Gloyn AL - Search Results

1

Mutations in HNF1A result in marked alterations of plasma glycan profile.

Thanabalasingham G, Huffman JE, Kattla JJ, Novokmet M, Rudan I, Gloyn AL, Hayward C, Adamczyk B, Reynolds RM, Muzinic A, Hassanali N, Pucic M, Bennett AJ, Essafi A, Polasek O, Mughal SA, Redzic I, Primorac D, Zgaga L, Kolcic I, Hansen T, Gasperikova D, Tjora E, Strachan MW, Nielsen T, Stanik J, Klimes I, Pedersen OB, Njølstad PR, Wild SH, Gyllensten U, Gornik O, Wilson JF, Hastie ND, Campbell H, McCarthy MI, Rudd PM, Owen KR, Lauc G, Wright AF. Thanabalasingham G, et al. Among authors: gloyn al. Diabetes. 2013 Apr;62(4):1329-37. doi: 10.2337/db12-0880. Epub 2012 Dec 28. Diabetes. 2013. PMID: 23274891 Free PMC article.

2

The genetics of type 2 diabetes.

Gloyn AL, McCarthy MI. Gloyn AL, et al. Best Pract Res Clin Endocrinol Metab. 2001 Sep;15(3):293-308. doi: 10.1053/beem.2001.0147. Best Pract Res Clin Endocrinol Metab. 2001. PMID: 11554772 Review.

3

The role of the HNF4alpha enhancer in type 2 diabetes.

Mitchell SM, Gloyn AL, Owen KR, Hattersley AT, Frayling TM. Mitchell SM, et al. Among authors: gloyn al. Mol Genet Metab. 2002 Jun;76(2):148-51. doi: 10.1016/S1096-7192(02)00027-6. Mol Genet Metab. 2002. PMID: 12083813

4

A putative functional polymorphism in the IGF-I gene: association studies with type 2 diabetes, adult height, glucose tolerance, and fetal growth in U.K. populations.

Frayling TM, Hattersley AT, McCarthy A, Holly J, Mitchell SM, Gloyn AL, Owen K, Davies D, Smith GD, Ben-Shlomo Y. Frayling TM, et al. Among authors: gloyn al. Diabetes. 2002 Jul;51(7):2313-6. doi: 10.2337/diabetes.51.7.2313. Diabetes. 2002. PMID: 12086966

5

Maturity-onset diabetes of the young caused by a balanced translocation where the 20q12 break point results in disruption upstream of the coding region of hepatocyte nuclear factor-4alpha (HNF4A) gene.

Gloyn AL, Ellard S, Shepherd M, Howell RT, Parry EM, Jefferson A, Levy ER, Hattersley AT. Gloyn AL, et al. Diabetes. 2002 Jul;51(7):2329-33. doi: 10.2337/diabetes.51.7.2329. Diabetes. 2002. PMID: 12086970

6

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

7

Insights into the biochemical and genetic basis of glucokinase activation from naturally occurring hypoglycemia mutations.

Gloyn AL, Noordam K, Willemsen MA, Ellard S, Lam WW, Campbell IW, Midgley P, Shiota C, Buettger C, Magnuson MA, Matschinsky FM, Hattersley AT. Gloyn AL, et al. Diabetes. 2003 Sep;52(9):2433-40. doi: 10.2337/diabetes.52.9.2433. Diabetes. 2003. PMID: 12941786

8

Genetics for Endocrinologists: The Molecular Genetic Basis of Endocrine Disorders.

McCarthy MI, Gloyn AL. McCarthy MI, et al. Among authors: gloyn al. Clin Endocrinol (Oxf). 2003 Dec;59(6):826. doi: 10.1046/j.1365-2265.2003.01927.x. Clin Endocrinol (Oxf). 2003. PMID: 14974932 No abstract available.

9

Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy.

Sagen JV, Raeder H, Hathout E, Shehadeh N, Gudmundsson K, Baevre H, Abuelo D, Phornphutkul C, Molnes J, Bell GI, Gloyn AL, Hattersley AT, Molven A, Søvik O, Njølstad PR. Sagen JV, et al. Among authors: gloyn al. Diabetes. 2004 Oct;53(10):2713-8. doi: 10.2337/diabetes.53.10.2713. Diabetes. 2004. PMID: 15448106

10

Assessment of the role of common genetic variation in the transient neonatal diabetes mellitus (TNDM) region in type 2 diabetes: a comparative genomic and tagging single nucleotide polymorphism approach.

Gloyn AL, Mackay DJ, Weedon MN, McCarthy MI, Walker M, Hitman G, Knight BA, Owen KR, Hattersley AT, Frayling TM. Gloyn AL, et al. Diabetes. 2006 Aug;55(8):2272-6. doi: 10.2337/db06-0216. Diabetes. 2006. PMID: 16873690

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