-
1
-
-
0030993133
-
Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element
-
Ripoche MA, Kress C, Poirier F, Dandolo L. Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element. Genes Dev 1997;11:1596-604.
-
(1997)
Genes Dev
, vol.11
, pp. 1596-1604
-
-
Ripoche, M.A.1
Kress, C.2
Poirier, F.3
Dandolo, L.4
-
2
-
-
0029165883
-
An enhancer deletion affects both H19 and Igf2 expression
-
Leighton PA, Saam JR, Ingram RS, Stewart CL, Tilghman SM. An enhancer deletion affects both H19 and Igf2 expression. Genes Dev 1995;9:2079-89.
-
(1995)
Genes Dev
, 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
-
3
-
-
0033785347
-
A skeletal muscle-specific mouse Igf2 repressor lies 40 kb downstream of the gene
-
Ainscough JF, John RM, Barton SC, Surani MA. A skeletal muscle-specific mouse Igf2 repressor lies 40 kb downstream of the gene. Development 2000;127:3923-30.
-
(2000)
Development
, vol.127
, pp. 3923-3930
-
-
Ainscough, J.F.1
John, R.M.2
Barton, S.C.3
Surani, M.A.4
-
4
-
-
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, Reik W. Disruption of mesodermal enhancers for Igf2 in the minute mutant. Development 2002;129:1657-68.
-
(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
-
5
-
-
0033870806
-
A transcriptional insulator at the imprinted H19/Igf2 locus
-
Kaffer CR, Srivastava M, Park KY, Ives E, Hsieh S, Batlle J, Grinberg A, Huang SP, Pfeifer K. A transcriptional insulator at the imprinted H19/Igf2 locus. Genes Dev 2000;14:1908-19.
-
(2000)
Genes Dev
, 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
-
6
-
-
0034127018
-
Comparative genomic sequencing identifies novel tissue-specific enhancers and sequence elements for methylation-sensitive factors implicated in Igf2/H19 imprinting
-
Ishihara K, Hatano N, Furuumi H, Kato R, Iwaki T, Miura K, Jinno Y, Sasaki H. Comparative genomic sequencing identifies novel tissue-specific enhancers and sequence elements for methylation-sensitive factors implicated in Igf2/H19 imprinting. Genome Res 2000;10:664-71.
-
(2000)
Genome Res
, vol.10
, pp. 664-671
-
-
Ishihara, K.1
Hatano, N.2
Furuumi, H.3
Kato, R.4
Iwaki, T.5
Miura, K.6
Jinno, Y.7
Sasaki, H.8
-
7
-
-
0036646951
-
An evolutionarily conserved putative insulator element near the 30 boundary of the imprinted Igf2/H19 domain
-
Ishihara K, Sasaki H. An evolutionarily conserved putative insulator element near the 30 boundary of the imprinted Igf2/H19 domain. Hum Mol Genet 2002;11:1627-36.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 1627-1636
-
-
Ishihara, K.1
Sasaki, H.2
-
8
-
-
3042587417
-
An enhancer element at the Igf2/H19 locus drives gene expression in both imprinted and non-imprinted tissues
-
Charalambous M, Menheniott TR, Bennett WR, Kelly SM, Dell G, Dandolo L, Ward A. An enhancer element at the Igf2/H19 locus drives gene expression in both imprinted and non-imprinted tissues. Dev Biol 2004;271:488-97.
-
(2004)
Dev Biol
, vol.271
, pp. 488-497
-
-
Charalambous, M.1
Menheniott, T.R.2
Bennett, W.R.3
Kelly, S.M.4
Dell, G.5
Dandolo, L.6
Ward, A.7
-
9
-
-
1842715884
-
Genomic imprinting: CTCF protects the boundaries
-
Lewis A, Murrell A. Genomic imprinting: CTCF protects the boundaries. Curr Biol 2004;14:R284-6.
-
(2004)
Curr Biol
, vol.14
, pp. R284-R286
-
-
Lewis, A.1
Murrell, A.2
-
10
-
-
0032878252
-
Methylation sequencing analysis refines the region of H19 epimutation in Wilms tumor
-
Frevel MA, Sowerby SJ, Petersen GB, Reeve AE. Methylation sequencing analysis refines the region of H19 epimutation in Wilms tumor. J Biol Chem 1999;274:29331-40.
