-
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. Nature Rev. Genet., 2, 21-32.
-
(2001)
Nature Rev. Genet.
, vol.2
, pp. 21-32
-
-
Reik, W.1
Walter, J.2
-
3
-
-
33645456062
-
Regulation of imprinted DNA methylation
-
Holmes,R. and Soloway,P.D. (2006) Regulation of imprinted DNA methylation. Cytogenet. Genome Res., 113, 122-129.
-
(2006)
Cytogenet. Genome Res.
, vol.113
, pp. 122-129
-
-
Holmes, R.1
Soloway, P.D.2
-
4
-
-
33645460549
-
How imprinting centres work
-
Lewis,A. and Reik,W. (2006) How imprinting centres work. Cytogenet. Genome Res., 113, 81-89.
-
(2006)
Cytogenet. Genome Res.
, vol.113
, pp. 81-89
-
-
Lewis, A.1
Reik, W.2
-
5
-
-
33746063711
-
CTCF binding at the H19 imprinting control region mediates maternally inherited higher-order chromatin conformation to restrict enhancer access to Igf2
-
Kurukuti,S., Tiwari,V.K., Tavoosidana,G., Pugacheva,E., Murrell,A., Zhao,Z., Lobanenkov,V., Reik,W. and Ohlsson,R. (2006) CTCF binding at the H19 imprinting control region mediates maternally inherited higher-order chromatin conformation to restrict enhancer access to Igf2. Proc. Natl Acad. Sci. USA, 103, 10684-10689.
-
(2006)
Proc. Natl Acad. Sci. USA
, vol.103
, pp. 10684-10689
-
-
Kurukuti, S.1
Tiwari, V.K.2
Tavoosidana, G.3
Pugacheva, E.4
Murrell, A.5
Zhao, Z.6
Lobanenkov, V.7
Reik, W.8
Ohlsson, R.9
-
6
-
-
0037322392
-
Epigenetic modifications in an imprinting cluster are controlled by a hierarchy of DMRs suggesting long-range chromatin interactions
-
Lopes,S., Lewis,A., Hajkova,P., Dean,W., Oswald,J., Forne,T., Murrell,A., Constancia,M., Bartolomei,M., Walter,J. et al. (2003) Epigenetic modifications in an imprinting cluster are controlled by a hierarchy of DMRs suggesting long-range chromatin interactions. Hum. Mol. Genet., 12, 295-305.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 295-305
-
-
Lopes, S.1
Lewis, A.2
Hajkova, P.3
Dean, W.4
Oswald, J.5
Forne, T.6
Murrell, A.7
Constancia, M.8
Bartolomei, M.9
Walter, J.10
-
7
-
-
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 Dev., 12, 3693-3702.
-
(1998)
Genes Dev.
, vol.12
, pp. 3693-3702
-
-
Thorvaldsen, J.L.1
Duran, K.L.2
Bartolomei, M.S.3
-
8
-
-
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
-
9
-
-
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
-
10
-
-
1842715884
-
Genomic imprinting: CTCF protects the boundaries
-
Lewis,A. and Murrell,A. (2004) Genomic imprinting: CTCF protects the boundaries. Curr. Biol., 14, R284-286.
-
(2004)
Curr. Biol.
, vol.14
-
-
Lewis, A.1
Murrell, A.2
-
11
-
-
0347986844
-
Transgenic RNAi reveals essential function for CTCF in H19 gene imprinting
-
Fedoriw,A.M., Stein,P., Svoboda,P., Schultz,R.M. and Bartolomei,M.S. (2004) Transgenic RNAi reveals essential function for CTCF in H19 gene imprinting. Science, 303, 238-240.
-
(2004)
Science
, vol.303
, pp. 238-240
-
-
Fedoriw, A.M.1
Stein, P.2
Svoboda, P.3
Schultz, R.M.4
Bartolomei, M.S.5
-
12
-
-
0033152214
-
A potential imprint control element: Identification of a conserved 42 bp sequence upstream of H19
-
Frevel,M.A., Hornberg,J.J. and Reeve,A.E. (1999) A potential imprint control element: Identification of a conserved 42 bp sequence upstream of H19. Trends Genet., 15, 216-218.
