Hattersley AT - Search Results

1

Insulin gene mutations as a cause of permanent neonatal diabetes.

Støy J, Edghill EL, Flanagan SE, Ye H, Paz VP, Pluzhnikov A, Below JE, Hayes MG, Cox NJ, Lipkind GM, Lipton RB, Greeley SA, Patch AM, Ellard S, Steiner DF, Hattersley AT, Philipson LH, Bell GI; Neonatal Diabetes International Collaborative Group. Støy J, et al. Among authors: hattersley at. Proc Natl Acad Sci U S A. 2007 Sep 18;104(38):15040-4. doi: 10.1073/pnas.0707291104. Epub 2007 Sep 12. Proc Natl Acad Sci U S A. 2007. PMID: 17855560 Free PMC article.

2

Missense glucokinase mutation in maturity-onset diabetes of the young and mutation screening in late-onset diabetes.

Stoffel M, Patel P, Lo YM, Hattersley AT, Lucassen AM, Page R, Bell JI, Bell GI, Turner RC, Wainscoat JS. Stoffel M, et al. Among authors: hattersley at. Nat Genet. 1992 Oct;2(2):153-6. doi: 10.1038/ng1092-153. Nat Genet. 1992. PMID: 1303265

3

Linkage analysis of maturity-onset diabetes of the young with microsatellite polymorphisms. No linkage to ADA or GLUT2 genes in two families.

Patel P, Lo YM, Hattersley A, Bell GI, Tybjaerg-Hansen A, Nerup J, Turner RC, Wainscoat JS. Patel P, et al. Diabetes. 1992 Aug;41(8):962-7. doi: 10.2337/diab.41.8.962. Diabetes. 1992. PMID: 1628771

4

Candidate gene studies in pedigrees with maturity-onset diabetes of the young not linked with glucokinase.

Zhang Y, Warren-Perry M, Saker PJ, Hattersley AT, Mackie AD, Baird JD, Greenwood RH, Stoffel M, Bell GI, Turner RC. Zhang Y, et al. Among authors: hattersley at. Diabetologia. 1995 Sep;38(9):1055-60. doi: 10.1007/BF00402175. Diabetologia. 1995. PMID: 8591819

5

Altered insulin secretory responses to glucose in diabetic and nondiabetic subjects with mutations in the diabetes susceptibility gene MODY3 on chromosome 12.

Byrne MM, Sturis J, Menzel S, Yamagata K, Fajans SS, Dronsfield MJ, Bain SC, Hattersley AT, Velho G, Froguel P, Bell GI, Polonsky KS. Byrne MM, et al. Among authors: hattersley at. Diabetes. 1996 Nov;45(11):1503-10. doi: 10.2337/diab.45.11.1503. Diabetes. 1996. PMID: 8866553

6

Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3).

Yamagata K, Oda N, Kaisaki PJ, Menzel S, Furuta H, Vaxillaire M, Southam L, Cox RD, Lathrop GM, Boriraj VV, Chen X, Cox NJ, Oda Y, Yano H, Le Beau MM, Yamada S, Nishigori H, Takeda J, Fajans SS, Hattersley AT, Iwasaki N, Hansen T, Pedersen O, Polonsky KS, Bell GI, et al. Yamagata K, et al. Among authors: hattersley at. Nature. 1996 Dec 5;384(6608):455-8. doi: 10.1038/384455a0. Nature. 1996. PMID: 8945470 Free article.

7

Mutations in the hepatocyte nuclear factor-1alpha gene are a common cause of maturity-onset diabetes of the young in the U.K.

Frayling TM, Bulamn MP, Ellard S, Appleton M, Dronsfield MJ, Mackie AD, Baird JD, Kaisaki PJ, Yamagata K, Bell GI, Bain SC, Hattersley AT. Frayling TM, et al. Among authors: hattersley at. Diabetes. 1997 Apr;46(4):720-5. doi: 10.2337/diab.46.4.720. Diabetes. 1997. PMID: 9075818

8

A rapid screening method for hepatocyte nuclear factor 1 alpha frameshift mutations; prevalence in maturity-onset diabetes of the young and late-onset non-insulin dependent diabetes.

Frayling TM, Bulman MP, Appleton M, Hattersley AT, Ellard S. Frayling TM, et al. Among authors: hattersley at. Hum Genet. 1997 Dec;101(3):351-4. doi: 10.1007/s004390050640. Hum Genet. 1997. PMID: 9439666

9

Mutations in hepatocyte nuclear factor 1beta are not a common cause of maturity-onset diabetes of the young in the U.K.

Beards F, Frayling T, Bulman M, Horikawa Y, Allen L, Appleton M, Bell GI, Ellard S, Hattersley AT. Beards F, et al. Among authors: hattersley at. Diabetes. 1998 Jul;47(7):1152-4. doi: 10.2337/diabetes.47.7.1152. Diabetes. 1998. PMID: 9648841 Review. No abstract available.

10

C282Y mutation in HFE (haemochromatosis) gene and type 2 diabetes.

Frayling T, Ellard S, Grove J, Walker M, Hattersley AT. Frayling T, et al. Among authors: hattersley at. Lancet. 1998 Jun 27;351(9120):1933-4. doi: 10.1016/S0140-6736(05)78618-9. Lancet. 1998. PMID: 9654270 No abstract available.

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