Morison IM - Search Results

1

Promoter haplotype of a new ABCA1 mutant influences expression of familial hypoalphalipoproteinemia.

Slatter TL, Williams MJ, Frikke-Schmidt R, Tybjaerg-Hansen A, Morison IM, McCormick SP. Slatter TL, et al. Among authors: morison im. Atherosclerosis. 2006 Aug;187(2):393-400. doi: 10.1016/j.atherosclerosis.2005.09.019. Epub 2005 Oct 12. Atherosclerosis. 2006. PMID: 16225879

2

Progression of the culprit lesion in unstable coronary artery disease with warfarin and aspirin versus aspirin alone: preliminary study.

Williams MJ, Morison IM, Parker JH, Stewart RA. Williams MJ, et al. Among authors: morison im. J Am Coll Cardiol. 1997 Aug;30(2):364-9. doi: 10.1016/s0735-1097(97)00153-8. J Am Coll Cardiol. 1997. PMID: 9247506 Free article. Clinical Trial.

3

Placental Hypomethylation Is More Pronounced in Genomic Loci Devoid of Retroelements.

Chatterjee A, Macaulay EC, Rodger EJ, Stockwell PA, Parry MF, Roberts HE, Slatter TL, Hung NA, Devenish CJ, Morison IM. Chatterjee A, et al. Among authors: morison im. G3 (Bethesda). 2016 Jul 7;6(7):1911-21. doi: 10.1534/g3.116.030379. G3 (Bethesda). 2016. PMID: 27172225 Free PMC article.

4

Silencing of Testin expression is a frequent event in spontaneous lymphomas from Trp53-mutant mice.

Weeks RJ, Ludgate JL, Le Mée G, Khanal R, Mehta S, Williams G, Slatter TL, Braithwaite AW, Morison IM. Weeks RJ, et al. Among authors: morison im. Sci Rep. 2020 Oct 1;10(1):16255. doi: 10.1038/s41598-020-73229-3. Sci Rep. 2020. PMID: 33004921 Free PMC article.

5

Identification and validation of DNA methylation changes in pre-eclampsia.

Almomani SN, Alsaleh AA, Weeks RJ, Chatterjee A, Day RC, Honda I, Homma H, Fukuzawa R, Slatter TL, Hung NA, Devenish C, Morison IM, Macaulay EC. Almomani SN, et al. Among authors: morison im. Placenta. 2021 Jul;110:16-23. doi: 10.1016/j.placenta.2021.05.005. Epub 2021 Jun 1. Placenta. 2021. PMID: 34098319

6

Human insulin-like growth factor type I and type II receptors are not imprinted.

Ogawa O, McNoe LA, Eccles MR, Morison IM, Reeve AE. Ogawa O, et al. Among authors: morison im. Hum Mol Genet. 1993 Dec;2(12):2163-5. doi: 10.1093/hmg/2.12.2163. Hum Mol Genet. 1993. PMID: 8111387

7

A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362X.

Heathcott RW, Morison IM, Gubler MC, Corbett R, Reeve AE. Heathcott RW, et al. Among authors: morison im. Hum Mutat. 2002 Apr;19(4):462. doi: 10.1002/humu.9031. Hum Mutat. 2002. PMID: 11933209 Review.

8

Silencing of TESTIN by dense biallelic promoter methylation is the most common molecular event in childhood acute lymphoblastic leukaemia.

Weeks RJ, Kees UR, Song S, Morison IM. Weeks RJ, et al. Among authors: morison im. Mol Cancer. 2010 Jun 24;9:163. doi: 10.1186/1476-4598-9-163. Mol Cancer. 2010. PMID: 20573277 Free PMC article.

9

Influence of the glutathione peroxidase 1 Pro200Leu polymorphism on the response of glutathione peroxidase activity to selenium supplementation: a randomized controlled trial.

Miller JC, Thomson CD, Williams SM, van Havre N, Wilkins GT, Morison IM, Ludgate JL, Skeaff CM. Miller JC, et al. Among authors: morison im. Am J Clin Nutr. 2012 Oct;96(4):923-31. doi: 10.3945/ajcn.112.043125. Epub 2012 Sep 5. Am J Clin Nutr. 2012. PMID: 22952184 Free article. Clinical Trial.

10

CYCS gene variants associated with thrombocytopenia.

Ledgerwood EC, Dunstan-Harrison C, Ong L, Morison IM. Ledgerwood EC, et al. Among authors: morison im. Platelets. 2019;30(5):672-674. doi: 10.1080/09537104.2018.1543866. Epub 2018 Nov 19. Platelets. 2019. PMID: 30452302 No abstract available.

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