-
1
-
-
0035839064
-
Imprinting and the epigenetic asymmetry between parental genomes
-
Ferguson-Smith, A.C. and Surani, M.A. (2001) Imprinting and the epigenetic asymmetry between parental genomes. Science, 293, 1086-1089.
-
(2001)
Science
, vol.293
, pp. 1086-1089
-
-
Ferguson-Smith, A.C.1
Surani, M.A.2
-
2
-
-
0035234557
-
Genomic imprinting: Parental influence on the genome
-
Reik, W. and Walter, J. (2001) Genomic imprinting: parental influence on the genome. Nat. Rev. Genet., 2, 21-32.
-
(2001)
Nat. Rev. Genet.
, vol.2
, pp. 21-32
-
-
Reik, W.1
Walter, J.2
-
3
-
-
0034068372
-
The uniqueness of the imprinting mechanism
-
Sleutels, F., Barlow, D.P. and Lyle, R. (2000) The uniqueness of the imprinting mechanism. Curr. Opin. Genet. Devl., 10, 229-233.
-
(2000)
Curr. Opin. Genet. Devl.
, vol.10
, pp. 229-233
-
-
Sleutels, F.1
Barlow, D.P.2
Lyle, R.3
-
4
-
-
0033593288
-
The sins of the fathers and mothers: Genomic imprinting in mammalian development
-
Tilghman, 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
-
-
Tilghman, S.M.1
-
6
-
-
0035208597
-
Parent-specific complementary patterns of histone H3 lysine 9 and H3 lysine 4 methylation at the Prader-Willi syndrome imprinting center
-
Xin, Z., Allis, C.D. and Wagstaff, J. (2001) Parent-specific complementary patterns of histone H3 lysine 9 and H3 lysine 4 methylation at the Prader-Willi syndrome imprinting center. Am. J. Hum. Genet., 69, 1389-1394.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 1389-1394
-
-
Xin, Z.1
Allis, C.D.2
Wagstaff, J.3
-
7
-
-
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
-
8
-
-
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. Nat. Genet., 9, 395-400.
-
(1995)
Nat. 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
-
9
-
-
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 Beaudet, A.L. (1994) Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region. Nat. Genet., 8, 5-7.
-
(1994)
Nat. Genet.
, vol.8
, pp. 5-7
-
-
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
-
10
-
-
0028862472
-
Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain
-
Reik, W., Brown, K.W., Schneid, H., Le Bouc, Y., Bickmore, W. and Maher, E.R. (1995) Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by 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
-
11
-
-
0034103656
-
De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch
-
Bielinska, B., Blaydes, S.M., Buiting, K., Yang, T., Krajewska-Walasek, M., Horsthemke, B. and Brannan, C.I. (2000) De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch. Nat. Genet., 25, 74-78.
-
(2000)
Nat. Genet.
, vol.25
, pp. 74-78
-
-
Bielinska, B.1
Blaydes, S.M.2
Buiting, K.3
Yang, T.4
Krajewska-Walasek, M.5
Horsthemke, B.6
Brannan, C.I.7
-
12
-
-
0034713275
-
CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus
-
Hark, A.T., Schoenherr, 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
Schoenherr, C.J.2
Katz, D.J.3
Ingram, R.S.4
Levorse, J.M.5
Tilghman, S.M.6
-
13
-
-
0034644120
-
Functional association of CTCF with the insulator upstream of the H19 gene is parent of origin-specific and methylation-sensitive
-
Kanduri, C., Pant, V., Loukinov, D., Pugacheva, E., Qi, C.F., Wolffe, A., Ohlsson, R. and Lobanenkov, V.V. (2000) Functional association of CTCF with the insulator upstream of the H19 gene is parent of origin-specific and methylation-sensitive. Curr. Biol., 10, 853-856.
-
(2000)
Curr. Biol.
