-
1
-
-
0028980026
-
Genomic imprinting of p57(KIP2), cyclin-dependent kinase inhibitor, in mouse
-
Hatada, I. and Mukai, T. (1995) Genomic imprinting of p57(KIP2), cyclin-dependent kinase inhibitor, in mouse. Nature Genet., 11, 204-206.
-
(1995)
Nature Genet.
, vol.11
, pp. 204-206
-
-
Hatada, I.1
Mukai, T.2
-
2
-
-
0028988159
-
P57KIP2, a structurally distinct member of the p21CIPI Cdk inhibitor family, is a candidate tumor suppressor gene
-
Matsuoka, S., Edwards, M.C., Bai, C., Parker, S., Zhang, P., Baldini, A., Harper, J.W. and Elledge, S.J. (1995) p57KIP2, a structurally distinct member of the p21CIPI Cdk inhibitor family, is a candidate tumor suppressor gene. Genes Dev., 9, 650-662.
-
(1995)
Genes Dev.
, vol.9
, pp. 650-662
-
-
Matsuoka, S.1
Edwards, M.C.2
Bai, C.3
Parker, S.4
Zhang, P.5
Baldini, A.6
Harper, J.W.7
Elledge, S.J.8
-
3
-
-
0028988158
-
Cloning of p57KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution
-
Lee, M.H., Reynisdottir, I. and Massague, J. (1995) Cloning of p57KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution. Genes Dev., 9, 639-649.
-
(1995)
Genes Dev.
, vol.9
, pp. 639-649
-
-
Lee, M.H.1
Reynisdottir, I.2
Massague, J.3
-
4
-
-
0029847299
-
Chromosome 11p15.5 regional imprinting: Comparative analysis of KIP2 and H19 in human tissues and Wilms' tumors
-
Chung, W.Y., Yuan, L., Feng, L., Hensle, T. and Tycko, B. (1996) Chromosome 11p15.5 regional imprinting: comparative analysis of KIP2 and H19 in human tissues and Wilms' tumors. Hum. Mol. Genet., 5, 1101-1108.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1101-1108
-
-
Chung, W.Y.1
Yuan, L.2
Feng, L.3
Hensle, T.4
Tycko, B.5
-
5
-
-
0029896367
-
Genomic imprinting of human p57(KIP2) and its reduced expression in Wilms' tumors
-
Hatada, I., Inazawa, J., Abe, T., Nakayama, M., Kaneko, Y., Jinno, Y., Niikawa, N., Ohashi, H., Fukushima, Y., Iida, K., Yutani, C., Takahashi, S., Chiba, Y., Ohishi, S. and Mukai, T. (1996) Genomic imprinting of human p57(KIP2) and its reduced expression in Wilms' tumors. Hum. Mol. Genet., 5, 783-788.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 783-788
-
-
Hatada, I.1
Inazawa, J.2
Abe, T.3
Nakayama, M.4
Kaneko, Y.5
Jinno, Y.6
Niikawa, N.7
Ohashi, H.8
Fukushima, Y.9
Iida, K.10
Yutani, C.11
Takahashi, S.12
Chiba, Y.13
Ohishi, S.14
Mukai, T.15
-
6
-
-
0029869293
-
Selective maternal-allele loss in human lung cancers of the maternally expressed p57(KIP2) gene at 11p15.5
-
Kondo, M., Matsuoka, S., Uchida, K., Osada, H., Nagatake, M., Takagi, K., Harper, J.W., Takahashi, T., Elledge, S.J. and Takahashi, T. (1996) Selective maternal-allele loss in human lung cancers of the maternally expressed p57(KIP2) gene at 11p15.5. Oncngene, 12, 1365-1368.
-
(1996)
Oncngene
, vol.12
, pp. 1365-1368
-
-
Kondo, M.1
Matsuoka, S.2
Uchida, K.3
Osada, H.4
Nagatake, M.5
Takagi, K.6
Harper, J.W.7
Takahashi, T.8
Elledge, S.J.9
Takahashi, T.10
-
7
-
-
0029978017
-
Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15
-
Matsuoka, S., Thompson, J.S., Edwards, M.C., Bartletta, J.M., Grundy, P., Kalikin, L.M., Harper, J.W., Elledge, S.J. and Feinberg, A.P. (1996) Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15. Proc. Natl Acad. Sci. USA, 93, 3026-3030.
