-
1
-
-
0028706337
-
A developmental context for multiple genetic alterations in Wilms' tumor
-
Feinberg, A. P. A developmental context for multiple genetic alterations in Wilms' tumor. J. Cell Sci., 18: 7-12, 1994.
-
(1994)
J. Cell Sci.
, vol.18
, pp. 7-12
-
-
Feinberg, A.P.1
-
2
-
-
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. N., Redeker, E., Verjaal, M., Feinberg, A. P., Little, P., Boavida, M., Coad, N., Steenman, M., Bliek, J., Niikawa, N., Tonoki, H., Nakamura, Y., de boer, E. G., Slater, R. M., John, R., Cowell, J. K., Junien, C., Henry, I., Tommerup, N., Weksberg, R., Pueschel, S. M., and Westerveld, A. Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann Syndrome and various human neoplasia. Eur. J. Hum. Genet., 2: 3-23, 1994.
-
(1994)
Eur. J. Hum. Genet.
, vol.2
, pp. 3-23
-
-
Mannens, M.1
Hoovers, J.M.N.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
Niikawa, N.11
Tonoki, H.12
Nakamura, Y.13
De Boer, E.G.14
Slater, R.M.15
John, R.16
Cowell, J.K.17
Junien, C.18
Henry, I.19
Tommerup, N.20
Weksberg, R.21
Pueschel, S.M.22
Westerveld, A.23
more..
-
3
-
-
0027172683
-
Relaxation of imprinted genes in human cancer
-
Rainier, S., Johnson, L. A., Dobry, C., Ping, A. J., Grundy, P. E., and Feinberg, A. P. Relaxation of imprinted genes in human cancer. Nature (Lond.), 362: 747-749, 1993.
-
(1993)
Nature (Lond.)
, vol.362
, pp. 747-749
-
-
Rainier, S.1
Johnson, L.A.2
Dobry, C.3
Ping, A.J.4
Grundy, P.E.5
Feinberg, A.P.6
-
4
-
-
0028356544
-
Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour
-
Steenman, M. J. C., Rainier, S., Dobry, C., Grundy, P., Horon, I., and Feinberg, A. P. Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour. Nat. Genet., 7: 433-439, 1994.
-
(1994)
Nat. Genet.
, vol.7
, pp. 433-439
-
-
Steenman, M.J.C.1
Rainier, S.2
Dobry, C.3
Grundy, P.4
Horon, I.5
Feinberg, A.P.6
-
6
-
-
0027285258
-
Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour
-
Ogawa, O., Eccles, M., Szeto, M. R., McNoe, L. A., Yun, K., Maw, M. A., Smith, P. J., and Reeve, A. E. Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour. Nature (Lond.), 362: 749-751, 1993.
-
(1993)
Nature (Lond.)
, vol.362
, pp. 749-751
-
-
Ogawa, O.1
Eccles, M.2
Szeto, M.R.3
McNoe, L.A.4
Yun, K.5
Maw, M.A.6
Smith, P.J.7
Reeve, A.E.8
-
7
-
-
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. Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome. Nat. Genet., 5: 143-150, 1993.
-
(1993)
Nat. Genet.
, vol.5
, pp. 143-150
-
-
Weksberg, R.1
Shen, D.R.2
Fei, Y.L.3
Song, Q.L.4
Squire, J.5
-
8
-
-
0027442239
-
Tumour-suppressor activity of H19 RNA
-
Hao, Y., Crenshaw, T., Moulton, T., Newcomb, E., and Tycko, B. Tumour-suppressor activity of H19 RNA. Nature (Lond.), 365: 764-767, 1993.
-
(1993)
Nature (Lond.)
, vol.365
, pp. 764-767
-
-
Hao, Y.1
Crenshaw, T.2
Moulton, T.3
Newcomb, E.4
Tycko, B.5
-
9
-
-
0029978017
-
KIP2, on chromosome 11p15
-
KIP2, on chromosome 11p15. Proc. Natl. Acad. Sci. USA, 93: 3026-3030, 1996.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 3026-3030
-
-
Matsuoka, S.1
Thompson, J.S.2
Edwards, M.C.3
Barletta, J.M.4
Grundy, P.5
Kalikin, L.M.6
Wade Harper, J.7
Elledge, S.J.8
Feinberg, A.P.9
-
10
-
-
16044364516
-
KIP2 is mutated in Beckwith-Wiedemann syndrome
-
KIP2 is mutated in Beckwith-Wiedemann syndrome. Nat. Genet., 14: 171-173, 1996.
