-
1
-
-
0142182088
-
Cell-type-specific repression of the maspin gene is disrupted frequently by demethylation at the promoter region in gastric intestinal metaplasia and cancer cells
-
Akiyama Y., Maesawa C., Ogasawara S., Terashima M., and Masuda T. 2003. Cell-type-specific repression of the maspin gene is disrupted frequently by demethylation at the promoter region in gastric intestinal metaplasia and cancer cells. Am. J. Pathol. 163: 1911.
-
(2003)
Am. J. Pathol.
, vol.163
, pp. 1911
-
-
Akiyama, Y.1
Maesawa, C.2
Ogasawara, S.3
Terashima, M.4
Masuda, T.5
-
2
-
-
0037924433
-
Histone modifications and silencing prior to DNA methylation of a tumor suppressor gene
-
Bachman K.E., Park B.H., Rhee I., Rajagopalan H., Herman J.G., Baylin S.B., Kinzler K.W., and Vogelstein B. 2003. Histone modifications and silencing prior to DNA methylation of a tumor suppressor gene. Cancer Cell 3: 89.
-
(2003)
Cancer Cell
, vol.3
, pp. 89
-
-
Bachman, K.E.1
Park, B.H.2
Rhee, I.3
Rajagopalan, H.4
Herman, J.G.5
Baylin, S.B.6
Kinzler, K.W.7
Vogelstein, B.8
-
4
-
-
0025809321
-
Parental imprinting of the mouse H19 gene
-
Bartolomei M.S., Zemel S., and Tilghman S.M. 1991. Parental imprinting of the mouse H19 gene. Nature 351: 153.
-
(1991)
Nature
, vol.351
, pp. 153
-
-
Bartolomei, M.S.1
Zemel, S.2
Tilghman, S.M.3
-
5
-
-
0032476054
-
Nephrogenic rests and the pathogenesis of Wilms tumor: Developmental and clinical considerations
-
Beckwith J.B. 1998. Nephrogenic rests and the pathogenesis of Wilms tumor: Developmental and clinical considerations. Am. J. Med. Genet. 79: 268.
-
(1998)
Am. J. Med. Genet.
, vol.79
, pp. 268
-
-
Beckwith, J.B.1
-
6
-
-
0025271523
-
Nephrogenic rests, nephroblastomatosis, and the pathogenesis of Wilms' tumor
-
Beckwith J.B., Kiviat N.B., and Bonadio J.F. 1990. Nephrogenic rests, nephroblastomatosis, and the pathogenesis of Wilms' tumor. Pediatr. Pathol. 10: 1.
-
(1990)
Pediatr. Pathol.
, vol.10
, pp. 1
-
-
Beckwith, J.B.1
Kiviat, N.B.2
Bonadio, J.F.3
-
8
-
-
0033377772
-
Oppositely imprinted genes p57 (Kip2) and IGF2 interact in a mouse model for Beckwith-Wiedemann syndrome
-
Caspary T., Cleary M.A., Perlman E.J., Zhang P., Elledge S.J., and Tilghman S.M. 1999. Oppositely imprinted genes p57 (Kip2) and IGF2 interact in a mouse model for Beckwith-Wiedemann syndrome. Genes Dev. 13: 3115.
-
(1999)
Genes Dev.
, vol.13
, pp. 3115
-
-
Caspary, T.1
Cleary, M.A.2
Perlman, E.J.3
Zhang, P.4
Elledge, S.J.5
Tilghman, S.M.6
-
9
-
-
17444450519
-
Activation of the MN/CA9 gene is associated with hypomethylation in human renal cell carcinoma cell lines
-
Cho M., Grabmaier K., Kitahori Y., Hiasa Y., Nakagawa Y., Uemura H., Hirao Y., Ohnishi T., Yoshikawa K., and Ooesterwijk E. 2000. Activation of the MN/CA9 gene is associated with hypomethylation in human renal cell carcinoma cell lines. Mol. Carcinog. 27: 184.
-
(2000)
Mol. Carcinog.
