-
1
-
-
0033923654
-
Sex-related differences in methionine metabolism and plasma homocysteine concentrations
-
Fukagawa NK, Martin JM, Wurthmann A, Prue AH, Ebenstein D, ORourke B: Sex-related differences in methionine metabolism and plasma homocysteine concentrations. Am. J. Clin. Nutr. 72(1), 22-29 (2000)
-
(2000)
Am. J. Clin. Nutr.
, vol.72
, Issue.1
, pp. 22-29
-
-
Fukagawa, N.K.1
Martin, J.M.2
Wurthmann, A.3
Prue, A.H.4
Ebenstein, D.5
Orourke, B.6
-
2
-
-
0041353558
-
An ICE pattern crystallizes
-
Spahn L, Barlow DP: An ICE pattern crystallizes. Nat. Genet. 35, 11-12 (2003).
-
(2003)
Nat. Genet.
, vol.35
, pp. 11-12
-
-
Spahn, L.1
Barlow, D.P.2
-
3
-
-
0027203606
-
Epigenetic mechanisms underlying the imprinting of the mouse H19 gene
-
Bartolomei MS, Webber AL, Brunkow ME, Tilghman SM: Epigenetic mechanisms underlying the imprinting of the mouse H19 gene. Genes Dev. 7, 1663-1673 (1993).
-
(1993)
Genes Dev.
, vol.7
, pp. 1663-1673
-
-
Bartolomei, M.S.1
Webber, A.L.2
Brunkow, M.E.3
Tilghman, S.M.4
-
4
-
-
0033152214
-
A potential imprint control element: Identification of a conserved 42 bp sequence upstream of H19
-
Frevel MA, Hornberg JJ, Reeve AE: A potential imprint control element: identification of a conserved 42 bp sequence upstream of H19. Trends Genet. 15, 216-218 (1999).
-
(1999)
Trends Genet.
, vol.15
, pp. 216-218
-
-
Frevel, M.A.1
Hornberg, J.J.2
Reeve, A.E.3
-
5
-
-
0028968205
-
A paternal-specific methylation imprint marks the alleles of the mouse H19 gene
-
Tremblay KD, Saam JR, Ingram RS, Tilghman SM, Bartolomei MS: A paternal-specific methylation imprint marks the alleles of the mouse H19 gene. Nat. Genet. 9, 407-413 (1995).
-
(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
-
6
-
-
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: 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).
-
(1997)
Mol. Cell. Biol.
, vol.17
, pp. 4322-4329
-
-
Tremblay, K.D.1
Duran, K.L.2
Bartolomei, M.S.3
-
7
-
-
0027236694
-
The ontogeny of allele-specific methylation associated with imprinted genes in the mouse
-
Brandeis M, Kafri T, Ariel M et al.: The ontogeny of allele-specific methylation associated with imprinted genes in the mouse. EMBO J. 12, 3669-3677 (1993).
-
(1993)
EMBO J.
, vol.12
, pp. 3669-3677
-
-
Brandeis, M.1
Kafri, T.2
Ariel, M.3
-
8
-
-
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 et al.: 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).
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 12509-12514
-
-
Moore, T.1
Constancia, M.2
Zubair, M.3
-
9
-
-
0027937839
-
Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes
-
Feil R, Walter J, Allen ND, Reik W: Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes. Development 120, 2933-2943 (1994).
-
(1994)
Development
, vol.120
, pp. 2933-2943
-
-
Feil, R.1
Walter, J.2
Allen, N.D.3
Reik, W.4
-
10
-
-
0027172684
-
Parental-origin-specific epigenetic modification of the mouse H19 gene
-
Ferguson-Smith AC, Sasaki H, Cattanach BM, Surani MA: Parental-origin-specific epigenetic modification of the mouse H19 gene. Nature 362, 751-755 (1993).
-
(1993)
Nature
, vol.362
, pp. 751-755
-
-
Ferguson-Smith, A.C.1
Sasaki, H.2
Cattanach, B.M.3
Surani, M.A.4
-
11
-
-
0032419812
-
Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2
-
Thorvaldsen JL, Duran KL, Bartolomei MS: Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. Genes Dev. 12, 3693-3702 (1998).
-
(1998)
Genes Dev.
, vol.12
, pp. 3693-3702
-
-
Thorvaldsen, J.L.1
Duran, K.L.2
Bartolomei, M.S.3
-
12
-
-
22544443322
-
Genomic imprinting recapitulated in the human b-globin locus
-
Tanimoto K, Shimotsuma M, Matsuzaki H et al.: Genomic imprinting recapitulated in the human b-globin locus. Proc. Natl Acad. Sci. USA 102, 10250-10255 (2005).
-
(2005)
Proc. Natl Acad. Sci. USA
, vol.102
, pp. 10250-10255
-
-
Tanimoto, K.1
Shimotsuma, M.2
Matsuzaki, H.3
-
13
-
-
1942422579
-
The H19 differentially methylated region marks the parental origin of a heterologous locus without gametic DNA methylation
-
Park KY, Sellars EA, Grinberg A, Huang SP, Pfeifer K: The H19 differentially methylated region marks the parental origin of a heterologous locus without gametic DNA methylation. Mol. Cell. Biol. 24, 3588-3595 (2004).
-
(2004)
Mol. Cell. Biol.
, vol.24
, pp. 3588-3595
-
-
Park, K.Y.1
Sellars, E.A.2
Grinberg, A.3
Huang, S.P.4
Pfeifer, K.5
-
14
-
-
76749128083
-
H19 imprinting control region methylation requires an imprinted environment only in the male germ line
-
Gebert C, Kunkel D, Grinberg A, Pfeifer K: H19 imprinting control region methylation requires an imprinted environment only in the male germ line. Mol. Cell. Biol. 30, 1108-1115 (2010).
-
(2010)
Mol. Cell. Biol.
, vol.30
, pp. 1108-1115
-
-
Gebert, C.1
Kunkel, D.2
Grinberg, A.3
Pfeifer, K.4
-
15
-
-
0035937404
-
Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene
-
Howell CY, Bestor TH, Ding F et al.: Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene. Cell 104, 829-838 (2001).
