Relaxation of imprinted genes in human cancer
Rainier, Shirley, Johnson, Laura A, Dobry, Craig J, Ping, April J, Grundy, Paul E, Feinberg, Andrew P
Published in Nature (London) (22.04.1993)
Published in Nature (London) (22.04.1993)
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Tumor-associated zinc finger mutations in the CTCF transcription factor selectively alter its DNA-binding specificity
FILIPPOVA, Galina N, QI, Chen-Feng, FEINBERG, Andrew P, CLETON-JANSEN, Anne-Marie, MOERLAND, Elna W, CORNELISSE, Cees J, SUZUKI, Hiroyoshi, KOMIYA, Akira, LINDBLOM, Annika, DORION-BONNET, Francoise, NEIMAN, Paul E, MORSE, Herbert C, ULMER, Jonathan E, COLLINS, Steven J, LOBANENKOV, Victor V, MOORE, James M, WARD, Michael D, HU, Ying J, LOUKINOV, Dmitri I, PUGACHEVA, Elena M, KLENOVA, Elena M, GRUNDY, Paul E
Published in Cancer research (Chicago, Ill.) (2002)
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Published in Cancer research (Chicago, Ill.) (2002)
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Loss of Imprinting of Insulin-Like Growth Factor-II (IGF2) Gene in Distinguishing Specific Biologic Subtypes of Wilms Tumor
Ravenel, Jason D., Broman, Karl W., Perlman, Elizabeth J., Niemitz, Emily L., Jayawardena, Tilanthi M., Bell, Daphne W., Haber, Daniel A., Uejima, Hiroshi, Feinberg, Andrew P.
Published in JNCI : Journal of the National Cancer Institute (21.11.2001)
Published in JNCI : Journal of the National Cancer Institute (21.11.2001)
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LIT1, an Imprinted Antisense RNA in the Human KvLQT1 Locus Identified by Screening for Differentially Expressed Transcripts Using Monochromosomal Hybrids
Mitsuya, Kohzoh, Meguro, Makiko, Lee, Maxwell P., Katoh, Motonobu, Schulz, Thomas C., Kugoh, Hiroyuki, Yoshida, Mitsuaki A., Niikawa, Norio, Feinberg, Andrew P., Oshimura, Mitsuo
Published in Human molecular genetics (01.07.1999)
Published in Human molecular genetics (01.07.1999)
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Monoallelic Expression and Methylation of Imprinted Genes in Human and Mouse Embryonic Germ Cell Lineages
Onyango, Patrick, Jiang, Shan, Uejima, Hiroshi, Shamblott, Michael J., Gearhart, John D., Cui, Hengmi, Feinberg, Andrew P.
Published in Proceedings of the National Academy of Sciences - PNAS (06.08.2002)
Published in Proceedings of the National Academy of Sciences - PNAS (06.08.2002)
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Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemia
Nakamura, Takuro, Largaespada, David A, Lee, Maxwell P, Johnson, Laura A, Ohyashiki, Kazuma, Toyama, Keisuke, Chen, Sai Juan, Willman, Cheryl L, Chen, I-Ming, Feinberg, Andrew P, Jenkins, Nancy A, Copeland, Neal G, Shaughnessy, John D
Published in Nature genetics (01.02.1996)
Published in Nature genetics (01.02.1996)
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Hot-stop PCR: a simple and general assay for linear quantitation of allele ratios
Feinberg, Andrew P, Uejima, Hiroshi, Lee, Maxwell P, Cui, Hengmi
Published in Nature genetics (01.08.2000)
Published in Nature genetics (01.08.2000)
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Temporal stability and age-related prevalence of loss of imprinting of the insulin-like growth factor-2 gene
Cruz-Correa, Marcia, Zhao, Ronghua, Oveido, Myriam, Bernabe, Raul D., Lacourt, Mercedes, Cardona, Alberto, Lopez-Enriquez, Reynold, Wexner, Steven, Cuffari, Carmen, Hylind, Linda, Platz, Elizabeth, Cui, Hengmi, Feinberg, Andrew P., Giardiello, Francis M.
Published in Epigenetics (16.02.2009)
Published in Epigenetics (16.02.2009)
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A new link between epigenetic progenitor lesions in cancer and the dynamics of signal transduction
Timp, Winston, Levchenko, Andre, Feinberg, Andrew P.
Published in Cell cycle (Georgetown, Tex.) (01.02.2009)
Published in Cell cycle (Georgetown, Tex.) (01.02.2009)
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BORIS, A Novel Male Germ-Line-Specific Protein Associated with Epigenetic Reprogramming Events, Shares the Same 11-Zinc-Finger Domain with CTCF, The Insulator Protein Involved in Reading Imprinting Marks in the Soma
Loukinov, Dmitri I., Pugacheva, Elena, Vatolin, Sergei, Pack, Svetlana D., Moon, Hanlim, Chernukhin, Igor, Mannan, Poonam, Larsson, Erik, Kanduri, Chandrasekhar, Vostrov, Alexander A., Cui, Hengmi, Niemitz, Emily L., John E. J. Rasko, Docquier, France M., Kistler, Malathi, Breen, Joseph J., Zhuang, Zhengping, Quitschke, Wolfgang W., Renkawitz, Rainer, Klenova, Elena M., Feinberg, Andrew P., Ohlsson, Rolf, Morse, Herbert C., Lobanenkov, Victor V.
Published in Proceedings of the National Academy of Sciences - PNAS (14.05.2002)
Published in Proceedings of the National Academy of Sciences - PNAS (14.05.2002)
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Addition of H19 ‘Loss of Methylation Testing’ for Beckwith-Wiedemann Syndrome (BWS) Increases the Diagnostic Yield
Lennerz, Jochen K, Timmerman, Robert J, Grange, Dorothy K, DeBaun, Michael R, Feinberg, Andrew P, Zehnbauer, Barbara A
Published in The Journal of molecular diagnostics : JMD (01.09.2010)
Published in The Journal of molecular diagnostics : JMD (01.09.2010)
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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, Maxwell P., DeBaun, Michael R., Mitsuya, Kohzoh, Galonek, Heidi L., Brandenburg, Sheri, Oshimura, Mitsuo, Feinberg, Andrew P.
Published in Proceedings of the National Academy of Sciences - PNAS (27.04.1999)
Published in Proceedings of the National Academy of Sciences - PNAS (27.04.1999)
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Comprehensive high-throughput arrays for relative methylation (CHARM)
Ladd-Acosta, Christine, Aryee, Martin J, Ordway, Jared M, Feinberg, Andrew P
Published in Current protocols in human genetics (01.04.2010)
Published in Current protocols in human genetics (01.04.2010)
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