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Quantitative traits associated with the Type 2 diabetes susceptibility allele in Kir6.2.
Weedon MN, Gloyn AL, Frayling TM, Hattersley AT, Davey Smith G, Ben-Shlomo Y. Weedon MN, et al. Among authors: gloyn al. Diabetologia. 2003 Jul;46(7):1021-3. doi: 10.1007/s00125-003-1135-3. Epub 2003 Jun 18. Diabetologia. 2003. PMID: 12819904 No abstract available.
Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features.
Proks P, Antcliff JF, Lippiat J, Gloyn AL, Hattersley AT, Ashcroft FM. Proks P, et al. Among authors: gloyn al. Proc Natl Acad Sci U S A. 2004 Dec 14;101(50):17539-44. doi: 10.1073/pnas.0404756101. Epub 2004 Dec 6. Proc Natl Acad Sci U S A. 2004. PMID: 15583126 Free PMC article.
Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patients.
Vaxillaire M, Populaire C, Busiah K, Cavé H, Gloyn AL, Hattersley AT, Czernichow P, Froguel P, Polak M. Vaxillaire M, et al. Among authors: gloyn al. Diabetes. 2004 Oct;53(10):2719-22. doi: 10.2337/diabetes.53.10.2719. Diabetes. 2004. PMID: 15448107
Activating mutations in the KCNJ11 gene encoding the ATP-sensitive K+ channel subunit Kir6.2 are rare in clinically defined type 1 diabetes diagnosed before 2 years.
Edghill EL, Gloyn AL, Gillespie KM, Lambert AP, Raymond NT, Swift PG, Ellard S, Gale EA, Hattersley AT. Edghill EL, et al. Among authors: gloyn al. Diabetes. 2004 Nov;53(11):2998-3001. doi: 10.2337/diabetes.53.11.2998. Diabetes. 2004. PMID: 15504982
Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes.
Gloyn AL, Pearson ER, Antcliff JF, Proks P, Bruining GJ, Slingerland AS, Howard N, Srinivasan S, Silva JM, Molnes J, Edghill EL, Frayling TM, Temple IK, Mackay D, Shield JP, Sumnik Z, van Rhijn A, Wales JK, Clark P, Gorman S, Aisenberg J, Ellard S, Njølstad PR, Ashcroft FM, Hattersley AT. Gloyn AL, et al. N Engl J Med. 2004 Apr 29;350(18):1838-49. doi: 10.1056/NEJMoa032922. N Engl J Med. 2004. PMID: 15115830
Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes.
Gloyn AL, Weedon MN, Owen KR, Turner MJ, Knight BA, Hitman G, Walker M, Levy JC, Sampson M, Halford S, McCarthy MI, Hattersley AT, Frayling TM. Gloyn AL, et al. Diabetes. 2003 Feb;52(2):568-72. doi: 10.2337/diabetes.52.2.568. Diabetes. 2003. PMID: 12540637
Human islet function following 20 years of cryogenic biobanking.
Manning Fox JE, Lyon J, Dai XQ, Wright RC, Hayward J, van de Bunt M, Kin T, Shapiro AM, McCarthy MI, Gloyn AL, Ungrin MD, Lakey JR, Kneteman NM, Warnock GL, Korbutt GS, Rajotte RV, MacDonald PE. Manning Fox JE, et al. Among authors: gloyn al. Diabetologia. 2015 Jul;58(7):1503-12. doi: 10.1007/s00125-015-3598-4. Epub 2015 May 1. Diabetologia. 2015. PMID: 25930156 Free PMC article.
Patterns of differential gene expression in a cellular model of human islet development, and relationship to type 2 diabetes predisposition.
Perez-Alcantara M, Honoré C, Wesolowska-Andersen A, Gloyn AL, McCarthy MI, Hansson M, Beer NL, van de Bunt M. Perez-Alcantara M, et al. Among authors: gloyn al. Diabetologia. 2018 Jul;61(7):1614-1622. doi: 10.1007/s00125-018-4612-4. Epub 2018 Apr 19. Diabetologia. 2018. PMID: 29675560 Free PMC article.
Human genetics as a model for target validation: finding new therapies for diabetes.
Thomsen SK, Gloyn AL. Thomsen SK, et al. Among authors: gloyn al. Diabetologia. 2017 Jun;60(6):960-970. doi: 10.1007/s00125-017-4270-y. Epub 2017 Apr 26. Diabetologia. 2017. PMID: 28447115 Free PMC article. Review.
Insights into metabolic disease from studying genetics in isolated populations: stories from Greece to Greenland.
Zeggini E, Gloyn AL, Hansen T. Zeggini E, et al. Among authors: gloyn al. Diabetologia. 2016 May;59(5):938-41. doi: 10.1007/s00125-016-3926-3. Epub 2016 Mar 18. Diabetologia. 2016. PMID: 26993633 Free PMC article. Review.
This review summarises a presentation given at the 'Exciting news in genetics of diabetes' symposium at the 2015 annual meeting of the EASD, with topics presented by Eleftheria Zeggini and Torben Hansen, and an overview by the Session Chair, Anna Gloyn....
This review summarises a presentation given at the 'Exciting news in genetics of diabetes' symposium at the 2015 annual meeting of the EASD, …
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