, vol.10
, pp. 853-856
-
-
Kanduri, C.1
Pant, V.2
Loukinov, D.3
Pugacheva, E.4
Qi, C.F.5
Wolffe, A.6
Ohlsson, R.7
Lobanenkov, V.V.8
-
14
-
-
0033870806
-
A transcriptional insulator at the imprinted H19/Igf2 locus
-
Kaffer, C.R., Srivastava, M., Park, K.Y, Ives, E., Hsieh, S., Batlle, J., Grinberg, A., Huang, S.P. and Pfeifer, K. (2000) A transcriptional insulator at the imprinted H19/Igf2 locus. Genes Devl., 14, 1908-1919.
-
(2000)
Genes Devl.
, vol.14
, pp. 1908-1919
-
-
Kaffer, C.R.1
Srivastava, M.2
Park, K.Y.3
Ives, E.4
Hsieh, S.5
Batlle, J.6
Grinberg, A.7
Huang, S.P.8
Pfeifer, K.9
-
15
-
-
0034193691
-
Maternal-specific footprints at putative CTCF sites in the H19 imprinting control region give evidence for insulator function
-
Szabo, P., Tang, S.H., Rentsendorj, A., Pfeifer, G.P. and Mann, J.R. (2000) Maternal-specific footprints at putative CTCF sites in the H19 imprinting control region give evidence for insulator function. Curr. Biol., 10, 607-610.
-
(2000)
Curr. Biol.
, vol.10
, pp. 607-610
-
-
Szabo, P.1
Tang, S.H.2
Rentsendorj, A.3
Pfeifer, G.P.4
Mann, J.R.5
-
16
-
-
0034713375
-
Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene
-
Bell, A.C. and Felsenfeld, G. (2000) Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene. Nature, 405, 482-485.
-
(2000)
Nature
, vol.405
, pp. 482-485
-
-
Bell, A.C.1
Felsenfeld, G.2
-
17
-
-
0033832962
-
Deletion of a silencer element disrupts H19 imprinting independently of a DNA methylation epigenetic switch
-
Drewell, R.A., Brenton, J.D., Ainscough, J.F., Barton, S.C., Hilton, K.J., Arney, K.L., Dandolo, L. and Surani, M.A. (2000) Deletion of a silencer element disrupts H19 imprinting independently of a DNA methylation epigenetic switch. Development, 127, 3419-3428.
-
(2000)
Development
, vol.127
, pp. 3419-3428
-
-
Drewell, R.A.1
Brenton, J.D.2
Ainscough, J.F.3
Barton, S.C.4
Hilton, K.J.5
Arney, K.L.6
Dandolo, L.7
Surani, M.A.8
-
18
-
-
0035796466
-
An upstream repressor element plays a role in Igf2 imprinting
-
Eden, S., Constancia, M., Hashmishony, T., Dean, W., Goldstein, B., Johnson, A.C., Keshet, I., Reik, W. and Cedar, H. (2001) An upstream repressor element plays a role in Igf2 imprinting. EMBO J., 20, 3518-3525.
-
(2001)
EMBO J.
, vol.20
, pp. 3518-3525
-
-
Eden, S.1
Constancia, M.2
Hashmishony, T.3
Dean, W.4
Goldstein, B.5
Johnson, A.C.6
Keshet, I.7
Reik, W.8
Cedar, H.9
-
19
-
-
0342572600
-
Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19
-
Constancia, M., Dean, W., Lopes, S., Moore, T., Kelsey, G. and Reik, W. (2000) Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19. Nat. Genet., 26, 203-206.
-
(2000)
Nat. Genet.
, vol.26
, pp. 203-206
-
-
Constancia, M.1
Dean, W.2
Lopes, S.3
Moore, T.4
Kelsey, G.5
Reik, W.6
-
20
-
-
0035680734
-
An intragenic methylated region in the imprinted Igf2 gene augments transcription
-
Murrell, A., Heeson, S., Bowden, L., Constancia, M., Dean, W., Kelsey, G. and Reik, W. (2001) An intragenic methylated region in the imprinted Igf2 gene augments transcription. EMBO Rep., 2, 1101-1106.
-
(2001)
EMBO Rep.
