-
5
-
-
0033118880
-
Stopped at the border: Boundaries and insulators
-
Bell AC, Felsenfeld G. 1999. S topped at the border: boundaries and insulators. Curr. Opin. Genet. Dev. 9:191-98
-
(1999)
Curr. Opin. Genet. Dev.
, vol.9
, pp. 191-198
-
-
Bell, A.C.1
Felsenfeld, G.2
-
6
-
-
0034713375
-
Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene
-
Bell AC, Felsenfeld G. 2000. Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene. Nature 405:482-85
-
(2000)
Nature
, vol.405
, pp. 482-485
-
-
Bell, A.C.1
Felsenfeld, G.2
-
7
-
-
0035930660
-
Dnmt3L and the establishment of maternal genomic imprints
-
Bourc'his D, Xu GL, Lin CS, Bollman B, Bestor TH. 2001. Dnmt3L and the establishment of maternal genomic imprints. Science 294:2536-39
-
(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
-
8
-
-
0027236694
-
The ontogeny of allele-specific methylation associated with imprinted genes in the mouse
-
Brandeis M, Kafri T, Ariel M, Chaillet JR, McCarrey J, et al. 1993. The ontogeny of allele-specific methylation associated with imprinted genes in the mouse. EMBO J. 12: 3669-77
-
(1993)
EMBO J.
, vol.12
, pp. 3669-3677
-
-
Brandeis, M.1
Kafri, T.2
Ariel, M.3
Chaillet, J.R.4
McCarrey, J.5
-
10
-
-
0034931032
-
The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice
-
Bressler J, Tsai TF, Wu MY, Tsai SF, Ramirez MA, et al. 2001. The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice. Nat. Genet. 28:232-40
-
(2001)
Nat. Genet.
, vol.28
, pp. 232-240
-
-
Bressler, J.1
Tsai, T.F.2
Wu, M.Y.3
Tsai, S.F.4
Ramirez, M.A.5
-
11
-
-
0036641071
-
X-chromosome inactivation: Closing in on proteins that bind Xist RNA
-
Brockdorff N. 2002. X-chromosome inactivation: closing in on proteins that bind Xist RNA. Trends Genet. 18:352-58
-
(2002)
Trends Genet.
, vol.18
, pp. 352-358
-
-
Brockdorff, N.1
-
12
-
-
0035003096
-
Disruption of the bipartite imprinting center in a family with Angelman syndrome
-
Buiting K, Barnicoat A, Lich C, Pembrey M, Malcolm S, Horsthemke B. 2001. Disruption of the bipartite imprinting center in a family with Angelman syndrome. Am. J. Hum. Genet. 68:1290-94
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 1290-1294
-
-
Buiting, K.1
Barnicoat, A.2
Lich, C.3
Pembrey, M.4
Malcolm, S.5
Horsthemke, B.6
-
13
-
-
0037371674
-
Epimutations in Prader-Willi and Angelman syndromes: A molecular study of 136 patients with an imprinting defect
-
Buiting K, Gross S, Lich C, Gillessen-Kaesbach G, El-Maarri O, Horsthemke B. 2003. Epimutations in Prader-Willi and Angelman syndromes: a molecular study of 136 patients with an imprinting defect. Am. J. Hum. Genet. 72:571-77
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 571-577
-
-
Buiting, K.1
Gross, S.2
Lich, C.3
Gillessen-Kaesbach, G.4
El-Maarri, O.5
Horsthemke, B.6
-
14
-
-
0031844688
-
Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster
-
Caspary T, Cleary MA, Baker CC, Guan XJ, Tilghman SM. 1998. Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster. Mol. Cell. Blol. 18: 3466-74
-
(1998)
Mol. Cell. Blol.
, vol.18
, pp. 3466-3474
-
-
Caspary, T.1
Cleary, M.A.2
Baker, C.C.3
Guan, X.J.4
Tilghman, S.M.5
-
15
-
-
0034687740
-
Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization
-
Cavaille J, Buiting K, Kiefmann M, Lalande M, Brannan CI, et al. 2000. Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization. Proc. Natl. Acad. Sci. USA 97:14311-16
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 14311-14316
-
-
Cavaille, J.1
Buiting, K.2
Kiefmann, M.3
Lalande, M.4
Brannan, C.I.5
-
16
-
-
0034749783
-
Retrotransposed genes such as Frat3 in the mouse chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion site
-
Chai JH, Locke DP, Ohta T, Greally JM, Nicholls RD. 2001. Retrotransposed genes such as Frat3 in the mouse chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion site. Mamm. Genome 12:813-21
-
(2001)
Mamm. Genome
, vol.12
, pp. 813-821
-
-
Chai, J.H.1
Locke, D.P.2
Ohta, T.3
Greally, J.M.4
Nicholls, R.D.5
-
17
-
-
0035336299
-
The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a
-
Chamberlain SJ, Brannan CI. 2001. The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a. Genomics 73:316-22
-
(2001)
Genomics
, vol.73
, pp. 316-322
-
-
Chamberlain, S.J.1
Brannan, C.I.2
-
18
-
-
0037059554
-
CTCF, a candidate transacting factor for X-inactivation choice
-
Chao W, Huynh KD, Spencer RJ, Davidow LS, Lee JT. 2002. CTCF, a candidate transacting factor for X-inactivation choice. Science 295:345-47
-
(2002)
Science
, vol.295
, pp. 345-347
-
-
Chao, W.1
Huynh, K.D.2
Spencer, R.J.3
Davidow, L.S.4
Lee, J.T.5
-
19
-
-
0036532224
-
X-chromosome inactivation and the search for chromosome-wide silencers
-
Cohen DE, Lee JT. 2002. X-chromosome inactivation and the search for chromosome-wide silencers. Curr. Opin. Genet. Dev. 12:219-24
-
(2002)
Curr. Opin. Genet. Dev.
