-
1
-
-
0023119242
-
Temporal and regional changes in DNA methylation in the embryonic, extraembryonic, and germ cell lineages during mouse development
-
Monk, M., Boubelik, M. and S. Lehnert (1987) Temporal and regional changes in DNA methylation in the embryonic, extraembryonic, and germ cell lineages during mouse development, Development, 99, 371-382.
-
(1987)
Development
, vol.99
, pp. 371-382
-
-
Monk, M.1
Boubelik, M.2
Lehnert, S.3
-
2
-
-
0023503627
-
Differences in DNA methylation during oogenesis and spermatogenesis and their persistence during early embryogenesis in the mouse
-
Sanford, J.P., Clark, H.J., Chapman, V.M. and J. Rossant (1987) Differences in DNA methylation during oogenesis and spermatogenesis and their persistence during early embryogenesis in the mouse, Genes Dev., 1, 1039-1046.
-
(1987)
Genes Dev.
, vol.1
, pp. 1039-1046
-
-
Sanford, J.P.1
Clark, H.J.2
Chapman, V.M.3
Rossant, J.4
-
3
-
-
0025322399
-
Sex difference in methylation of single-copy genes in human meiotic germ cells: Implications for X chromosome inactivation, parental imprinting, and origin of CpG mutations
-
Driscoll, D.J. and B.R. Migeon (1990) Sex difference in methylation of single-copy genes in human meiotic germ cells: implications for X chromosome inactivation, parental imprinting, and origin of CpG mutations, Somatic Cell Mol. Genet., 16, 267-282.
-
(1990)
Somatic Cell Mol. Genet.
, vol.16
, pp. 267-282
-
-
Driscoll, D.J.1
Migeon, B.R.2
-
4
-
-
0025800593
-
Methylation levels of maternal and paternal genomes during preimplantation development
-
Hewlett, S.K. and W. Reik (1991) Methylation levels of maternal and paternal genomes during preimplantation development, Development, 113, 119-127.
-
(1991)
Development
, vol.113
, pp. 119-127
-
-
Hewlett, S.K.1
Reik, W.2
-
5
-
-
0026740497
-
Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line
-
Kafri, T., Ariel, M., Brandeis, M., Shemer, R., Urven, L., McCarrey, J., Cedar, H. and A. Razin (1992) Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line, Genes Dev., 6, 705-714.
-
(1992)
Genes Dev.
, vol.6
, pp. 705-714
-
-
Kafri, T.1
Ariel, M.2
Brandeis, M.3
Shemer, R.4
Urven, L.5
McCarrey, J.6
Cedar, H.7
Razin, A.8
-
6
-
-
0025869047
-
Demethylation of CpG islands in embryonic cells
-
Frank, D., Keshet, I., Shani, M., Levine, A., Razin, A. and H. Cedar (1991) Demethylation of CpG islands in embryonic cells, Nature, 351, 239-241.
-
(1991)
Nature
, vol.351
, pp. 239-241
-
-
Frank, D.1
Keshet, I.2
Shani, M.3
Levine, A.4
Razin, A.5
Cedar, H.6
-
7
-
-
0021237658
-
Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis
-
Surani, M.A.H., Barton, S.C. and M.L. Norrris (1984) Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis, Nature, 308, 548-550.
-
(1984)
Nature
, vol.308
, pp. 548-550
-
-
Surani, M.A.H.1
Barton, S.C.2
Norrris, M.L.3
-
8
-
-
0021145377
-
Role of paternal and maternal genomes in mouse development
-
Barton, S.C., Surani, M.A.H. and Norris, M.L. (1984) Role of paternal and maternal genomes in mouse development, Nature, 311, 374-376.
-
(1984)
Nature
, vol.311
, pp. 374-376
-
-
Barton, S.C.1
Surani, M.A.H.2
Norris, M.L.3
-
9
-
-
0021139084
-
Completion of mouse embryogenesis requires both the maternal and paternal genomes
-
McGrath, J. and D. Solter (1984) Completion of mouse embryogenesis requires both the maternal and paternal genomes, Cell, 37, 179-183.
-
(1984)
Cell
, vol.37
, pp. 179-183
-
-
McGrath, J.1
Solter, D.2
-
10
-
-
0023196308
-
Genomic imprinting determines methylation of parental alleles in transgenic mice
-
Reik, W., Collick, A., Norris, M.L., Barton, S.C. and M.A. Surani (1987) Genomic imprinting determines methylation of parental alleles in transgenic mice, Nature, 328, 248-251.