-
(1999)
Trends Genet.
, vol.15
, pp. 216-218
-
-
Frevel, M.A.1
Hornberg, J.J.2
Reeve, A.E.3
-
13
-
-
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
-
14
-
-
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
-
15
-
-
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
-
16
-
-
0035393429
-
Loss of imprinting of insulin-like growth factor-II in Wilms' tumor commonly involves altered methylation but not mutations of CTCF or its binding site
-
Cui,H., Niemitz,E.L., Ravenel,J.D., Onyango,P., Brandenburg,S.A., Lobanenkov,V.V. and Feinberg,A.P. (2001) Loss of imprinting of insulin-like growth factor-II in Wilms' tumor commonly involves altered methylation but not mutations of CTCF or its binding site. Cancer Res., 61, 4947-4950.
-
(2001)
Cancer Res.
, vol.61
, pp. 4947-4950
-
-
Cui, H.1
Niemitz, E.L.2
Ravenel, J.D.3
Onyango, P.4
Brandenburg, S.A.5
Lobanenkov, V.V.6
Feinberg, A.P.7
-
17
-
-
0037112364
-
Loss of imprinting in colorectal cancer linked to hypomethylation of H19 and IGF2
-
Cui,H., Onyango,P., Brandenburg,S., Wu,Y., Hsieh,C.L. and Feinberg,A.P. (2002) Loss of imprinting in colorectal cancer linked to hypomethylation of H19 and IGF2. Cancer Res., 62, 6442-6446.
-
(2002)
Cancer Res.
, vol.62
, pp. 6442-6446
-
-
Cui, H.1
Onyango, P.2
Brandenburg, S.3
Wu, Y.4
Hsieh, C.L.5
Feinberg, A.P.6
-
18
-
-
25144454048
-
Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome
-
Gicquel,C., Rossignol,S., Cabrol,S., Houang,M., Steunou,V., Barbu,V., Danton,F., Thibaud,N., Le Merrer,M., Burglen,L. et al. (2005) Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome. Nature Genet., 37, 1003-1007.
-
(2005)
Nature Genet.
, vol.37
, pp. 1003-1007
-
-
Gicquel, C.1
Rossignol, S.2
Cabrol, S.3
Houang, M.4
Steunou, V.5
Barbu, V.6
Danton, F.7
Thibaud, N.8
Le Merrer, M.9
Burglen, L.10
-
19
-
-
0141673489
-
CTCF binding at the insulin-like growth factor-II (IGF2)/H19 imprinting control region is insufficient to regulate IGF2/H19 expression in human tissues
-
Ulaner,G.A., Yang,Y., Hu,J.F., Li,T., Vu,T.H. and Hoffman,A.R. (2003) CTCF binding at the insulin-like growth factor-II (IGF2)/H19 imprinting control region is insufficient to regulate IGF2/H19 expression in human tissues. Endocrinology, 144, 4420-4426.
-
(2003)
Endocrinology
, vol.144
, pp. 4420-4426
-
-
Ulaner, G.A.1
Yang, Y.2
Hu, J.F.3
Li, T.4
Vu, T.H.5
Hoffman, A.R.6
-
20
-
-
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. et al. (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
-
21
-
-
0038104379
-
Familial aggregation of abnormal methylation of parental alleles at the IGF2/H19 and IGF2R differentially methylated regions
-
Sandovici,I., Leppert,M., Hawk,P.R., Suarez,A., Linares,Y. and Sapienza,C. (2003) Familial aggregation of abnormal methylation of parental alleles at the IGF2/H19 and IGF2R differentially methylated regions. Hum. Mol. Genet., 12, 1569-1578.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 1569-1578
-
-
Sandovici, I.1
Leppert, M.2
Hawk, P.R.3
Suarez, A.4
Linares, Y.5
Sapienza, C.6
-
22
-
-
0037182866
-
Placental-specific IGF-II is a major modulator of placental and fetal growth
-
Constancia,M., Hemberger,M., Hughes,J., Dean,W., Ferguson-Smith,A., Fundele,R., Stewart,F., Kelsey,G., Fowden,A., Sibley,C. et al. (2002) Placental-specific IGF-II is a major modulator of placental and fetal growth. Nature, 417, 945-948.