, vol.12
, pp. 219-224
-
-
Cohen, D.E.1
Lee, J.T.2
-
20
-
-
0034081857
-
Histone macroH2A1 is concentrated in the inactive X chromosome of female preimplantation mouse embryos
-
Costanzi C, Stein P, Worrad DM, Schultz RM, Pehrson JR. 2000. Histone macroH2A1 is concentrated in the inactive X chromosome of female preimplantation mouse embryos. Development 127:2283-89
-
(2000)
Development
, vol.127
, pp. 2283-2289
-
-
Costanzi, C.1
Stein, P.2
Worrad, D.M.3
Schultz, R.M.4
Pehrson, J.R.5
-
21
-
-
0035308792
-
Elucidation of the minimal sequence required to imprint H19 transgenes
-
Cranston MJ, Spinka TL, Elson DA, Bartolomei MS. 2001. Elucidation of the minimal sequence required to imprint H19 transgenes. Genomics 73:98-107
-
(2001)
Genomics
, vol.73
, pp. 98-107
-
-
Cranston, M.J.1
Spinka, T.L.2
Elson, D.A.3
Bartolomei, M.S.4
-
22
-
-
0033499692
-
Functional analysis of the DXPas34 locus, a 3′ regulator of Xist expression
-
Debrand E, Chureau C, Arnaud D, Avner P, Heard E. 1999. Functional analysis of the DXPas34 locus, a 3′ regulator of Xist expression. Mol. Cell. Biol. 19:8513-25
-
(1999)
Mol. Cell. Biol.
, vol.19
, pp. 8513-8525
-
-
Debrand, E.1
Chureau, C.2
Arnaud, D.3
Avner, P.4
Heard, E.5
-
23
-
-
0025967857
-
Parental imprinting of the mouse insulin-like growth factor II gene
-
DeChiara TM, Robertson EJ, Efstratiadis A. 1991. Parental imprinting of the mouse insulin-like growth factor II gene. Cell 64: 849-59
-
(1991)
Cell
, vol.64
, pp. 849-859
-
-
DeChiara, T.M.1
Robertson, E.J.2
Efstratiadis, A.3
-
24
-
-
0033754151
-
Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which is highly expressed in brain
-
de los Santos T, Schweizer J, Rees CA, Francke U. 2000. Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which is highly expressed in brain. Am. J. Hum. Genet. 67:1067-82
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 1067-1082
-
-
De Los Santos, T.1
Schweizer, J.2
Rees, C.A.3
Francke, U.4
-
25
-
-
0033832962
-
Deletion of a silencer element disrupts H19 imprinting independently of a DNa methylation epigenetic switch
-
Drewell RA, Brenton JD, Ainscough JF, Barton SC, Hilton KJ, et al. 2000. Deletion of a silencer element disrupts H19 imprinting independently of a DNA methylation epigenetic switch. Development 127:3419-28
-
(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
-
26
-
-
0035090961
-
Maternal methylation imprints on human chromosome 15 are established during or after fertilization
-
El-Maarri O, Buiting K, Peery EG, Kroisel PM, Balaban B, et al. 2001. Maternal methylation imprints on human chromosome 15 are established during or after fertilization. Nat Genet. 27:341-44
-
(2001)
Nat Genet.
, vol.27
, pp. 341-344
-
-
El-Maarri, O.1
Buiting, K.2
Peery, E.G.3
Kroisel, P.M.4
Balaban, B.5
-
27
-
-
0034326859
-
Sequence and functional comparison in the Beckwith-Wiedemann region: Implications for a novel imprinting centre and extended imprinting
-
Engemann S, Strodicke M, Paulsen M, Franck O, Reinhardt R, et al. 2000. Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting. Hum. Mol. Genet. 9:2691-706
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2691-2706
-
-
Engemann, S.1
Strodicke, M.2
Paulsen, M.3
Franck, O.4
Reinhardt, R.5
-
28
-
-
17144438935
-
The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletion
-
Farber C, Dittrich B, Buiting K, Horsthemke B. 1999. The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletion. Hum. Mol. Genet. 8:337-43
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 337-343
-
-
Farber, C.1
Dittrich, B.2
Buiting, K.3
Horsthemke, B.4
-
29
-
-
0036831864
-
Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1
-
Fitzpatrick GV, Soloway PD, Higgins MJ. 2002. Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1. Nat. Genet. 32:426-31
-
(2002)
Nat. Genet.
, vol.32
, pp. 426-431
-
-
Fitzpatrick, G.V.1
Soloway, P.D.2
Higgins, M.J.3
-
30
-
-
0037011058
-
Allele-specific histone lysine methylation marks regulatory regions at imprinted mouse genes
-
Fournier C, Goto Y, Ballestar E, Delaval K, Hever AM, et al. 2002. Allele-specific histone lysine methylation marks regulatory regions at imprinted mouse genes. EMBO J. 21:6560-70
-
(2002)
EMBO J.
, vol.21
, pp. 6560-6570
-
-
Fournier, C.1
Goto, Y.2
Ballestar, E.3
Delaval, K.4
Hever, A.M.5
-
31
-
-
0032878252
-
Methylation sequencing analysis refines the region of H19 epimutation in Wilms tumor
-
Frevel MA, Sowerby SJ, Petersen GB, Reeve AE. 1999. Methylation sequencing analysis refines the region of H19 epimutation in Wilms tumor. J. Biol. Chem. 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
-
32
-
-
0035869208
-
Association of acetylated histones with paternally expressed genes in the Prader-Willi deletion region
-
Fulmer-Smentek SB, Francke U. 2001. Association of acetylated histones with paternally expressed genes in the Prader-Willi deletion region. Hum. Mol. Genet. 10:645-52
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 645-652
-
-
Fulmer-Smentek, S.B.1
Francke, U.2
-
33
-
-
0036724342
-
Evidence for the role of PWCR1/HBII-85 C/D box small nucleolar RNAs in Prader-Willi syndrome
-
Gallagher RC, Pils B, Albalwi M, Francke U. 2002. Evidence for the role of PWCR1/HBII-85 C/D box small nucleolar RNAs in Prader-Willi syndrome. Am. J. Hum. Genet. 71:669-78
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 669-678
-
-
Gallagher, R.C.1
Pils, B.2
Albalwi, M.3
Francke, U.4
-
34
-
-
0027158855
-
Parental genomic imprinting of the human IGF2 gene
-
Giannoukakis N, Deal C, Paquette J, Goodyer CG, Polychronakos C. 1993. Parental genomic imprinting of the human IGF2 gene. Nat. Genet. 4:98-101
-
(1993)
Nat. Genet.