-
(2001)
Cell
, vol.104
, pp. 829-838
-
-
Howell, C.Y.1
Bestor, T.H.2
Ding, F.3
-
16
-
-
0027378582
-
Role for DNA methylation in genomic imprinting
-
Li E, Beard C, Jaenisch R: Role for DNA methylation in genomic imprinting. Nature 366, 362-365 (1993).
-
(1993)
Nature
, vol.366
, pp. 362-365
-
-
Li, E.1
Beard, C.2
Jaenisch, R.3
-
17
-
-
0030734880
-
Modulation of Igf2 genomic imprinting in mice induced by 5-azacytidine, an inhibitor of DNA methylation
-
Hu JF, Nguyen PH, Pham NV, Vu TH, Hoffman AR: Modulation of Igf2 genomic imprinting in mice induced by 5-azacytidine, an inhibitor of DNA methylation. Mol. Endocrinol. 11, 1891-1898 (1997).
-
(1997)
Mol. Endocrinol.
, vol.11
, pp. 1891-1898
-
-
Hu, J.F.1
Nguyen, P.H.2
Pham, N.V.3
Vu, T.H.4
Hoffman, A.R.5
-
18
-
-
0037011058
-
Allele-specific histone lysine methylation marks regulatory regions at imprinted mouse genes
-
Fournier C, Goto Y, Ballestar E et al.: Allele-specific histone lysine methylation marks regulatory regions at imprinted mouse genes. Embo J. 21, 6560-6570 (2002).
-
(2002)
Embo J.
, vol.21
, pp. 6560-6570
-
-
Fournier, C.1
Goto, Y.2
Ballestar, E.3
-
19
-
-
69449092535
-
Histone methylation is mechanistically linked to DNA methylation at imprinting control regions in mammals
-
Henckel A, Nakabayashi K, Sanz LA, Feil R, Hata K, Arnaud P: Histone methylation is mechanistically linked to DNA methylation at imprinting control regions in mammals. Hum. Mol. Genet. 18, 3375-3383 (2009).
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 3375-3383
-
-
Henckel, A.1
Nakabayashi, K.2
Sanz, L.A.3
Feil, R.4
Hata, K.5
Arnaud, P.6
-
20
-
-
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 et al.: Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes. Nat. Genet. 36, 1296-1300 (2004).
-
(2004)
Nat. Genet.
, vol.36
, pp. 1296-1300
-
-
Umlauf, D.1
Goto, Y.2
Cao, R.3
-
21
-
-
34547400458
-
Active and repressive chromatin are interspersed without spreading in an imprinted gene cluster in the mammalian genome
-
Regha K, Sloane MA, Huang R et al.: Active and repressive chromatin are interspersed without spreading in an imprinted gene cluster in the mammalian genome. Mol. Cell 27, 353-366 (2007).
-
(2007)
Mol. Cell
, vol.27
, pp. 353-366
-
-
Regha, K.1
Sloane, M.A.2
Huang, R.3
-
22
-
-
37549006834
-
The transcriptional status but not the imprinting control region determines allele-specific histone modifications at the imprinted H19 locus
-
Verona RI, Thorvaldsen JL, Reese KJ, Bartolomei MS: The transcriptional status but not the imprinting control region determines allele-specific histone modifications at the imprinted H19 locus. Mol. Cell. Biol. 28, 71-82 (2008).
-
(2008)
Mol. Cell. Biol.
, vol.28
, pp. 71-82
-
-
Verona, R.I.1
Thorvaldsen, J.L.2
Reese, K.J.3
Bartolomei, M.S.4
-
23
-
-
33846972618
-
Differential histone modifications mark mouse imprinting control regions during spermatogenesis
-
Delaval K, Govin J, Cerqueira F, Rousseaux S, Khochbin S, Feil R: Differential histone modifications mark mouse imprinting control regions during spermatogenesis. EMBO J. 26, 720-729 (2007).
-
(2007)
EMBO J.
, vol.26
, pp. 720-729
-
-
Delaval, K.1
Govin, J.2
Cerqueira, F.3
Rousseaux, S.4
Khochbin, S.5
Feil, R.6
-
24
-
-
34547624303
-
Genome-wide maps of chromatin state in pluripotent and lineage-committed cells
-
Mikkelsen TS, Ku M, Jaffe DB et al.: Genome-wide maps of chromatin state in pluripotent and lineage-committed cells. Nature 448, 553-560 (2007).
-
(2007)
Nature
, vol.448
, pp. 553-560
-
-
Mikkelsen, T.S.1
Ku, M.2
Jaffe, D.B.3
-
25
-
-
33645216984
-
Regulated expression of two sets of paternally imprinted genes is necessary for mouse parthenogenetic development to term
-
Wu Q, Kumagai T, Kawahara M et al.: Regulated expression of two sets of paternally imprinted genes is necessary for mouse parthenogenetic development to term. Reproduction 131, 481-488 (2006).
-
(2006)
Reproduction
, vol.131
, pp. 481-488
-
-
Wu, Q.1
Kumagai, T.2
Kawahara, M.3
-
26
-
-
9644266664
-
Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation
-
DOI 10.1038/ng1468
-
Lewis A, Mitsuya K, Umlauf D et al.: Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation. Nat. Genet. 36, 1291-1295 (2004). (Pubitemid 39577937)
-
(2004)
Nature Genetics
, vol.36
, Issue.12
, 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
-
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 et al.: Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting. Hum. Mol. Genet. 9, 2691-2706 (2000).
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2691-2706
-
-
Engemann, S.1
Strodicke, M.2
Paulsen, M.3
-
28
-
-
0036831864
-
Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1
-
Fitzpatrick GV, Soloway PD, Higgins MJ: Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1. Nat. Genet. 32, 426-431 (2002).
-
(2002)
Nat. Genet.
, vol.32
, pp. 426-431
-
-
Fitzpatrick, G.V.1
Soloway, P.D.2
Higgins, M.J.3
-
29
-
-
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 et al.: 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, 5203-5208 (1999).
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
, pp. 5203-5208
-
-
Lee, M.P.1
Debaun, M.R.2
Mitsuya, K.3
-
30
-
-
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 et al.: 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, 8064-8069 (1999).