-
(1987)
Nature
, vol.328
, pp. 248-251
-
-
Reik, W.1
Collick, A.2
Norris, M.L.3
Barton, S.C.4
Surani, M.A.5
-
11
-
-
0023220910
-
Degree of methylation of transgenes is dependent on gamete of origin
-
Sapienza, C., Peterson, A.C., Rossant, J. and R. Balling (1987) Degree of methylation of transgenes is dependent on gamete of origin, Nature, 328, 251-254.
-
(1987)
Nature
, vol.328
, pp. 251-254
-
-
Sapienza, C.1
Peterson, A.C.2
Rossant, J.3
Balling, R.4
-
12
-
-
0023274924
-
Maternal inhibition of hepatitis B surface antigen gene expression in transgenic mice correlates with de novo methylation
-
Hadchouel, M., Farza, H., Simon, D., Tiollais, P. and C. Pourcel (1987) Maternal inhibition of hepatitis B surface antigen gene expression in transgenic mice correlates with de novo methylation, Nature, 329, 454-456.
-
(1987)
Nature
, vol.329
, pp. 454-456
-
-
Hadchouel, M.1
Farza, H.2
Simon, D.3
Tiollais, P.4
Pourcel, C.5
-
13
-
-
0023614187
-
Parental legacy determines methylation and expression of an autosomal transgene: A molecular mechanism for parental imprinting
-
Swain, J.L., Stewart, T.A. and P. Leder (1987) Parental legacy determines methylation and expression of an autosomal transgene: A molecular mechanism for parental imprinting, Cell, 50, 719-727.
-
(1987)
Cell
, vol.50
, pp. 719-727
-
-
Swain, J.L.1
Stewart, T.A.2
Leder, P.3
-
14
-
-
0029054424
-
Regulation of genomic imprinting by gametic and embryonic processes
-
Chaillet, R., Bader, D.S. and P. Leder (1995) Regulation of genomic imprinting by gametic and embryonic processes, Genes Dev., 9, 1177-1187.
-
(1995)
Genes Dev.
, vol.9
, pp. 1177-1187
-
-
Chaillet, R.1
Bader, D.S.2
Leder, P.3
-
15
-
-
0028245837
-
Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineage
-
Michaud, E.J., van Vugt, M.J., Bultman, S.J., Sweet, H.O., Davisson, M.T. and R.P. Woychik (1994) Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineage, Genes Dev., 8, 1463-1472.
-
(1994)
Genes Dev.
, vol.8
, pp. 1463-1472
-
-
Michaud, E.J.1
Van Vugt, M.J.2
Bultman, S.J.3
Sweet, H.O.4
Davisson, M.T.5
Woychik, R.P.6
-
16
-
-
0028048664
-
Neomorphic agouti mutations in obese yellow mice
-
Duhl, D.M.J., Vrieling, H., Miller, K.A., Wolff, G.L. and G.S. Barsh (1994) Neomorphic agouti mutations in obese yellow mice, Nature Genet., 8, 59-65.
-
(1994)
Nature Genet.
, vol.8
, pp. 59-65
-
-
Duhl, D.M.J.1
Vrieling, H.2
Miller, K.A.3
Wolff, G.L.4
Barsh, G.S.5
-
17
-
-
0025716294
-
DNA methylation: Evolution of a bacterial immune function into a regulator of genome structure and activity in higher eukaryotes
-
Bestor, T.H. (1990) DNA methylation: evolution of a bacterial immune function into a regulator of genome structure and activity in higher eukaryotes, Phil. Trans. Royal Soc. Lond. B326, 179-187.
-
(1990)
Phil. Trans. Royal Soc. Lond.
, vol.B326
, pp. 179-187
-
-
Bestor, T.H.1
-
18
-
-
0027280881
-
Methylation and imprinting: From host defense to gene regulation?
-
Barlow, D.P. (1993) Methylation and imprinting: from host defense to gene regulation?, Science, 260, 309-10.
-
(1993)
Science
, vol.260
, pp. 309-310
-
-
Barlow, D.P.1
-
19
-
-
0028851082
-
Characteristics of imprinted genes
-
Neumann, B., Kubicka, P. and D.P. Barlow (1995) Characteristics of imprinted genes, Nature Genet., 9, 12-13.
-
(1995)
Nature Genet.
