-
1
-
-
0036144048
-
DNA methylation patterns and epigenetic memory
-
Bird, A. (2002) DNA methylation patterns and epigenetic memory. Genes Dev., 16, 6-21.
-
(2002)
Genes Dev.
, vol.16
, pp. 6-21
-
-
Bird, A.1
-
2
-
-
0036733675
-
Chromatin modification and epigenetic reprogramming in mammalian development
-
Li, E. (2002) Chromatin modification and epigenetic reprogramming in mammalian development. Nat. Rev. Genet., 3, 662-673.
-
(2002)
Nat. Rev. Genet.
, vol.3
, pp. 662-673
-
-
Li, E.1
-
3
-
-
0035839136
-
Translating the histone code
-
Jenuwein, T. and Allis, C.D. (2001) Translating the histone code. Science, 293, 1074-1780.
-
(2001)
Science
, vol.293
, pp. 1074-1780
-
-
Jenuwein, T.1
Allis, C.D.2
-
4
-
-
0027172683
-
Relaxation of imprinted genes in human cancer
-
Rainier, S., Johnson, L.A., Dobry, C.J., Ping, A.P., Grundy, P.E. and Feinberg, A.P. (1993) Relaxation of imprinted genes in human cancer. Nature, 362, 747-749.
-
(1993)
Nature
, vol.362
, pp. 747-749
-
-
Rainier, S.1
Johnson, L.A.2
Dobry, C.J.3
Ping, A.P.4
Grundy, P.E.5
Feinberg, A.P.6
-
5
-
-
0027285258
-
Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumor
-
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' tumor. Nature, 362, 749-751.
-
(1993)
Nature
, vol.362
, pp. 749-751
-
-
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
-
6
-
-
0033036021
-
Genomic imprinting: Implications for human disease
-
Falls, J.G., Pulford, D.J., Wylie, A.A. and Jirtle, R.L. (1999) Genomic imprinting: implications for human disease. Am. J. Pathol., 154, 635-647.
-
(1999)
Am. J. Pathol.
, vol.154
, pp. 635-647
-
-
Falls, J.G.1
Pulford, D.J.2
Wylie, A.A.3
Jirtle, R.L.4
-
7
-
-
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, 1276-1280.
-
(1998)
Nat. Med.
, vol.4
, pp. 1276-1280
-
-
Cui, H.1
Horon, I.L.2
Ohlsson, R.3
Hamilton, S.R.4
Feinberg, A.P.5
-
8
-
-
0027180213
-
The insulin-like growth factor type-2 receptor gene is imprinted in the mouse but not in humans
-
Kalscheuer, V.M., Mariman, E.C., Schepens, M.T., Rehder, H. and Ropers, H.H. (1993) The insulin-like growth factor type-2 receptor gene is imprinted in the mouse but not in humans. Nat. Genet., 5, 74-78.
-
(1993)
Nat. Genet.
, vol.5
, pp. 74-78
-
-
Kalscheuer, V.M.1
Mariman, E.C.2
Schepens, M.T.3
Rehder, H.4
Ropers, H.H.5
-
9
-
-
0027716060
-
Functional polymorphism in the parental imprinting of the human IGF2R gene
-
Xu, Y., Goodyer, C.G., Deal, C. and Polychronakos, C. (1993) Functional polymorphism in the parental imprinting of the human IGF2R gene. Biochem. Biophys. Res. Commun., 197, 747-754.
-
(1993)
Biochem. Biophys. Res. Commun.
, vol.197
, pp. 747-754
-
-
Xu, Y.1
Goodyer, C.G.2
Deal, C.3
Polychronakos, C.4
-
10
-
-
0030920665
-
Polymorphic and tissue-specific imprinting of the human Wilms tumor gene, WT1
-
Nishiwaki, K., Niikawa, N. and Ishikawa, M. (1997) Polymorphic and tissue-specific imprinting of the human Wilms tumor gene, WT1. Jpn. J. Hum. Genet., 42, 205-211.
-
(1997)
Jpn. J. Hum. Genet.
, vol.42
, pp. 205-211
-
-
Nishiwaki, K.1
Niikawa, N.2
Ishikawa, M.3
-
11
-
-
0034811734
-
Epigenetic heterogeneity at imprinted loci in normal populations
-
Sakatani, T., Wei, M., Katoh, M., Okita, C., Wada, D., Mitsuya, K., Meguro, M., Ikeguchi, M., Ito, H., Tycko, B. and Oshimura, M. (2001) Epigenetic heterogeneity at imprinted loci in normal populations. Biochem. Biophys. Res. Commun., 283, 1124-1130.
