Harries LW - Search Results

1

A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity.

Frayling TM, Timpson NJ, Weedon MN, Zeggini E, Freathy RM, Lindgren CM, Perry JR, Elliott KS, Lango H, Rayner NW, Shields B, Harries LW, Barrett JC, Ellard S, Groves CJ, Knight B, Patch AM, Ness AR, Ebrahim S, Lawlor DA, Ring SM, Ben-Shlomo Y, Jarvelin MR, Sovio U, Bennett AJ, Melzer D, Ferrucci L, Loos RJ, Barroso I, Wareham NJ, Karpe F, Owen KR, Cardon LR, Walker M, Hitman GA, Palmer CN, Doney AS, Morris AD, Smith GD, Hattersley AT, McCarthy MI. Frayling TM, et al. Among authors: harries lw. Science. 2007 May 11;316(5826):889-94. doi: 10.1126/science.1141634. Epub 2007 Apr 12. Science. 2007. PMID: 17434869 Free PMC article.

2

Molecular genetics of the human cytochrome P450 monooxygenase superfamily.

Smith G, Stubbins MJ, Harries LW, Wolf CR. Smith G, et al. Among authors: harries lw. Xenobiotica. 1998 Dec;28(12):1129-65. doi: 10.1080/004982598238868. Xenobiotica. 1998. PMID: 9890157 Review. No abstract available.

3

Abnormal splicing of hepatocyte nuclear factor 1 alpha in maturity-onset diabetes of the young.

Bulman MP, Harries LW, Hansen T, Shepherd M, Kelly WF, Hattersley AT, Ellard S. Bulman MP, et al. Among authors: harries lw. Diabetologia. 2002 Oct;45(10):1463-7. doi: 10.1007/s00125-002-0919-1. Epub 2002 Sep 11. Diabetologia. 2002. PMID: 12378390

4

Messenger RNA transcripts of the hepatocyte nuclear factor-1alpha gene containing premature termination codons are subject to nonsense-mediated decay.

Harries LW, Hattersley AT, Ellard S. Harries LW, et al. Diabetes. 2004 Feb;53(2):500-4. doi: 10.2337/diabetes.53.2.500. Diabetes. 2004. PMID: 14747304

5

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. Diabetologia. 2004 May;47(5):937-42. doi: 10.1007/s00125-004-1383-x. Epub 2004 Apr 15. Diabetologia. 2004. PMID: 15085338

6

Permanent neonatal diabetes due to paternal germline mosaicism for an activating mutation of the KCNJ11 Gene encoding the Kir6.2 subunit of the beta-cell potassium adenosine triphosphate channel.

Gloyn AL, Cummings EA, Edghill EL, Harries LW, Scott R, Costa T, Temple IK, Hattersley AT, Ellard S. Gloyn AL, et al. Among authors: harries lw. J Clin Endocrinol Metab. 2004 Aug;89(8):3932-5. doi: 10.1210/jc.2004-0568. J Clin Endocrinol Metab. 2004. PMID: 15292329

7

Analysis of haematopoietic chimaerism by quantitative real-time polymerase chain reaction.

Harries LW, Wickham CL, Evans JC, Rule SA, Joyner MV, Ellard S. Harries LW, et al. Bone Marrow Transplant. 2005 Feb;35(3):283-90. doi: 10.1038/sj.bmt.1704764. Bone Marrow Transplant. 2005. PMID: 15531894

8

The position of premature termination codons in the hepatocyte nuclear factor -1 beta gene determines susceptibility to nonsense-mediated decay.

Harries LW, Bingham C, Bellanne-Chantelot C, Hattersley AT, Ellard S. Harries LW, et al. Hum Genet. 2005 Nov;118(2):214-24. doi: 10.1007/s00439-005-0023-y. Epub 2005 Nov 15. Hum Genet. 2005. PMID: 16133182 Clinical Trial.

9

Rapid and sensitive real-time polymerase chain reaction method for detection and quantification of 3243A>G mitochondrial point mutation.

Singh R, Ellard S, Hattersley A, Harries LW. Singh R, et al. Among authors: harries lw. J Mol Diagn. 2006 May;8(2):225-30. doi: 10.2353/jmoldx.2006.050067. J Mol Diagn. 2006. PMID: 16645209 Free PMC article.

10

Isomers of the TCF1 gene encoding hepatocyte nuclear factor-1 alpha show differential expression in the pancreas and define the relationship between mutation position and clinical phenotype in monogenic diabetes.

Harries LW, Ellard S, Stride A, Morgan NG, Hattersley AT. Harries LW, et al. Hum Mol Genet. 2006 Jul 15;15(14):2216-24. doi: 10.1093/hmg/ddl147. Epub 2006 Jun 7. Hum Mol Genet. 2006. PMID: 16760222

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