, vol.9
, pp. 12-13
-
-
Neumann, B.1
Kubicka, P.2
Barlow, D.P.3
-
20
-
-
0030115772
-
Creation of genomic methylation patterns
-
Bestor, T.H. and B. Tycko (1996) Creation of genomic methylation patterns. Nature Genet., 12, 363-367.
-
(1996)
Nature Genet.
, vol.12
, pp. 363-367
-
-
Bestor, T.H.1
Tycko, B.2
-
21
-
-
0028004378
-
Evidence that a complex of SIR proteins interacts with the silencer and telomere-binding protein RAP1
-
Moretti, P., Freeman, K., Coodly, L. and D. Shore (1994) Evidence that a complex of SIR proteins interacts with the silencer and telomere-binding protein RAP1, Genes Dev., 8, 2257-2269.
-
(1994)
Genes Dev.
, vol.8
, pp. 2257-2269
-
-
Moretti, P.1
Freeman, K.2
Coodly, L.3
Shore, D.4
-
22
-
-
0025967857
-
Paternal imprinting of the mouse insulin-like growth factor II gene
-
DeChiara, T.M., Robertson, E.J. and A. Efstratiadis (1991) Paternal imprinting of the mouse insulin-like growth factor II gene, Cell, 64, 849-859.
-
(1991)
Cell
, vol.64
, pp. 849-859
-
-
Dechiara, T.M.1
Robertson, E.J.2
Efstratiadis, A.3
-
23
-
-
0026098090
-
The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus
-
Barlow, D,P, Stoger, R., Hermann, B.G., Saito, K. and N. Schweifer (1991) The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus, Nature, 349, 84-87.
-
(1991)
Nature
, vol.349
, pp. 84-87
-
-
Barlow, D.1
Stoger, R.2
Hermann, B.G.3
Saito, K.4
Schweifer, N.5
-
24
-
-
0025809321
-
Parental imprinting of the mouse H19 gene
-
Bartolomei, M.S., Zemel, S. and S.M. Tilghman (1991) Parental imprinting of the mouse H19 gene, Nature, 351, 153-155.
-
(1991)
Nature
, vol.351
, pp. 153-155
-
-
Bartolomei, M.S.1
Zemel, S.2
Tilghman, S.M.3
-
25
-
-
0026849544
-
Monoallelic expression of the human H19 gene
-
Zhang, Y. and B. Tycko (1992) Monoallelic expression of the human H19 gene. Nature Genet., 1, 40-44.
-
(1992)
Nature Genet.
, vol.1
, pp. 40-44
-
-
Zhang, Y.1
Tycko, B.2
-
26
-
-
0027172683
-
Relaxation of imprinted genes in human cancer
-
Rainier, S., Johnson, L., Dobry, C.J., Ping, A.J., Grundy, P.E. and A.P. Feinberg (1993) Relaxation of imprinted genes in human cancer, Nature, 362, 747-749.
-
(1993)
Nature
, vol.362
, pp. 747-749
-
-
Rainier, S.1
Johnson, L.2
Dobry, C.J.3
Ping, A.J.4
Grundy, P.E.5
Feinberg, A.P.6
-
27
-
-
0027496294
-
Imprinting of human H19: Allele-specific CpG methylation, loss of the active allele in Wilms' tumor and potential for somatic allele switching
-
Zhang, Y., Shields, T., Crenshaw, T., Hao, Y., Moulton, T. and B. Tycko (1993) Imprinting of human H19: allele-specific CpG methylation, loss of the active allele in Wilms' tumor and potential for somatic allele switching, Am. J. Hum. Genet., 53, 113-124.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 113-124
-
-
Zhang, Y.1
Shields, T.2
Crenshaw, T.3
Hao, Y.4
Moulton, T.5
Tycko, B.6
-
28
-
-
0027322519
-
IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome
-
Ohlsson, R., Nystrom, A., Pfeifer-Ohlsson, S., Tohonen, V., Hedbourg, F., Schofield, P., Flam, F. and T.J. Ekstrom (1993) IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome, Nature Genet., 4, 94-97.
-
(1993)
Nature Genet.
, vol.4
, pp. 94-97
-
-
Ohlsson, R.1
Nystrom, A.2
Pfeifer-Ohlsson, S.3
Tohonen, V.4
Hedbourg, F.5
Schofield, P.6
Flam, F.7
Ekstrom, T.J.8
-
29
-
-
0027158855
-
Parental genomic imprinting of the human IGF2 gene
-
Giannoukakis, N., Deal, C., Paquette, J., Goodyer, C.G. and C. Polychronakos (1993) Parental genomic imprinting of the human IGF2 gene, Nature Genet., 4, 98-101.