, vol.2
, pp. 1101-1106
-
-
Murrell, A.1
Heeson, S.2
Bowden, L.3
Constancia, M.4
Dean, W.5
Kelsey, G.6
Reik, W.7
-
21
-
-
0027937839
-
Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes
-
Feil, R., Walter, J., Allen, N.D. and Reik, W. (1994) Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes. Development, 120, 2933-2943.
-
(1994)
Development
, vol.120
, pp. 2933-2943
-
-
Feil, R.1
Walter, J.2
Allen, N.D.3
Reik, W.4
-
22
-
-
0030730287
-
Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2
-
Moore, T., Constancia, M., Zubair, M., Bailleul, B., Feil, R., Sasaki, H. and Reik, W. (1997) Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2. Proc. Natl Acad. Sci. USA, 94, 12509-12514.
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 12509-12514
-
-
Moore, T.1
Constancia, M.2
Zubair, M.3
Bailleul, B.4
Feil, R.5
Sasaki, H.6
Reik, W.7
-
23
-
-
0030931672
-
Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans
-
. Forné, T., Oswald, J., Dean, W., Saam, J.R., Bailleul, B., Dandolo, L., Tilghman, S.M., Walter, J. and Reik, W. (1997) Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans. Proc. Natl Acad. Sci. USA, 94, 10243-10248.
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 10243-10248
-
-
Forné, T.1
Oswald, J.2
Dean, W.3
Saam, J.R.4
Bailleul, B.5
Dandolo, L.6
Tilghman, S.M.7
Walter, J.8
Reik, W.9
-
24
-
-
0031279892
-
The pre-implantation ontogeny of the H19 methylation imprint
-
Olek, A. and Walter, J. (1997) The pre-implantation ontogeny of the H19 methylation imprint. Nat. Genet., 17, 275-276.
-
(1997)
Nat. Genet.
, vol.17
, pp. 275-276
-
-
Olek, A.1
Walter, J.2
-
25
-
-
0030802395
-
A 5′ 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development
-
Tremblay, K.D., Duran, K.L. and Bartolomei, M.S. (1997) A 5′ 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development. Mol. Cell. Biol., 17, 4322-4329.
-
(1997)
Mol. Cell. Biol.
, vol.17
, pp. 4322-4329
-
-
Tremblay, K.D.1
Duran, K.L.2
Bartolomei, M.S.3
-
26
-
-
0034176639
-
Active demethylation of the paternal genome in the mouse zygote
-
Oswald, J., Engemann, S., Lane, N., Mayer, W., Olek, A., Fundele, R., Dean, W., Reik, W. and Walter, J. (2000) Active demethylation of the paternal genome in the mouse zygote. Curr. Biol., 10, 475-478.
-
(2000)
Curr. Biol.
, vol.10
, pp. 475-478
-
-
Oswald, J.1
Engemann, S.2
Lane, N.3
Mayer, W.4
Olek, A.5
Fundele, R.6
Dean, W.7
Reik, W.8
Walter, J.9
-
27
-
-
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, 34-39.
-
(1995)
Nature
, vol.375
, pp. 34-39
-
-
Leighton, P.A.1
Ingram, R.S.2
Eggenschwiler, J.3
Efstratiadis, A.4
Tilghman, S.M.5
-
28
-
-
0032419812
-
Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2
-
Thorvaldsen, J.L., Duran, K.L. and Bartolomei, M.S. (1998) Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. Genes Devl., 12, 3693-3702.
-
(1998)
Genes Devl.
, vol.12
, pp. 3693-3702
-
-
Thorvaldsen, J.L.1
Duran, K.L.2
Bartolomei, M.S.3
-
29
-
-
0035111294
-
Extensive tissue-specific variation of allelic methylation in the Igf2 gene during mouse fetal development: Relation to expression and imprinting
-
Weber, M., Milligan, L., Delalbre, A., Antoine, E., Brunel, C., Cathala, G. and Forne, T. (2001) Extensive tissue-specific variation of allelic methylation in the Igf2 gene during mouse fetal development: relation to expression and imprinting. Mech. Devl., 101, 133-141.
-
(2001)
Mech. Devl.