-
(1996)
Nat. Genet.
, vol.14
, pp. 171-173
-
-
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
-
11
-
-
0030610261
-
KIP2 mutation in Beckwith Wiedemann syndrome
-
KIP2 mutation in Beckwith Wiedemann syndrome. Am. J. Hum. Genet., 61: 304-309, 1997.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 304-309
-
-
Lee, M.P.1
DeBaun, M.2
Randhawa, G.3
Reichard, B.A.4
Elledge, S.J.5
Feinberg, A.P.6
-
12
-
-
0030610260
-
KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms' tumors
-
KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms' tumors. Am. J. Hum. Genet., 61: 295-303, 1997.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 295-303
-
-
O'Keefe, D.1
Dao, D.2
Zhao, L.3
Sanderson, R.4
Warburton, D.5
Weiss, L.6
Anyane-Yeboa, K.7
Tycko, B.8
-
13
-
-
0031046285
-
VLQT1 shows tissue-specific imprinting and is physically disrupted by Beckwith Wiedemann syndrome chromosomal rearrangements
-
VLQT1 shows tissue-specific imprinting and is physically disrupted by Beckwith Wiedemann syndrome chromosomal rearrangements. Nat. Genet., 15: 181-185, 1997.
-
(1997)
Nat. Genet.
, vol.15
, pp. 181-185
-
-
Lee, M.P.1
Hu, R.-J.2
Johnson, L.A.3
Feinberg, A.P.4
-
14
-
-
0027231784
-
Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from human chromosome 11
-
Washington DC
-
Koi, M., Johnson, L. A., Kalikin, L. M., Little, P. F. R., Nakamura, Y., and Feinberg, A. P. Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from human chromosome 11. Science (Washington DC), 260: 361-364, 1993.
-
(1993)
Science
, vol.260
, pp. 361-364
-
-
Koi, M.1
Johnson, L.A.2
Kalikin, L.M.3
Little, P.F.R.4
Nakamura, Y.5
Feinberg, A.P.6
-
15
-
-
0030176271
-
A novel gene product that couples TCR signaling to Fas(CD95) expression in activation-induced cell death
-
Park, C. G., Lee, S. Y., Kandala, G., Lee, S. Y., and Choi, Y. A novel gene product that couples TCR signaling to Fas(CD95) expression in activation-induced cell death. Immunity, 4: 583-591, 1996.
-
(1996)
Immunity
, vol.4
, pp. 583-591
-
-
Park, C.G.1
Lee, S.Y.2
Kandala, G.3
Lee, S.Y.4
Choi, Y.5
-
16
-
-
0031573423
-
A 2.5-Mb transcript map of a tumor-suppressing subchromosomal transferable fragment from 11p15.5, and isolation and sequence analysis of three novel genes
-
Hu, R-J., Lee, M. P., Connors, T. D., Johnson, L. A., Burn, T. C., Su, K., Landes, G. M., and Feinberg, A. P. A 2.5-Mb transcript map of a tumor-suppressing subchromosomal transferable fragment from 11p15.5, and isolation and sequence analysis of three novel genes. Genomics, 46: 9-17, 1997.
-
(1997)
Genomics
, vol.46
, pp. 9-17
-
-
Hu, R.-J.1
Lee, M.P.2
Connors, T.D.3
Johnson, L.A.4
Burn, T.C.5
Su, K.6
Landes, G.M.7
Feinberg, A.P.8
-
17
-
-
0029807080
-
KIP2 gene, is biallelically expressed in fetal and adult tissues
-
KIP2 gene, is biallelically expressed in fetal and adult tissues. Hum. Mol. Genet., 5: 1743-1748, 1996.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1743-1748
-
-
Hu, R.-J.1
Lee, M.P.2
Johnson, L.A.3
Feinberg, A.P.4
-
18
-
-
0020793569
-
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
-
Feinberg, A. P., and Vogelstein, B. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal. Biochem., 132: 6-13, 1983.
