Bingham C - Search Results

1

In silico searching of human and mouse genome data identifies known and unknown HNF1 binding sites upstream of beta-cell genes.

Lockwood CR, Bingham C, Frayling TM. Lockwood CR, et al. Among authors: bingham c. Mol Genet Metab. 2003 Feb;78(2):145-51. doi: 10.1016/s1096-7192(02)00225-1. Mol Genet Metab. 2003. PMID: 12618086

2

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: bingham c. Diabetes. 2001 Feb;50 Suppl 1:S94-100. doi: 10.2337/diabetes.50.2007.s94. Diabetes. 2001. PMID: 11272211

3

Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1beta gene mutation.

Bingham C, Ellard S, van't Hoff WG, Simmonds HA, Marinaki AM, Badman MK, Winocour PH, Stride A, Lockwood CR, Nicholls AJ, Owen KR, Spyer G, Pearson ER, Hattersley AT. Bingham C, et al. Kidney Int. 2003 May;63(5):1645-51. doi: 10.1046/j.1523-1755.2003.00903.x. Kidney Int. 2003. PMID: 12675839 Free article.

4

Contrasting diabetes phenotypes associated with hepatocyte nuclear factor-1alpha and -1beta mutations.

Pearson ER, Badman MK, Lockwood CR, Clark PM, Ellard S, Bingham C, Hattersley AT. Pearson ER, et al. Among authors: bingham c. Diabetes Care. 2004 May;27(5):1102-7. doi: 10.2337/diacare.27.5.1102. Diabetes Care. 2004. PMID: 15111528

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

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. 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.

7

The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype.

Hamilton AJ, Bingham C, McDonald TJ, Cook PR, Caswell RC, Weedon MN, Oram RA, Shields BM, Shepherd M, Inward CD, Hamilton-Shield JP, Kohlhase J, Ellard S, Hattersley AT. Hamilton AJ, et al. Among authors: bingham c. J Med Genet. 2014 Mar;51(3):165-9. doi: 10.1136/jmedgenet-2013-102066. Epub 2013 Nov 27. J Med Genet. 2014. PMID: 24285859 Free PMC article.

8

Solitary functioning kidney and diverse genital tract malformations associated with hepatocyte nuclear factor-1beta mutations.

Bingham C, Ellard S, Cole TR, Jones KE, Allen LI, Goodship JA, Goodship TH, Bakalinova-Pugh D, Russell GI, Woolf AS, Nicholls AJ, Hattersley AT. Bingham C, et al. Kidney Int. 2002 Apr;61(4):1243-51. doi: 10.1046/j.1523-1755.2002.00272.x. Kidney Int. 2002. PMID: 11918730 Free article.

9

Abnormal splicing of hepatocyte nuclear factor-1 beta in the renal cysts and diabetes syndrome.

Harries LW, Ellard S, Jones RW, Hattersley AT, Bingham C. Harries LW, et al. Among authors: bingham c. Diabetologia. 2004 May;47(5):937-42. doi: 10.1007/s00125-004-1383-x. Epub 2004 Apr 15. Diabetologia. 2004. PMID: 15085338

10

The generalized aminoaciduria seen in patients with hepatocyte nuclear factor-1alpha mutations is a feature of all patients with diabetes and is associated with glucosuria.

Bingham C, Ellard S, Nicholls AJ, Pennock CA, Allen J, James AJ, Satchell SC, Salzmann MB, Hattersley AT. Bingham C, et al. Diabetes. 2001 Sep;50(9):2047-52. doi: 10.2337/diabetes.50.9.2047. Diabetes. 2001. PMID: 11522670

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