, vol.27
, pp. 184
-
-
Cho, M.1
Grabmaier, K.2
Kitahori, Y.3
Hiasa, Y.4
Nakagawa, Y.5
Uemura, H.6
Hirao, Y.7
Ohnishi, T.8
Yoshikawa, K.9
Ooesterwijk, E.10
-
10
-
-
0028356419
-
A second signal supplied by insulin-like growth factor II in oncogene-induced tumorigenesis
-
Christofori G., Naik P., and Hanahan D. 1994. A second signal supplied by insulin-like growth factor II in oncogene-induced tumorigenesis. Nature 369: 414.
-
(1994)
Nature
, vol.369
, pp. 414
-
-
Christofori, G.1
Naik, P.2
Hanahan, D.3
-
11
-
-
0031761362
-
Loss of imprinting in normal tissue of colorectal cancer patients with microsatellite instability
-
Cui H., Horon I.L., Ohlsson R., Hamilton S.R., and Feinberg A.P. 1998. Loss of imprinting in normal tissue of colorectal cancer patients with microsatellite instability. Nat. Med. 4: 1276.
-
(1998)
Nat. Med.
, vol.4
, pp. 1276
-
-
Cui, H.1
Horon, I.L.2
Ohlsson, R.3
Hamilton, S.R.4
Feinberg, A.P.5
-
12
-
-
0037436509
-
Loss of IGF2 imprinting: A potential marker of colorectal cancer risk
-
Cui H., Cruz-Correa M., Giardiello F.M., Hutcheon D.F., Kafonek D.R., Brandenburg S., Wu Y., He X., Powe N.R., and Feinberg A.P. 2003. Loss of IGF2 imprinting: A potential marker of colorectal cancer risk. Science 299: 1753.
-
(2003)
Science
, vol.299
, pp. 1753
-
-
Cui, H.1
Cruz-Correa, M.2
Giardiello, F.M.3
Hutcheon, D.F.4
Kafonek, D.R.5
Brandenburg, S.6
Wu, Y.7
He, X.8
Powe, N.R.9
Feinberg, A.P.10
-
13
-
-
85015806874
-
IGF2, H19, p57KIP2, and LIT1 and the Beckwith-Wiedemann syndrome
-
(ed. C.J. Epstein et al.). Oxford University Press, New York
-
DeBaun M.R. and Feinberg A.P. 2004. IGF2, H19, p57KIP2, and LIT1 and the Beckwith-Wiedemann syndrome. In Inborn errors of development: The molecular basis of clinical disorders of morphogenesis (ed. C.J. Epstein et al.). Oxford University Press, New York.
-
(2004)
Inborn Errors of Development: The Molecular Basis of Clinical Disorders of Morphogenesis
-
-
DeBaun, M.R.1
Feinberg, A.P.2
-
14
-
-
0036182963
-
Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects
-
DeBaun M.R., Niemitz E.L., McNeil D.E., Brandenburg S.A., Lee M.P., and Feinberg A.P. 2002. Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects. Am. J. Hum. Genet. 70: 604.
-
(2002)
Am. J. Hum. Genet.
, vol.70
, pp. 604
-
-
DeBaun, M.R.1
Niemitz, E.L.2
McNeil, D.E.3
Brandenburg, S.A.4
Lee, M.P.5
Feinberg, A.P.6
-
15
-
-
0025967857
-
Parental imprinting of the mouse insulin-like growth factor II gene
-
DeChiara T.M., Robertson E.J., and Efstratiadis A. 1991. Parental imprinting of the mouse insulin-like growth factor II gene. Cell 64: 849.
-
(1991)
Cell
, vol.64
, pp. 849
-
-
DeChiara, T.M.1
Robertson, E.J.2
Efstratiadis, A.3
-
16
-
-
0033118754
-
Imprinting of a genomic domain of 11p15 and loss of imprinting in cancer: An introduction
-
Feinberg A.P. 1999. Imprinting of a genomic domain of 11p15 and loss of imprinting in cancer: An introduction. Cancer Res. 59: 1743s.
-
(1999)
Cancer Res.
, vol.59
-
-
Feinberg, A.P.1
-
17
-
-
1042278765
-
The history of cancer epigenetics
-
Feinberg A.P. and Tycko B. 2004. The history of cancer epigenetics. Nat. Rev. Cancer 4: 143.