-
(1999)
J Biol Chem
, vol.274
, pp. 29331-29340
-
-
Frevel, M.A.1
Sowerby, S.J.2
Petersen, G.B.3
Reeve, A.E.4
-
11
-
-
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 FA, Tsai YC, Thayer MJ, Jones PA. Large scale mapping of methylcytosines in CTCF-binding sites in the human H19 promoter and aberrant hypomethylation in human bladder cancer. Hum Mol Genet 2001;10:2619-26.
-
(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
-
12
-
-
33645820241
-
Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human
-
Monk D, Sanches R, Arnaud P, Apostolidou S, Hills FA, Abu-Amero S, Murrell A, Friess H, Reik W, Stanier P, Constancia M, Moore GE. Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human. Hum Mol Genet 2006;15:1259-69.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 1259-1269
-
-
Monk, D.1
Sanches, R.2
Arnaud, P.3
Apostolidou, S.4
Hills, F.A.5
Abu-Amero, S.6
Murrell, A.7
Friess, H.8
Reik, W.9
Stanier, P.10
Constancia, M.11
Moore, G.E.12
-
13
-
-
0034967806
-
Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome
-
Gaston V, Le Bouc Y, Soupre V, Burglen L, Donadieu J, Oro H, Audry G, Vazquez MP, Gicquel C. Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome. Eur J Hum Genet 2001;9:409-18.
-
(2001)
Eur J Hum Genet
, vol.9
, pp. 409-418
-
-
Gaston, V.1
Le Bouc, Y.2
Soupre, V.3
Burglen, L.4
Donadieu, J.5
Oro, H.6
Audry, G.7
Vazquez, M.P.8
Gicquel, C.9
-
14
-
-
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, Bertrand AM, Netchine I, Le Bouc Y. Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome. Nat Genet 2005;37:1003-7.
-
(2005)
Nat 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
Bertrand, A.M.11
Netchine, I.12
Le Bouc, Y.13
-
15
-
-
34547764390
-
11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations
-
Netchine I, Rossignol S, Dufourg MN, Azzi S, Rousseau A, Perin L, Houang M, Steunou V, Esteva B, Thibaud N, Demay MC, Danton F, Petriczko E, Bertrand AM, Heinrichs C, Carel JC, Loeuille GA, Pinto G, Jacquemont ML, Gicquel C, Cabrol S, Le Bouc Y. 11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations. J Clin Endocrinol Metab 2007;92:3148-54.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 3148-3154
-
-
Netchine, I.1
Rossignol, S.2
Dufourg, M.N.3
Azzi, S.4
Rousseau, A.5
Perin, L.6
Houang, M.7
Steunou, V.8
Esteva, B.9
Thibaud, N.10
Demay, M.C.11
Danton, F.12
Petriczko, E.13
Bertrand, A.M.14
Heinrichs, C.15
Carel, J.C.16
Loeuille, G.A.17
Pinto, G.18
Jacquemont, M.L.19
Gicquel, C.20
Cabrol, S.21
Le Bouc, Y.22
more..
-
16
-
-
0027231511
-
Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome
-
Schneid H, Seurin D, Vazquez MP, Gourmelen M, Cabrol S, Le Bouc Y. Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome. J Med Genet 1993;30:353-62.
-
(1993)
J Med Genet
, vol.30
, pp. 353-362
-
-
Schneid, H.1
Seurin, D.2
Vazquez, M.P.3
Gourmelen, M.4
Cabrol, S.5
Le Bouc, Y.6
-
17
-
-
80053952320
-
CTCF function is modulated by neighboring DNA binding factors
-
Weth O, Renkawitz R. CTCF function is modulated by neighboring DNA binding factors. Biochem Cell Biol 2011;89:459-68.