-
(1996)
Proc. Natl Acad. Sci. USA
, vol.93
, pp. 3026-3030
-
-
Matsuoka, S.1
Thompson, J.S.2
Edwards, M.C.3
Bartletta, J.M.4
Grundy, P.5
Kalikin, L.M.6
Harper, J.W.7
Elledge, S.J.8
Feinberg, A.P.9
-
8
-
-
0032410152
-
Mechanism of imprinting on mouse distal chromosome 7
-
Ainscough, J.F., John, R.M. and Surani, M.A. (1998) Mechanism of imprinting on mouse distal chromosome 7. Genet. Res., 72, 237-245.
-
(1998)
Genet. Res.
, vol.72
, pp. 237-245
-
-
Ainscough, J.F.1
John, R.M.2
Surani, M.A.3
-
9
-
-
0031750223
-
Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5
-
Paulsen, M., Davies, K.R., Bowden, L.M., Villar, A.J., Franck, O., Fuermann, M., Dean, W.L., Moore, T.F., Rodrigues, N., Davies, K.E., Hu, R.J., Feinberg, A.P., Maher, E.R., Reik, W. and Walter, J. (1998) Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5. Hum. Mol. Genet., 7, 1149-1159.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1149-1159
-
-
Paulsen, M.1
Davies, K.R.2
Bowden, L.M.3
Villar, A.J.4
Franck, O.5
Fuermann, M.6
Dean, W.L.7
Moore, T.F.8
Rodrigues, N.9
Davies, K.E.10
Hu, R.J.11
Feinberg, A.P.12
Maher, E.R.13
Reik, W.14
Walter, J.15
-
10
-
-
0025738681
-
Uniparental paternal disomy in a genetic cancer-predisposing syndrome
-
Henry, I., Bonaiti-Pellie, C., Chehensse, V., Beldjord, C., Schwartz, C., Utermann, G. and Junien, C. (1991) Uniparental paternal disomy in a genetic cancer-predisposing syndrome. Nature, 351, 665-667.
-
(1991)
Nature
, vol.351
, pp. 665-667
-
-
Henry, I.1
Bonaiti-Pellie, C.2
Chehensse, V.3
Beldjord, C.4
Schwartz, C.5
Utermann, G.6
Junien, C.7
-
11
-
-
0020511170
-
Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome
-
Waziri, M., Patil, S.R., Hanson, J.W. and Bartley, J.A. (1983) Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome. J. Pediatr., 102, 873-876.
-
(1983)
J. Pediatr.
, vol.102
, pp. 873-876
-
-
Waziri, M.1
Patil, S.R.2
Hanson, J.W.3
Bartley, J.A.4
-
12
-
-
0021256768
-
Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases
-
Turleau, C., de Grouchy, J., Chavin-Colin, F., Martelli, H., Voyer, M. and Charlas, R. (1984) Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases. Hum. Genet., 67, 219-221.
-
(1984)
Hum. Genet.
, vol.67
, pp. 219-221
-
-
Turleau, C.1
De Grouchy, J.2
Chavin-Colin, F.3
Martelli, H.4
Voyer, M.5
Charlas, R.6
-
13
-
-
0023011534
-
An infant with Beckwith-Wiedemann syndrome and chromosomal duplication 11p13-pter: Correlation of symptoms between 11p trisomy and Beckwith-Wiedemann syndrome
-
Okano, Y., Osasa, Y., Yamamoto, H., Hase, Y., Tsuruhara, T. and Fujita, H. (1986) An infant with Beckwith-Wiedemann syndrome and chromosomal duplication 11p13-pter: correlation of symptoms between 11p trisomy and Beckwith-Wiedemann syndrome. Jinrui Idengaku Zasshi, 31, 365-372.
-
(1986)
Jinrui Idengaku Zasshi
, vol.31
, pp. 365-372
-
-
Okano, Y.1
Osasa, Y.2
Yamamoto, H.3
Hase, Y.4
Tsuruhara, T.5
Fujita, H.6
-
14
-
-
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. Nature Genet., 5, 143-150.
-
(1993)
Nature Genet.