-
(2004)
Nat. Rev. Cancer
, vol.4
, pp. 143
-
-
Feinberg, A.P.1
Tycko, B.2
-
18
-
-
0020699979
-
Hypomethylation distinguishes genes of some human cancers from their normal counterparts
-
Feinberg A.P. and Vogelstein B. 1983. Hypomethylation distinguishes genes of some human cancers from their normal counterparts. Nature 301: 89.
-
(1983)
Nature
, vol.301
, pp. 89
-
-
Feinberg, A.P.1
Vogelstein, B.2
-
19
-
-
20144388146
-
Loss of acetylation at Lys16 and trimethylation at Lys20 of histone H4 is a common hallmark of human cancer
-
Fraga M.F., Ballestar E., Villar-Garea A., Boix-Chornet M., Espada J., Schotta G., Bonaldi T., Haydon C., Ropero S., Petrie K., Iyer N.G., Perez-Rosado A., Calvo E., Lopez J.A., Cano A., Calasanz M.J., Colomer D., Piris M.A., Ahn N., Imhof A., Caldas C., Jenuwein T., and Esteller M. 2005. Loss of acetylation at Lys16 and trimethylation at Lys20 of histone H4 is a common hallmark of human cancer. Nat. Genet. 37: 391.
-
(2005)
Nat. Genet.
, vol.37
, pp. 391
-
-
Fraga, M.F.1
Ballestar, E.2
Villar-Garea, A.3
Boix-Chornet, M.4
Espada, J.5
Schotta, G.6
Bonaldi, T.7
Haydon, C.8
Ropero, S.9
Petrie, K.10
Iyer, N.G.11
Perez-Rosado, A.12
Calvo, E.13
Lopez, J.A.14
Cano, A.15
Calasanz, M.J.16
Colomer, D.17
Piris, M.A.18
Ahn, N.19
Imhof, A.20
Caldas, C.21
Jenuwein, T.22
Esteller, M.23
more..
-
20
-
-
0021101229
-
The 5-methylcytosine content of DNA from human tumors
-
Gama-Sosa M.A., Slagel V.A., Trewyn R.W., Oxenhandler R., Kuo K.C., Gehrke C.W., and Ehrlich M. 1983. The 5-methylcytosine content of DNA from human tumors. Nucleic Acids Res. 11: 6883.
-
(1983)
Nucleic Acids Res.
, vol.11
, pp. 6883
-
-
Gama-Sosa, M.A.1
Slagel, V.A.2
Trewyn, R.W.3
Oxenhandler, R.4
Kuo, K.C.5
Gehrke, C.W.6
Ehrlich, M.7
-
21
-
-
0242584449
-
Induction of tumors in mice by genomic hypomethylation
-
Gaudet F., Hodgson J.G., Eden A., Jackson-Grusby L., Dausman J., Gray J.W., Leonhardt H., and Jaenisch R. 2003. Induction of tumors in mice by genomic hypomethylation. Science 300: 489.
-
(2003)
Science
, vol.300
, pp. 489
-
-
Gaudet, F.1
Hodgson, J.G.2
Eden, A.3
Jackson-Grusby, L.4
Dausman, J.5
Gray, J.W.6
Leonhardt, H.7
Jaenisch, R.8
-
22
-
-
0027442239
-
Tumour-suppressor activity of H19 RNA
-
Hao Y., Crenshaw T., Moulton T., Newcomb E., and Tycko B. 1993. Tumour-suppressor activity of H19 RNA. Nature 365: 764.
-
(1993)
Nature
, vol.365
, pp. 764
-
-
Hao, Y.1
Crenshaw, T.2
Moulton, T.3
Newcomb, E.4
Tycko, B.5
-
23
-
-
16044364516
-
An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome
-
Hatada I., Ohashi H., Fukushima Y., Kaneko Y., Inoue M., Komoto Y., Okada A., Ohishi S., Nabetani A., Morisaki H., Nakayama M., Niikawa N., and Mukai T. 1996. An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome. Nat. Genet. 14: 171.
-
(1996)
Nat. Genet.
, vol.14
, pp. 171
-
-
Hatada, I.1
Ohashi, H.2
Fukushima, Y.3
Kaneko, Y.4
Inoue, M.5
Komoto, Y.6
Okada, A.7
Ohishi, S.8
Nabetani, A.9
Morisaki, H.10
Nakayama, M.11
Niikawa, N.12
Mukai, T.13
-
24
-
-
0032527755
-
IGF2 imprinting does not require its own DNA methylation or H19 RNA
-
Jones B.K., Levorse J.M., and Tilghman S.M. 1998. IGF2 imprinting does not require its own DNA methylation or H19 RNA. Genes Dev. 12: 2200.