-
(2011)
Biochem Cell Biol
, vol.89
, pp. 459-468
-
-
Weth, O.1
Renkawitz, R.2
-
18
-
-
77950523023
-
Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders
-
Demars J, Shmela ME, Rossignol S, Okabe J, Netchine I, Azzi S, Cabrol S, Le Caignec C, David A, Le Bouc Y, El-Osta A, Gicquel C. Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders. Hum Mol Genet 2010;19:803-14.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 803-814
-
-
Demars, J.1
Shmela, M.E.2
Rossignol, S.3
Okabe, J.4
Netchine, I.5
Azzi, S.6
Cabrol, S.7
Le Caignec, C.8
David, A.9
Le Bouc, Y.10
El-Osta, A.11
Gicquel, C.12
-
19
-
-
84855812755
-
Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1
-
Poole RL, Leith DJ, Docherty LE, Shmela ME, Gicquel C, Splitt M, Temple IK, Mackay DJ. Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1. Eur J Hum Genet 2011;20:240-3.
-
(2011)
Eur J Hum Genet
, vol.20
, pp. 240-243
-
-
Poole, R.L.1
Leith, D.J.2
Docherty, L.E.3
Shmela, M.E.4
Gicquel, C.5
Splitt, M.6
Temple, I.K.7
Mackay, D.J.8
-
20
-
-
84937511764
-
A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient.
-
Nov 8
-
Higashimoto K, Jozaki K, Kosho T, Matsubara K, Fuke T, Yamada D, Yatsuki H, Maeda T, Ohtsuka Y, Nishioka K, Joh K, Koseki H, Ogata T, Soejima H. A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient. Clin Genet 2013. Nov 8. doi:10.1111/cge.12318.
-
(2013)
Clin Genet
-
-
Higashimoto, K.1
Jozaki, K.2
Kosho, T.3
Matsubara, K.4
Fuke, T.5
Yamada, D.6
Yatsuki, H.7
Maeda, T.8
Ohtsuka, Y.9
Nishioka, K.10
Joh, K.11
Koseki, H.12
Ogata, T.13
Soejima, H.14
-
21
-
-
84871577497
-
Induction of DNA demethylation depending on two sets of Sox2 and adjacent Oct3/4 binding sites (Sox-Oct motifs) within the mouse H19/insulin-like growth factor 2 (Igf2) imprinted control region
-
Hori N, Yamane M, Kouno K, Sato K. Induction of DNA demethylation depending on two sets of Sox2 and adjacent Oct3/4 binding sites (Sox-Oct motifs) within the mouse H19/insulin-like growth factor 2 (Igf2) imprinted control region. J Biol Chem 2012;287:44006-16.
-
(2012)
J Biol Chem
, vol.287
, pp. 44006-44016
-
-
Hori, N.1
Yamane, M.2
Kouno, K.3
Sato, K.4
-
22
-
-
84887001456
-
Sox-Oct motifs contribute to maintenance of the unmethylated H19 ICR in YAC transgenic mice
-
Sakaguchi R, Okamura E, Matsuzaki H, Fukamizu A, Tanimoto K. Sox-Oct motifs contribute to maintenance of the unmethylated H19 ICR in YAC transgenic mice. Hum Mol Genet 2013;22:4627-37.
-
(2013)
Hum Mol Genet
, vol.22
, pp. 4627-4637
-
-
Sakaguchi, R.1
Okamura, E.2
Matsuzaki, H.3
Fukamizu, A.4
Tanimoto, K.5
-
23
-
-
70450162112
-
Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci
-
Azzi S, Rossignol S, Steunou V, Sas T, Thibaud N, Danton F, Le Jule M, Heinrichs C, Cabrol S, Gicquel C, Le Bouc Y, Netchine I. Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci. Hum Mol Genet 2009;18:4724-33.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 4724-4733
-
-
Azzi, S.1
Rossignol, S.2
Steunou, V.3
Sas, T.4
Thibaud, N.5
Danton, F.6
Le Jule, M.7
Heinrichs, C.8
Cabrol, S.9
Gicquel, C.10
Le Bouc, Y.11
Netchine, I.12
-
24
-
-
79551551535
-
Allele-specific methylated multiplex real-time quantitative PCR (ASMM RTQ-PCR), a powerful method for diagnosing loss of imprinting of the 11p15 region in Russell Silver and Beckwith Wiedemann syndromes
-
Azzi S, Steunou V, Rousseau A, Rossignol S, Thibaud N, Danton F, Le Jule M, Gicquel C, Le Bouc Y, Netchine I. Allele-specific methylated multiplex real-time quantitative PCR (ASMM RTQ-PCR), a powerful method for diagnosing loss of imprinting of the 11p15 region in Russell Silver and Beckwith Wiedemann syndromes. Hum Mutat 2011;32:249-58.