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
, pp. 8064-8069
-
-
Smilinich, N.J.1
Day, C.D.2
Fitzpatrick, G.V.3
-
31
-
-
33846818301
-
A developmental window of opportunity for imprinted gene silencing mediated by DNA methylation and the Kcnq1ot1 noncoding RNA
-
Green K, Lewis A, Dawson C et al.: A developmental window of opportunity for imprinted gene silencing mediated by DNA methylation and the Kcnq1ot1 noncoding RNA. Mamm. Genome 18, 32-42 (2007).
-
(2007)
Mamm. Genome
, vol.18
, pp. 32-42
-
-
Green, K.1
Lewis, A.2
Dawson, C.3
-
32
-
-
54049138948
-
Kcnq1ot1 antisense noncoding RNA mediates lineage-specific transcriptional silencing through chromatin-level regulation
-
Pandey RR, Mondal T, Mohammad F et al.: Kcnq1ot1 antisense noncoding RNA mediates lineage-specific transcriptional silencing through chromatin-level regulation. Mol. Cell 32, 232-246 (2008).
-
(2008)
Mol. Cell
, vol.32
, pp. 232-246
-
-
Pandey, R.R.1
Mondal, T.2
Mohammad, F.3
-
33
-
-
38549179917
-
G9a histone methyltransferase contributes to imprinting in the mouse placenta
-
Wagschal A, Sutherland HG, Woodfine K et al.: G9a histone methyltransferase contributes to imprinting in the mouse placenta. Mol. Cell. Biol. 28, 1104-1113 (2008).
-
(2008)
Mol. Cell. Biol.
, vol.28
, pp. 1104-1113
-
-
Wagschal, A.1
Sutherland, H.G.2
Woodfine, K.3
-
34
-
-
0032878170
-
Parental origin-specific expression of Mash2 is established at the time of implantation with its imprinting mechanism highly resistant to genome-wide demethylation
-
Tanaka M, Puchyr M, Gertsenstein M et al.: Parental origin-specific expression of Mash2 is established at the time of implantation with its imprinting mechanism highly resistant to genome-wide demethylation. Mech. Dev. 87, 129-142 (1999).
-
(1999)
Mech. Dev.
, vol.87
, pp. 129-142
-
-
Tanaka, M.1
Puchyr, M.2
Gertsenstein, M.3
-
35
-
-
0031844688
-
CC, Guan XJ, Tilghman SM: Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster
-
Baker
-
Caspary T, Cleary MA, Baker CC, Guan XJ, Tilghman SM: Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster. Mol. Cell. Biol. 18, 3466-3474 (1998).
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 3466-3474
-
-
Caspary, T.1
Cleary, M.A.2
-
36
-
-
38649114329
-
Specific expression of long noncoding RNAs in the mouse brain
-
Mercer TR, Dinger ME, Sunkin SM, Mehler MF, Mattick JS: Specific expression of long noncoding RNAs in the mouse brain. Proc. Natl Acad. Sci. USA 105, 716-721 (2008).
-
(2008)
Proc. Natl Acad. Sci. USA
, vol.105
, pp. 716-721
-
-
Mercer, T.R.1
Dinger, M.E.2
Sunkin, S.M.3
Mehler, M.F.4
Mattick, J.S.5
-
37
-
-
69549128557
-
The function of non-coding RNAs in genomic imprinting
-
Koerner MV, Pauler FM, Huang R, Barlow DP: The function of non-coding RNAs in genomic imprinting. Development 136, 1771-1783 (2009).
-
(2009)
Development
, vol.136
, pp. 1771-1783
-
-
Koerner, M.V.1
Pauler, F.M.2
Huang, R.3
Barlow, D.P.4
-
38
-
-
40649106258
-
Non-coding RNAs in imprinted gene clusters
-
Royo H, Cavaille J: Non-coding RNAs in imprinted gene clusters. Biol. Cell 100, 149-166 (2008).
-
(2008)
Biol. Cell
, vol.100
, pp. 149-166
-
-
Royo, H.1
Cavaille, J.2
-
39
-
-
39049093762
-
Regulation of imprinting in clusters: Noncoding RNAs versus insulators
-
Wan LB, Bartolomei MS: Regulation of imprinting in clusters: noncoding RNAs versus insulators. Adv. Genet. 61, 207-223 (2008).
-
(2008)
Adv. Genet.
, vol.61
, pp. 207-223
-
-
Wan, L.B.1
Bartolomei, M.S.2
-
40
-
-
0034118382
-
The imprinted antisense RNA at the Igf2r locus overlaps but does not imprint Mas1
-
Lyle R, Watanabe D, te Vruchte D et al.: The imprinted antisense RNA at the Igf2r locus overlaps but does not imprint Mas1. Nat. Genet. 25, 19-21 (2000).
-
(2000)
Nat. Genet.
, vol.25
, pp. 19-21
-
-
Lyle, R.1
Watanabe, D.2
Te Vruchte, D.3
-
41
-
-
33747603960
-
The imprinted Air ncRNA is an atypical RNAPII transcript that evades splicing and escapes nuclear export
-
Seidl CI, Stricker SH, Barlow DP: The imprinted Air ncRNA is an atypical RNAPII transcript that evades splicing and escapes nuclear export. EMBO J. 25, 3565-3575 (2006).
-
(2006)
EMBO J.
, vol.25
, pp. 3565-3575
-
-
Seidl, C.I.1
Stricker, S.H.2
Barlow, D.P.3
-
42
-
-
0037075032
-
The non-coding Air RNA is required for silencing autosomal imprinted genes
-
Sleutels F, Zwart R, Barlow DP: The non-coding Air RNA is required for silencing autosomal imprinted genes. Nature 415, 810-813 (2002).
-
(2002)
Nature
, vol.415
, pp. 810-813
-
-
Sleutels, F.1
Zwart, R.2
Barlow, D.P.3
-
43
-
-
0041312649
-
Imprinted silencing of Slc22a2 and Slc22a3 does not need transcriptional overlap between Igf2r and Air
-
Sleutels F, Tjon G, Ludwig T, Barlow DP: Imprinted silencing of Slc22a2 and Slc22a3 does not need transcriptional overlap between Igf2r and Air. EMBO J. 22, 3696-3704 (2003).