-
(1993)
Nature Genet.
, vol.4
, pp. 98-101
-
-
Giannoukakis, N.1
Deal, C.2
Paquette, J.3
Goodyer, C.G.4
Polychronakos, C.5
-
30
-
-
0027018063
-
Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region
-
Leff, S.E., Brannan, C.I., Reed, M.L., Ozcelik, T., Francke, U., Copeland, N.J and N.A. Jenkins (1992) Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region, Nature Genet., 2, 259-264.
-
(1992)
Nature Genet.
, vol.2
, pp. 259-264
-
-
Leff, S.E.1
Brannan, C.I.2
Reed, M.L.3
Ozcelik, T.4
Francke, U.5
Copeland, N.J.6
Jenkins, N.A.7
-
31
-
-
0027730805
-
Functional imprinting and epigenetic modification of the human SNRPN gene
-
Glenn, C.C., Porter, K.A., Jong, M.T.C., Nicholls, R.D. and D.J. Driscoll (1993) Functional imprinting and epigenetic modification of the human SNRPN gene, Hum. Mol. Genet., 2, 2001-2005.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 2001-2005
-
-
Glenn, C.C.1
Porter, K.A.2
Jong, M.T.C.3
Nicholls, R.D.4
Driscoll, D.J.5
-
32
-
-
0027172684
-
Parental-origin-specific epigenetic modification of the mouse H19 gene
-
Ferguson-Smith, A.C., Sasaki, H., Cattanach, B.M. and M.A. Surani (1993) Parental-origin-specific epigenetic modification of the mouse H19 gene, Nature, 362, 751-755.
-
(1993)
Nature
, vol.362
, pp. 751-755
-
-
Ferguson-Smith, A.C.1
Sasaki, H.2
Cattanach, B.M.3
Surani, M.A.4
-
33
-
-
0027236694
-
The ontogeny of allele-specific methylation associated with imprinted genes in the mouse
-
Brandeis, M., Kafri, T., Ariel, M., Chaillet, J.R., McCarrey, J., Razin, A. and H. Cedar (1993) The ontogeny of allele-specific methylation associated with imprinted genes in the mouse, EMBO J., 12, 3669-3677.
-
(1993)
EMBO J.
, vol.12
, pp. 3669-3677
-
-
Brandeis, M.1
Kafri, T.2
Ariel, M.3
Chaillet, J.R.4
McCarrey, J.5
Razin, A.6
Cedar, H.7
-
34
-
-
0027203606
-
Epigenetic mechanisms underlying the imprinting of the mouse H19 gene
-
Bartolomei, M.S., Webber, A.L., Brunkow, M.E. and S.M. Tilghman (1993) Epigenetic mechanisms underlying the imprinting of the mouse H19 gene, Genes Dev., 7, 1663-1673.
-
(1993)
Genes Dev.
, vol.7
, pp. 1663-1673
-
-
Bartolomei, M.S.1
Webber, A.L.2
Brunkow, M.E.3
Tilghman, S.M.4
-
35
-
-
0028968205
-
A paternal-specific methylation imprint marks the alleles of the mouse H19 gene
-
Tremblay, K.D., Saam, J.R., Ingram, R.S., Tilghman, S.M. and M.S. Bartolomei (1995) A paternal-specific methylation imprint marks the alleles of the mouse H19 gene, Nature Genet., 9, 407-413.
-
(1995)
Nature Genet.
, vol.9
, pp. 407-413
-
-
Tremblay, K.D.1
Saam, J.R.2
Ingram, R.S.3
Tilghman, S.M.4
Bartolomei, M.S.5
-
36
-
-
0027400888
-
Maternal-specific methylation of the imprinted Igf2r locus identifies the expressed locus as carrying the imprinting signal
-
Stoger, R., Kubicka, P., Liu, C.-G., Kafri, T., Razin, A., Cedar, H. and D.P. Barlow (1993) Maternal-specific methylation of the imprinted Igf2r locus identifies the expressed locus as carrying the imprinting signal, Cell, 73, 61-72.
