Semple RK - Search Results

1

Monogenic polycystic ovary syndrome due to a mutation in the lamin A/C gene is sensitive to thiazolidinediones but not to metformin.

Gambineri A, Semple RK, Forlani G, Genghini S, Grassi I, Hyden CS, Pagotto U, O'Rahilly S, Pasquali R. Gambineri A, et al. Among authors: semple rk. Eur J Endocrinol. 2008 Sep;159(3):347-53. doi: 10.1530/EJE-08-0272. Eur J Endocrinol. 2008. PMID: 18728124

2

Severe hypo-alpha-lipoproteinemia during treatment with rosiglitazone.

Sarker A, Semple RK, Dinneen SF, O'Rahilly S, Martin SC. Sarker A, et al. Among authors: semple rk. Diabetes Care. 2004 Nov;27(11):2577-80. doi: 10.2337/diacare.27.11.2577. Diabetes Care. 2004. PMID: 15504988

3

Two novel missense mutations in g protein-coupled receptor 54 in a patient with hypogonadotropic hypogonadism.

Semple RK, Achermann JC, Ellery J, Farooqi IS, Karet FE, Stanhope RG, O'rahilly S, Aparicio SA. Semple RK, et al. J Clin Endocrinol Metab. 2005 Mar;90(3):1849-55. doi: 10.1210/jc.2004-1418. Epub 2004 Dec 14. J Clin Endocrinol Metab. 2005. PMID: 15598687 Free article.

4

A dominant negative human peroxisome proliferator-activated receptor (PPAR){alpha} is a constitutive transcriptional corepressor and inhibits signaling through all PPAR isoforms.

Semple RK, Meirhaeghe A, Vidal-Puig AJ, Schwabe JW, Wiggins D, Gibbons GF, Gurnell M, Chatterjee VK, O'Rahilly S. Semple RK, et al. Endocrinology. 2005 Apr;146(4):1871-82. doi: 10.1210/en.2004-1405. Epub 2005 Jan 20. Endocrinology. 2005. PMID: 15661858

5

PPAR gamma and human metabolic disease.

Semple RK, Chatterjee VK, O'Rahilly S. Semple RK, et al. J Clin Invest. 2006 Mar;116(3):581-9. doi: 10.1172/JCI28003. J Clin Invest. 2006. PMID: 16511590 Free PMC article. Review.

6

Elevated plasma adiponectin in humans with genetically defective insulin receptors.

Semple RK, Soos MA, Luan J, Mitchell CS, Wilson JC, Gurnell M, Cochran EK, Gorden P, Chatterjee VK, Wareham NJ, O'Rahilly S. Semple RK, et al. J Clin Endocrinol Metab. 2006 Aug;91(8):3219-23. doi: 10.1210/jc.2006-0166. Epub 2006 May 16. J Clin Endocrinol Metab. 2006. PMID: 16705075

7

Functional characterization of a novel insulin receptor mutation contributing to Rabson-Mendenhall syndrome.

Tuthill A, Semple RK, Day R, Soos MA, Sweeney E, Seymour PJ, Didi M, O'rahilly S. Tuthill A, et al. Among authors: semple rk. Clin Endocrinol (Oxf). 2007 Jan;66(1):21-6. doi: 10.1111/j.1365-2265.2006.02678.x. Clin Endocrinol (Oxf). 2007. PMID: 17201797

8

Adiponectin receptor genes: mutation screening in syndromes of insulin resistance and association studies for type 2 diabetes and metabolic traits in UK populations.

Collins SC, Luan J, Thompson AJ, Daly A, Semple RK, O'Rahilly S, Wareham NJ, Barroso I. Collins SC, et al. Among authors: semple rk. Diabetologia. 2007 Mar;50(3):555-62. doi: 10.1007/s00125-006-0534-7. Epub 2007 Jan 10. Diabetologia. 2007. PMID: 17216283 Free PMC article.

9

A clinical approach to severe insulin resistance.

Savage DB, Semple RK, Chatterjee VKK, Wales JKH, Ross RJM, O'Rahilly S. Savage DB, et al. Among authors: semple rk. Endocr Dev. 2007;11:122-132. doi: 10.1159/000111067. Endocr Dev. 2007. PMID: 17986832 Review.

10

Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophy.

Kim CA, Delépine M, Boutet E, El Mourabit H, Le Lay S, Meier M, Nemani M, Bridel E, Leite CC, Bertola DR, Semple RK, O'Rahilly S, Dugail I, Capeau J, Lathrop M, Magré J. Kim CA, et al. Among authors: semple rk. J Clin Endocrinol Metab. 2008 Apr;93(4):1129-34. doi: 10.1210/jc.2007-1328. Epub 2008 Jan 22. J Clin Endocrinol Metab. 2008. PMID: 18211975 Free article.

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