Hattersley AT - Search Results

1

Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects.

Ellard S, Flanagan SE, Girard CA, Patch AM, Harries LW, Parrish A, Edghill EL, Mackay DJ, Proks P, Shimomura K, Haberland H, Carson DJ, Shield JP, Hattersley AT, Ashcroft FM. Ellard S, et al. Among authors: hattersley at. Am J Hum Genet. 2007 Aug;81(2):375-82. doi: 10.1086/519174. Epub 2007 Jun 29. Am J Hum Genet. 2007. PMID: 17668386 Free PMC article.

2

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

3

A missense mutation in the hepatocyte nuclear factor 4 alpha gene in a UK pedigree with maturity-onset diabetes of the young.

Bulman MP, Dronsfield MJ, Frayling T, Appleton M, Bain SC, Ellard S, Hattersley AT. Bulman MP, et al. Among authors: hattersley at. Diabetologia. 1997 Jul;40(7):859-62. doi: 10.1007/s001250050760. Diabetologia. 1997. PMID: 9243109

4

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

5

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.

6

Mutations in the glucokinase gene of the fetus result in reduced birth weight.

Hattersley AT, Beards F, Ballantyne E, Appleton M, Harvey R, Ellard S. Hattersley AT, et al. Nat Genet. 1998 Jul;19(3):268-70. doi: 10.1038/953. Nat Genet. 1998. PMID: 9662401

7

Genetic testing for maturity onset diabetes of the young in childhood hyperglycaemia.

Matyka KA, Beards F, Appleton M, Ellard S, Hattersley A, Dunger DB. Matyka KA, et al. Arch Dis Child. 1998 Jun;78(6):552-4. doi: 10.1136/adc.78.6.552. Arch Dis Child. 1998. PMID: 9713013 Free PMC article.

8

Allelic drop-out in exon 2 of the hepatocyte nuclear factor-1alpha gene hinders the identification of mutations in three families with maturity-onset diabetes of the young.

Ellard S, Bulman MP, Frayling TM, Allen LI, Dronsfield MJ, Tack CJ, Hattersley AT. Ellard S, et al. Among authors: hattersley at. Diabetes. 1999 Apr;48(4):921-3. doi: 10.2337/diabetes.48.4.921. Diabetes. 1999. PMID: 10102714 No abstract available.

9

A gene for autosomal recessive spondylocostal dysostosis maps to 19q13.1-q13.3.

Turnpenny PD, Bulman MP, Frayling TM, Abu-Nasra TK, Garrett C, Hattersley AT, Ellard S. Turnpenny PD, et al. Among authors: hattersley at. Am J Hum Genet. 1999 Jul;65(1):175-82. doi: 10.1086/302464. Am J Hum Genet. 1999. PMID: 10364530 Free PMC article.

10

Non-penetrance in a MODY 3 family with a mutation in the hepatic nuclear factor 1alpha gene: implications for predictive testing.

Miedzybrodzka Z, Hattersley AT, Ellard S, Pearson D, de Silva D, Harvey R, Haites N. Miedzybrodzka Z, et al. Among authors: hattersley at. Eur J Hum Genet. 1999 Sep;7(6):729-32. doi: 10.1038/sj.ejhg.5200358. Eur J Hum Genet. 1999. PMID: 10482964

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