Feinberg AP - Search Results

1

Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemia.

Nakamura T, Largaespada DA, Lee MP, Johnson LA, Ohyashiki K, Toyama K, Chen SJ, Willman CL, Chen IM, Feinberg AP, Jenkins NA, Copeland NG, Shaughnessy JD Jr. Nakamura T, et al. Among authors: feinberg ap. Nat Genet. 1996 Feb;12(2):154-8. doi: 10.1038/ng0296-154. Nat Genet. 1996. PMID: 8563753

2

A novel general strategy for cloning tumor suppressor genes using radiation-reduced chromosomal superfragments.

Koi M, Johnson LA, Feinberg AP. Koi M, et al. Among authors: feinberg ap. Tohoku J Exp Med. 1992 Oct;168(2):167-8. doi: 10.1620/tjem.168.167. Tohoku J Exp Med. 1992. PMID: 1306300 Free article.

3

Loss of imprinting in human cancer.

Feinberg AP, Kalikin LM, Johnson LA, Thompson JS. Feinberg AP, et al. Cold Spring Harb Symp Quant Biol. 1994;59:357-64. doi: 10.1101/sqb.1994.059.01.040. Cold Spring Harb Symp Quant Biol. 1994. PMID: 7587088 No abstract available.

4

Relaxation of imprinted genes in human cancer.

Rainier S, Johnson LA, Dobry CJ, Ping AJ, Grundy PE, Feinberg AP. Rainier S, et al. Among authors: feinberg ap. Nature. 1993 Apr 22;362(6422):747-9. doi: 10.1038/362747a0. Nature. 1993. PMID: 8385745 Free article.

5

Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11.

Koi M, Johnson LA, Kalikin LM, Little PF, Nakamura Y, Feinberg AP. Koi M, et al. Among authors: feinberg ap. Science. 1993 Apr 16;260(5106):361-4. doi: 10.1126/science.8469989. Science. 1993. PMID: 8469989

6

Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments.

Hoovers JM, Kalikin LM, Johnson LA, Alders M, Redeker B, Law DJ, Bliek J, Steenman M, Benedict M, Wiegant J, Lengauer C, Taillon-Miller P, Schlessinger D, Edwards MC, Elledge SJ, Ivens A, Westerveld A, Little P, Mannens M, Feinberg AP. Hoovers JM, et al. Among authors: feinberg ap. Proc Natl Acad Sci U S A. 1995 Dec 19;92(26):12456-60. doi: 10.1073/pnas.92.26.12456. Proc Natl Acad Sci U S A. 1995. PMID: 8618920 Free PMC article.

7

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: feinberg ap. Hum Mol Genet. 1996 Nov;5(11):1743-8. doi: 10.1093/hmg/5.11.1743. Hum Mol Genet. 1996. PMID: 8923002

8

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. Among authors: feinberg ap. Nat Genet. 1997 Feb;15(2):181-5. doi: 10.1038/ng0297-181. Nat Genet. 1997. PMID: 9020845

9

Aberrant splicing but not mutations of TSG101 in human breast cancer.

Lee MP, Feinberg AP. Lee MP, et al. Among authors: feinberg ap. Cancer Res. 1997 Aug 1;57(15):3131-4. Cancer Res. 1997. PMID: 9242438

10

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. Among authors: feinberg ap. Am J Hum Genet. 1997 Aug;61(2):304-9. doi: 10.1086/514858. Am J Hum Genet. 1997. PMID: 9311734 Free PMC article.

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