-
(1993)
Cell
, vol.73
, pp. 61-72
-
-
Stoger, R.1
Kubicka, P.2
Liu, C.-G.3
Kafri, T.4
Razin, A.5
Cedar, H.6
Barlow, D.P.7
-
37
-
-
0028143457
-
Comparative analysis of the Igf-2/H19 imprinted domain: Identification of a highly conserved intergenic DNase I hypersensitive region
-
Koide, T., Ainscough, J., Wijgerde, M. and M.A. Surani (1994) Comparative analysis of the Igf-2/H19 imprinted domain: identification of a highly conserved intergenic DNase I hypersensitive region, Genomics, 24, 1-8.
-
(1994)
Genomics
, vol.24
, pp. 1-8
-
-
Koide, T.1
Ainscough, J.2
Wijgerde, M.3
Surani, M.A.4
-
38
-
-
0028862472
-
Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by an altered imprinting pattern in the IGF2-H19 domain
-
Reik, W., Brown, K.W., Schneid, H., Le Bouc, Y, Bickmore W. and E.R. Maher (1995) Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by an altered imprinting pattern in the IGF2-H19 domain, Hum. Mol. Genet., 4, 2379-2385.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 2379-2385
-
-
Reik, W.1
Brown, K.W.2
Schneid, H.3
Le Bouc, Y.4
Bickmore, W.5
Maher, E.R.6
-
39
-
-
0030052505
-
Gene structure, DNA methylation and imprinted expression of the human SNRPN gene
-
Glenn, C.C., Saitoh, S., Jong, M.T.C., Filbrandt, M.M., Surti, U., Driscoll, D.J. and R.D. Nicholls (1996) Gene structure, DNA methylation and imprinted expression of the human SNRPN gene. Am. J. Hum. Genet., 58, 335-346.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 335-346
-
-
Glenn, C.C.1
Saitoh, S.2
Jong, M.T.C.3
Filbrandt, M.M.4
Surti, U.5
Driscoll, D.J.6
Nicholls, R.D.7
-
40
-
-
0028859287
-
Gamete-specific methylation correlates with imprinting of the murine Xist gene
-
Ariel, M., Robinson, E., McCarrey, J.R. and H. Cedar, (1995) Gamete-specific methylation correlates with imprinting of the murine Xist gene, Nature Genet., 9, 312-315.
-
(1995)
Nature Genet.
, vol.9
, pp. 312-315
-
-
Ariel, M.1
Robinson, E.2
McCarrey, J.R.3
Cedar, H.4
-
41
-
-
0028809295
-
Methylation of the mouse Xist gene in spern and eggs correlates with imprinted Xist expression and paternal X-inactivation
-
Zuccotti, M. and M. Monk (1995) Methylation of the mouse Xist gene in spern and eggs correlates with imprinted Xist expression and paternal X-inactivation, Nature Genet., 9, 316-320.
-
(1995)
Nature Genet.
, vol.9
, pp. 316-320
-
-
Zuccotti, M.1
Monk, M.2
-
42
-
-
0027169927
-
Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients
-
Glenn, C., Nicholls, R.D., Robinson, W.P., Saitoh, S., Niikawa, N., Schinzel, A. Horsthemke, B. and D. Driscoll (1993) Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients, Hum. Mol. Genet., 2, 1377-1382.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1377-1382
-
-
Glenn, C.1
Nicholls, R.D.2
Robinson, W.P.3
Saitoh, S.4
Niikawa, N.5
Schinzel, A.6
Horsthemke, B.7
Driscoll, D.8
-
43
-
-
0028336989
-
Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method
-
Hayashizaki, Y., Shibata, H., Hirotsune, S., Sugino, H., Okazaki, Y., Sasaki, N., Hirose, K., Imoto, H., Okuizumi, H., Muramatsu, M., Komatsubara, H., Shiroishi, T, Moriwaki, K, Katsuki, M., Hatano, N., Sasaki, H., Ueda, T., Mise, N., Takagi, N., Plass, C. and V.M. Chapman (1994) Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method, Nature Genet., 6, 33-40.
-
(1994)
Nature Genet.
, vol.6
, pp. 33-40
-
-
Hayashizaki, Y.1
Shibata, H.2
Hirotsune, S.3
Sugino, H.4
Okazaki, Y.5
Sasaki, N.6
Hirose, K.7
Imoto, H.8
Okuizumi, H.9
Muramatsu, M.10
Komatsubara, H.11
Shiroishi, T.12
Moriwaki, K.13
Katsuki, M.14
Hatano, N.15
Sasaki, H.16
Ueda, T.17
Mise, N.18
Takagi, N.19
Plass, C.20
Chapman, V.M.21
more..