, vol.5
, pp. 143-150
-
-
Weksberg, R.1
Shen, D.R.2
Fei, Y.L.3
Song, Q.L.4
Squire, J.5
-
15
-
-
0030827119
-
Imprinting of IGF2 and H19: Lack of reciprocity in sporadic Beckwith-Wiedemann syndrome
-
Joyce, J.A., Lam, W.K., Catchpoole, D.J., Jenks, P., Reik, W., Maher, E.R. and Schofield, P.N. (1997) Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome. Hum. Mol. Genet., 6, 1543-1548.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1543-1548
-
-
Joyce, J.A.1
Lam, W.K.2
Catchpoole, D.J.3
Jenks, P.4
Reik, W.5
Maher, E.R.6
Schofield, P.N.7
-
16
-
-
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. Nature Genet., 14, 171-173.
-
(1996)
Nature 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
-
17
-
-
0030610260
-
Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors
-
O'Keefe, D., Dao, D., Zhao, L., Sanderson, R., Warburton, D., Weiss, L., Anyane-Yeboa, K. and Tycko, B. (1997) Coding mutations in p57KIP2 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)
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
-
18
-
-
0030610261
-
Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome
-
Lee, M.P., DeBaun, M., Randhawa, G., Reichard, B.A., Elledge, S.J. and Feinberg, A.P. (1997) Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome. Am. J. Hum. Genet., 61, 304-309.
-
(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
-
19
-
-
0028130305
-
Disproportionate growth in mice with Igf-2 transgenes
-
Ward, A., Bates, P., Fisher, R., Richardson, L. and Graham, C.F. (1994) Disproportionate growth in mice with Igf-2 transgenes. Proc. Natl Acad. Sci. USA, 91, 10365-10369.
-
(1994)
Proc. Natl Acad. Sci. USA
, vol.91
, pp. 10365-10369
-
-
Ward, A.1
Bates, P.2
Fisher, R.3
Richardson, L.4
Graham, C.F.5
-
20
-
-
0028061877
-
Consequences of postnatally elevated insulin-like growth factor-II in transgenic mice: Endocrine changes and effects on body and organ growth
-
Wolf, E., Kramer, R., Blum, W.F., Foll, J. and Brem, G. (1994) Consequences of postnatally elevated insulin-like growth factor-II in transgenic mice: endocrine changes and effects on body and organ growth. Endocrinology, 135, 1877-1886.
-
(1994)
Endocrinology
, vol.135
, pp. 1877-1886
-
-
Wolf, E.1
Kramer, R.2
Blum, W.F.3
Foll, J.4
Brem, G.5
-
21
-
-
0030660180
-
Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes
-
Eggenschwiler, J., Ludwig, T., Fisher, P., Leighton, P.A., Tilghman, S.M. and Efstratiadis, A. (1997) Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes. Genes Dev., 11, 3128-3142.
-
(1997)
Genes Dev.
, vol.11
, pp. 3128-3142
-
-
Eggenschwiler, J.1
Ludwig, T.2
Fisher, P.3
Leighton, P.A.4
Tilghman, S.M.5
Efstratiadis, A.6
-
22
-
-
0030735169
-
Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome
-
Sun, F.L., Dean, W.L., Kelsey, G., Allen, N.D. and Reik, W. (1997) Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome. Nature, 389, 809-815.
-
(1997)
Nature
, vol.389
, pp. 809-815
-
-
Sun, F.L.1
Dean, W.L.2
Kelsey, G.3
Allen, N.D.4
Reik, W.5
-
23
-
-
1842335753
-
KIP2 indicates a role in Beckwith-Wiedemann syndrome
-
KIP2 indicates a role in Beckwith-Wiedemann syndrome. Nature, 387, 151-158.
-
(1997)
Nature
, vol.387
, pp. 151-158
-
-
Zhang, P.1
Liegeois, N.J.2
Wong, C.3
Finegold, M.4
Hou, H.5
Thompson, J.C.6
Silverman, A.7
Harper, J.W.8
Depinho, R.A.9
Elledge, S.J.10
-
25
-
-
13344278697
-
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments
-
Hoovers, J.M.N., Kalikin, L.M., Johnson, L.A., Alders, M., Redeker, B., Law, D.J., Bliek, J., Steenman, M., Benedict, M., Wiegant, J., Lengauer, C., Taillon-Miller, P., Schlessinger, D., Edwards, M.C., Elledge, S.J., Ivens, A., Westerveld, A., Little, P., Mannens, M. and Feinberg, A.P. (1995) Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments. Proc. Natl Acad. Sci. USA, 92, 12456-12460.
