Allen LI - Search Results

1

Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes.

Macfarlane WM, Frayling TM, Ellard S, Evans JC, Allen LI, Bulman MP, Ayres S, Shepherd M, Clark P, Millward A, Demaine A, Wilkin T, Docherty K, Hattersley AT. Macfarlane WM, et al. Among authors: allen li. J Clin Invest. 1999 Nov;104(9):R33-9. doi: 10.1172/JCI7449. J Clin Invest. 1999. PMID: 10545530 Free PMC article.

2

Hepatocyte nuclear factor-1beta: a new kindred with renal cysts and diabetes and gene expression in normal human development.

Kolatsi-Joannou M, Bingham C, Ellard S, Bulman MP, Allen LIS, Hattersley AT, Woolf AS. Kolatsi-Joannou M, et al. J Am Soc Nephrol. 2001 Oct;12(10):2175-2180. doi: 10.1681/ASN.V12102175. J Am Soc Nephrol. 2001. PMID: 11562418

3

Mutations in the hepatocyte nuclear factor-1beta gene are associated with familial hypoplastic glomerulocystic kidney disease.

Bingham C, Bulman MP, Ellard S, Allen LI, Lipkin GW, Hoff WG, Woolf AS, Rizzoni G, Novelli G, Nicholls AJ, Hattersley AT. Bingham C, et al. Among authors: allen li. Am J Hum Genet. 2001 Jan;68(1):219-24. doi: 10.1086/316945. Epub 2000 Nov 20. Am J Hum Genet. 2001. PMID: 11085914 Free PMC article.

4

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. Diabetes. 1998 Jul;47(7):1152-4. doi: 10.2337/diabetes.47.7.1152. Diabetes. 1998. PMID: 9648841 Review. No abstract available.

5

Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 beta.

Bingham C, Ellard S, Allen L, Bulman M, Shepherd M, Frayling T, Berry PJ, Clark PM, Lindner T, Bell GI, Ryffel GU, Nicholls AJ, Hattersley AT. Bingham C, et al. Kidney Int. 2000 Mar;57(3):898-907. doi: 10.1046/j.1523-1755.2000.057003898.x. Kidney Int. 2000. PMID: 10720943 Free article.

6

beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors.

Frayling TM, Evans JC, Bulman MP, Pearson E, Allen L, Owen K, Bingham C, Hannemann M, Shepherd M, Ellard S, Hattersley AT. Frayling TM, et al. Diabetes. 2001 Feb;50 Suppl 1:S94-100. doi: 10.2337/diabetes.50.2007.s94. Diabetes. 2001. PMID: 11272211

7

Identification of 21 novel glucokinase (GCK) mutations in UK and European Caucasians with maturity-onset diabetes of the young (MODY).

Thomson KL, Gloyn AL, Colclough K, Batten M, Allen LI, Beards F, Hattersley AT, Ellard S. Thomson KL, et al. Among authors: allen li. Hum Mutat. 2003 Nov;22(5):417. doi: 10.1002/humu.9186. Hum Mutat. 2003. PMID: 14517956

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: allen li. Diabetes. 1999 Apr;48(4):921-3. doi: 10.2337/diabetes.48.4.921. Diabetes. 1999. PMID: 10102714 No abstract available.

9

Parent-offspring trios: a resource to facilitate the identification of type 2 diabetes genes.

Frayling TM, Walker M, McCarthy MI, Evans JC, Allen LI, Lynn S, Ayres S, Millauer B, Turner C, Turner RC, Sampson MJ, Hitman GA, Ellard S, Hattersley AT. Frayling TM, et al. Among authors: allen li. Diabetes. 1999 Dec;48(12):2475-9. doi: 10.2337/diabetes.48.12.2475. Diabetes. 1999. PMID: 10580439

10

A high prevalence of glucokinase mutations in gestational diabetic subjects selected by clinical criteria.

Ellard S, Beards F, Allen LI, Shepherd M, Ballantyne E, Harvey R, Hattersley AT. Ellard S, et al. Among authors: allen li. Diabetologia. 2000 Feb;43(2):250-3. doi: 10.1007/s001250050038. Diabetologia. 2000. PMID: 10753050

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