-
(2002)
Nature
, vol.417
, pp. 945-948
-
-
Constancia, M.1
Hemberger, M.2
Hughes, J.3
Dean, W.4
Ferguson-Smith, A.5
Fundele, R.6
Stewart, F.7
Kelsey, G.8
Fowden, A.9
Sibley, C.10
-
23
-
-
33645308782
-
Programming placental nutrient transport capacity
-
Fowden,A.L., Ward,J.W., Wooding,F.P., Forhead,A.J. and Constancia,M. (2006) Programming placental nutrient transport capacity. J. Physiol., 572, 5-15.
-
(2006)
J. Physiol.
, vol.572
, pp. 5-15
-
-
Fowden, A.L.1
Ward, J.W.2
Wooding, F.P.3
Forhead, A.J.4
Constancia, M.5
-
24
-
-
33645454706
-
The H19 gene: Regulation and function of a non-coding RNA
-
Gabory,A., Ripoche,M.A., Yoshimizu,T. and Dandolo,L. (2006) The H19 gene: Regulation and function of a non-coding RNA. Cytogenet. Genome Res., 113, 188-193.
-
(2006)
Cytogenet. Genome Res.
, vol.113
, pp. 188-193
-
-
Gabory, A.1
Ripoche, M.A.2
Yoshimizu, T.3
Dandolo, L.4
-
25
-
-
11144358198
-
A gene atlas of the mouse and human protein-encoding transcriptomes
-
Su,A.I., Wiltshire,T., Batalov,S., Lapp,H., Ching,K.A., Block,D., Zhang,J., Soden,R., Hayakawa,M., Kreiman,G. et al. (2004) A gene atlas of the mouse and human protein-encoding transcriptomes. Proc. Natl Acad. Sci. USA, 101, 6062-6067.
-
(2004)
Proc. Natl Acad. Sci. USA
, vol.101
, pp. 6062-6067
-
-
Su, A.I.1
Wiltshire, T.2
Batalov, S.3
Lapp, H.4
Ching, K.A.5
Block, D.6
Zhang, J.7
Soden, R.8
Hayakawa, M.9
Kreiman, G.10
-
26
-
-
0037339486
-
Altered imprinting, promoter usage, and expression of insulin-like growth factor-II gene in gestational trophoblastic diseases
-
Kim,S.J., Park,S.E., Lee,C., Lee,S.Y., Kim,I.H., An,H.J. and Oh,Y.K. (2003) Altered imprinting, promoter usage, and expression of insulin-like growth factor-II gene in gestational trophoblastic diseases. Gynecol. Oncol., 88, 411-418.
-
(2003)
Gynecol. Oncol.
, vol.88
, pp. 411-418
-
-
Kim, S.J.1
Park, S.E.2
Lee, C.3
Lee, S.Y.4
Kim, I.H.5
An, H.J.6
Oh, Y.K.7
-
27
-
-
0029043178
-
Establishment of functional imprinting of the H19 gene in human developing placentae
-
Jinno,Y., Ikeda,Y., Yun,K., Maw,M., Masuzaki,H., Fukuda,H., Inuzuka,K., Fujishita,A., Ohtani,Y., Okimoto,T. et al. (1995) Establishment of functional imprinting of the H19 gene in human developing placentae. Nature Genet., 10, 318-324.
-
(1995)
Nature Genet.
, vol.10
, pp. 318-324
-
-
Jinno, Y.1
Ikeda, Y.2
Yun, K.3
Maw, M.4
Masuzaki, H.5
Fukuda, H.6
Inuzuka, K.7
Fujishita, A.8
Ohtani, Y.9
Okimoto, T.10
-
28
-
-
0038002236
-
Analysis and quantification of multiple methylation variable positions in CpG islands by Pyrosequencing
-
Tost,J., Dunker,J. and Gut,I.G. (2003) Analysis and quantification of multiple methylation variable positions in CpG islands by Pyrosequencing. Biotechniques, 35, 152-156.