-
(1998)
Genes Dev.
, vol.12
, pp. 2200
-
-
Jones, B.K.1
Levorse, J.M.2
Tilghman, S.M.3
-
25
-
-
0036274359
-
The fundamental role of epigenetic events in cancer
-
Jones P.A. and Baylin S.B. 2002. The fundamental role of epigenetic events in cancer. Nat. Rev. Genet. 3: 415.
-
(2002)
Nat. Rev. Genet.
, vol.3
, pp. 415
-
-
Jones, P.A.1
Baylin, S.B.2
-
26
-
-
0034112090
-
Loss of imprinting and elevated expression of wild-type p73 in human gastric adenocarcinoma
-
Kang M.J., Park B.J., Byun D.S., Park J.I., Kim H.J., Park J.H., and Chi S.G. 2000. Loss of imprinting and elevated expression of wild-type p73 in human gastric adenocarcinoma. Clin. Cancer Res. 6: 1767.
-
(2000)
Clin. Cancer Res.
, vol.6
, pp. 1767
-
-
Kang, M.J.1
Park, B.J.2
Byun, D.S.3
Park, J.I.4
Kim, H.J.5
Park, J.H.6
Chi, S.G.7
-
27
-
-
15044356152
-
Epigenetics: Surveillance team against cancer
-
Klein G. 2005. Epigenetics: Surveillance team against cancer. Nature 434: 150.
-
(2005)
Nature
, vol.434
, pp. 150
-
-
Klein, G.1
-
28
-
-
0023529174
-
Prince Takamatsu memorial lecture. Rare cancers: Clues to genetic mechanisms
-
Knudson A.G., Jr. 1987. Prince Takamatsu memorial lecture. Rare cancers: Clues to genetic mechanisms. Princess Takamatsu Symp. 18: 221.
-
(1987)
Princess Takamatsu Symp.
, vol.18
, pp. 221
-
-
Knudson Jr., A.G.1
-
29
-
-
0032992678
-
Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting
-
Lee M.P., Brandenburg S., Landes G.M., Adams M., Miller G., and Feinberg A.P. 1999a. Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting. Hum. Mol. Genet. 8: 683.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 683
-
-
Lee, M.P.1
Brandenburg, S.2
Landes, G.M.3
Adams, M.4
Miller, G.5
Feinberg, A.P.6
-
30
-
-
0033609117
-
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 M.P., DeBaun M.R., Mitsuya K., Galonek H.L., Brandenburg S., Oshimura M., and Feinberg A.P. 1999b. 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. Proc. Natl. Acad. Sci. 96: 5203.
-
(1999)
Proc. Natl. Acad. Sci.
, vol.96
, pp. 5203
-
-
Lee, M.P.1
DeBaun, M.R.2
Mitsuya, K.3
Galonek, H.L.4
Brandenburg, S.5
Oshimura, M.6
Feinberg, A.P.7
-
31
-
-
0029024277
-
Disruption of imprinting caused by deletion of the H19 gene region in mice
-
Leighton P.A., Ingram R.S., Eggenschwiler J., Efstratiadis A., and Tilghman S.M. 1995. Disruption of imprinting caused by deletion of the H19 gene region in mice. Nature 375: 34.
-
(1995)
Nature
, vol.375
, pp. 34
-
-
Leighton, P.A.1
Ingram, R.S.2
Eggenschwiler, J.3
Efstratiadis, A.4
Tilghman, S.M.5
-
33
-
-
0028316620
-
Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia
-
Mannens M., Hoovers J.M., Redeker E., Verjaal M., Feinberg A.P., Little P., Boavida M., Coad N., Steenman M., and Bliek J., et al. 1994. Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia. Eur. J. Hum. Genet. 2: 3.
-
(1994)
Eur. J. Hum. Genet.