-
(2011)
Hum Mutat
, vol.32
, pp. 249-258
-
-
Azzi, S.1
Steunou, V.2
Rousseau, A.3
Rossignol, S.4
Thibaud, N.5
Danton, F.6
Le Jule, M.7
Gicquel, C.8
Le Bouc, Y.9
Netchine, I.10
-
25
-
-
84880509448
-
Simultaneous hyper- and hypomethylation at imprinted loci in a subset of patients with GNAS epimutations underlies a complex and different mechanism of multilocus methylation defect in pseudohypoparathyroidism type 1b
-
Maupetit-Mehouas S, Azzi S, Steunou V, Sakakini N, Silve C, Reynes C, Perez de Nanclares G, Keren B, Chantot S, Barlier A, Linglart A, Netchine I. Simultaneous hyper- and hypomethylation at imprinted loci in a subset of patients with GNAS epimutations underlies a complex and different mechanism of multilocus methylation defect in pseudohypoparathyroidism type 1b. Hum Mutat 2013;34:1172-80.
-
(2013)
Hum Mutat
, vol.34
, pp. 1172-1180
-
-
Maupetit-Mehouas, S.1
Azzi, S.2
Steunou, V.3
Sakakini, N.4
Silve, C.5
Reynes, C.6
Perez de Nanclares, G.7
Keren, B.8
Chantot, S.9
Barlier, A.10
Linglart, A.11
Netchine, I.12
-
26
-
-
84911458699
-
Extensive investigation of the IGF2/H19 Imprinting Control Region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann Syndrome
-
Abi Habib W, Azzi S, Brioude F, Steunou V, Thibaud N, Das Neves C, Le Jule M, Chantot-Bastaraud S, Keren B, Lyonnet S, Michot C, Rossi M, Pasquier L, Gicquel C, Rossignol S, Le Bouc Y, Netchine I. Extensive investigation of the IGF2/H19 Imprinting Control Region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann Syndrome. Hum Mol Genet 2014;23:5763-73.
-
(2014)
Hum Mol Genet
, vol.23
, pp. 5763-5773
-
-
Abi Habib, W.1
Azzi, S.2
Brioude, F.3
Steunou, V.4
Thibaud, N.5
Das Neves, C.6
Le Jule, M.7
Chantot-Bastaraud, S.8
Keren, B.9
Lyonnet, S.10
Michot, C.11
Rossi, M.12
Pasquier, L.13
Gicquel, C.14
Rossignol, S.15
Le Bouc, Y.16
Netchine, I.17
-
27
-
-
84892371264
-
Beckwith-Wiedemann and Russell-Silver Syndromes: from new molecular insights to the comprehension of imprinting regulation
-
Azzi S, Abi Habib W, Netchine I. Beckwith-Wiedemann and Russell-Silver Syndromes: from new molecular insights to the comprehension of imprinting regulation. Curr Opin Endocrinol Diabetes Obes 2014;21:30-8.
-
(2014)
Curr Opin Endocrinol Diabetes Obes
, vol.21
, pp. 30-38
-
-
Azzi, S.1
Abi Habib, W.2
Netchine, I.3
-
28
-
-
38449113853
-
DNA methylation analysis by pyrosequencing
-
Tost J, Gut IG. DNA methylation analysis by pyrosequencing. Nat Protoc 2007;2:2265-75.
-
(2007)
Nat Protoc
, vol.2
, pp. 2265-2275
-
-
Tost, J.1
Gut, I.G.2
-
29
-
-
84973587732
-
A coefficient of agreement for nominal scales
-
Cohen J. A coefficient of agreement for nominal scales. Educ Psychol Meas 1960;20:37-46.
-
(1960)
Educ Psychol Meas
, vol.20
, pp. 37-46
-
-
Cohen, J.1
-
30
-
-
84908693428
-
Complex tissue-specific epigenotypes in russell-silver syndrome associated with 11p15 ICR1 hypomethylation
-
Azzi S, Blaise A, Steunou V, Harbison MD, Salem J, Brioude F, Rossignol S, Habib WA, Thibaud N, Neves CD, Jule ML, Brachet C, Heinrichs C, Bouc YL, Netchine I. Complex tissue-specific epigenotypes in russell-silver syndrome associated with 11p15 ICR1 hypomethylation. Hum Mutat 2014;35: 1211-20.