-
(1995)
Proc. Natl Acad. Sci. USA
, vol.92
, pp. 12456-12460
-
-
Hoovers, J.M.N.1
Kalikin, L.M.2
Johnson, L.A.3
Alders, M.4
Redeker, B.5
Law, D.J.6
Bliek, J.7
Steenman, M.8
Benedict, M.9
Wiegant, J.10
Lengauer, C.11
Taillon-Miller, P.12
Schlessinger, D.13
Edwards, M.C.14
Elledge, S.J.15
Ivens, A.16
Westerveld, A.17
Little, P.18
Mannens, M.19
Feinberg, A.P.20
more..
-
26
-
-
0031046285
-
Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements
-
Lee, M.P., Hu, R.-J., Johnson, L.A. and Feinberg, A.P. (1997) Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements. Nature Genet., 15, 181-185.
-
(1997)
Nature Genet.
, vol.15
, pp. 181-185
-
-
Lee, M.P.1
Hu, R.-J.2
Johnson, L.A.3
Feinberg, A.P.4
-
27
-
-
0028939902
-
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15
-
Buiting, K., Saitoh, S., Gross, S., Dittrich, B., Schwartz, S., Nicholls, R.D. and Horsthemke, B. (1995) Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nature Genet., 9, 395-400.
-
(1995)
Nature Genet.
, vol.9
, pp. 395-400
-
-
Buiting, K.1
Saitoh, S.2
Gross, S.3
Dittrich, B.4
Schwartz, S.5
Nicholls, R.D.6
Horsthemke, B.7
-
28
-
-
0033073395
-
Imprinting-mutation mechanisms in Prader-Willi syndrome
-
Ohta, T., Gray, T.A., Rogan, P.K., Buiting, K., Gabriel, J.M., Saitoh, S., Muralidhar, B., Bilienska, B., Krajewska-Walasek, M., Driscoll, D.J., Horsthemke, B., Butler, M.G. and Nicholls, R.D. (1999) Imprinting-mutation mechanisms in Prader-Willi syndrome. Am. J. Hum. Genet., 64, 397-413.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 397-413
-
-
Ohta, T.1
Gray, T.A.2
Rogan, P.K.3
Buiting, K.4
Gabriel, J.M.5
Saitoh, S.6
Muralidhar, B.7
Bilienska, B.8
Krajewska-Walasek, M.9
Driscoll, D.J.10
Horsthemke, B.11
Butler, M.G.12
Nicholls, R.D.13
-
29
-
-
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. (1999) 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. USA, 96, 5203-5208.
-
(1999)
Proc, Natl Acad. Sci. USA
, vol.96
, pp. 5203-5208
-
-
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
-
30
-
-
0030840328
-
Imprinting of Igf2 and H19 from a 130kb YAC transgene
-
Ainscough, J.F.-X., Koide, T., Tada, M., Barton, S. and Surani, M.A. (1997) Imprinting of Igf2 and H19 from a 130kb YAC transgene. Development, 124, 3621-3632.
-
(1997)
Development
, vol.124
, pp. 3621-3632
-
-
Ainscough, J.F.-X.1
Koide, T.2
Tada, M.3
Barton, S.4
Surani, M.A.5
-
31
-
-
0031893360
-
Epigenotype switching of imprintable loci in embryonic germ cells
-
Tada, T., Tada, M., Hilton, K., Barton, S.C., Sado, T., Takagi, N. and Surani, M.A. (1998) Epigenotype switching of imprintable loci in embryonic germ cells. Dev. Genes Evol., 207, 551-561.
-
(1998)
Dev. Genes Evol.