, vol.2
, pp. 3
-
-
Mannens, M.1
Hoovers, J.M.2
Redeker, E.3
Verjaal, M.4
Feinberg, A.P.5
Little, P.6
Boavida, M.7
Coad, N.8
Steenman, M.9
Bliek, J.10
-
34
-
-
0028227938
-
Epigenetic lesions at the H19 locus in Wilms' tumour patients
-
Moulton T., Crenshaw T., Hao Y., Moosikasuwan J., Lin N., Dembitzer F., Hensle T., Weiss L., McMorrow L., and Loew T., et al. 1994. Epigenetic lesions at the H19 locus in Wilms' tumour patients. Nat. Genet. 7: 440.
-
(1994)
Nat. Genet.
, vol.7
, pp. 440
-
-
Moulton, T.1
Crenshaw, T.2
Hao, Y.3
Moosikasuwan, J.4
Lin, N.5
Dembitzer, F.6
Hensle, T.7
Weiss, L.8
McMorrow, L.9
Loew, T.10
-
35
-
-
16644397923
-
Loss of imprinting of PEG1/MEST in lung cancer cell lines
-
Nakanishi H., Suda T., Katoh M., Watanabe A., Igishi T., Kodani M., Matsumoto S., Nakamoto M., Shigeoka Y., Okabe T., Oshimura M., and Shimizu E. 2004. Loss of imprinting of PEG1/MEST in lung cancer cell lines. Oncol. Rep. 12: 1273.
-
(2004)
Oncol. Rep.
, vol.12
, pp. 1273
-
-
Nakanishi, H.1
Suda, T.2
Katoh, M.3
Watanabe, A.4
Igishi, T.5
Kodani, M.6
Matsumoto, S.7
Nakamoto, M.8
Shigeoka, Y.9
Okabe, T.10
Oshimura, M.11
Shimizu, E.12
-
36
-
-
16844384464
-
Discovery of aberrant expression of R-RAS by cancer-linked DNA hypomethylation in gastric cancer using microarrays
-
Nishigaki M., Aoyagi K., Danjoh I., Fukaya M., Yanagihara K., Sakamoto H., Yoshida T., and Sasaki H. 2005. Discovery of aberrant expression of R-RAS by cancer-linked DNA hypomethylation in gastric cancer using microarrays. Cancer Res. 65: 2115.
-
(2005)
Cancer Res.
, vol.65
, pp. 2115
-
-
Nishigaki, M.1
Aoyagi, K.2
Danjoh, I.3
Fukaya, M.4
Yanagihara, K.5
Sakamoto, H.6
Yoshida, T.7
Sasaki, H.8
-
37
-
-
0027285258
-
Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour
-
Ogawa O., Eccles M.R., Szeto J., McNoe L.A., Yun K., Maw M.A., Smith P.J., and Reeve A.E. 1993. Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour. Nature 362: 749.
-
(1993)
Nature
, vol.362
, pp. 749
-
-
Ogawa, O.1
Eccles, M.R.2
Szeto, J.3
McNoe, L.A.4
Yun, K.5
Maw, M.A.6
Smith, P.J.7
Reeve, A.E.8
-
38
-
-
16544382864
-
Loss of IGF2 imprinting: Mechanisms and consequences
-
Ohlsson R. 2004. Loss of IGF2 imprinting: Mechanisms and consequences. Novartis Found. Symp. 262: 108.
-
(2004)
Novartis Found. Symp.
, vol.262
, pp. 108
-
-
Ohlsson, R.1
-
39
-
-
0027322519
-
IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome
-
Ohlsson R., Nystrom A., Pfeifer-Ohlsson S., Tohonen V., Hedborg F., Schofield P., Flam F., and Ekstrom T.J. 1993. IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome. Nat. Genet. 4: 94.
-
(1993)
Nat. Genet.
, vol.4
, pp. 94
-
-
Ohlsson, R.1
Nystrom, A.2
Pfeifer-Ohlsson, S.3
Tohonen, V.4
Hedborg, F.5
Schofield, P.6
Flam, F.7
Ekstrom, T.J.8
-
40
-
-
0024518392
-
Genetic linkage of Beckwith-Wiedemann syndrome to 11p15
-
Ping A.J., Reeve A.E., Law D.J., Young M.R., Boehnke M., and Feinberg A.P. 1989. Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. Am. J. Hum. Genet. 44: 720.
-
(1989)
Am. J. Hum. Genet.