, vol.4
, pp. 98-101
-
-
Giannoukakis, N.1
Deal, C.2
Paquette, J.3
Goodyer, C.G.4
Polychronakos, C.5
-
35
-
-
0034928861
-
DNA methylation is linked to deacetylation of histone H3, but not H4, on the imprinted genes Snrpn and U2af1-rs1
-
Gregory RI, Randall TE, Johnson CA, Khosla S, Hatada I, et al. 2001. DNA methylation is linked to deacetylation of histone H3, but not H4, on the imprinted genes Snrpn and U2af1-rs1. Mol. Cell. Biol. 21:5426-36
-
(2001)
Mol. Cell. Biol.
, vol.21
, pp. 5426-5436
-
-
Gregory, R.I.1
Randall, T.E.2
Johnson, C.A.3
Khosla, S.4
Hatada, I.5
-
36
-
-
0035102797
-
Establishment and maintenance of DNA methylation patterns in mouse Ndn: Implications for maintenance of imprinting in target genes of the imprinting center
-
Hanel ML, 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. 21:2384-92
-
(2001)
Mol. Cell. Biol.
, vol.21
, pp. 2384-2392
-
-
Hanel, M.L.1
Wevrick, R.2
-
37
-
-
0034713275
-
CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus
-
Hark AT, Schoenherr CJ, Katz DJ, Ingram RS, Levorse JM, Tilghrnan SM. 2000. CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus. Nature 405:486-89
-
(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
Tilghrnan, S.M.6
-
38
-
-
0036333103
-
Dnmt3L cooperates with the Dnmt3 family of de novo DNA methyltransferases to establish maternal imprints in mice
-
Hata K, Okano M, Lei H, Li E. 2002. Dnmt3L cooperates with the Dnmt3 family of de novo DNA methyltransferases to establish maternal imprints in mice. Development 129: 1983-93
-
(2002)
Development
, vol.129
, pp. 1983-1993
-
-
Hata, K.1
Okano, M.2
Lei, H.3
Li, E.4
-
39
-
-
0035861875
-
Methylation of histone H3 at Lys-9 is an early mark on the X chromosome during X inactivation
-
Heard E, Rougeulle C, Arnaud D, Avner P, Allis CD, Spector DL. 2001. Methylation of histone H3 at Lys-9 is an early mark on the X chromosome during X inactivation. Cell 107:727-38
-
(2001)
Cell
, vol.107
, pp. 727-738
-
-
Heard, E.1
Rougeulle, C.2
Arnaud, D.3
Avner, P.4
Allis, C.D.5
Spector, D.L.6
-
40
-
-
0033026969
-
Imprinted methylation and its effect on expression of the mouse Zfp127 gene
-
Hershko A, Razin A, Shemer R. 1999. Imprinted methylation and its effect on expression of the mouse Zfp127 gene. Gene 234:323-27
-
(1999)
Gene
, vol.234
, pp. 323-327
-
-
Hershko, A.1
Razin, A.2
Shemer, R.3
-
41
-
-
0034284693
-
Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome
-
Horike S, Mitsuya K, Meguro M, Kotobuki N, Kashiwagi A, et al. 2000. Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome. Hum. Mol. Genet. 9:2075-83
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2075-2083
-
-
Horike, S.1
Mitsuya, K.2
Meguro, M.3
Kotobuki, N.4
Kashiwagi, A.5
-
42
-
-
0035937404
-
Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene
-
Howell CY, Bestor TH, Ding F, Latham KE, Mertineit C, et al. 2001. Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene. Cell 104:829-38
-
(2001)
Cell
, vol.104
, pp. 829-838
-
-
Howell, C.Y.1
Bestor, T.H.2
Ding, F.3
Latham, K.E.4
Mertineit, C.5
-
43
-
-
0033551109
-
Lack of reciprocal genomic imprinting of sense and antisense RNA of mouse insulin-like growth factor II receptor in the central nervous system
-
Hu JF, Balaguru KA, Ivaturi RD, Oruganti H, Li T, et al. 1999. Lack of reciprocal genomic imprinting of sense and antisense RNA of mouse insulin-like growth factor II receptor in the central nervous system. Biochem. Biophys. Res. Commun. 257:604-8
-
(1999)
Biochem. Biophys. Res. Commun.
, vol.257
, pp. 604-608
-
-
Hu, J.F.1
Balaguru, K.A.2
Ivaturi, R.D.3
Oruganti, H.4
Li, T.5
-
44
-
-
0032230178
-
Tissue-specific imprinting of the mouse insulin-like growth factor II receptor gene correlates with differential allele-specific DNA methylation
-
Hu JF, Oruganti H, Vu TH, Huffman AR. 1998. Tissue-specific imprinting of the mouse insulin-like growth factor II receptor gene correlates with differential allele-specific DNA methylation. Mol. Endocrinol. 12:220-32
-
(1998)
Mol. Endocrinol.