-
(2001)
Biochem. Biophys. Res. Commun.
, vol.283
, pp. 1124-1130
-
-
Sakatani, T.1
Wei, M.2
Katoh, M.3
Okita, C.4
Wada, D.5
Mitsuya, K.6
Meguro, M.7
Ikeguchi, M.8
Ito, H.9
Tycko, B.10
Oshimura, M.11
-
12
-
-
0035895208
-
Loss of imprinting of the insulin-like growth factor II gene occurs by biallelic methylation in a core region of H19-associated CTCF-binding sites in colorectal cancer
-
Nakagawa, H., Chadwick, R.B., Peltomaki, P., Plass, C., Nakamura, Y. and de La Chapelle, A. (2001) Loss of imprinting of the insulin-like growth factor II gene occurs by biallelic methylation in a core region of H19-associated CTCF-binding sites in colorectal cancer. Proc. Natl Acad. Sci. USA, 98, 591-596.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 591-596
-
-
Nakagawa, H.1
Chadwick, R.B.2
Peltomaki, P.3
Plass, C.4
Nakamura, Y.5
de La Chapelle, A.6
-
13
-
-
0034162161
-
Symmetric and asymmetric DNA methylation in the human IGF2-H19 imprinted region
-
Vu, T.H., Li, T., Nguyen, D., Nguyen, B.T., Yao, X.M., Hu, J.F. and Hoffman, A.R. (2000) Symmetric and asymmetric DNA methylation in the human IGF2-H19 imprinted region. Genomics, 64, 132-143.
-
(2000)
Genomics
, vol.64
, pp. 132-143
-
-
Vu, T.H.1
Li, T.2
Nguyen, D.3
Nguyen, B.T.4
Yao, X.M.5
Hu, J.F.6
Hoffman, A.R.7
-
14
-
-
0034658545
-
H19 and Igf2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream H19
-
Srivastava, M., Hsieh, S., Grinberg, A., Williams-Simons, L., Huang, S.P. and Pfeifer, K. (2000) H19 and Igf2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream H19. Genes Dev., 14, 1186-1195.
-
(2000)
Genes Dev.
, vol.14
, pp. 1186-1195
-
-
Srivastava, M.1
Hsieh, S.2
Grinberg, A.3
Williams-Simons, L.4
Huang, S.P.5
Pfeifer, K.6
-
15
-
-
0034713275
-
CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus
-
Hark, A.T., Schroenherr, C.J., Katz, D.J., Ingram, R.S., Levorse, J.M. and Tilghman, S.M. (2000) CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus. Nature, 405, 486-489.
-
(2000)
Nature
, vol.405
, pp. 486-489
-
-
Hark, A.T.1
Schroenherr, C.J.2
Katz, D.J.3
Ingram, R.S.4
Levorse, J.M.5
Tilghman, S.M.6
-
16
-
-
0035510088
-
Large scale mapping of methylcytosines in CTCF-binding sites in the human H19 promoter and aberrant hypomethylation in human bladder cancer
-
Takai, D., Gonzales, F.A., Tsai, Y.C., Thayer, M.J. and Jones, P.A. (2001) Large scale mapping of methylcytosines in CTCF-binding sites in the human H19 promoter and aberrant hypomethylation in human bladder cancer. Hum. Mol. Genet., 10, 2619-2626.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 2619-2626
-
-
Takai, D.1
Gonzales, F.A.2
Tsai, Y.C.3
Thayer, M.J.4
Jones, P.A.5
-
17
-
-
0028864462
-
Conservation of a maternal-specific methylation signal at the human IGF2R locus
-
Smrzka, O.W., Fae, I., Stoger, R., Kurzbauer, R., Fisher, G.F., Henn, T., Weith, A. and Barlow, D.P. (1995) Conservation of a maternal-specific methylation signal at the human IGF2R locus. Hum. Mol. Genet., 4, 1945-1952.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1945-1952
-
-
Smrzka, O.W.1
Fae, I.2
Stoger, R.3
Kurzbauer, R.4
Fisher, G.F.5
Henn, T.6
Weith, A.7
Barlow, D.P.8
-
18
-
-
0026546877
-
A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands
-
Frommer, M., McDonald, L.E., Millar, D.S., Collis, C.M., Watt, F., Grigg, G.W., Molloy, P.L. and Paul, C.L. (1992) A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands. Proc. Natl Acad. Sci. USA, 89, 1827-1831.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 1827-1831
-
-
Frommer, M.1
McDonald, L.E.2
Millar, D.S.3
Collis, C.M.4
Watt, F.5
Grigg, G.W.6
Molloy, P.L.7
Paul, C.L.8
-
19
-
-
0028096611
-
High sensitivity mapping of methylated cytosines
-
Clark, S.J., Harrison, J., Paul, C.L. and Frommer, M. (1994) High sensitivity mapping of methylated cytosines. Nucl. Acids Res., 22, 2990-2997.