, vol.44
, pp. 720
-
-
Ping, A.J.1
Reeve, A.E.2
Law, D.J.3
Young, M.R.4
Boehnke, M.5
Feinberg, A.P.6
-
41
-
-
0027172683
-
Relaxation of imprinted genes in human cancer
-
Rainier S., Johnson L.A., Dobry C.J., Ping A.J., Grundy P.E., and Feinberg A.P. 1993. Relaxation of imprinted genes in human cancer. Nature 362: 747.
-
(1993)
Nature
, vol.362
, pp. 747
-
-
Rainier, S.1
Johnson, L.A.2
Dobry, C.J.3
Ping, A.J.4
Grundy, P.E.5
Feinberg, A.P.6
-
42
-
-
0035930134
-
Loss of imprinting of insulin-like growth factor-II (IGF2) gene in distinguishing specific biologic subtypes of Wilms tumor
-
Ravenel J.D., Broman K.W., Perlman E.J., Niemitz E.L., Jayawardena T.M., Bell D.W., Haber D.A., Uejima H., and Feinberg A.P. 2001. Loss of imprinting of insulin-like growth factor-II (IGF2) gene in distinguishing specific biologic subtypes of Wilms tumor. J. Natl. Cancer Inst. 93: 1698.
-
(2001)
J. Natl. Cancer Inst.
, vol.93
, pp. 1698
-
-
Ravenel, J.D.1
Broman, K.W.2
Perlman, E.J.3
Niemitz, E.L.4
Jayawardena, T.M.5
Bell, D.W.6
Haber, D.A.7
Uejima, H.8
Feinberg, A.P.9
-
43
-
-
0030993133
-
Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element
-
Ripoche M.A., Kress C., Poirier F., and Dandolo L. 1997. Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element. Genes Dev. 11: 1596.
-
(1997)
Genes Dev.
, vol.11
, pp. 1596
-
-
Ripoche, M.A.1
Kress, C.2
Poirier, F.3
Dandolo, L.4
-
44
-
-
22844457491
-
DNA methylation and human disease
-
Robertson K.D. 2005. DNA methylation and human disease. Nat. Rev. Genet. 6: 597.
-
(2005)
Nat. Rev. Genet.
, vol.6
, pp. 597
-
-
Robertson, K.D.1
-
45
-
-
20144374299
-
Loss of imprinting of IGF2 alters intestinal maturation and tumorigenesis in mice
-
Sakatani T., Kaneda A., Iacobuzio-Donahue C.A., Carter M.G., de Boom Witzel S., Okano H., Ko M.S., Ohlsson R., Longo D.L., and Feinberg A.P. 2005. Loss of imprinting of IGF2 alters intestinal maturation and tumorigenesis in mice. Science 307: 1976.
-
(2005)
Science
, vol.307
, pp. 1976
-
-
Sakatani, T.1
Kaneda, A.2
Iacobuzio-Donahue, C.A.3
Carter, M.G.4
De Boom Witzel, S.5
Okano, H.6
Ko, M.S.7
Ohlsson, R.8
Longo, D.L.9
Feinberg, A.P.10
-
46
-
-
27644466889
-
Epigenetic down-regulation of CDKN1C/p57KIP2 in pancreatic ductal neoplasms identified by gene expression profiling
-
Sato N., Matsubayashi H., Abe T., Fukushima N., and Goggins M. 2005. Epigenetic down-regulation of CDKN1C/p57KIP2 in pancreatic ductal neoplasms identified by gene expression profiling. Clin. Cancer Res. 11: 4681.
-
(2005)
Clin. Cancer Res.
, vol.11
, pp. 4681
-
-
Sato, N.1
Matsubayashi, H.2
Abe, T.3
Fukushima, N.4
Goggins, M.5
-
47
-
-
0038002683
-
The EZH2 polycomb transcriptional repressor: A marker or mover of metastatic prostate cancer?
-
Sellers W.R. and Loda M. 2002. The EZH2 polycomb transcriptional repressor: A marker or mover of metastatic prostate cancer? Cancer Cell 2: 349.
-
(2002)
Cancer Cell
, vol.2
, pp. 349
-
-
Sellers, W.R.1
Loda, M.2
-
48
-
-
0028827816
-
Insulin-like growth factor II gene expression by congenital mesoblastic nephroma
-
Sharifah N.A., Yun K., and McLay J. 1995. Insulin-like growth factor II gene expression by congenital mesoblastic nephroma. Diagn. Mol. Pathol. 4: 279.