-
(2003)
EMBO J.
, vol.22
, pp. 3696-3704
-
-
Sleutels, F.1
Tjon, G.2
Ludwig, T.3
Barlow, D.P.4
-
44
-
-
56549111129
-
The Air noncoding RNA epigenetically silences transcription by targeting G9a to chromatin
-
Nagano T, Mitchell JA, Sanz LA et al.: The Air noncoding RNA epigenetically silences transcription by targeting G9a to chromatin. Science 322, 1717-1720 (2008).
-
(2008)
Science
, vol.322
, pp. 1717-1720
-
-
Nagano, T.1
Mitchell, J.A.2
Sanz, L.A.3
-
45
-
-
55349100420
-
Polycomb group proteins Ezh2 and Rnf2 direct genomic contraction and imprinted repression in early mouse embryos
-
Terranova R, Yokobayashi S, Stadler MB et al.: Polycomb group proteins Ezh2 and Rnf2 direct genomic contraction and imprinted repression in early mouse embryos. Dev. Cell 15, 668-679 (2008).
-
(2008)
Dev. Cell
, vol.15
, pp. 668-679
-
-
Terranova, R.1
Yokobayashi, S.2
Stadler, M.B.3
-
46
-
-
0037083376
-
Capturing chromosome conformation
-
Dekker J, Rippe K, Dekker M, Kleckner N: Capturing chromosome conformation. Science 295, 1306-1311 (2002).
-
(2002)
Science
, vol.295
, pp. 1306-1311
-
-
Dekker, J.1
Rippe, K.2
Dekker, M.3
Kleckner, N.4
-
47
-
-
33750203582
-
Circular chromosome conformation capture (4C) uncovers extensive networks of epigenetically regulated intra- and interchromosomal interactions
-
Zhao Z, Tavoosidana G, Sjolinder M et al.: Circular chromosome conformation capture (4C) uncovers extensive networks of epigenetically regulated intra- and interchromosomal interactions. Nat. Genet. 38, 1341-1347 (2006).
-
(2006)
Nat. Genet.
, vol.38
, pp. 1341-1347
-
-
Zhao, Z.1
Tavoosidana, G.2
Sjolinder, M.3
-
48
-
-
33749400168
-
Chromosome conformation capture carbon copy (5C): A massively parallel solution for mapping interactions between genomic elements
-
Dostie J, Richmond TA, Arnaout RA et al.: Chromosome conformation capture carbon copy (5C): a massively parallel solution for mapping interactions between genomic elements. Genome Res. 16, 1299-1309 (2006).
-
(2006)
Genome Res.
, vol.16
, pp. 1299-1309
-
-
Dostie, J.1
Richmond, T.A.2
Arnaout, R.A.3
-
49
-
-
66149167455
-
ChIP-based methods for the identification of long-range chromatin interactions
-
Fullwood MJ, Ruan Y: ChIP-based methods for the identification of long-range chromatin interactions. J. Cell Biochem. 107, 30-39 (2009).
-
(2009)
J. Cell Biochem.
, vol.107
, pp. 30-39
-
-
Fullwood, M.J.1
Ruan, Y.2
-
50
-
-
33750212321
-
Nuclear organization of active and inactive chromatin domains uncovered by chromosome conformation capture-on-chip (4C)
-
Simonis M, Klous P, Splinter E et al.: Nuclear organization of active and inactive chromatin domains uncovered by chromosome conformation capture-on-chip (4C). Nat. Genet. 38, 1348-1354 (2006).
-
(2006)
Nat. Genet.
, vol.38
, pp. 1348-1354
-
-
Simonis, M.1
Klous, P.2
Splinter, E.3
-
51
-
-
70349873824
-
Comprehensive mapping of long-range interactions reveals folding principles of the human genome
-
Lieberman-Aiden E, van Berkum NL, Williams L et al.: Comprehensive mapping of long-range interactions reveals folding principles of the human genome. Science 326, 289-293 (2009).
-
(2009)
Science
, vol.326
, pp. 289-293
-
-
Lieberman-Aiden, E.1
Van Berkum, N.L.2
Williams, L.3
-
52
-
-
77950525321
-
Loss of IGF2 imprinting is associated with abrogation of long-range intrachromosomal interactions in human cancer cells
-
Vu TH, Nguyen AH, Hoffman AR: Loss of IGF2 imprinting is associated with abrogation of long-range intrachromosomal interactions in human cancer cells. Hum. Mol. Genet. 19, 901-919.
-
Hum. Mol. Genet.
, vol.19
, pp. 901-919
-
-
Vu, T.H.1
Nguyen, A.H.2
Hoffman, A.R.3
-
53
-
-
73649145481
-
Cohesin is required for higher-order chromatin conformation at the imprinted IGF2-H19 locus
-
Nativio R, Wendt KS, Ito Y et al.: Cohesin is required for higher-order chromatin conformation at the imprinted IGF2-H19 locus. PLoS Genet. 5, E1000739 (2009).
-
(2009)
PLoS Genet.
, vol.5
-
-
Nativio, R.1
Wendt, K.S.2
Ito, Y.3
-
54
-
-
44649186971
-
A complex deoxyribonucleic acid looping configuration associated with the silencing of the maternal Igf2 allele
-
Qiu X, Vu TH, Lu Q et al.: A complex deoxyribonucleic acid looping configuration associated with the silencing of the maternal Igf2 allele. Mol. Endocrinol. 22, 1476-1488 (2008).
-
(2008)
Mol. Endocrinol.
, vol.22
, pp. 1476-1488
-
-
Qiu, X.1
Vu, T.H.2
Lu, Q.3
-
55
-
-
3543018516
-
Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loops
-
Murrell A, Heeson S, Reik W: Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loops. Nat. Genet. 36, 889-893 (2004).
-
(2004)
Nat. Genet.
, vol.36
, pp. 889-893
-
-
Murrell, A.1
Heeson, S.2
Reik, W.3
-
56
-
-
53549127289
-
CTCF regulates allelic expression of Igf2 by orchestrating a promoter-polycomb repressive complex 2 intrachromosomal loop
-
Li T, Hu JF, Qiu X et al.: CTCF regulates allelic expression of Igf2 by orchestrating a promoter-polycomb repressive complex 2 intrachromosomal loop. Mol. Cell. Biol. 28, 6473-6482 (2008).