, vol.101
, pp. 133-141
-
-
Weber, M.1
Milligan, L.2
Delalbre, A.3
Antoine, E.4
Brunel, C.5
Cathala, G.6
Forne, T.7
-
30
-
-
0029165883
-
An enhancer deletion affects both H19 and Igf2 expression
-
Leighton, P.A., Saam, J.R., Ingram, R.S., Stewart, C.L. and Tilghman, S.M. (1995) An enhancer deletion affects both H19 and Igf2 expression. Genes Devl., 9, 2079-2089.
-
(1995)
Genes Devl.
, vol.9
, pp. 2079-2089
-
-
Leighton, P.A.1
Saam, J.R.2
Ingram, R.S.3
Stewart, C.L.4
Tilghman, S.M.5
-
31
-
-
0030986103
-
Formation of methylation patterns in the mammalian genome
-
Turker, M.S. and Bestor, T.H. (1997) Formation of methylation patterns in the mammalian genome. Mutat. Res., 386, 119-130.
-
(1997)
Mutat. Res.
, vol.386
, pp. 119-130
-
-
Turker, M.S.1
Bestor, T.H.2
-
32
-
-
0028143457
-
Comparative analysis of Igf-2/H19 imprinted domain: Identification of a highly conserved intergenic DNase I hypersensitive region
-
Koide, T., Ainscough, J., Wijgerde, M. and Surani, M.A. (1994) Comparative analysis of 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
-
33
-
-
0035282661
-
Did genomic imprinting and X chromosome inactivation arise from stochastic expression?
-
Ohlsson, R., Paldi, A. and Graves, J.A. (2001) Did genomic imprinting and X chromosome inactivation arise from stochastic expression? Trends Genet., 17, 136-141.
-
(2001)
Trends Genet.
, vol.17
, pp. 136-141
-
-
Ohlsson, R.1
Paldi, A.2
Graves, J.A.3
-
34
-
-
0035093826
-
Evolution of imprinting mechanisms: The battle of the sexes begins in the zygote
-
Reik, W. and Walter, J. (2001) Evolution of imprinting mechanisms: the battle of the sexes begins in the zygote. Nat. Genet., 27, 255-256.
-
(2001)
Nat. Genet.
, vol.27
, pp. 255-256
-
-
Reik, W.1
Walter, J.2
-
35
-
-
0033615717
-
DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development
-
Okano, M., Bell, D.W, Haber, D.A. and Li, E. (1999) DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development. Cell, 99, 247-257.
-
(1999)
Cell
, vol.99
, pp. 247-257
-
-
Okano, M.1
Bell, D.W.2
Haber, D.A.3
Li, E.4
-
36
-
-
0029621799
-
Allele-specific expression and total expression levels of imprinted genes during early mouse development: Implications for imprinting mechanisms
-
Szabo, P.E. and Mann, J.R. (1995) Allele-specific expression and total expression levels of imprinted genes during early mouse development: implications for imprinting mechanisms. Genes Devl., 9, 3097-3108.
-
(1995)
Genes Devl.
, vol.9
, pp. 3097-3108
-
-
Szabo, P.E.1
Mann, J.R.2
-
37
-
-
0036333199
-
Disruption of mesodermal enhancers for Igf2 in the minute mutant
-
Davies, K., Bowden, L., Smith, P., Dean, W., Hill, D., Furuumi, H., Sasaki, H., Cattanach, B. and Reik, W. (2002) Disruption of mesodermal enhancers for Igf2 in the minute mutant. Development, 129, 1657-1668.
-
(2002)
Development
, vol.129
, pp. 1657-1668
-
-
Davies, K.1
Bowden, L.2
Smith, P.3
Dean, W.4
Hill, D.5
Furuumi, H.6
Sasaki, H.7
Cattanach, B.8
Reik, W.9
-
38
-
-
0029411508
-
A chromatin model of IGF2/H19 imprinting
-
Banerjee, S. and Smallwood, A. (1995) A chromatin model of IGF2/H19 imprinting. Nat. Genet., 11, 237-238.