, vol.12
, pp. 220-232
-
-
Hu, J.F.1
Oruganti, H.2
Vu, T.H.3
Huffman, A.R.4
-
45
-
-
0035878537
-
Distant cis-elements regulate imprinted expression of the mouse p57(Kip2) (Cdkn1c) gene: Implications for the human disorder, Beckwith-Wiedemann syndrome
-
John RM, Ainscough JF, Barton SC, Surani MA. 2001. Distant cis-elements regulate imprinted expression of the mouse p57(Kip2) (Cdkn1c) gene: implications for the human disorder, Beckwith-Wiedemann syndrome. Hum. Mol. Genet. 10:1601-9
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1601-1609
-
-
John, R.M.1
Ainscough, J.F.2
Barton, S.C.3
Surani, M.A.4
-
46
-
-
0033870806
-
A transcriptional insulator at the imprinted H19/Igf2 locus
-
Kaffer CR, Srivastava M, Park KY, Ives E, Hsieh S, et al. 2000. A transcriptional insulator at the imprinted H19/Igf2 locus. Genes Dev. 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
-
47
-
-
0027180213
-
The insulin-like growth factor type-2 receptor gene is imprinted in the mouse but not in humans
-
Kalscheuer VM, Mariman EC, Schepens MT, Rehder H, Ropers 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.5
-
48
-
-
0037124080
-
A differentially methylated imprinting control region within the Kcnq1 locus harbors a methylation-sensitive chromatin insulator
-
Kanduri C, Fitzpatrick G, Mukhopadhyay R, Kanduri M, Lobanenkov V, et al. 2002. A differentially methylated imprinting control region within the Kcnq1 locus harbors a methylation-sensitive chromatin insulator. J. Biol. Chem. 277:18106-10
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 18106-18110
-
-
Kanduri, C.1
Fitzpatrick, G.2
Mukhopadhyay, R.3
Kanduri, M.4
Lobanenkov, V.5
-
49
-
-
0034177668
-
The 5′ flank of mouse H19 in an unusual chromatin conformation unidirectionally blocks enhancer-promoter communication
-
Kanduri C, Holmgren C, Pilartz M, Franklin G, Kanduri M, et al. 2000a. The 5′ flank of mouse H19 in an unusual chromatin conformation unidirectionally blocks enhancer-promoter communication. Curr. Biol. 10:449-57
-
(2000)
Curr. Biol.
, vol.10
, pp. 449-457
-
-
Kanduri, C.1
Holmgren, C.2
Pilartz, M.3
Franklin, G.4
Kanduri, M.5
-
50
-
-
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 CF, et al. 2000b. Functional association of CTCF with the insulator upstream of the H19 gene is parent of origin-specific and methylation-sensitive, Curr. Biol. 10:853-56
-
(2000)
Curr. Biol.
, vol.10
, pp. 853-856
-
-
Kanduri, C.1
Pant, V.2
Loukinov, D.3
Pugacheva, E.4
Qi, C.F.5
-
51
-
-
0037322797
-
Methylation-sensitive binding of transcription factor YY1 to an insulator sequence within the paternally expressed imprinted gene, Peg3
-
Kim J, Kollhoff A, Bergmann A, Stubbs L. 2003. Methylation-sensitive binding of transcription factor YY1 to an insulator sequence within the paternally expressed imprinted gene, Peg3. Hum. Mol. Genet. 12:233-45
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 233-245
-
-
Kim, J.1
Kollhoff, A.2
Bergmann, A.3
Stubbs, L.4
-
52
-
-
0034730332
-
Disruption of imprinted X inactivation by parent-of-origin effects at Tsix
-
Lee JT. 2000. Disruption of imprinted X inactivation by parent-of-origin effects at Tsix. Cell 103:17-27
-
(2000)
Cell
, vol.103
, pp. 17-27
-
-
Lee, J.T.1
-
53
-
-
0033609117
-
Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting
-
Lee MP, DeBaun MR, Mitsuya K, Galonek HL, Brandenburg S, et al. 1999. Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting. Proc. Natl. Acad. Sci. USA 96:5203-8
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 5203-5208
-
-
Lee, M.P.1
DeBaun, M.R.2
Mitsuya, K.3
Galonek, H.L.4
Brandenburg, S.5
-
54
-
-
0031052901
-
Paternal repression of the imprinted mouse Igf2r locus occurs during implantation and is stable in all tissues of the post-implantation mouse embryo
-
Lerchner W, Barlow DP. 1997. Paternal repression of the imprinted mouse Igf2r locus occurs during implantation and is stable in all tissues of the post-implantation mouse embryo. Mech. Dev. 61:141-49
-
(1997)
Mech. Dev.
, vol.61
, pp. 141-149
-
-
Lerchner, W.1
Barlow, D.P.2
-
55
-
-
0027378582
-
Role for DNA methylation in genomic imprinting
-
Li E, Beard C, Jaenisch R. 1993. Role for DNA methylation in genomic imprinting. Nature 366:362-65
-
(1993)
Nature
, vol.366
, pp. 362-365
-
-
Li, E.1
Beard, C.2
Jaenisch, R.3
-
56
-
-
0036205914
-
Methylation dynamics of imprinted genes in mouse germ cells
-
Lucifero D, Mertineit C, Clarke HJ, Bestor TH, Trasler JM. 2002. Methylation dynamics of imprinted genes in mouse germ cells. Genomics 79:530-38
-
(2002)
Genomics
, vol.79
, pp. 530-538
-
-
Lucifero, D.1
Mertineit, C.2
Clarke, H.J.3
Bestor, T.H.4
Trasler, J.M.5
-
57
-
-
0034118382
-
The imprinted antisense RNA at the Igf2r locus overlaps but does not imprint Mas1
-
Lyle R, Watanabe D, te Vruchte D, Lerchner W, Smrzka OW, et al. 2000. The imprinted antisense RNA at the Igf2r locus overlaps but does not imprint Mas1. Nat. Genet. 25:19-21
-
(2000)
Nat. Genet.
, vol.25
, pp. 19-21
-
-
Lyle, R.1
Watanabe, D.2
Te Vruchte, D.3
Lerchner, W.4
Smrzka, O.W.5
-
58
-
-
0033975096
-
Beckwith-Wiedemann syndrome: Imprinting in clusters revisited
-
Maher ER, Reik W. 2000. Beckwith-Wiedemann syndrome: imprinting in clusters revisited. J. Clin. Invest. 105:247-52
-
(2000)
J. Clin. Invest.
, vol.105
, pp. 247-252
-
-
Maher, E.R.1
Reik, W.2
-
59
-
-
0037321187
-
A differentially methylated region within the gene Kcnq1 functions as an imprinted promoter and silencer
-
Mancini-DiNardo D, Steele SJ, Ingram RS, Tilghman SM. 2003. A differentially methylated region within the gene Kcnq1 functions as an imprinted promoter and silencer. Hum. Mol. Genet. 12:283-94
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 283-294
-
-
Mancini-DiNardo, D.1
Steele, S.J.2
Ingram, R.S.3
Tilghman, S.M.4
-
60
-
-
0031044166
-
Xist-deficient mice are defective in dosage compensation but not spermatogenesis
-
Marahrens Y, Panning B, Dausman J, Strauss W, Jaenisch R. 1997. Xist-deficient mice are defective in dosage compensation but not spermatogenesis. Genes Dev. 11:156-66
-
(1997)
Genes Dev.