-
(2008)
Mol. Cell. Biol.
, vol.28
, pp. 6473-6482
-
-
Li, T.1
Hu, J.F.2
Qiu, X.3
-
57
-
-
25144468033
-
CTCF binding and higher order chromatin structure of the H19 locus are maintained in mitotic chromatin
-
Burke LJ, Zhang R, Bartkuhn M et al.: CTCF binding and higher order chromatin structure of the H19 locus are maintained in mitotic chromatin. EMBO J. 24, 3291-3300 (2005).
-
(2005)
EMBO J.
, vol.24
, pp. 3291-3300
-
-
Burke, L.J.1
Zhang, R.2
Bartkuhn, M.3
-
58
-
-
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 VK, Tavoosidana G et al.: 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).
-
(2006)
Proc. Natl Acad. Sci. USA
, vol.103
, pp. 10684-10689
-
-
Kurukuti, S.1
Tiwari, V.K.2
Tavoosidana, G.3
-
59
-
-
34247576603
-
Analysis of the H19 ICR insulator
-
Yoon YS, Jeong S, Rong Q, Park KY, Chung JH, Pfeifer K: Analysis of the H19 ICR insulator. Mol. Cell. Biol. 27, 3499-3510 (2007).
-
(2007)
Mol. Cell. Biol.
, vol.27
, pp. 3499-3510
-
-
Yoon, Y.S.1
Jeong, S.2
Rong, Q.3
Park, K.Y.4
Chung, J.H.5
Pfeifer, K.6
-
60
-
-
11244328520
-
Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome
-
Horike S, Cai S, Miyano M, Cheng JF, Kohwi-Shigematsu T: Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome. Nat. Genet. 37, 31-40 (2005).
-
(2005)
Nat. Genet.
, vol.37
, pp. 31-40
-
-
Horike, S.1
Cai, S.2
Miyano, M.3
Cheng, J.F.4
Kohwi-Shigematsu, T.5
-
61
-
-
49649116680
-
Genomic matrix attachment region and chromosome conformation capture quantitative real time PCR assays identify novel putative regulatory elements at the imprinted Dlk1/Gtl2 locus
-
Braem C, Recolin B, Rancourt RC et al.: Genomic matrix attachment region and chromosome conformation capture quantitative real time PCR assays identify novel putative regulatory elements at the imprinted Dlk1/Gtl2 locus. J. Biol. Chem. 283, 18612-18620 (2008).
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 18612-18620
-
-
Braem, C.1
Recolin, B.2
Rancourt, R.C.3
-
62
-
-
76249083210
-
ATRX partners with cohesin and MeCP2 and contributes to developmental silencing of imprinted genes in the brain
-
Kernohan KD, Jiang Y, Tremblay DC et al.: ATRX partners with cohesin and MeCP2 and contributes to developmental silencing of imprinted genes in the brain. Dev. Cell. 18, 191-202 (2010).
-
(2010)
Dev. Cell.
, vol.18
, pp. 191-202
-
-
Kernohan, K.D.1
Jiang, Y.2
Tremblay, D.C.3
-
63
-
-
38549129312
-
CTCF is the master organizer of domain-wide allele-specific chromatin at the H19/Igf2 imprinted region
-
Han L, Lee DH, Szabo PE: CTCF is the master organizer of domain-wide allele-specific chromatin at the H19/Igf2 imprinted region. Mol. Cell. Biol. 28, 1124-1135 (2008).
-
(2008)
Mol. Cell. Biol.
, vol.28
, pp. 1124-1135
-
-
Han, L.1
Lee, D.H.2
Szabo, P.E.3
-
64
-
-
33747885707
-
CTCF-dependent chromatin insulator is linked to epigenetic remodeling
-
Ishihara K, Oshimura M, Nakao M: CTCF-dependent chromatin insulator is linked to epigenetic remodeling. Mol. Cell 23, 733-742 (2006).
-
(2006)
Mol. Cell
, vol.23
, pp. 733-742
-
-
Ishihara, K.1
Oshimura, M.2
Nakao, M.3
-
65
-
-
38849121606
-
Cohesins functionally associate with CTCF on mammalian chromosome arms
-
Parelho V, Hadjur S, Spivakov M et al.: Cohesins functionally associate with CTCF on mammalian chromosome arms. Cell 132, 422-433 (2008).
-
(2008)
Cell
, vol.132
, pp. 422-433
-
-
Parelho, V.1
Hadjur, S.2
Spivakov, M.3
-
66
-
-
39149121436
-
Cohesin mediates transcriptional insulation by CCCTC-binding factor
-
Wendt KS, Yoshida K, Itoh T et al.: Cohesin mediates transcriptional insulation by CCCTC-binding factor. Nature 451, 796-801 (2008).
-
(2008)
Nature
, vol.451
, pp. 796-801
-
-
Wendt, K.S.1
Yoshida, K.2
Itoh, T.3
-
67
-
-
0030886602
-
A direct link between sister chromatid cohesion and chromosome condensation revealed through the analysis of MCD1 in S. cerevisiae
-
Guacci V, Koshland D, Strunnikov A: A direct link between sister chromatid cohesion and chromosome condensation revealed through the analysis of MCD1 in S. cerevisiae. Cell 91, 47-57 (1997).
-
(1997)
Cell
, vol.91
, pp. 47-57
-
-
Guacci, V.1
Koshland, D.2
Strunnikov, A.3
-
68
-
-
0032127940
-
Identification of Xenopus SMC protein complexes required for sister chromatid cohesion
-
Losada A, Hirano M, Hirano T: Identification of Xenopus SMC protein complexes required for sister chromatid cohesion. Genes Dev. 12, 1986-1997 (1998).
-
(1998)
Genes Dev.
, vol.12
, pp. 1986-1997
-
-
Losada, A.1
Hirano, M.2
Hirano, T.3
-
69
-
-
0030885925
-
Cohesins: Chromosomal proteins that prevent premature separation of sister chromatids
-
Michaelis C, Ciosk R, Nasmyth K: Cohesins: chromosomal proteins that prevent premature separation of sister chromatids. Cell 91, 35-45 (1997).