-
(2003)
Biotechniques
, vol.35
, pp. 152-156
-
-
Tost, J.1
Dunker, J.2
Gut, I.G.3
-
29
-
-
4444346815
-
De novo quantitative bisulfite sequencing using the pyrosequencing technology
-
Dupont,J.M., Tost,J., Jammes,H. and Gut,I.G. (2004) De novo quantitative bisulfite sequencing using the pyrosequencing technology. Anal. Biochem., 333, 119-127.
-
(2004)
Anal. Biochem.
, vol.333
, pp. 119-127
-
-
Dupont, J.M.1
Tost, J.2
Jammes, H.3
Gut, I.G.4
-
30
-
-
33746485733
-
Serial pyrosequencing for quantitative DNA methylation analysis
-
Tost,J., El Abdalaoui,H. and Gut,I.G. (2006) Serial pyrosequencing for quantitative DNA methylation analysis. Biotechniques, 40, 721-726.
-
(2006)
Biotechniques
, vol.40
, pp. 721-726
-
-
Tost, J.1
El Abdalaoui, H.2
Gut, I.G.3
-
31
-
-
0348202422
-
Analysis and accurate quantification of CpG methylation by MALDI mass spectrometry
-
Tost,J., Schatz,P., Schuster,M., Berlin,K. and Gut,I.G. (2003) Analysis and accurate quantification of CpG methylation by MALDI mass spectrometry. Nucleic Acids Res., 31, e50.
-
(2003)
Nucleic Acids Res.
, vol.31
-
-
Tost, J.1
Schatz, P.2
Schuster, M.3
Berlin, K.4
Gut, I.G.5
-
32
-
-
4444365791
-
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome
-
Sparago,A., Cerrato,F., Vernucci,M., Ferrero,G.B., Silengo,M.C. and Riccio,A. (2004) Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome. Nature Genet., 36, 958-960.
-
(2004)
Nature Genet.
, vol.36
, pp. 958-960
-
-
Sparago, A.1
Cerrato, F.2
Vernucci, M.3
Ferrero, G.B.4
Silengo, M.C.5
Riccio, A.6
-
33
-
-
20144363310
-
Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor
-
Prawitt,D., Enklaar,T., Gartner-Rupprecht,B., Spangenberg,C., Oswald,M., Lausch,E., Schmidtke,P., Reutzel,D., Fees,S., Lucito,R. et al. (2005) Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor. Proc. Natl Acad. Sci. USA, 102, 4085-4090.
-
(2005)
Proc. Natl Acad. Sci. USA
, vol.102
, pp. 4085-4090
-
-
Prawitt, D.1
Enklaar, T.2
Gartner-Rupprecht, B.3
Spangenberg, C.4
Oswald, M.5
Lausch, E.6
Schmidtke, P.7
Reutzel, D.8
Fees, S.9
Lucito, R.10
-
34
-
-
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
-
35
-
-
33644858912
-
H19-DMR allele-specific methylation analysis reveals epigenetic heterogeneity of CTCF binding site 6 but not of site 5 in head-and-neck carcinomas: A pilot case-control analysis
-
De Castro Valente Esteves,L.I., De Karla Cervigne,N., Do Carmo Javaroni,A., Magrin,J., Kowalski,L.P., Rainho,C.A. and Rogatto,S.R. (2006) H19-DMR allele-specific methylation analysis reveals epigenetic heterogeneity of CTCF binding site 6 but not of site 5 in head-and-neck carcinomas: A pilot case-control analysis. Int. J. Mol. Med., 17, 397-404.
-
(2006)
Int. J. Mol. Med.