-
(1994)
Nucl. Acids Res.
, vol.22
, pp. 2990-2997
-
-
Clark, S.J.1
Harrison, J.2
Paul, C.L.3
Frommer, M.4
-
20
-
-
0036566806
-
Heteroduplexes in mixed-template amplifications: Formation, consequence and elimination by 'reconditioning PCR'
-
Thompson, J.R., Marcelino, L.A. and Polz, M.F. (2002) Heteroduplexes in mixed-template amplifications: formation, consequence and elimination by 'reconditioning PCR'. Nucl. Acids Res., 30, 2083-2088.
-
(2002)
Nucl. Acids Res.
, vol.30
, pp. 2083-2088
-
-
Thompson, J.R.1
Marcelino, L.A.2
Polz, M.F.3
-
21
-
-
0034081245
-
Heteroduplex resolution using T7 endonuclease I in microbial community analyses
-
680, 681
-
Lowell, J.L. and Klein, D.A. (2000) Heteroduplex resolution using T7 endonuclease I in microbial community analyses. Biotechniques, 28, 676-678, 680, 681.
-
(2000)
Biotechniques
, vol.28
, pp. 676-678
-
-
Lowell, J.L.1
Klein, D.A.2
-
22
-
-
0035407651
-
Bisulfite genomic sequencing: Systematic investigation of critical experimental parameters
-
Grunau, C., Clark, S.J. and Rosenthal, A. (2001) Bisulfite genomic sequencing: systematic investigation of critical experimental parameters. Nucl. Acids Res., 29, e65.
-
(2001)
Nucl. Acids Res.
, vol.29
-
-
Grunau, C.1
Clark, S.J.2
Rosenthal, A.3
-
23
-
-
0036311202
-
Identification and resolution of artifacts in bisulfite sequencing
-
Warnecke, P.M., Stirzaker, C., Song, J., Grunau, C., Melki, J.R. and Clark, S.J. (2002) Identification and resolution of artifacts in bisulfite sequencing. Methods, 27, 101-107.
-
(2002)
Methods
, vol.27
, pp. 101-107
-
-
Warnecke, P.M.1
Stirzaker, C.2
Song, J.3
Grunau, C.4
Melki, J.R.5
Clark, S.J.6
-
24
-
-
0025170997
-
Mechanisms of DNA-mismatch correction
-
Grilley, M., Holmes, J., Yashar, B. and Modrich, P. (1990) Mechanisms of DNA-mismatch correction. Mutat. Res., 236, 253-267.
-
(1990)
Mutat. Res.
, vol.236
, pp. 253-267
-
-
Grilley, M.1
Holmes, J.2
Yashar, B.3
Modrich, P.4
-
25
-
-
0034426034
-
Hot-stop PCR: A simple and general assay for linear quantification of allele ratios
-
Uejima, H., Lee, M.P., Cui, H. and Feinberg, A.P. (2000) Hot-stop PCR: a simple and general assay for linear quantification of allele ratios. Nat. Genet., 25, 375-376.
-
(2000)
Nat. Genet.
, vol.25
, pp. 375-376
-
-
Uejima, H.1
Lee, M.P.2
Cui, H.3
Feinberg, A.P.4
-
26
-
-
0028804071
-
M6P/IGF2R gene is mutated in human hepatocellular carcinomas with loss of heterozigosity
-
De Souza, A.T., Hankins, G.R., Washington, M.K., Orton, T.C. and Jirtle, R.L. (1995) M6P/IGF2R gene is mutated in human hepatocellular carcinomas with loss of heterozigosity. Nat. Genet., 11, 447-449.
-
(1995)
Nat. Genet.
, vol.11
, pp. 447-449
-
-
De Souza, A.T.1
Hankins, G.R.2
Washington, M.K.3
Orton, T.C.4
Jirtle, R.L.5
-
27
-
-
0029934868
-
M6P/IGF2R receptor: A candidate breast tumor suppressor gene
-
Hankins, G.R., De Souza, A.T., Bentley, R.C., Patel, M.R., Marks, J.R., Iglehart, J.D. and Jirtle, R.L. (1996) M6P/IGF2R receptor: a candidate breast tumor suppressor gene. Oncogene, 12, 2003-2009.