-
44
-
-
0028980026
-
Genomic imprinting of p57Kip2, a cyclin-dependent kinase inhibitor, in mouse
-
Hatada, I. and T. Mukai (1995) Genomic imprinting of p57Kip2, a 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
-
45
-
-
0029024277
-
Disruption of imprinting caused by deletion of the H19 gene region in mice
-
Leighton, P.A., Ingram, R.S., Eggenschwiler, J., Efstratiatis, A. and S.M. Tilghman (1995) Disruption of imprinting caused by deletion of the H19 gene region in mice. Nature, 375, 34-39.
-
(1995)
Nature
, vol.375
, pp. 34-39
-
-
Leighton, P.A.1
Ingram, R.S.2
Eggenschwiler, J.3
Efstratiatis, A.4
Tilghman, S.M.5
-
46
-
-
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 B. Tycko (1996) Chromosome 11p15.5 regional imprinting: comparative analysis of KIP2 and H19 in human tissues and Wilms' tumors. Hum. Mol. Genet., 8, 1101-1108.
-
(1996)
Hum. Mol. Genet.
, vol.8
, pp. 1101-1108
-
-
Chung, W.-Y.1
Yuan, L.2
Feng, L.3
Hensle, T.4
Tycko, B.5
-
47
-
-
0029869293
-
Selective maternal allele loss in human lung cancers of the maternally expressed p57KIP2 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 T. Takahashi (1996) Selective maternal allele loss in human lung cancers of the maternally expressed p57KIP2 gene at 11p15.5. Oncogene, 12, 1365-1368.
-
(1996)
Oncogene
, 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
-
48
-
-
0029978017
-
Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15
-
Matsuoka, S., Thompson, J.S., Edwards, M.C., Barletta, J.M., Grundy, P., Kalikin, L.M., Harper, J.W., Elledge, S.J. and A.P. Feinberg (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
Barletta, J.M.4
Grundy, P.5
Kalikin, L.M.6
Harper, J.W.7
Elledge, S.J.8
Feinberg, A.P.9
-
49
-
-
0024619007
-
Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion
-
Knoll, J.H.M., Nicholls, R.D., Magenis, R.E., Graham, J.M. Jr, Lalande, M. and S.A. Latt (1989) Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion., Am. J. Med. Genet., 32, 285-290.
-
(1989)
Am. J. Med. Genet.
, vol.32
, pp. 285-290
-
-
Knoll, J.H.M.1
Nicholls, R.D.2
Magenis, R.E.3
Graham J.M., Jr.4
Lalande, M.5
Latt, S.A.6
-
50
-
-
0024440608
-
Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome
-
Nicholls, R.D., Knoll, J.H.M., Butler, M.G., Karam, S. and M. Lalande (1989) Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome, Nature, 342, 281-285.
-
(1989)
Nature
, vol.342
, pp. 281-285
-
-
Nicholls, R.D.1
Knoll, J.H.M.2
Butler, M.G.3
Karam, S.4
Lalande, M.5
-
51
-
-
0026080417
-
Uniparental paternal disomy in Angelman's syndrome
-
Malcolm, S., Clayton-Smith, J,. Nichols, M., Robb, S., Webb, T., Armour, J.A.L., Jeffreys, A.J. and M.E. Pembrey (1991) Uniparental paternal disomy in Angelman's syndrome, Lancet, 337, 694-697.
-
(1991)
Lancet
, vol.337
, pp. 694-697
-
-
Malcolm, S.1
Clayton-Smith, J.2
Nichols, M.3
Robb, S.4
Webb, T.5
Armour, J.A.L.6
Jeffreys, A.J.7
Pembrey, M.E.8
-
52
-
-
0026893703
-
Maternal but not paternal transmission of 15q11-13-linked nondeletion Angleman syndrome leads to phenotypic expression
-
Wagstaff, J., Knoll, J.H.M., Glatt, K.A., Shugart, Y.Y., Sommer, A. and M. Lalande (1992) Maternal but not paternal transmission of 15q11-13-linked nondeletion Angleman syndrome leads to phenotypic expression, Nature Genet., 1, 291-294
-
(1992)
Nature Genet.
, vol.1
, pp. 291-294
-
-
Wagstaff, J.1
Knoll, J.H.M.2
Glatt, K.A.3
Shugart, Y.Y.4
Sommer, A.5
Lalande, M.6
-
53
-
-
0027738562
-
Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN gene, Hum
-
Buiting, K. Dittrich, B., Gross, S., Greger, V., Lalande, M., Robinson, W., Mutirangura, A. et al. (1993) Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN gene, Hum. Mol. Genet., 2, 1991-1994.