-
(1995)
Diagn. Mol. Pathol.
, vol.4
, pp. 279
-
-
Sharifah, N.A.1
Yun, K.2
McLay, J.3
-
49
-
-
0028356544
-
Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour
-
Steenman M.J., Rainier S., Dobry C.J., Grundy P., Horon I.L., and Feinberg A.P. 1994. Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour. Nat. Genet. 7: 433.
-
(1994)
Nat. Genet.
, vol.7
, pp. 433
-
-
Steenman, M.J.1
Rainier, S.2
Dobry, C.J.3
Grundy, P.4
Horon, I.L.5
Feinberg, A.P.6
-
50
-
-
0027131705
-
Infrequency of ras, p53, WT1, or RB gene alterations in Wilms tumors
-
Waber P.G., Chen J., and Nisen P.D. 1993. Infrequency of ras, p53, WT1, or RB gene alterations in Wilms tumors. Cancer 72: 3732.
-
(1993)
Cancer
, vol.72
, pp. 3732
-
-
Waber, P.G.1
Chen, J.2
Nisen, P.D.3
-
51
-
-
0027420362
-
Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome
-
Weksberg R., Shen D.R., Fei Y.L., Song Q.L., and Squire J. 1993. Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome. Nat. Genet. 5: 143.
-
(1993)
Nat. Genet.
, vol.5
, pp. 143
-
-
Weksberg, R.1
Shen, D.R.2
Fei, Y.L.3
Song, Q.L.4
Squire, J.5
-
52
-
-
1542318319
-
Loss of insulin-like growth factor-II imprinting and the presence of screen-detected colorectal adenomas in women
-
Woodson K., Flood A., Green L., Tangrea J.A., Hanson J., Cash B., and Schoenfeld P. 2004. Loss of insulin-like growth factor-II imprinting and the presence of screen-detected colorectal adenomas in women. J. Natl. Cancer Inst. 96: 407.
-
(2004)
J. Natl. Cancer Inst.
, vol.96
, pp. 407
-
-
Woodson, K.1
Flood, A.2
Green, L.3
Tangrea, J.A.4
Hanson, J.5
Cash, B.6
Schoenfeld, P.7
-
53
-
-
26444473234
-
Opposing effects of DNA hypomethylation on intestinal and liver carcinogenesis
-
Yamada Y., Jackson-Grusby L., Linhart H., Meissner A., Eden A., Lin H., and Jaenisch R. 2005. Opposing effects of DNA hypomethylation on intestinal and liver carcinogenesis. Proc. Natl. Acad. Sci. 102: 13580.
-
(2005)
Proc. Natl. Acad. Sci.
, vol.102
, pp. 13580
-
-
Yamada, Y.1
Jackson-Grusby, L.2
Linhart, H.3
Meissner, A.4
Eden, A.5
Lin, H.6
Jaenisch, R.7
-
54
-
-
13044283423
-
NOEY2 (ARHI), an imprinted putative tumor suppressor gene in ovarian and breast carcinomas
-
Yu Y., Xu F., Peng H., Fang X., Zhao S., Li Y., Cuevas B., Kuo W.L., Gray J.W., Siciliano M., Mills G.B., and Bast R.C., Jr. 1999. NOEY2 (ARHI), an imprinted putative tumor suppressor gene in ovarian and breast carcinomas. Proc. Natl. Acad. Sci. 96: 214.
-
(1999)
Proc. Natl. Acad. Sci.
, vol.96
, pp. 214
-
-
Yu, Y.1
Xu, F.2
Peng, H.3
Fang, X.4
Zhao, S.5
Li, Y.6
Cuevas, B.7
Kuo, W.L.8
Gray, J.W.9
Siciliano, M.10
Mills, G.B.11
Bast Jr., R.C.12
-
55
-
-
0026849544
-
Monoallelic expression of the human H19 gene
-
Zhang Y. and Tycko B. 1992. Monoallelic expression of the human H19 gene. Nat. Genet. 1: 40.
-
(1992)
Nat. Genet.
, vol.1
, pp. 40
-
-
Zhang, Y.1
Tycko, B.2
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