-
(1997)
Cell
, vol.91
, pp. 35-45
-
-
Michaelis, C.1
Ciosk, R.2
Nasmyth, K.3
-
70
-
-
0033083727
-
Yeast cohesin complex requires a conserved protein, Eco1p(Ctf7), to establish cohesion between sister chromatids during DNA replication
-
Toth A, Ciosk R, Uhlmann F, Galova M, Schleiffer A, Nasmyth K: Yeast cohesin complex requires a conserved protein, Eco1p(Ctf7), to establish cohesion between sister chromatids during DNA replication. Genes Dev. 13, 320-333 (1999).
-
(1999)
Genes Dev.
, vol.13
, pp. 320-333
-
-
Toth, A.1
Ciosk, R.2
Uhlmann, F.3
Galova, M.4
Schleiffer, A.5
Nasmyth, K.6
-
71
-
-
0037017393
-
Condensin and cohesin display different arm conformations with characteristic hinge angles
-
Anderson DE, Losada A, Erickson HP, Hirano T: Condensin and cohesin display different arm conformations with characteristic hinge angles. J. Cell. Biol. 156, 419-424 (2002).
-
(2002)
J. Cell. Biol.
, vol.156
, pp. 419-424
-
-
Anderson, D.E.1
Losada, A.2
Erickson, H.P.3
Hirano, T.4
-
72
-
-
0037459376
-
Chromosomal cohesin forms a ring
-
Gruber S, Haering CH, Nasmyth K: Chromosomal cohesin forms a ring. Cell 112, 765-777 (2003).
-
(2003)
Cell
, vol.112
, pp. 765-777
-
-
Gruber, S.1
Haering, C.H.2
Nasmyth, K.3
-
73
-
-
0021139084
-
Completion of mouse embryogenesis requires both the maternal and paternal genomes
-
McGrath J, Solter D: Completion of mouse embryogenesis requires both the maternal and paternal genomes. Cell 37, 179-183 (1984).
-
(1984)
Cell
, vol.37
, pp. 179-183
-
-
McGrath, J.1
Solter, D.2
-
74
-
-
0021740225
-
Inability of mouse blastomere nuclei transferred to enucleated zygotes to support development in vitro
-
McGrath J, Solter D: Inability of mouse blastomere nuclei transferred to enucleated zygotes to support development in vitro. Science 226, 1317-1319 (1984).
-
(1984)
Science
, vol.226
, pp. 1317-1319
-
-
McGrath, J.1
Solter, D.2
-
75
-
-
0021237658
-
Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis
-
Surani MA, Barton SC, Norris ML: Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis. Nature 308, 548-550 (1984).
-
(1984)
Nature
, vol.308
, pp. 548-550
-
-
Surani, M.A.1
Barton, S.C.2
Norris, M.L.3
-
76
-
-
77957350883
-
The importance of imprinting in the human placenta
-
Frost JM, Moore GE: The importance of imprinting in the human placenta. PLoS Genet. 6, E1001015 (2010).
-
(2010)
PLoS Genet.
, vol.6
-
-
Frost, J.M.1
Moore, G.E.2
-
78
-
-
0028832361
-
Distribution of parthenogenetic cells in the mouse brain and their influence on brain development and behavior
-
Allen ND, Logan K, Lally G, Drage DJ, Norris ML, Keverne EB: Distribution of parthenogenetic cells in the mouse brain and their influence on brain development and behavior. Proc. Natl Acad. Sci. USA 92, 10782-10786 (1995).
-
(1995)
Proc. Natl Acad. Sci. USA
, vol.92
, pp. 10782-10786
-
-
Allen, N.D.1
Logan, K.2
Lally, G.3
Drage, D.J.4
Norris, M.L.5
Keverne, E.B.6
-
79
-
-
0025368338
-
Androgenetic mouse embryonic stem cells are pluripotent and cause skeletal defects in chimeras: Implications for genetic imprinting
-
Mann JR, Gadi I, Harbison ML, Abbondanzo SJ, Stewart CL: Androgenetic mouse embryonic stem cells are pluripotent and cause skeletal defects in chimeras: implications for genetic imprinting. Cell 62, 251-260 (1990).
-
(1990)
Cell
, vol.62
, pp. 251-260
-
-
Mann, J.R.1
Gadi, I.2
Harbison, M.L.3
Abbondanzo, S.J.4
Stewart, C.L.5
-
80
-
-
0029881013
-
Genomic imprinting and the differential roles of parental genomes in brain development
-
Keverne EB, Fundele R, Narasimha M, Barton SC, Surani MA: Genomic imprinting and the differential roles of parental genomes in brain development. Brain Res. Dev. Brain Res. 92, 91-100 (1996).
-
(1996)
Brain Res. Dev. Brain Res.
, vol.92
, pp. 91-100
-
-
Keverne, E.B.1
Fundele, R.2
Narasimha, M.3
Barton, S.C.4
Surani, M.A.5
-
81
-
-
9044253328
-
Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein
-
Kuroiwa Y, Kaneko-Ishino T, Kagitani F et al.: Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein. Nat. Genet. 12, 186-190 (1996).
-
(1996)
Nat. Genet.
, vol.12
, pp. 186-190
-
-
Kuroiwa, Y.1
Kaneko-Ishino, T.2
Kagitani, F.3
-
82
-
-
76249090489
-
BioGPS: An extensible and customizable portal for querying and organizing gene annotation resources
-
Wu C, Orozco C, Boyer J et al.: BioGPS: an extensible and customizable portal for querying and organizing gene annotation resources. Genome Biol. 10, R130 (2009).
-
(2009)
Genome Biol.
, vol.10
-
-
Wu, C.1
Orozco, C.2
Boyer, J.3
-
83
-
-
0036299197
-
Paternal expression of a novel imprinted gene, Peg12/Frat3, in the mouse 7C region homologous to the Prader-Willi syndrome region
-
Kobayashi S, Kohda T, Ichikawa H et al.: Paternal expression of a novel imprinted gene, Peg12/Frat3, in the mouse 7C region homologous to the Prader-Willi syndrome region. Biochem. Biophys. Res. Commun. 290, 403-408 (2002).