-
(1993)
Mol. Genet.
, vol.2
, pp. 1991-1994
-
-
Buiting, K.1
Dittrich, B.2
Gross, S.3
Greger, V.4
Lalande, M.5
Robinson, W.6
Mutirangura, A.7
-
54
-
-
0013476457
-
The ZNF127 gene encodes a novel C3HC4 zinc-finger protein and its expression is regulated by genomic imprinting
-
Abstr.
-
Jong, M.T.C., Carey, A.H., Stewart, C.L., Rinchik, E.M., Glenn, C.C., Driscoll, D.J. and R.D. Nicholls (1993) The ZNF127 gene encodes a novel C3HC4 zinc-finger protein and its expression is regulated by genomic imprinting, Am. J. Hum. Genet., 53, Abstr. 697.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 697
-
-
Jong, M.T.C.1
Carey, A.H.2
Stewart, C.L.3
Rinchik, E.M.4
Glenn, C.C.5
Driscoll, D.J.6
Nicholls, R.D.7
-
55
-
-
0028124726
-
Identification of a novel paternally expressed gene in the Prader-Willi syndrome region
-
Wevrick, R., Kerns, J.A. and U. Francke (1994) Identification of a novel paternally expressed gene in the Prader-Willi syndrome region, Hum. Mol. Genet., 3, 1877-1882.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1877-1882
-
-
Wevrick, R.1
Kerns, J.A.2
Francke, U.3
-
56
-
-
0028133293
-
Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region
-
Sutcliffe, J.S., Nakao, M., Christian, S,. Orstavik, K.H., Tommerup, N., Ledbetter, D.H. and A.L. Beaudet (1994) Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region, Nature Genet., 8, 52-58.
-
(1994)
Nature Genet.
, vol.8
, pp. 52-58
-
-
Sutcliffe, J.S.1
Nakao, M.2
Christian, S.3
Orstavik, K.H.4
Tommerup, N.5
Ledbetter, D.H.6
Beaudet, A.L.7
-
57
-
-
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 B. Horsthemke (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
-
58
-
-
0029063587
-
Visualization of chromosomal domains with boundary element-associated factor BEAF-32
-
Zhao, K., Hart, C.M. and U.K. Laemmli (1995) Visualization of chromosomal domains with boundary element-associated factor BEAF-32, Cell, 81, 879-889.
-
(1995)
Cell
, vol.81
, pp. 879-889
-
-
Zhao, K.1
Hart, C.M.2
Laemmli, U.K.3
-
59
-
-
0013280347
-
Genomic imprinting in Wilms' tumor
-
in press
-
Tycko, B. (1996) Genomic imprinting in Wilms' tumor. Med. Ped. Oncol., in press.
-
(1996)
Med. Ped. Oncol.
-
-
Tycko, B.1
-
60
-
-
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. 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, 3-23.
-
(1994)
Eur. J. Hum. Genet.
, vol.2
, pp. 3-23
-
-
Mannens, M.1
Hoovers, J.M.2
Redeker, E.3
Verjaal, M.4
Feinberg, A.P.5
Little, P.6
-
61
-
-
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 J. Squire (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
-
62
-
-
0028356544
-
Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumor
-
Steenman, M.J.C., Rainier, S., Dobry, C.J., Grundy, P., Horon, I.L. and A.P. Feinberg (1994) Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumor, Nature Genet., 7, 433-439.
-
(1994)
Nature Genet.
, vol.7
, pp. 433-439
-
-
Steenman, M.J.C.1
Rainier, S.2
Dobry, C.J.3
Grundy, P.4
Horon, I.L.5
Feinberg, A.P.6
-
63
-
-
0028227938
-
Epigenetic lesions at the H19 locus in Wilms' tumor patients
-
Moulton, T., Crenshaw, T., Hao, Y., Moosikasuwan, J., Lin, N., Dembitzer, F., Hensle, T., Weiss, L., McMorrow, L., Loew, T., Kraus, W., Gerald, W. and B. Tycko (1994) Epigenetic lesions at the H19 locus in Wilms' tumor patients, Nature Genet., 7, 440-447.
-
(1994)
Nature Genet.