, vol.11
, pp. 156-166
-
-
Marahrens, Y.1
Panning, B.2
Dausman, J.3
Strauss, W.4
Jaenisch, R.5
-
61
-
-
0035875092
-
Control of Xist expression for imprinted and random X chromosome inactivation in mice
-
Matsui J, Goto Y, Takagi N. 2001. Control of Xist expression for imprinted and random X chromosome inactivation in mice. Hum. Mol. Genet. 10:1393-401
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1393-1401
-
-
Matsui, J.1
Goto, Y.2
Takagi, N.3
-
63
-
-
0032535289
-
Bisulfite genomic sequencing-derived methylation profile of the Xist gene throughout early mouse development
-
McDonald LE, Paterson CA, Kay GF. 1998. Bisulfite genomic sequencing-derived methylation profile of the Xist gene throughout early mouse development. Genomics 54:379-86
-
(1998)
Genomics
, vol.54
, pp. 379-386
-
-
McDonald, L.E.1
Paterson, C.A.2
Kay, G.F.3
-
64
-
-
0037022129
-
Histone H3 lysine 9 methylation occurs rapidly at the onset of random X chromosome inactivation
-
Mermoud JE, Popova B, Peters AH, Jenuwein T, Brockdorff N. 2002. Histone H3 lysine 9 methylation occurs rapidly at the onset of random X chromosome inactivation. Curr. Biol. 12:247-51
-
(2002)
Curr. Biol.
, vol.12
, pp. 247-251
-
-
Mermoud, J.E.1
Popova, B.2
Peters, A.H.3
Jenuwein, T.4
Brockdorff, N.5
-
65
-
-
0032813924
-
LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids
-
Mitsuya K, Meguro M, Lee MP, Katoh M, Schulz TC, et al. 1999. LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids. Hum. Mol. Genet. 8:1209-17
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1209-1217
-
-
Mitsuya, K.1
Meguro, M.2
Lee, M.P.3
Katoh, M.4
Schulz, T.C.5
-
66
-
-
0035875043
-
Tsix-mediated repression of Xist accumulation is not sufficient for normal random X inactivation
-
Morey C, Arnaud D, Avner P, Clerc P. 2001. Tsix-mediated repression of Xist accumulation is not sufficient for normal random X inactivation. Hum. Mol. Genet. 10:1403-11
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1403-1411
-
-
Morey, C.1
Arnaud, D.2
Avner, P.3
Clerc, P.4
-
67
-
-
0035879217
-
Loss of Xist imprinting in diploid parthenogenetic preimplantation embryos
-
Nesterova TB, Barton SC, Surani MA, Brockdorff N. 2001. Loss of Xist imprinting in diploid parthenogenetic preimplantation embryos. Dev. Biol. 235:343-50
-
(2001)
Dev. Biol.
, vol.235
, pp. 343-350
-
-
Nesterova, T.B.1
Barton, S.C.2
Surani, M.A.3
Brockdorff, N.4
-
68
-
-
0035777024
-
Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes
-
Nicholls RD, Knepper JL. 2001. Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes. Annu. Rev. Genomics Hum. Genet. 2:153-75
-
(2001)
Annu. Rev. Genomics Hum. Genet.
, vol.2
, pp. 153-175
-
-
Nicholls, R.D.1
Knepper, J.L.2
-
69
-
-
0027322519
-
IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome
-
Ohlsson R, Nystrom A, Pfeifer-Ohlsson S, Tohonen V, Hedborg F, et al. 1993. IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome. Nat. Genet. 4:94-97
-
(1993)
Nat. Genet.
, vol.4
, pp. 94-97
-
-
Ohlsson, R.1
Nystrom, A.2
Pfeifer-Ohlsson, S.3
Tohonen, V.4
Hedborg, F.5
-
70
-
-
0035336255
-
Allelic IGF2R repression does not correlate with expression of antisense RNA in human extraembryonic tissues
-
Oudejans CB, Westerman B, Wouters D, Gooyer S, Leegwater PA, et al. 2001. Allelic IGF2R repression does not correlate with expression of antisense RNA in human extraembryonic tissues. Genomics 73:331-37
-
(2001)
Genomics
, vol.73
, pp. 331-337
-
-
Oudejans, C.B.1
Westerman, B.2
Wouters, D.3
Gooyer, S.4
Leegwater, P.A.5
-
71
-
-
0030693368
-
Genomic imprinting in the rat: Linkage of Igf2 and H19 genes and opposite parental allele-specific expression during embryogenesis
-
Overall M, Bakker M, Spencer J, Parker N, Smith P, Dziadek M. 1997. Genomic imprinting in the rat: linkage of Igf2 and H19 genes and opposite parental allele-specific expression during embryogenesis. Genomics 45:416-20
-
(1997)
Genomics
, vol.45
, pp. 416-420
-
-
Overall, M.1
Bakker, M.2
Spencer, J.3
Parker, N.4
Smith, P.5
Dziadek, M.6
-
72
-
-
0037338544
-
The nucleotides responsible for the direct physical contact between the chromatin insulator protein CTCF and the H19 imprinting control region manifest parent of origin-specific long-distance insulation and methylation-free domains
-
Pant V, Mariano P, Kanduri C, Mattsson A, Lobanenkov V, et al. 2003. The nucleotides responsible for the direct physical contact between the chromatin insulator protein CTCF and the H19 imprinting control region manifest parent of origin-specific long-distance insulation and methylation-free domains. Genes Dev. 17:586-90
-
(2003)
Genes Dev.
