lango, H, Timpson, N, Perry, JR, Rayner, N, Freathy, R, Barrett, J, Shields, B, Morris, A, Ellard, S, Groves, C, Harries, L, Marchini, J, Owen, K, Knight, B, Cardon, L, Walker, M, Hitman, G, Morris, A, Doney, A, McCarthy, M