, vol.7
, pp. 440-447
-
-
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
Kraus, W.11
Gerald, W.12
Tycko, B.13
-
64
-
-
0028935017
-
Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor
-
Taniguchi, T., Sullivan, M.J., Osamu, O. and A. Reeve (1995) Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor, Proc. Natl. Acad. Sci. USA, 92, 2159-2163.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 2159-2163
-
-
Taniguchi, T.1
Sullivan, M.J.2
Osamu, O.3
Reeve, A.4
-
65
-
-
0028815477
-
Genomic imprinting of Mash2, a mouse gene required for trophoblast development
-
Guillemot, F., Caspary, T., Tilghman, S.M., Copeland, N.G., Gilbert, D.J., Jenkins, N.A. anderson, D.J.., Joyner, A.L., Rossant, J. and A. Nagy (1995) Genomic imprinting of Mash2, a mouse gene required for trophoblast development, Nature Genet., 9, 235-241.
-
(1995)
Nature Genet.
, vol.9
, pp. 235-241
-
-
Guillemot, F.1
Caspary, T.2
Tilghman, S.M.3
Copeland, N.G.4
Gilbert, D.J.5
Jenkins, N.A.6
Anderson, D.J.7
Joyner, A.L.8
Rossant, J.9
Nagy, A.10
-
66
-
-
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., Goy, A., Zelenetz, A.D., Selleri, L. and B. Tycko (1995) 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)
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
Goy, A.8
Zelenetz, A.D.9
Selleri, L.10
Tycko, B.11
-
67
-
-
13344278697
-
Multiple genetic loci within 11p15 defined by Beckwith-Weidemann 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 A. Feinberg (1995) Multiple genetic loci within 11p15 defined by Beckwith-Weidemann 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.20
more..
-
68
-
-
0020986251
-
5-methylcytosine, gene regulation and cancer
-
Riggs, A.D. and P.A. Jones (1983) 5-methylcytosine, gene regulation and cancer, Adv. Cancer Res., 40, 1-28.
-
(1983)
Adv. Cancer Res.
, vol.40
, pp. 1-28
-
-
Riggs, A.D.1
Jones, P.A.2
-
69
-
-
0026708177
-
Targeted mutation of the DNA methyltransferase gene results in embryonic lethality
-
Li, E., Bestor, T.H. and R. Jaenisch (1992) Targeted mutation of the DNA methyltransferase gene results in embryonic lethality, Cell, 69, 915-926.
-
(1992)
Cell
, vol.69
, pp. 915-926
-
-
Li, E.1
Bestor, T.H.2
Jaenisch, R.3
-
70
-
-
0027378582
-
Role for DNA methylation in genomic imprinting
-
Li, E., Beard C. and R. Jaenisch. (1993) Role for DNA methylation in genomic imprinting, JOURNAL, 366, 362-365.
-
(1993)
JOURNAL
, vol.366
, pp. 362-365
-
-
Li, E.1
Beard, C.2
Jaenisch, R.3
-
71
-
-
0027274649
-
Treatment with azacytidine of patients with end-stage beta-thalassemia
-
Lowrey, C.H. and A.W. Nienhuis (1993) Treatment with azacytidine of patients with end-stage beta-thalassemia, New Engl. J. Med., 329, 845-848.
-
(1993)
New Engl. J. Med.
, vol.329
, pp. 845-848
-
-
Lowrey, C.H.1
Nienhuis, A.W.2
-
72
-
-
0023657424
-
Methylation of the Hprt gene on the inactive X occurs after chromosome inactivation
-
Lock, L.F., Takagi, N. and G.R. Martin (1987) Methylation of the Hprt gene on the inactive X occurs after chromosome inactivation, Cell, 48, 39-46.
-
(1987)
Cell
, vol.48
, pp. 39-46
-
-
Lock, L.F.1
Takagi, N.2
Martin, G.R.3
-
73
-
-
0029360421
-
Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies
-
Paldi, A., Gyapay, G. and J. Jami (1995) Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies, Curr. Biol., 5, 1030-1035.
-
(1995)
Curr. Biol.
, vol.5
, pp. 1030-1035
-
-
Paldi, A.1
Gyapay, G.2
Jami, J.3
-
74
-
-
0025965092
-
Sex, maps, and imprinting
-
Thomas, B.J. and R. Rothstein (1991) Sex, maps, and imprinting, Cell, 64, 1-3.
-
(1991)
Cell
, vol.64
, pp. 1-3
-
-
Thomas, B.J.1
Rothstein, R.2
|