, vol.17
, pp. 397-404
-
-
De Castro Valente Esteves, L.I.1
De Karla Cervigne, N.2
Do Carmo Javaroni, A.3
Magrin, J.4
Kowalski, L.P.5
Rainho, C.A.6
Rogatto, S.R.7
-
36
-
-
33646193822
-
Inherited epigenetic variation - Revisiting soft inheritance
-
Richards,E.J. (2006) Inherited epigenetic variation - revisiting soft inheritance. Nature Rev. Genet., 7, 395-401.
-
(2006)
Nature Rev. Genet.
, vol.7
, pp. 395-401
-
-
Richards, E.J.1
-
37
-
-
0032751471
-
Epigenetic inheritance at the agouti locus in the mouse
-
Morgan,H.D., Sutherland,H.G., Martin,D.I. and Whitelaw,E. (1999) Epigenetic inheritance at the agouti locus in the mouse. Nature Genet., 23, 314-318.
-
(1999)
Nature Genet.
, vol.23
, pp. 314-318
-
-
Morgan, H.D.1
Sutherland, H.G.2
Martin, D.I.3
Whitelaw, E.4
-
38
-
-
0037418193
-
Transgenerational inheritance of epigenetic states at the murine Axin(Fu) allele occurs after maternal and paternal transmission
-
Rakyan,V.K., Chong,S., Champ,M.E., Cuthbert,P.C., Morgan,H.D., Luu,K.V. and Whitelaw,E. (2003) Transgenerational inheritance of epigenetic states at the murine Axin(Fu) allele occurs after maternal and paternal transmission. Proc. Natl Acad. Sci. USA, 100, 2538-2543.
-
(2003)
Proc. Natl Acad. Sci. USA
, vol.100
, pp. 2538-2543
-
-
Rakyan, V.K.1
Chong, S.2
Champ, M.E.3
Cuthbert, P.C.4
Morgan, H.D.5
Luu, K.V.6
Whitelaw, E.7
-
39
-
-
27744447434
-
MLH1 germline epimutations as a factor in hereditary nonpolyposis colorectal cancer
-
Hitchins,M., Williams,R., Cheong,K., Halani,N., Lin,V.A., Packham,D., Ku,S., Buckle,A., Hawkins,N., Burn,J. et al. (2005) MLH1 germline epimutations as a factor in hereditary nonpolyposis colorectal cancer. Gastroenterology, 129, 1392-1399.
-
(2005)
Gastroenterology
, vol.129
, pp. 1392-1399
-
-
Hitchins, M.1
Williams, R.2
Cheong, K.3
Halani, N.4
Lin, V.A.5
Packham, D.6
Ku, S.7
Buckle, A.8
Hawkins, N.9
Burn, J.10
-
40
-
-
2442424419
-
Germline epimutation of MLH1 in individuals with multiple cancers
-
Suter,C.M., Martin,D.I. and Ward,R.L. (2004) Germline epimutation of MLH1 in individuals with multiple cancers. Nature Genet., 36, 497-501.
-
(2004)
Nature Genet.
, vol.36
, pp. 497-501
-
-
Suter, C.M.1
Martin, D.I.2
Ward, R.L.3
-
41
-
-
9644266664
-
Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation
-
Lewis,A., Mitsuya,K., Umlauf,D., Smith,P., Dean,W., Walter,J., Higgins,M., Feil,R. and Reik,W. (2004) Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation. Nature Genet., 36, 1291-1295.
-
(2004)
Nature Genet.
, vol.36
, pp. 1291-1295
-
-
Lewis, A.1
Mitsuya, K.2
Umlauf, D.3
Smith, P.4
Dean, W.5
Walter, J.6
Higgins, M.7
Feil, R.8
Reik, W.9
-
42
-
-
9644281546
-
Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes
-
Umlauf,D., Goto,Y., Cao,R., Cerqueira,F., Wagschal,A., Zhang,Y. and Feil,R. (2004) Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes. Nature Genet., 36, 1296-1300.
-
(2004)
Nature Genet.
, vol.36
, pp. 1296-1300
-
-
Umlauf, D.1
Goto, Y.2
Cao, R.3
Cerqueira, F.4
Wagschal, A.5
Zhang, Y.6
Feil, R.7
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