-
(1996)
Oncogene
, vol.12
, pp. 2003-2009
-
-
Hankins, G.R.1
De Souza, A.T.2
Bentley, R.C.3
Patel, M.R.4
Marks, J.R.5
Iglehart, J.D.6
Jirtle, R.L.7
-
28
-
-
0030889737
-
Aberrant imprinting of the insulin-like growth factor II receptor gene in Wilms' tumor
-
Xu, Y.Q., Grundy, P. and Polychronakos, C. (1997) Aberrant imprinting of the insulin-like growth factor II receptor gene in Wilms' tumor. Oncogene, 14, 1041-1046.
-
(1997)
Oncogene
, vol.14
, pp. 1041-1046
-
-
Xu, Y.Q.1
Grundy, P.2
Polychronakos, C.3
-
29
-
-
0033593288
-
The sins of the fathers and mothers: Genomic imprinting in mammalian development
-
Tilgman, S.M. (1999) The sins of the fathers and mothers: genomic imprinting in mammalian development. Cell, 96, 185-193.
-
(1999)
Cell
, vol.96
, pp. 185-193
-
-
Tilgman, S.M.1
-
30
-
-
0027378582
-
Role for DNA methylation in genomic imprinting
-
Li, E., Beard, C. and Jaenisch, R. (1993) Role for DNA methylation in genomic imprinting. Nature, 366, 362-365.
-
(1993)
Nature
, vol.366
, pp. 362-365
-
-
Li, E.1
Beard, C.2
Jaenisch, R.3
-
31
-
-
0032797231
-
Multipoint analysis of human chromosome 11p15/mouse distal chromosome 7: Inclusion of H19/IGF2 in the minimal WT2 region, gene specificity of H19 silencing in Wilms' tumorigenesis and methylation hyper-dependence of H19 imprinting
-
Dao, D., Walsh, C.P., Yuan, L., Gorelov, D., Feng, L., Hensle, T., Nisen, P., Yamashiro, D.J., Bestor, T.H. and Tycko, B. (1999) Multipoint analysis of human chromosome 11p15/mouse distal chromosome 7: Inclusion of H19/IGF2 in the minimal WT2 region, gene specificity of H19 silencing in Wilms' tumorigenesis and methylation hyper-dependence of H19 imprinting. Hum. Mol. Genet., 8, 1337-1352.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1337-1352
-
-
Dao, D.1
Walsh, C.P.2
Yuan, L.3
Gorelov, D.4
Feng, L.5
Hensle, T.6
Nisen, P.7
Yamashiro, D.J.8
Bestor, T.H.9
Tycko, B.10
-
32
-
-
0026678490
-
Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation
-
Allen, R.C., Zoghbi, H.Y., Moseley, A.B., Rosenblatt, H.M. and Belmont, J.W. (1992) Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation. Am. J. Hum. Genet., 51, 1229-1239.
-
(1992)
Am. J. Hum. Genet.
, vol.51
, pp. 1229-1239
-
-
Allen, R.C.1
Zoghbi, H.Y.2
Moseley, A.B.3
Rosenblatt, H.M.4
Belmont, J.W.5
-
33
-
-
0028823339
-
Sex-specific transmission-ratio distorsion of X-chromosome alleles in the offspring of females with nonrandom X-inactivation
-
Naumova, A.K., Bird, L.M., Slamka, C., Fonseca, M., Verner, A.E., Wang, M., Leppert, M., Morgan, K. and Sapienza, C. (1995) Sex-specific transmission-ratio distorsion of X-chromosome alleles in the offspring of females with nonrandom X-inactivation, Dev. Genet., 17, 198-205.
-
(1995)
Dev. Genet.
, vol.17
, pp. 198-205
-
-
Naumova, A.K.1
Bird, L.M.2
Slamka, C.3
Fonseca, M.4
Verner, A.E.5
Wang, M.6
Leppert, M.7
Morgan, K.8
Sapienza, C.9
-
34
-
-
0034565915
-
Natural selection and the function of genome imprinting: Beyond the silenced minority
-
Pardo-Manuel de Villena, F., de la Casa Esperon, E. and Sapienza, C. (2000) Natural selection and the function of genome imprinting: beyond the silenced minority. Trends Genet., 16, 573-579.
-
(2000)
Trends Genet.
, vol.16
, pp. 573-579
-
-
Pardo-Manuel de Villena, F.1
de la Casa Esperon, E.2
Sapienza, C.3
|