Global microRNA expression profiles in insulin target tissues in a spontaneous rat model of type 2 diabetes
Herrera, B. M., Lockstone, H. E., Taylor, J. M., Ria, M., Barrett, A., Collins, S., Kaisaki, P., Argoud, K., Fernandez, C., Travers, M. E., Grew, J. P., Randall, J. C., Gloyn, A. L., Gauguier, D., McCarthy, M. I., Lindgren, C. M.
Published in Diabetologia (01.06.2010)
Published in Diabetologia (01.06.2010)
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Journal Article
Cellular characterisation of the GCKR P446L variant associated with type 2 diabetes risk
Rees, M. G., Wincovitch, S., Schultz, J., Waterstradt, R., Beer, N. L., Baltrusch, S., Collins, F. S., Gloyn, A. L.
Published in Diabetologia (01.01.2012)
Published in Diabetologia (01.01.2012)
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Journal Article
A global initiative to deliver precision health in diabetes
Cefalu, W. T., Franks, P. W., Rosenblum, N. D., Zaghloul, N. A., Florez, J. C., Giorgino, F., Ji, L., Ma, R. C. W., Mathieu, C., Misra, S., Ramirez, A. H., Roden, M., Scherer, P. E., Sheu, W. H. -H., Stehouwer, C. D. A., Woo, M., Pragnell, M., Anand, S. S., Carnethon, M., Chambers, J. C., Dennis, J. M., Gloyn, A. L., Herder, C., Holt, R. I. G., Manuel, D. G., Redondo, M. J., Tandon, N., Tsang, J. S., Udler, M. S., Rich, S. S.
Published in Nature medicine (11.07.2024)
Published in Nature medicine (11.07.2024)
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Journal Article
A large multi-centre European study validates high-sensitivity C-reactive protein (hsCRP) as a clinical biomarker for the diagnosis of diabetes subtypes
Thanabalasingham, G., Shah, N., Vaxillaire, M., Hansen, T., Tuomi, T., Gašperíková, D., Szopa, M., Tjora, E., James, T. J., Kokko, P., Loiseleur, F., Andersson, E., Gaget, S., Isomaa, B., Nowak, N., Raeder, H., Stanik, J., Njolstad, P. R., Malecki, M. T., Klimes, I., Groop, L., Pedersen, O., Froguel, P., McCarthy, M. I., Gloyn, A. L., Owen, K. R.
Published in Diabetologia (01.11.2011)
Published in Diabetologia (01.11.2011)
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Journal Article
Apolipoprotein M can discriminate HNF1A-MODY from Type 1 diabetes
Mughal, S. A., Park, R., Nowak, N., Gloyn, A. L., Karpe, F., Matile, H., Malecki, M. T., McCarthy, M. I., Stoffel, M., Owen, K. R.
Published in Diabetic medicine (01.02.2013)
Published in Diabetic medicine (01.02.2013)
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Journal Article
Heterogeneity in disease severity in a family with a novel G68V GCK activating mutation causing persistent hyperinsulinaemic hypoglycaemia of infancy
Wabitsch, M., Lahr, G., Van de Bunt, M., Marchant, C., Lindner, M., Von Puttkamer, J., Fenneberg, A., Debatin, K. M., Klein, R., Ellard, S., Clark, A., Gloyn, A. L.
Published in Diabetic medicine (01.12.2007)
Published in Diabetic medicine (01.12.2007)
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Journal Article
Association studies of variants in promoter and coding regions of beta-cell ATP-sensitive K-channel genes SUR1 and Kir6.2 with Type 2 diabetes mellitus (UKPDS 53)
Gloyn, A. L., Hashim, Y., Ashcroft, S. J. H., Ashfield, R., Wiltshire, S., Turner, R. C.
Published in Diabetic medicine (01.03.2001)
Published in Diabetic medicine (01.03.2001)
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Journal Article
The previously reported T342P GCK missense variant is not a pathogenic mutation causing MODY
Steele, A. M., Tribble, N. D., Caswell, R., Wensley, K. J., Hattersley, A. T., Gloyn, A. L., Ellard, S.
Published in Diabetologia (01.08.2011)
Published in Diabetologia (01.08.2011)
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Journal Article
Prevalence of GCK mutations in individuals screened for fasting hyperglycaemia
Gloyn, A. L, van de Bunt, M, Stratton, I. M, Lonie, L, Tucker, L, Ellard, S, Holman, R. R
Published in Diabetologia (2009)
Published in Diabetologia (2009)
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Journal Article
role for coding functional variants in HNF4A in type 2 diabetes susceptibility
Jafar-Mohammadi, B, Groves, C. J, Gjesing, A. P, Herrera, B. M, Winckler, W, Stringham, H. M, Morris, A. P, Lauritzen, T, Doney, A. S. F, Morris, A. D, Weedon, M. N, Swift, A. J, Kuusisto, J, Laakso, M, Altshuler, D, Hattersley, A. T, Collins, F. S, Boehnke, M, Hansen, T, Pedersen, O, Palmer, C. N. A, Frayling, T. M, Gloyn, A. L, McCarthy, M. I
Published in Diabetologia (01.01.2011)
Published in Diabetologia (01.01.2011)
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Journal Article
Permanent neonatal diabetes in an Asian infant
Porter, J.R., Shaw, N.J., Barrett, T.G., Hattersley, A.T., Ellard, S., Gloyn, A.L.
Published in The Journal of pediatrics (2005)
Published in The Journal of pediatrics (2005)
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Journal Article
Prevalence and clinical characteristics of maternally inherited diabetes and deafness caused by the mt3243A > G mutation in young adult diabetic subjects in Sri Lanka
Katulanda, P., Groves, C. J., Barrett, A., Sheriff, R., Matthews, D. R., McCarthy, M. I., Gloyn, A. L.
Published in Diabetic medicine (01.03.2008)
Published in Diabetic medicine (01.03.2008)
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Journal Article
Asian MODY: are we missing an important diagnosis?
Porter, J. R., Rangasami, J. J., Ellard, S., Gloyn, A. L., Shields, B. M., Edwards, J., Anderson, J. M., Shaw, N. J., Hattersley, A. T., Frayling, T. M., Plunkett, M., Barrett, T. G.
Published in Diabetic medicine (01.11.2006)
Published in Diabetic medicine (01.11.2006)
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Journal Article
Mutations in HHEX are not a common cause of monogenic forms of beta cell dysfunction
MINTON, J. A. L, VAN DE BUNT, M, BOUSTRED, C, HUSSAIN, K, HATTERSLEY, A. T, ELLARD, S, GLOYN, A. L
Published in Diabetologia (01.09.2007)
Published in Diabetologia (01.09.2007)
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Journal Article
Mutations in the third gene shown to alter fasting glucose levels in the population (G6PC2) are not a common cause of monogenic forms of pancreatic B-cell dysfunction
Edghill, E. L., McCulloch, L., Fulton, P., Beer, N., Hattersley, A. T., Gloyn, A. L.
Published in Diabetic medicine (01.01.2009)
Published in Diabetic medicine (01.01.2009)
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Journal Article
Complete glucokinase deficiency is not a common cause of permanent neonatal diabetes
Gloyn, A L, Ellard, S, Shield, J P, Temple, I K, Mackay, D J G, Polak, M, Barrett, T, Hattersley, A T
Published in Diabetologia (01.02.2002)
Published in Diabetologia (01.02.2002)
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