, vol.17
, pp. 586-590
-
-
Pant, V.1
Mariano, P.2
Kanduri, C.3
Mattsson, A.4
Lobanenkov, V.5
-
73
-
-
0035839097
-
Epigenetic aspects of X-chromosome dosage compensation
-
Park Y, Kuroda MI. 2001. Epigenetic aspects of X-chromosome dosage compensation. Science 293:1083-85
-
(2001)
Science
, vol.293
, pp. 1083-1085
-
-
Park, Y.1
Kuroda, M.I.2
-
74
-
-
0036846536
-
The imprinting mechanism of the Prader-Willi/Angelman regional control center
-
Perk J, Makedonski K, Lande L, Cedar H, Razin A, Shemer R. 2002. The imprinting mechanism of the Prader-Willi/Angelman regional control center. EMBO J. 21:5807-14
-
(2002)
EMBO J.
, vol.21
, pp. 5807-5814
-
-
Perk, J.1
Makedonski, K.2
Lande, L.3
Cedar, H.4
Razin, A.5
Shemer, R.6
-
76
-
-
0035173738
-
Methylation profiles of DXPas34 during the onset of X-inactivation
-
Prissette M, El-Maarri O, Arnaud D, Walter J, Avner P. 2001. Methylation profiles of DXPas34 during the onset of X-inactivation. Hum. Mol. Genet. 10:31-38
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 31-38
-
-
Prissette, M.1
El-Maarri, O.2
Arnaud, D.3
Walter, J.4
Avner, P.5
-
77
-
-
9844265406
-
The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis
-
Qian N, Frank D, O'Keefe D, Dao D, Zhao L, et al. 1997. The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis. Hum. Mol. Genet. 6:2021-29
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 2021-2029
-
-
Qian, N.1
Frank, D.2
O'Keefe, D.3
Dao, D.4
Zhao, L.5
-
78
-
-
0026732759
-
Parental imprinting of the human H19 gene
-
Rachmilewitz J, Goshen R, Ariel I, Schneider T, de Groot N, Hochberg A. 1992. Parental imprinting of the human H19 gene. FEBS Lett 309:25-28
-
(1992)
FEBS Lett
, vol.309
, pp. 25-28
-
-
Rachmilewitz, J.1
Goshen, R.2
Ariel, I.3
Schneider, T.4
De Groot, N.5
Hochberg, A.6
-
79
-
-
0037154972
-
Epigenetic codes for heterochromatin formation and silencing: Rounding up the usual suspects
-
Richards FJ, Elgin SC. 2002. Epigenetic codes for heterochromatin formation and silencing: rounding up the usual suspects. Cell 108:489-500
-
(2002)
Cell
, vol.108
, pp. 489-500
-
-
Richards, F.J.1
Elgin, S.C.2
-
80
-
-
0032492629
-
Absence of an obvious molecular imprinting mechanism in a human fetus with monoallelic IGF2R expression
-
Riesewijk AM, Xu YQ, Schepens MT, Mariman EM, Polychronakos C, et al. 1998. Absence of an obvious molecular imprinting mechanism in a human fetus with monoallelic IGF2R expression. Biochem. Biophys. Res. Commun. 245:272-77
-
(1998)
Biochem. Biophys. Res. Commun.
, vol.245
, pp. 272-277
-
-
Riesewijk, A.M.1
Xu, Y.Q.2
Schepens, M.T.3
Mariman, E.M.4
Polychronakos, C.5
-
81
-
-
0035509699
-
The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A
-
Runte M, Huttenhofer A, Gross S, Kiefmann M, Horsthemke B, Buiting K. 2001. The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A. Hum. Mol. Genet. 10:2687-700
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 2687-2700
-
-
Runte, M.1
Huttenhofer, A.2
Gross, S.3
Kiefmann, M.4
Horsthemke, B.5
Buiting, K.6
-
82
-
-
0034665756
-
X inactivation in the mouse embryo deficient for Dnmt1: Distinct effect of hypomethylation on imprinted and random X inactivation
-
Sado T, Fenner MH, Tan SS, Tam P, Shioda T, Li E. 2000. X inactivation in the mouse embryo deficient for Dnmt1: distinct effect of hypomethylation on imprinted and random X inactivation. Dev. Biol. 225:294-303
-
(2000)
Dev. Biol.
, vol.225
, pp. 294-303
-
-
Sado, T.1
Fenner, M.H.2
Tan, S.S.3
Tam, P.4
Shioda, T.5
Li, E.6
-
83
-
-
0035030004
-
Regulation of imprinted X-chromosome inactivation in mice by Tsix
-
Sado T, Wang Z, Sasaki H, Li E. 2001. Regulation of imprinted X-chromosome inactivation in mice by Tsix. Development 128:1275-86
-
(2001)
Development
, vol.128
, pp. 1275-1286
-
-
Sado, T.1
Wang, Z.2
Sasaki, H.3
Li, E.4
-
84
-
-
0033924890
-
Parent-of-origin specific histone acetylation and reactivation of a key imprinted gene locus in Prader-Willi syndrome
-
Saitoh S, Wada T. 2000. Parent-of-origin specific histone acetylation and reactivation of a key imprinted gene locus in Prader-Willi syndrome. Am. J. Hum. Genet. 66:1958-62
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 1958-1962
-
-
Saitoh, S.1
Wada, T.2
-
85
-
-
0037228669
-
CTCF maintains differential methylation at the Igf2/H19 locus
-
Schoenherr CJ, Levorse JM, Tilghman SM. 2003. CTCF maintains differential methylation at the Igf2/H19 locus. Nat. Genet. 33:66-69
-
(2003)
Nat. Genet.
, vol.33
, pp. 66-69
-
-
Schoenherr, C.J.1
Levorse, J.M.2
Tilghman, S.M.3
-
86
-
-
0031848147
-
Methylation analysis of the PWS/AS region does not support an enhancer-competition model
-
Schumacher A, Buiting K, Zeschnigk M, Doerfler W, Horsthemke B. 1998. Methylation analysis of the PWS/AS region does not support an enhancer-competition model. Nat. Genet. 19:324-25
-
(1998)
Nat. Genet.