-
(1983)
Anal. Biochem.
, vol.132
, pp. 6-13
-
-
Feinberg, A.P.1
Vogelstein, B.2
-
19
-
-
9844265406
-
The IPL gene on chromosome 11p15.5 is imprinted in human and mice and is similar to TDAG51, implicated in Fas expression and apoptosis
-
Qian, N., Frank, D., O'Keefe, D., Dao, D., Zhao, L., Yuan, L., Wang, Q., Keating, M., Walsh, C., and Tycko, B. The IPL gene on chromosome 11p15.5 is imprinted in human and mice and is similar to TDAG51, implicated in Fas expression and apoptosis. Hum. Mol. Genet., 6: 2021-2029, 1997.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 2021-2029
-
-
Qian, N.1
Frank, D.2
O'Keefe, D.3
Dao, D.4
Zhao, L.5
Yuan, L.6
Wang, Q.7
Keating, M.8
Walsh, C.9
Tycko, B.10
-
20
-
-
0029817663
-
Fas expression and function in normal and malignant breast cell lines
-
Keane, M. M., Ettenberg, S. A., Lowrey, G. A., Russell, E. K., and Lipkowitz, S. Fas expression and function in normal and malignant breast cell lines. Cancer Res., 56: 4791-4798, 1996.
-
(1996)
Cancer Res.
, vol.56
, pp. 4791-4798
-
-
Keane, M.M.1
Ettenberg, S.A.2
Lowrey, G.A.3
Russell, E.K.4
Lipkowitz, S.5
-
21
-
-
0030667376
-
Requirement for the CD95 receptor-ligand pathway in c-myc-induced apoptosis
-
Washington DC
-
Hueber, A-O., Zornig, M., Lyon, D., Suda, T., Nagata, S., and Evan, G. I. Requirement for the CD95 receptor-ligand pathway in c-myc-induced apoptosis. Science (Washington DC), 278: 1305-1309, 1997.
-
(1997)
Science
, vol.278
, pp. 1305-1309
-
-
Hueber, A.-O.1
Zornig, M.2
Lyon, D.3
Suda, T.4
Nagata, S.5
Evan, G.I.6
-
22
-
-
0028263811
-
c-myc-induced apoptosis in fibroblasts is inhibited by specific cytokines
-
Harrington, E. A., Bennett, A. F., and Evan, G. I. c-myc-induced apoptosis in fibroblasts is inhibited by specific cytokines. EMBO J., 13: 3286-3295, 1994.
-
(1994)
EMBO J.
, vol.13
, pp. 3286-3295
-
-
Harrington, E.A.1
Bennett, A.F.2
Evan, G.I.3
-
23
-
-
0026036288
-
Genomic imprinting and the strange case of the insulin-like growth factor II receptor
-
Haig, D., and Graham, C. Genomic imprinting and the strange case of the insulin-like growth factor II receptor. Cell, 64: 1045-1046, 1991.
-
(1991)
Cell
, vol.64
, pp. 1045-1046
-
-
Haig, D.1
Graham, C.2
-
24
-
-
0029126018
-
A novel L23-related gene 40 kb downstream of the imprinted H19 gene is biallelically expressed in mid-fetal and adult human tissues
-
Tsang, P., Gilles, F., Yuan, L., Kuo, Y-H., Lupu, F., Samara, G., Moosikasuwan, J., Goye, A., Zelenetz, A. D., Selleri, L., and Tycko, B. A novel L23-related gene 40 kb downstream of the imprinted H19 gene is biallelically expressed in mid-fetal and adult human tissues. Hum. Mol. Genet., 4: 1499-1507, 1995.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1499-1507
-
-
Tsang, P.1
Gilles, F.2
Yuan, L.3
Kuo, Y.-H.4
Lupu, F.5
Samara, G.6
Moosikasuwan, J.7
Goye, A.8
Zelenetz, A.D.9
Selleri, L.10
Tycko, B.11
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