-
(2014)
Hum Mutat
, vol.35
, pp. 1211-1220
-
-
Azzi, S.1
Blaise, A.2
Steunou, V.3
Harbison, M.D.4
Salem, J.5
Brioude, F.6
Rossignol, S.7
Habib, W.A.8
Thibaud, N.9
Neves, C.D.10
Jule, M.L.11
Brachet, C.12
Heinrichs, C.13
Bouc, Y.L.14
Netchine, I.15
-
31
-
-
84890244971
-
CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome
-
Brioude F, Oliver-Petit I, Blaise A, Praz F, Rossignol S, Jule ML, Thibaud N, Faussat AM, Tauber M, Bouc YL, Netchine I. CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome. J Med Genet 2013;50:823-30.
-
(2013)
J Med Genet
, vol.50
, pp. 823-830
-
-
Brioude, F.1
Oliver-Petit, I.2
Blaise, A.3
Praz, F.4
Rossignol, S.5
Jule, M.L.6
Thibaud, N.7
Faussat, A.M.8
Tauber, M.9
Bouc, Y.L.10
Netchine, I.11
-
32
-
-
84862540114
-
Epigenetic and genetic diagnosis of Silver-Russell syndrome
-
Eggermann T, Spengler S, Gogiel M, Begemann M, Elbracht M. Epigenetic and genetic diagnosis of Silver-Russell syndrome. Expert Rev Mol Diagn 2012;12:459-71.
-
(2012)
Expert Rev Mol Diagn
, vol.12
, pp. 459-471
-
-
Eggermann, T.1
Spengler, S.2
Gogiel, M.3
Begemann, M.4
Elbracht, M.5
-
33
-
-
84883826863
-
IGF2/H19 hypomethylation is tissue, cell, and CpG site dependent and not correlated with body asymmetry in adolescents with Silver-Russell syndrome
-
Kannenberg K, Weber K, Binder C, Urban C, Kirschner HJ, Binder G. IGF2/H19 hypomethylation is tissue, cell, and CpG site dependent and not correlated with body asymmetry in adolescents with Silver-Russell syndrome. Clin Epigenetics 2012;4:15.
-
(2012)
Clin Epigenetics
, vol.4
, pp. 15
-
-
Kannenberg, K.1
Weber, K.2
Binder, C.3
Urban, C.4
Kirschner, H.J.5
Binder, G.6
-
34
-
-
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, Reik W. Epigenetic modifications in an imprinting cluster are controlled by a hierarchy of DMRs suggesting long-range chromatin interactions. Hum Mol Genet 2003;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
Reik, W.11
-
35
-
-
79952605614
-
Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome
-
Nativio R, Sparago A, Ito Y, Weksberg R, Riccio A, Murrell A. Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome. Hum Mol Genet 2011;20:1363-74.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 1363-1374
-
-
Nativio, R.1
Sparago, A.2
Ito, Y.3
Weksberg, R.4
Riccio, A.5
Murrell, A.6
-
36
-
-
84878568511
-
Induced DNA demethylation can reshape chromatin topology at the IGF2-H19 locus
-
Ito Y, Nativio R, Murrell A. Induced DNA demethylation can reshape chromatin topology at the IGF2-H19 locus. Nucleic Acids Res 2013;41:5290-302.
-
(2013)
Nucleic Acids Res
, vol.41
, pp. 5290-5302
-
-
Ito, Y.1
Nativio, R.2
Murrell, A.3
-
37
-
-
84891960330
-
Oct4/Sox2 binding sites contribute to maintaining hypomethylation of the maternal igf2/h19 imprinting control region
-
Zimmerman DL, Boddy CS, Schoenherr CS. Oct4/Sox2 binding sites contribute to maintaining hypomethylation of the maternal igf2/h19 imprinting control region. PLoS ONE 2013;8:e81962.
-
(2013)
PLoS ONE
, vol.8
-
-
Zimmerman, D.L.1
Boddy, C.S.2
Schoenherr, C.S.3
|