, vol.19
, pp. 324-325
-
-
Schumacher, A.1
Buiting, K.2
Zeschnigk, M.3
Doerfler, W.4
Horsthemke, B.5
-
87
-
-
0033035048
-
In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit
-
Schweizer J, Zynger D, Francke U. 1999. In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit. Hum. Mol. Genet. 8:555-66
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 555-566
-
-
Schweizer, J.1
Zynger, D.2
Francke, U.3
-
88
-
-
18844472627
-
Stabilization of Xist RNA mediates initiation of X chromosome inactivation
-
Sheardown SA, Duthie SM, Johnston CM, Newall AE, Formstone EJ, et al. 1997. Stabilization of Xist RNA mediates initiation of X chromosome inactivation. Cell 91:99-107
-
(1997)
Cell
, vol.91
, pp. 99-107
-
-
Sheardown, S.A.1
Duthie, S.M.2
Johnston, C.M.3
Newall, A.E.4
Formstone, E.J.5
-
89
-
-
0030886796
-
Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern
-
Shemer R, Birger Y, Riggs AD, Razin A. 1997. Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern. Proc. Natl. Acad. Sci. USA 94:10267-72
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 10267-10272
-
-
Shemer, R.1
Birger, Y.2
Riggs, A.D.3
Razin, A.4
-
90
-
-
0037075032
-
The non-coding Air RNA is required for silencing autosomal imprinted genes
-
Sleutels F, Zwart R, Barlow DP. 2002. The non-coding Air RNA is required for silencing autosomal imprinted genes. Nature 415:810-13
-
(2002)
Nature
, vol.415
, pp. 810-813
-
-
Sleutels, F.1
Zwart, R.2
Barlow, D.P.3
-
91
-
-
0033529207
-
A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome
-
Smilinich NJ, Day CD, Fitzpatrick GV, Caldwell GM, Lossie AC, et al. 1999. A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome. Proc. Natl. Acad. Sci. USA 96:8064-69
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 8064-8069
-
-
Smilinich, N.J.1
Day, C.D.2
Fitzpatrick, G.V.3
Caldwell, G.M.4
Lossie, A.C.5
-
92
-
-
0028864462
-
Conservation of a maternal-specific methylation signal at the human IGF2R locus
-
Smrzka OW, Fae I, Stoger R, Kurzbauer R, Fischer GF, et al. 1995. Conservation of a maternal-specific methylation signal at the human IGF2R locus. Hum. Mol. Genet. 4:1945-52
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1945-1952
-
-
Smrzka, O.W.1
Fae, I.2
Stoger, R.3
Kurzbauer, R.4
Fischer, G.F.5
-
93
-
-
0034658545
-
H19 and Igf2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream of H19
-
Srivastava M, Hsieh S, Grinberg A, Williams-Simons L, Huang SP, Pfeifer K. 2000. H19 and Igf2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream of H19. Genes Dev. 14:1186-95
-
(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
-
94
-
-
0027400888
-
Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal
-
Stöger R, Kubicka P, Liu C-G, Kafri T, Razin A, et al. 1993. Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal. Cell 73:61-71
-
(1993)
Cell
, vol.73
, pp. 61-71
-
-
Stöger, R.1
Kubicka, P.2
Liu, C.-G.3
Kafri, T.4
Razin, A.5
-
95
-
-
0034193691
-
Maternal-specific footprints at putative CTCF sites in the H19 imprinting control region give evidence for insulator function
-
Szabo PE, Tang S-H, Rentsendorj A, Pfeifer GP, Mann JR. 2000. Maternal-specific footprints at putative CTCF sites in the H19 imprinting control region give evidence for insulator function. Curr. Biol. 10:607-10
-
(2000)
Curr. Biol.
, vol.10
, pp. 607-610
-
-
Szabo, P.E.1
Tang, S.-H.2
Rentsendorj, A.3
Pfeifer, G.P.4
Mann, J.R.5
-
96
-
-
0036151866
-
Epigenetic analysis of the Dlk1-Gtl2 imprinted domain on mouse chromosome 12: Implications for imprinting control from comparison with Igf2-H19
-
Takada S, Paulsen M, Tevendale M, Tsai CE, Kelsey G, et al. 2002. Epigenetic analysis of the Dlk1-Gtl2 imprinted domain on mouse chromosome 12: implications for imprinting control from comparison with Igf2-H19. Hum. Mol. Genet. 11:77-86
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 77-86
-
-
Takada, S.1
Paulsen, M.2
Tevendale, M.3
Tsai, C.E.4
Kelsey, G.5
-
97
-
-
0032419812
-
Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2
-
Thorvaldsen JL, Duran KL, Bartolomei MS. 1998. Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. Genes Dev. 12:3693-702
-
(1998)
Genes Dev.
, vol.12
, pp. 3693-3702
-
-
Thorvaldsen, J.L.1
Duran, K.L.2
Bartolomei, M.S.3
-
98
-
-
0036211514
-
Analysis of sequence upstream of the endogenous H19 gene reveals elements both essential and dispensable for imprinting
-
Thorvaldsen JL, Mann MR, Nwoko O, Duran KL, Bartolomei MS. 2002. Analysis of sequence upstream of the endogenous H19 gene reveals elements both essential and dispensable for imprinting. Mol. Cell. Biol. 22: 2450-62
-
(2002)
Mol. Cell. Biol.
, vol.22
, pp. 2450-2462
-
-
Thorvaldsen, J.L.1
Mann, M.R.2
Nwoko, O.3
Duran, K.L.4
Bartolomei, M.S.5
-
99
-
-
0030802395
-
A 5′ 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development
-
Tremblay KD, Duran KL, Bartolomei MS. 1997. A 5′ 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development. Mol. Cell. Biol. 17:4322-29
-
(1997)
Mol. Cell. Biol.
