Authors:
Ravenel, JD
Broman, KW
Perlman, EJ
Niemitz, EL
Jayawardena, TM
Bell, DW
Haber, DA
Uejima, H
Feinberg, AP
Citation: Jd. Ravenel et al., Loss of imprinting of insulin-like growth factor-II (IGF2) gene in distinguishing specific biologic subtypes of Wilms tumor, J NAT CANC, 93(22), 2001, pp. 1698-1703
Authors:
Onyango, P
Miller, W
Lehoczky, J
Leung, CT
Birren, B
Wheelan, S
Dewar, K
Feinberg, AP
Citation: P. Onyango et al., Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain (vol 10, pg 1697, 2000), GENOME RES, 11(2), 2001, pp. 308-308
Authors:
Cui, HM
Niemitz, EL
Ravenel, JD
Onyango, P
Brandenburg, SA
Lobanenkov, VV
Feinberg, AP
Citation: Hm. Cui et al., Loss of imprinting of insulin-like growth factor-II in Wilms' tumor commonly involves altered methylation hut not mutations of CTCF or its binding site, CANCER RES, 61(13), 2001, pp. 4947-4950
Authors:
Onyango, P
Miller, W
Lehoczky, J
Leung, CT
Birren, B
Wheelan, S
Dewar, K
Feinberg, AP
Citation: P. Onyango et al., Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain, GENOME RES, 10(11), 2000, pp. 1697-1710
Authors:
Krasner, A
Wallace, L
Thiagalingam, A
Jones, C
Lengauer, C
Minahan, L
Ma, YK
Kalikin, L
Feinberg, AP
Jabs, EW
Tunnacliffe, A
Baylin, SB
Ball, DW
Nelkin, BD
Citation: A. Krasner et al., Cloning and chromosomal localization of the human BARX2 homeobox protein gene, GENE, 250(1-2), 2000, pp. 171-180
Authors:
Lee, MP
Ravenel, JD
Hu, RJ
Lustig, LR
Tomaselli, G
Berger, RD
Brandenburg, SA
Litzi, TJ
Bunton, TE
Limb, C
Francis, H
Gorelikow, M
Gu, H
Washington, K
Argani, P
Goldenring, JR
Coffey, RJ
Feinberg, AP
Citation: Mp. Lee et al., Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice, J CLIN INV, 106(12), 2000, pp. 1447-1455
Authors:
Alders, M
Ryan, A
Hodges, M
Bliek, J
Feinberg, AP
Privitera, O
Westerveld, A
Little, PFR
Mannens, M
Citation: M. Alders et al., Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome, AM J HU GEN, 66(5), 2000, pp. 1473-1484
Authors:
Mitsuya, K
Meguro, M
Lee, MP
Katoh, M
Schulz, TC
Kugoh, H
Yoshida, MA
Niikawa, N
Feinberg, AP
Oshimura, M
Citation: K. Mitsuya et al., LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids (vol 8, 1209, 1999), HUM MOL GEN, 8(8), 1999, pp. 1585-1585
Authors:
Mitsuya, K
Meguro, M
Lee, MP
Katoh, M
Schulz, TC
Kugoh, H
Yoshida, MA
Niikawa, N
Feinberg, AP
Oshimura, M
Citation: K. Mitsuya et al., LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids, HUM MOL GEN, 8(7), 1999, pp. 1209-1217
Authors:
Lee, MP
DeBaun, MR
Mitsuya, K
Galonek, HL
Brandenburg, S
Oshimura, M
Feinberg, AP
Citation: Mp. Lee et al., Loss of imprinting of a paternally expressed transcript, with antisense orientation to K(V)LQT1, occurs frequently in Beckwith-Wiedemann syndrome andis independent of insulin-like growth factor II imprinting, P NAS US, 96(9), 1999, pp. 5203-5208
Citation: Ap. Feinberg, Imprinting of a genomic domain of 11p15 and loss of imprinting in cancer: An introduction, CANCER RES, 59(7), 1999, pp. 1743S-1746S
Authors:
Ohlsson, R
Cui, HM
He, LM
Pfeifer, S
Malmikumpu, H
Jiang, S
Feinberg, AP
Hedborg, F
Citation: R. Ohlsson et al., Mosaic allelic insulin-like growth factor 2 expression patterns reveal a link between Wilms' tumorigenesis and epigenetic heterogeneity, CANCER RES, 59(16), 1999, pp. 3889-3892