Murphy SK - Search Results

1

Insulin-like growth factor 2/H19 methylation at birth and risk of overweight and obesity in children.

Perkins E, Murphy SK, Murtha AP, Schildkraut J, Jirtle RL, Demark-Wahnefried W, Forman MR, Kurtzberg J, Overcash F, Huang Z, Hoyo C. Perkins E, et al. Among authors: murphy sk. J Pediatr. 2012 Jul;161(1):31-9. doi: 10.1016/j.jpeds.2012.01.015. Epub 2012 Feb 17. J Pediatr. 2012. PMID: 22341586 Free PMC article.

2

Imprinted genes as potential genetic and epigenetic toxicologic targets.

Murphy SK, Jirtle RL. Murphy SK, et al. Environ Health Perspect. 2000 Mar;108 Suppl 1(Suppl 1):5-11. doi: 10.1289/ehp.00108s15. Environ Health Perspect. 2000. PMID: 10698719 Free PMC article. Review.

3

Novel imprinted DLK1/GTL2 domain on human chromosome 14 contains motifs that mimic those implicated in IGF2/H19 regulation.

Wylie AA, Murphy SK, Orton TC, Jirtle RL. Wylie AA, et al. Among authors: murphy sk. Genome Res. 2000 Nov;10(11):1711-8. doi: 10.1101/gr.161600. Genome Res. 2000. PMID: 11076856 Free PMC article.

4

Imprinting of PEG3, the human homologue of a mouse gene involved in nurturing behavior.

Murphy SK, Wylie AA, Jirtle RL. Murphy SK, et al. Genomics. 2001 Jan 1;71(1):110-7. doi: 10.1006/geno.2000.6419. Genomics. 2001. PMID: 11161803

5

The neuronatin gene resides in a "micro-imprinted" domain on human chromosome 20q11.2.

Evans HK, Wylie AA, Murphy SK, Jirtle RL. Evans HK, et al. Among authors: murphy sk. Genomics. 2001 Sep;77(1-2):99-104. doi: 10.1006/geno.2001.6612. Genomics. 2001. PMID: 11543638

6

Exclusion of maternal uniparental disomy of chromosome 14 in patients referred for Prader-Willi syndrome using a multiplex methylation polymerase chain reaction assay.

Dietz LG, Wylie AA, Rauen KA, Murphy SK, Jirtle RL, Cotter PD. Dietz LG, et al. Among authors: murphy sk. J Med Genet. 2003 Apr;40(4):e46. doi: 10.1136/jmg.40.4.e46. J Med Genet. 2003. PMID: 12676919 Free PMC article. No abstract available.

7

Imprinting evolution and the price of silence.

Murphy SK, Jirtle RL. Murphy SK, et al. Bioessays. 2003 Jun;25(6):577-88. doi: 10.1002/bies.10277. Bioessays. 2003. PMID: 12766947 Review.

8

Epigenetic detection of human chromosome 14 uniparental disomy.

Murphy SK, Wylie AA, Coveler KJ, Cotter PD, Papenhausen PR, Sutton VR, Shaffer LG, Jirtle RL. Murphy SK, et al. Hum Mutat. 2003 Jul;22(1):92-7. doi: 10.1002/humu.10237. Hum Mutat. 2003. PMID: 12815599

9

Phylogenetic footprint analysis of IGF2 in extant mammals.

Weidman JR, Murphy SK, Nolan CM, Dietrich FS, Jirtle RL. Weidman JR, et al. Among authors: murphy sk. Genome Res. 2004 Sep;14(9):1726-32. doi: 10.1101/gr.2774804. Genome Res. 2004. PMID: 15342558 Free PMC article.

10

Abnormal postnatal maintenance of elevated DLK1 transcript levels in callipyge sheep.

Murphy SK, Freking BA, Smith TP, Leymaster K, Nolan CM, Wylie AA, Evans HK, Jirtle RL. Murphy SK, et al. Mamm Genome. 2005 Mar;16(3):171-83. doi: 10.1007/s00335-004-2421-1. Mamm Genome. 2005. PMID: 15834634

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