, vol.17
, pp. 4322-4329
-
-
Tremblay, K.D.1
Duran, K.L.2
Bartolomei, M.S.3
-
100
-
-
0028968205
-
A paternal-specific methylation imprint marks the alleles of the mouse H19 gene
-
Tremblay KD, Saam JR, Ingram RS, Tilghman SM, Bartolomei MS. 1995. A paternal-specific methylation imprint marks the alleles of the mouse H19 gene. Nat. Genet. 9: 407-13
-
(1995)
Nat. 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
-
101
-
-
0028224130
-
Genomic imprinting - Defusing the ovarian time bomb
-
Varmuza S, Mann M. 1994. Genomic imprinting - defusing the ovarian time bomb. Trends Genet. 10:118-23
-
(1994)
Trends Genet.
, vol.10
, pp. 118-123
-
-
Varmuza, S.1
Mann, M.2
-
102
-
-
0037072661
-
Regulation of heterochromatic silencing and histone H3 lysine-9 methylation by RNAi
-
Volpe TA, Kidner C, Hall IM, Teng G, Grewal SI, Martienssen RA. 2002. Regulation of heterochromatic silencing and histone H3 lysine-9 methylation by RNAi. Science 297:1833-37
-
(2002)
Science
, vol.297
, pp. 1833-1837
-
-
Volpe, T.A.1
Kidner, C.2
Hall, I.M.3
Teng, G.4
Grewal, S.I.5
Martienssen, R.A.6
-
103
-
-
0034724290
-
An imprinted transcript, antisense to Nesp, adds complexity to the cluster of imprinted genes at the mouse Gnas locus
-
Wroe SF, Kelsey G, Skinner JA, Bodle D, Ball ST, et al. 2000. An imprinted transcript, antisense to Nesp, adds complexity to the cluster of imprinted genes at the mouse Gnas locus. Proc. Natl. Acad. Sci. USA 97:3342-46
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 3342-3346
-
-
Wroe, S.F.1
Kelsey, G.2
Skinner, J.A.3
Bodle, D.4
Ball, S.T.5
-
104
-
-
0036479009
-
Chromosomal silencing and localization are mediated by different domains of Xist RNA
-
Wutz A, Rasmussen TP, Jaenisch R. 2002. Chromosomal silencing and localization are mediated by different domains of Xist RNA. Nat. Genet. 30:167-74
-
(2002)
Nat. Genet.
, vol.30
, pp. 167-174
-
-
Wutz, A.1
Rasmussen, T.P.2
Jaenisch, R.3
-
105
-
-
0030694713
-
Imprinted expression of the Igf2r gene depends on an intronic CpG island
-
Wutz A, Smrzka OW, Schweifer N, Schellander K, Wagner EF, Barlow DP. 1997. Imprinted expression of the Igf2r gene depends on an intronic CpG island. Nature 389:745-49
-
(1997)
Nature
, vol.389
, pp. 745-749
-
-
Wutz, A.1
Smrzka, O.W.2
Schweifer, N.3
Schellander, K.4
Wagner, E.F.5
Barlow, D.P.6
-
106
-
-
0034743736
-
Non-imprinted Igf2r expression decreases growth and rescues the Tme mutation in mice
-
Wutz A, Theussl HC, Dausman J, Jaenisch R, Barlow DP, Wagner EF. 2001. Non-imprinted Igf2r expression decreases growth and rescues the Tme mutation in mice. Development 128:1881-87
-
(2001)
Development
, vol.128
, pp. 1881-1887
-
-
Wutz, A.1
Theussl, H.C.2
Dausman, J.3
Jaenisch, R.4
Barlow, D.P.5
Wagner, E.F.6
-
107
-
-
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 CD, 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. 69:1389-94
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 1389-1394
-
-
Xin, Z.1
Allis, C.D.2
Wagstaff, J.3
-
109
-
-
0031747932
-
A mouse model for Prader-Willi syndrome imprinting-centre mutations
-
Yang T, Adamson TE, Resnick JL, Leff S, Wevrick R, et al. 1998. A mouse model for Prader-Willi syndrome imprinting-centre mutations. Nat. Genet. 19:25-31
-
(1998)
Nat. Genet.
, vol.19
, pp. 25-31
-
-
Yang, T.1
Adamson, T.E.2
Resnick, J.L.3
Leff, S.4
Wevrick, R.5
-
110
-
-
0036911383
-
Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: Large-scale DNa methylation analysis reveals that DMR-Lit1 is a putative imprinting control region
-
Yatsuki H, Joh K, Higashimoto K, Soejima H, Arai Y, et al. 2002. Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: Large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region. Genome Res. 12:1860-70
-
(2002)
Genome Res.
, vol.12
, pp. 1860-1870
-
-
Yatsuki, H.1
Joh, K.2
Higashimoto, K.3
Soejima, H.4
Arai, Y.5
-
111
-
-
0026849544
-
Monoallelic expression of the human H19 gene
-
Zhang Y, Tycko B. 1992. Monoallelic expression of the human H19 gene. Nat. Genet. 1:40-44
-
(1992)
Nat. Genet.
, vol.1
, pp. 40-44
-
-
Zhang, Y.1
Tycko, B.2
-
112
-
-
0036364553
-
Mouse Xist expression begins at zygotic genome activation and is timed by a zygotic clock
-
Zuccotti M, Boiani M, Ponce R, Guizzardi S, Scandroglio R, et al. 2002. Mouse Xist expression begins at zygotic genome activation and is timed by a zygotic clock. Mol. Reprod. Dev. 61:14-20
-
(2002)
Mol. Reprod. Dev.
, vol.61
, pp. 14-20
-
-
Zuccotti, M.1
Boiani, M.2
Ponce, R.3
Guizzardi, S.4
Scandroglio, R.5
-
113
-
-
0035883743
-
Bidirectional action of the Igf2r imprint control element on upstream and downstream imprinted genes
-
Zwart R, Sleutels F, Wutz A, Schinkel AH, Barlow DP. 2001. Bidirectional action of the Igf2r imprint control element on upstream and downstream imprinted genes. Genes Dev. 15:2361-66
-
(2001)
Genes Dev.
, vol.15
, pp. 2361-2366
-
-
Zwart, R.1
Sleutels, F.2
Wutz, A.3
Schinkel, A.H.4
Barlow, D.P.5
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