, vol.207
, pp. 551-561
-
-
Tada, T.1
Tada, M.2
Hilton, K.3
Barton, S.C.4
Sado, T.5
Takagi, N.6
Surani, M.A.7
-
32
-
-
0031813176
-
Disruption of primary imprinting during oocyte growth leads to the modified expression of imprinted genes during embryogenesis
-
Obata, Y., Kaneko-Ishino, T., Koide, T., Takai, Y., Ueda, T., Domeki, I., Shiroishi, T., Ishino, F. and Kono, T. (1998) Disruption of primary imprinting during oocyte growth leads to the modified expression of imprinted genes during embryogenesis. Development, 125, 1553-1560.
-
(1998)
Development
, vol.125
, pp. 1553-1560
-
-
Obata, Y.1
Kaneko-Ishino, T.2
Koide, T.3
Takai, Y.4
Ueda, T.5
Domeki, I.6
Shiroishi, T.7
Ishino, F.8
Kono, T.9
-
33
-
-
0033045798
-
Developmental potential of mouse primordial germ cells
-
Kato, Y., Iii, W.M., Hilton, K., Barton, S.C., Tsunoda, Y. and Surani, M.A. (1999) Developmental potential of mouse primordial germ cells. Development, 126, 1823-1832.
-
(1999)
Development
, vol.126
, pp. 1823-1832
-
-
Kato, Y.1
Iii, W.M.2
Hilton, K.3
Barton, S.C.4
Tsunoda, Y.5
Surani, M.A.6
-
34
-
-
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. (1999) Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting. Hum. Mol. Genet., 8, 683-690.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 683-690
-
-
Lee, M.P.1
Brandenburg, S.2
Landes, G.M.3
Adams, M.4
Miller, G.5
Feinberg, A.P.6
-
35
-
-
0029670462
-
Characterization of the human p57KIP2 gene: Alternative splicing, insertion/deletion polymorphisms in VNTR sequences in the coding region, and mutational analysis
-
Tokino, T., Urano, T., Furuhata, T., Matsushima, M., Miyatsu, T., Sasaki, S. and Nakamura, Y. (1996) Characterization of the human p57KIP2 gene: alternative splicing, insertion/deletion polymorphisms in VNTR sequences in the coding region, and mutational analysis. Hum. Genet., 97, 625-631.
-
(1996)
Hum. Genet.
, vol.97
, pp. 625-631
-
-
Tokino, T.1
Urano, T.2
Furuhata, T.3
Matsushima, M.4
Miyatsu, T.5
Sasaki, S.6
Nakamura, Y.7
-
36
-
-
1842364873
-
Embryonic germ cells induce epigenetic reprogramming of somatic nucleus in hybrid cells
-
Tada, M., Tada, T., Lefebvre, L., Barton, S.C. and Surani, M.A. (1997) Embryonic germ cells induce epigenetic reprogramming of somatic nucleus in hybrid cells. EMBO J., 16, 6510-6520.
-
(1997)
EMBO J.
, vol.16
, pp. 6510-6520
-
-
Tada, M.1
Tada, T.2
Lefebvre, L.3
Barton, S.C.4
Surani, M.A.5
-
37
-
-
0031149162
-
DNA methylation: A molecular lock
-
Siegfried, Z. and Cedar, H. (1997) DNA methylation: a molecular lock. Curr. Biol., 7, R305-R307.
-
(1997)
Curr. Biol.
, vol.7
-
-
Siegfried, Z.1
Cedar, H.2
-
38
-
-
0002958296
-
Embryo-derived stem cell lines
-
Robertson, E.J. (ed.), IRL Press, Oxford
-
Robertson, E.J. (1987) Embryo-derived stem cell lines. In Robertson, E.J. (ed.), Teratocarcinomas and Embryonic Stem Cells: A Practical Approach. IRL Press, Oxford, pp. 71-112.
-
(1987)
Teratocarcinomas and Embryonic Stem Cells: A Practical Approach
, pp. 71-112
-
-
Robertson, E.J.1
-
39
-
-
0030034110
-
Withdrawal of differentiation inhibitory activity/ leukemia inhibitory factor up-regulates D-type cyclins and cyclin-dependent kinase inhibitors in mouse embryonic stem cells
-
Savatier, P., Lapillonne, H., van Grunsven, L.A., Rudkin, B.B. and Samarut, J. (1996) Withdrawal of differentiation inhibitory activity/ leukemia inhibitory factor up-regulates D-type cyclins and cyclin-dependent kinase inhibitors in mouse embryonic stem cells. Oncogene, 12, 309-322.