-
(2002)
Biochem. Biophys. Res. Commun.
, vol.290
, pp. 403-408
-
-
Kobayashi, S.1
Kohda, T.2
Ichikawa, H.3
-
85
-
-
0031687985
-
Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest
-
Lefebvre L, Viville S, Barton SC, Ishino F, Keverne EB, Surani MA: Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest. Nat. Genet. 20, 163-169 (1998).
-
(1998)
Nat. Genet.
, vol.20
, pp. 163-169
-
-
Lefebvre, L.1
Viville, S.2
Barton, S.C.3
Ishino, F.4
Keverne, E.B.5
Surani, M.A.6
-
86
-
-
0033537716
-
Regulation of maternal behavior and offspring growth by paternally expressed Peg3
-
Li L, Keverne EB, Aparicio SA, Ishino F, Barton SC, Surani MA: Regulation of maternal behavior and offspring growth by paternally expressed Peg3. Science 284, 330-333 (1999).
-
(1999)
Science
, vol.284
, pp. 330-333
-
-
Li, L.1
Keverne, E.B.2
Aparicio, S.A.3
Ishino, F.4
Barton, S.C.5
Surani, M.A.6
-
87
-
-
4744376102
-
Expression patterns of the novel imprinted genes Nap1l5 and Peg13 and their non-imprinted host genes in the adult mouse brain
-
Davies W, Smith RJ, Kelsey G, Wilkinson LS: Expression patterns of the novel imprinted genes Nap1l5 and Peg13 and their non-imprinted host genes in the adult mouse brain. Gene Expr. Patterns 4, 741-747 (2004).
-
(2004)
Gene Expr. Patterns
, vol.4
, pp. 741-747
-
-
Davies, W.1
Smith, R.J.2
Kelsey, G.3
Wilkinson, L.S.4
-
88
-
-
0042786856
-
Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain
-
Lee S, Walker CL, Wevrick R: Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain. Gene Expr. Patterns 3, 599-609 (2003).
-
(2003)
Gene Expr. Patterns
, vol.3
, pp. 599-609
-
-
Lee, S.1
Walker, C.L.2
Wevrick, R.3
-
89
-
-
33846252240
-
Genome-wide atlas of gene expression in the adult mouse brain
-
Lein ES, Hawrylycz MJ, Ao N et al.: Genome-wide atlas of gene expression in the adult mouse brain. Nature 445, 168-176 (2007).
-
(2007)
Nature
, vol.445
, pp. 168-176
-
-
Lein, E.S.1
Hawrylycz, M.J.2
Ao, N.3
-
90
-
-
0025809321
-
Parental imprinting of the mouse H19 gene
-
Bartolomei MS, Zemel S, Tilghman SM: Parental imprinting of the mouse H19 gene. Nature 351, 153-155 (1991).
-
(1991)
Nature
, vol.351
, pp. 153-155
-
-
Bartolomei, M.S.1
Zemel, S.2
Tilghman, S.M.3
-
91
-
-
0032954668
-
Zim1, a maternally expressed mouse Kruppel-type zinc-finger gene located in proximal chromosome 7
-
Kim J, Lu X, Stubbs L: Zim1, a maternally expressed mouse Kruppel-type zinc-finger gene located in proximal chromosome 7. Hum. Mol. Genet. 8, 847-854 (1999).
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 847-854
-
-
Kim, J.1
Lu, X.2
Stubbs, L.3
-
92
-
-
69449084565
-
The expression analysis of Grb10 during mouse embryonic development
-
Liu Q, Wang Y, Chen Y et al.: The expression analysis of Grb10 during mouse embryonic development. Yi Chuan 31, 732-740 (2009).
-
(2009)
Yi Chuan
, vol.31
, pp. 732-740
-
-
Liu, Q.1
Wang, Y.2
Chen, Y.3
-
93
-
-
0035207879
-
The spatial and temporal expression pattern of Nesp and its antisense Nespas, in mid-gestation mouse embryos
-
Ball ST, Williamson CM, Hayes C, Hacker T, Peters J: The spatial and temporal expression pattern of Nesp and its antisense Nespas, in mid-gestation mouse embryos. Mech. Dev. 100, 79-81 (2001).
-
(2001)
Mech. Dev.
, vol.100
, pp. 79-81
-
-
Ball, S.T.1
Williamson, C.M.2
Hayes, C.3
Hacker, T.4
Peters, J.5
-
94
-
-
0033616719
-
A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2
-
Peters J, Wroe SF, Wells CA et al.: A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2. Proc. Natl Acad. Sci. USA 96, 3830-3835 (1999).
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
, pp. 3830-3835
-
-
Peters, J.1
Wroe, S.F.2
Wells, C.A.3
-
95
-
-
33344465477
-
Expression pattern of the maternally imprinted gene Gtl2 in the forebrain during embryonic development and adulthood
-
McLaughlin D, Vidaki M, Renieri E, Karagogeos D: Expression pattern of the maternally imprinted gene Gtl2 in the forebrain during embryonic development and adulthood. Gene Expr. Patterns 6, 394-399 (2006).
-
(2006)
Gene Expr. Patterns
, vol.6
, pp. 394-399
-
-
McLaughlin, D.1
Vidaki, M.2
Renieri, E.3
Karagogeos, D.4
-
96
-
-
0025320906
-
A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting
-
DeChiara TM, Efstratiadis A, Robertson EJ: A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting. Nature 345, 78-80 (1990).
-
(1990)
Nature
, vol.345
, pp. 78-80
-
-
Dechiara, T.M.1
Efstratiadis, A.2
Robertson, E.J.3
-
97
-
-
77956972424
-
Grb10 interacts with Bim L and inhibits apoptosis
-
Hu ZQ, Zhang JY, Ji CN, Xie Y, Chen JZ, Mao YM: Grb10 interacts with Bim L and inhibits apoptosis. Mol. Biol. Rep. 37(7), 3547-3552 (2010).
-
(2010)
Mol. Biol. Rep.
