Shepherd M - Search Results

1

Intrauterine hyperglycemia is associated with an earlier diagnosis of diabetes in HNF-1alpha gene mutation carriers.

Stride A, Shepherd M, Frayling TM, Bulman MP, Ellard S, Hattersley AT. Stride A, et al. Among authors: shepherd m. Diabetes Care. 2002 Dec;25(12):2287-91. doi: 10.2337/diacare.25.12.2287. Diabetes Care. 2002. PMID: 12453975

2

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: shepherd m. J Clin Invest. 1999 Nov;104(9):R33-9. doi: 10.1172/JCI7449. J Clin Invest. 1999. PMID: 10545530 Free PMC article.

3

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. Among authors: shepherd m. Kidney Int. 2000 Mar;57(3):898-907. doi: 10.1046/j.1523-1755.2000.057003898.x. Kidney Int. 2000. PMID: 10720943 Free article.

4

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: shepherd m. Diabetologia. 2000 Feb;43(2):250-3. doi: 10.1007/s001250050038. Diabetologia. 2000. PMID: 10753050

5

Predictive genetic testing in diabetes: a case study of multiple perspectives.

Shepherd M, Hattersley AT, Sparkes AC. Shepherd M, et al. Qual Health Res. 2000 Mar;10(2):242-59. doi: 10.1177/104973200129118390. Qual Health Res. 2000. PMID: 10788286

6

Sensitivity to sulphonylureas in patients with hepatocyte nuclear factor-1alpha gene mutations: evidence for pharmacogenetics in diabetes.

Pearson ER, Liddell WG, Shepherd M, Corrall RJ, Hattersley AT. Pearson ER, et al. Among authors: shepherd m. Diabet Med. 2000 Jul;17(7):543-5. doi: 10.1046/j.1464-5491.2000.00305.x. Diabet Med. 2000. PMID: 10972586

7

Proposed mechanism for a novel insertion/deletion frameshift mutation (I414G415ATCG-->CCA) in the hepatocyte nuclear factor 1 alpha (HNF-1 alpha) gene which causes maturity-onset diabetes of the young (MODY).

Ellard S, Bulman MP, Frayling TM, Shepherd M, Hattersley AT. Ellard S, et al. Among authors: shepherd m. Hum Mutat. 2000 Sep;16(3):273. doi: 10.1002/1098-1004(200009)16:3<273::AID-HUMU18>3.0.CO;2-Z. Hum Mutat. 2000. PMID: 10980542

8

beta-cell genes and diabetes: quantitative and qualitative differences in the pathophysiology of hepatic nuclear factor-1alpha and glucokinase mutations.

Pearson ER, Velho G, Clark P, Stride A, Shepherd M, Frayling TM, Bulman MP, Ellard S, Froguel P, Hattersley AT. Pearson ER, et al. Among authors: shepherd m. Diabetes. 2001 Feb;50 Suppl 1:S101-7. doi: 10.2337/diabetes.50.2007.s101. Diabetes. 2001. PMID: 11272165

9

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. Among authors: shepherd m. Diabetes. 2001 Feb;50 Suppl 1:S94-100. doi: 10.2337/diabetes.50.2007.s94. Diabetes. 2001. PMID: 11272211

10

Predictive genetic testing in maturity-onset diabetes of the young (MODY).

Shepherd M, Ellis I, Ahmad AM, Todd PJ, Bowen-Jones D, Mannion G, Ellard S, Sparkes AC, Hattersley AT. Shepherd M, et al. Diabet Med. 2001 May;18(5):417-21. doi: 10.1046/j.1464-5491.2001.00447.x. Diabet Med. 2001. PMID: 11472455

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