-
(1996)
Oncogene
, vol.12
, pp. 309-322
-
-
Savatier, P.1
Lapillonne, H.2
Van Grunsven, L.A.3
Rudkin, B.B.4
Samarut, J.5
-
40
-
-
0031788639
-
LCR-dependent gene expression in beta-globin YAC transgenics: Detailed structural studies validate functional analysis even in the presence of fragmented YACs
-
Peterson, K.R., Navas, P.A., Li, Q. and Stamatoyannopoulos, G. (1998) LCR-dependent gene expression in beta-globin YAC transgenics: detailed structural studies validate functional analysis even in the presence of fragmented YACs. Hum. Mol. Genet., 7, 2079-2088.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 2079-2088
-
-
Peterson, K.R.1
Navas, P.A.2
Li, Q.3
Stamatoyannopoulos, G.4
-
41
-
-
0030581164
-
Influence of PAX6 gene dosage on development: Overexpression causes severe eye abnormalities
-
Schedl, A., Ross, A., Lee, M., Engelkamp, D., Rashbass, P., van Heyningen, V. and Hastie, N.D. (1996) Influence of PAX6 gene dosage on development: overexpression causes severe eye abnormalities. Cell, 86, 71-82.
-
(1996)
Cell
, vol.86
, pp. 71-82
-
-
Schedl, A.1
Ross, A.2
Lee, M.3
Engelkamp, D.4
Rashbass, P.5
Van Heyningen, V.6
Hastie, N.D.7
-
42
-
-
0032565753
-
Imprinting of the mouse Igf2r gene depends on an intronic CpG island
-
Wutz, A. and Barlow, D.P. (1998) Imprinting of the mouse Igf2r gene depends on an intronic CpG island. Mol. Cell. Endocrinol., 140, 9-14.
-
(1998)
Mol. Cell. Endocrinol.
, vol.140
, pp. 9-14
-
-
Wutz, A.1
Barlow, D.P.2
-
43
-
-
0030298416
-
The vagaries of variegating transgenes
-
Martin, D.I. and Whitelaw, E. (1996) The vagaries of variegating transgenes. Bioessays, 18, 919-923.
-
(1996)
Bioessays
, vol.18
, pp. 919-923
-
-
Martin, D.I.1
Whitelaw, E.2
-
44
-
-
0031984304
-
Repeat-induced gene silencing in mammals
-
Garrick, D., Fiering, S., Martin, D.I. and Whitelaw, E. (1998) Repeat-induced gene silencing in mammals. Nature Genet., 18, 56-59.
-
(1998)
Nature Genet.
, vol.18
, pp. 56-59
-
-
Garrick, D.1
Fiering, S.2
Martin, D.I.3
Whitelaw, E.4
-
45
-
-
0027303619
-
Parental imprinting of an Igf-2 transgene
-
Lee, J.E., Tantravahi, U., Boyle, A.L. and Efstratiadis, A. (1993) Parental imprinting of an Igf-2 transgene. Mol. Reprod. Dev., 35, 382-390.
-
(1993)
Mol. Reprod. Dev.
, vol.35
, pp. 382-390
-
-
Lee, J.E.1
Tantravahi, U.2
Boyle, A.L.3
Efstratiadis, A.4
-
46
-
-
10544222019
-
Human huntingtin derived from YAC transgenes compensates for loss of murine huntingtin by rescue of the embryonic lethal phenotype
-
Hedgson, J.G., Smith, D.J., McCutcheon, K., Koide, H.B., Nishiyama, K., Dinulos, M.B., Stevens, M.E., Bissada, N., Nasir, J., Kanazawa, I., Disteche, C.M., Rubin, E.M. and Hayden, M.R. (1996) Human huntingtin derived from YAC transgenes compensates for loss of murine huntingtin by rescue of the embryonic lethal phenotype. Hum. Mol. Genet., 5, 1875-1885.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1875-1885
-
-
Hedgson, J.G.1
Smith, D.J.2
McCutcheon, K.3
Koide, H.B.4
Nishiyama, K.5
Dinulos, M.B.6
Stevens, M.E.7
Bissada, N.8
Nasir, J.9
Kanazawa, I.10
Disteche, C.M.11
Rubin, E.M.12
Hayden, M.R.13
-
47
-
-
0030853895
-
Complementation of null CF mice with a human CFTR YAC transgene
-
Manson, A.L., Trezise, A.E., MacVinish, L.J., Kasschau, K.D., Birchall, N., Episkopou, V., Vassaux, G., Evans, M.J., Colledge, W.H., Cuthbert, A.W. and Huxley, C. (1997) Complementation of null CF mice with a human CFTR YAC transgene. EMBO J., 16, 4238-4249.
