Lee MP - Search Results

1

Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects.

DeBaun MR, Niemitz EL, McNeil DE, Brandenburg SA, Lee MP, Feinberg AP. DeBaun MR, et al. Among authors: lee mp. Am J Hum Genet. 2002 Mar;70(3):604-11. doi: 10.1086/338934. Epub 2002 Jan 28. Am J Hum Genet. 2002. PMID: 11813134 Free PMC article.

2

Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome.

Lee MP, DeBaun M, Randhawa G, Reichard BA, Elledge SJ, Feinberg AP. Lee MP, et al. Am J Hum Genet. 1997 Aug;61(2):304-9. doi: 10.1086/514858. Am J Hum Genet. 1997. PMID: 9311734 Free PMC article.

3

A novel human homologue of yeast nucleosome assembly protein, 65 kb centromeric to the p57KIP2 gene, is biallelically expressed in fetal and adult tissues.

Hu RJ, Lee MP, Johnson LA, Feinberg AP. Hu RJ, et al. Among authors: lee mp. Hum Mol Genet. 1996 Nov;5(11):1743-8. doi: 10.1093/hmg/5.11.1743. Hum Mol Genet. 1996. PMID: 8923002

4

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

Lee MP, Hu RJ, Johnson LA, Feinberg AP. Lee MP, et al. Nat Genet. 1997 Feb;15(2):181-5. doi: 10.1038/ng0297-181. Nat Genet. 1997. PMID: 9020845

5

Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting.

Lee MP, Brandenburg S, Landes GM, Adams M, Miller G, Feinberg AP. Lee MP, et al. Hum Mol Genet. 1999 Apr;8(4):683-90. doi: 10.1093/hmg/8.4.683. Hum Mol Genet. 1999. PMID: 10072438

6

Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting.

Lee MP, DeBaun MR, Mitsuya K, Galonek HL, Brandenburg S, Oshimura M, Feinberg AP. Lee MP, et al. Proc Natl Acad Sci U S A. 1999 Apr 27;96(9):5203-8. doi: 10.1073/pnas.96.9.5203. Proc Natl Acad Sci U S A. 1999. PMID: 10220444 Free PMC article.

7

LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids.

Mitsuya K, Meguro M, Lee MP, Katoh M, Schulz TC, Kugoh H, Yoshida MA, Niikawa N, Feinberg AP, Oshimura M. Mitsuya K, et al. Among authors: lee mp. Hum Mol Genet. 1999 Jul;8(7):1209-17. doi: 10.1093/hmg/8.7.1209. Hum Mol Genet. 1999. PMID: 10369866

8

Genomic imprinting of a human apoptosis gene homologue, TSSC3.

Lee MP, Feinberg AP. Lee MP, et al. Cancer Res. 1998 Mar 1;58(5):1052-6. Cancer Res. 1998. PMID: 9500470

9

Lack of parental origin specificity of altered alleles at 11p15 in testicular germ cell tumors.

Kraggerud SM, Lee MP, Skotheim RI, Stenwig AE, Fosså SD, Feinberg AP, Lothe RA. Kraggerud SM, et al. Among authors: lee mp. Cancer Genet Cytogenet. 2003 Nov;147(1):1-8. doi: 10.1016/s0165-4608(03)00160-2. Cancer Genet Cytogenet. 2003. PMID: 14580764

10

Strain-dependent developmental relaxation of imprinting of an endogenous mouse gene, Kvlqt1.

Jiang S, Hemann MA, Lee MP, Feinberg AP. Jiang S, et al. Among authors: lee mp. Genomics. 1998 Nov 1;53(3):395-9. doi: 10.1006/geno.1998.5511. Genomics. 1998. PMID: 9799609 Free article.

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