-
(1995)
Nat. Genet.
, vol.11
, pp. 237-238
-
-
Banerjee, S.1
Smallwood, A.2
-
39
-
-
0036898580
-
Long-range chromatin regulatory interactions in vivo
-
Carter, D., Chakalova, L., Osborne, C.S., Dai, Y. and Fraser, P. (2002) Long-range chromatin regulatory interactions in vivo. Nat. Genet., 32, 623-626.
-
(2002)
Nat. Genet.
, vol.32
, pp. 623-626
-
-
Carter, D.1
Chakalova, L.2
Osborne, C.S.3
Dai, Y.4
Fraser, P.5
-
40
-
-
0036532237
-
Gene silencing, cell fate and nuclear organisation
-
Fisher, A.G. and Merkenschlager, M. (2002) Gene silencing, cell fate and nuclear organisation. Curr. Opin. Genet. Devl., 12, 193-197.
-
(2002)
Curr. Opin. Genet. Devl.
, vol.12
, pp. 193-197
-
-
Fisher, A.G.1
Merkenschlager, M.2
-
41
-
-
0037071535
-
Spatial organization of active and inactive genes and noncoding DNA within chromosome territories
-
Mahy, N.L., Perry; P.E., Gilchrist, S., Baldock, R.A. and Bickmore, W.A. (2002) Spatial organization of active and inactive genes and noncoding DNA within chromosome territories. J. Cell Biol., 157, 579-589.
-
(2002)
J. Cell Biol.
, vol.157
, pp. 579-589
-
-
Mahy, N.L.1
Perry, P.E.2
Gilchrist, S.3
Baldock, R.A.4
Bickmore, W.A.5
-
42
-
-
0037154983
-
The contribution of nuclear compartmentalization to gene regulation
-
Carmo-Fonseca, M. (2002) The contribution of nuclear compartmentalization to gene regulation. Cell, 108, 513-521.
-
(2002)
Cell
, vol.108
, pp. 513-521
-
-
Carmo-Fonseca, M.1
-
43
-
-
0036333103
-
Dnmt3L cooperates with the Dnmt3 family of de novo DNA methyltransferases to establish maternal imprints in mice
-
Hata, K., Okano, M., Lei, H. and Li, E. (2002) Dnmt3L cooperates with the Dnmt3 family of de novo DNA methyltransferases to establish maternal imprints in mice. Development, 129, 1983-1993.
-
(2002)
Development
, vol.129
, pp. 1983-1993
-
-
Hata, K.1
Okano, M.2
Lei, H.3
Li, E.4
-
44
-
-
0035930660
-
Dnmt3L and the establishment of maternal genomic imprints
-
Bourc'his, D., Xu, G.L., Lin, C.S., Bollman, B. and Bestor, T.H. (2001) Dnmt3L and the establishment of maternal genomic imprints. Science, 294, 2536-2539.
-
(2001)
Science
, vol.294
, pp. 2536-2539
-
-
Bourc'his, D.1
Xu, G.L.2
Lin, C.S.3
Bollman, B.4
Bestor, T.H.5
-
45
-
-
0032076307
-
Imprinting in Prader-Willi and Angelman syndromes
-
Nicholls, R.D., Saitoh, S. and Horsthemke, B. (1998) Imprinting in Prader-Willi and Angelman syndromes. Trends Genet., 14, 194-200.
-
(1998)
Trends Genet.
, vol.14
, pp. 194-200
-
-
Nicholls, R.D.1
Saitoh, S.2
Horsthemke, B.3
-
46
-
-
0030886796
-
Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern
-
Shemer, R., Birger, Y., Riggs, A.D. and Razin, A. (1997) Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern. Proc. Natl Acad. Sci. USA, 94, 10267-10272.
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 10267-10272
-
-
Shemer, R.1
Birger, Y.2
Riggs, A.D.3
Razin, A.4
-
47
-
-
0035102797
-
Establishment and maintenance of DNA methylation patterns in mouse Ndn: Implications for maintenance of imprinting in target genes of the imprinting center
-
Hanel, M.L. and Wevrick, R. (2001) Establishment and maintenance of DNA methylation patterns in mouse Ndn: implications for maintenance of imprinting in target genes of the imprinting center. Mol. Cell. Biol., 21, 2384-2392.