-
(1997)
EMBO J.
, vol.16
, pp. 4238-4249
-
-
Manson, A.L.1
Trezise, A.E.2
MacVinish, L.J.3
Kasschau, K.D.4
Birchall, N.5
Episkopou, V.6
Vassaux, G.7
Evans, M.J.8
Colledge, W.H.9
Cuthbert, A.W.10
Huxley, C.11
-
48
-
-
0030758466
-
The X-linked immunodeficiency defect in the mouse is corrected by expression of human Bruton's tyrosine kinase from a yeast artificial chromosome transgene
-
Maas, A., Dingjan, G.M., Savelkoul, H.F., Kinnon, C., Grosveld, F. and Hendriks, R.W. (1997) The X-linked immunodeficiency defect in the mouse is corrected by expression of human Bruton's tyrosine kinase from a yeast artificial chromosome transgene. Eur. J. Immunol, 27, 2180-2187.
-
(1997)
Eur. J. Immunol
, vol.27
, pp. 2180-2187
-
-
Maas, A.1
Dingjan, G.M.2
Savelkoul, H.F.3
Kinnon, C.4
Grosveld, F.5
Hendriks, R.W.6
-
49
-
-
0032479079
-
Going the distance: A current view of enhancer action
-
Blackwood, E.M. and Kadonaga, J.T. (1998) Going the distance: a current view of enhancer action. Science, 281, 60-63.
-
(1998)
Science
, vol.281
, pp. 60-63
-
-
Blackwood, E.M.1
Kadonaga, J.T.2
-
50
-
-
0032509990
-
Location of enhancers is essential for the imprinting of H19 and Igf2 genes
-
Webber, A.L., Ingram, R.S., Levorse, J.M. and Tilghman, S.M. (1998) Location of enhancers is essential for the imprinting of H19 and Igf2 genes. Nature, 391, 711-715.
-
(1998)
Nature
, vol.391
, pp. 711-715
-
-
Webber, A.L.1
Ingram, R.S.2
Levorse, J.M.3
Tilghman, S.M.4
-
51
-
-
0029807080
-
A novel human homologue of yeast nucleosome assembly protein, 65 kb centromeric to the ps7KIP2 gene, is biallelically expressed in fetal and adult tissues
-
Hu, R.J., Lee, M.P., Johnson, L.A. and Feinberg, A.P. (1996) A novel human homologue of yeast nucleosome assembly protein, 65 kb centromeric to the pS7KIP2 gene, is biallelically expressed in fetal and adult tissues. Hum. Mol. Genet., 5, 1743-1748.
-
(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
-
52
-
-
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. (1997) 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)
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
-
53
-
-
0031844688
-
Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster
-
Caspary, T., Cleary, M.A., Baker, C.C., Guan, X.J. and Tilghman, S.M. (1998) Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster. Mol. Cell. Biol., 18, 3466-3474.
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 3466-3474
-
-
Caspary, T.1
Cleary, M.A.2
Baker, C.C.3
Guan, X.J.4
Tilghman, S.M.5
-
54
-
-
0004136246
-
-
Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
-
Sambrook, J., Fritsch, E.F. and Maniatis, T. (1989) Molecular Cloning: A Laboratory Manual, 2nd edn. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
-
(1989)
Molecular Cloning: A Laboratory Manual, 2nd Edn.
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
55
-
-
0003799070
-
-
Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
-
Hogan, B., Beddington, R., Constantin., F. and Lacy, E. (1994) Manipulating the Mouse Embryo: A Laboratory Manual, 2nd edn. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
-
(1994)
Manipulating the Mouse Embryo: A Laboratory Manual, 2nd Edn.
-
-
Hogan, B.1
Beddington, R.2
Constantin, F.3
Lacy, E.4
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