-
(2001)
Mol. Cell. Biol.
, vol.21
, pp. 2384-2392
-
-
Hanel, M.L.1
Wevrick, R.2
-
48
-
-
0032782842
-
Genomic imprinting and chromatin insulation in Beckwith-Wiedemann syndrome
-
Greally, J.M. (1999) Genomic imprinting and chromatin insulation in Beckwith-Wiedemann syndrome. Mol. Biotechnol., 11, 159-173.
-
(1999)
Mol. Biotechnol.
, vol.11
, pp. 159-173
-
-
Greally, J.M.1
-
49
-
-
0035883743
-
Bidirectional action of the Igf2r imprint control element on upstream and downstream imprinted genes
-
Zwart, R., Sleutels, F., Wutz, A., Schinkel, A.H. and Barlow, D.P. (2001) Bidirectional action of the Igf2r imprint control element on upstream and downstream imprinted genes. Genes Devl., 15, 2361-2366.
-
(2001)
Genes Devl.
, vol.15
, pp. 2361-2366
-
-
Zwart, R.1
Sleutels, F.2
Wutz, A.3
Schinkel, A.H.4
Barlow, D.P.5
-
50
-
-
0033762171
-
A GNAS1 imprinting defect in pseudohypoparathyroidism type IB
-
Liu, J., Litman, D., Rosenberg, M.J., Yu, S., Biesecker, L.G. and Weinstein, L.S. (2000) A GNAS1 imprinting defect in pseudohypoparathyroidism type IB. J. Clin. Invest., 106, 1167-1174.
-
(2000)
J. Clin. Invest.
, vol.106
, pp. 1167-1174
-
-
Liu, J.1
Litman, D.2
Rosenberg, M.J.3
Yu, S.4
Biesecker, L.G.5
Weinstein, L.S.6
-
51
-
-
0003799070
-
-
Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
-
Hogan, B., Beddington, R., Costantini, F. and Lacy, E. (1994) Manipulating the Mouse Embryo. A Laboratory Manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
-
(1994)
Manipulating the Mouse Embryo. A Laboratory Manual
-
-
Hogan, B.1
Beddington, R.2
Costantini, F.3
Lacy, E.4
-
52
-
-
0030471926
-
A modified and improved method for bisulphite based cytosine methylation analysis
-
Olek, A., Oswald, J. and Walter, J. (1996) A modified and improved method for bisulphite based cytosine methylation analysis. Nucleic Acids Res., 24, 5064-5066.
-
(1996)
Nucleic Acids Res.
, vol.24
, pp. 5064-5066
-
-
Olek, A.1
Oswald, J.2
Walter, J.3
-
53
-
-
0025739379
-
Simplified mammalian DNA isolation procedure
-
Laird, P.W, Zijderveld, A., Linders, K., Rudnicki, M.A., Jaenisch, R. and Berns, A. (1991) Simplified mammalian DNA isolation procedure. Nucl. Acids Res., 19, 4293.
-
(1991)
Nucl. Acids Res.
, vol.19
, pp. 4293
-
-
Laird, P.W.1
Zijderveld, A.2
Linders, K.3
Rudnicki, M.A.4
Jaenisch, R.5
Berns, A.6
-
55
-
-
0032528048
-
Bisulfite sequencing in preimplantation embryos: DNA methylation profile of the upstream region of the mouse imprinted H19 gene
-
Warnecke, P.M., Mann, J.R., Frommer, M. and Clark, S.J. (1998) Bisulfite sequencing in preimplantation embryos: DNA methylation profile of the upstream region of the mouse imprinted H19 gene. Genomics, 51, 182-190.
-
(1998)
Genomics
, vol.51
, pp. 182-190
-
-
Warnecke, P.M.1
Mann, J.R.2
Frommer, M.3
Clark, S.J.4
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