, vol.37
, Issue.7
, pp. 3547-3552
-
-
Hu, Z.Q.1
Zhang, J.Y.2
Ji, C.N.3
Xie, Y.4
Chen, J.Z.5
Mao, Y.M.6
-
98
-
-
0038246289
-
Calcr, a brain-specific imprinted mouse calcitonin receptor gene in the imprinted cluster of the proximal region of chromosome 6
-
Hoshiya H, Meguro M, Kashiwagi A, Okita C, Oshimura M: Calcr, a brain-specific imprinted mouse calcitonin receptor gene in the imprinted cluster of the proximal region of chromosome 6. J. Hum. Genet. 48, 208-211 (2003).
-
(2003)
J. Hum. Genet.
, vol.48
, pp. 208-211
-
-
Hoshiya, H.1
Meguro, M.2
Kashiwagi, A.3
Okita, C.4
Oshimura, M.5
-
99
-
-
0031228039
-
The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain
-
Rougeulle C, Glatt H, Lalande M: The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain. Nat. Genet. 17, 14-15 (1997).
-
(1997)
Nat. Genet.
, vol.17
, pp. 14-15
-
-
Rougeulle, C.1
Glatt, H.2
Lalande, M.3
-
100
-
-
0031230614
-
Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain
-
Vu TH, Hoffman AR: Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain. Nat. Genet. 17, 12-13 (1997).
-
(1997)
Nat. Genet.
, vol.17
, pp. 12-13
-
-
Vu, T.H.1
Hoffman, A.R.2
-
101
-
-
0025967857
-
Parental imprinting of the mouse insulin-like growth factor II gene
-
DeChiara TM, Robertson EJ, Efstratiadis A: Parental imprinting of the mouse insulin-like growth factor II gene. Cell 64, 849-859 (1991).
-
(1991)
Cell
, vol.64
, pp. 849-859
-
-
Dechiara, T.M.1
Robertson, E.J.2
Efstratiadis, A.3
-
102
-
-
0346363764
-
The mouse Murr1 gene is imprinted in the adult brain, presumably due to transcriptional interference by the antisense-oriented U2af1-rs1 gene
-
Wang Y, Joh K, Masuko S et al.: The mouse Murr1 gene is imprinted in the adult brain, presumably due to transcriptional interference by the antisense-oriented U2af1-rs1 gene. Mol. Cell. Biol. 24, 270-279 (2004).
-
(2004)
Mol. Cell. Biol.
, vol.24
, pp. 270-279
-
-
Wang, Y.1
Joh, K.2
Masuko, S.3
-
103
-
-
77955285002
-
Sex-specific parent-of-origin allelic expression in the mouse brain
-
Gregg C, Zhang J, Butler JE, Haig D, Dulac C: Sex-specific parent-of-origin allelic expression in the mouse brain. Science 329(5992), 682-685 (2010).
-
(2010)
Science
, vol.329
, Issue.5992
, pp. 682-685
-
-
Gregg, C.1
Zhang, J.2
Butler, J.E.3
Haig, D.4
Dulac, C.5
-
104
-
-
77955299096
-
High-resolution analysis of parent-of-origin allelic expression in the mouse brain
-
Gregg C, Zhang J, Weissbourd B et al.: High-resolution analysis of parent-of-origin allelic expression in the mouse brain. Science 329(5992), 643-648 (2010).
-
(2010)
Science
, vol.329
, Issue.5992
, pp. 643-648
-
-
Gregg, C.1
Zhang, J.2
Weissbourd, B.3
-
105
-
-
34548304069
-
Activation of p53 by MEG3 non-coding RNA
-
Zhou Y, Zhong Y, Wang Y et al.: Activation of p53 by MEG3 non-coding RNA. J. Biol. Chem. 282, 24731-24742 (2007).
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 24731-24742
-
-
Zhou, Y.1
Zhong, Y.2
Wang, Y.3
-
106
-
-
0030698872
-
Interneuron migration from basal forebrain to neocortex: Dependence on Dlx genes
-
Anderson SA, Eisenstat DD, Shi L, Rubenstein JL: Interneuron migration from basal forebrain to neocortex: dependence on Dlx genes. Science 278, 474-476 (1997).
-
(1997)
Science
, vol.278
, pp. 474-476
-
-
Anderson, S.A.1
Eisenstat, D.D.2
Shi, L.3
Rubenstein, J.L.4
-
107
-
-
0036337338
-
Ectopic expression of the Dlx genes induces glutamic acid decarboxylase and Dlx expression
-
Stuhmer T, Anderson SA, Ekker M, Rubenstein JL: Ectopic expression of the Dlx genes induces glutamic acid decarboxylase and Dlx expression. Development 129, 245-252 (2002).
-
(2002)
Development
, vol.129
, pp. 245-252
-
-
Stuhmer, T.1
Anderson, S.A.2
Ekker, M.3
Rubenstein, J.L.4
-
108
-
-
0030687684
-
Evidence for uniparental, paternal expression of the human GABAA receptor subunit genes, using microcell-mediated chromosome transfer
-
Meguro M, Mitsuya K, Sui H et al.: Evidence for uniparental, paternal expression of the human GABAA receptor subunit genes, using microcell-mediated chromosome transfer. Hum. Mol. Genet. 6, 2127-2133 (1997).
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 2127-2133
-
-
Meguro, M.1
Mitsuya, K.2
Sui, H.3
-
109
-
-
0026357494
-
The GABAA receptor b 3 subunit gene: Characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7
-
Wagstaff J, Chaillet JR, Lalande M: The GABAA receptor b 3 subunit gene: characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7. Genomics 11, 1071-1078 (1991).
-
(1991)
Genomics
, vol.11
, pp. 1071-1078
-
-
Wagstaff, J.1
Chaillet, J.R.2
Lalande, M.3
-
110
-
-
20444403730
-
GABAA receptor b3 subunit gene-deficient heterozygous mice show parent-of-origin and gender-related differences in b3 subunit levels, EEG, and behavior
-
Liljelund P, Handforth A, Homanics GE, Olsen RW: GABAA receptor b3 subunit gene-deficient heterozygous mice show parent-of-origin and gender-related differences in b3 subunit levels, EEG, and behavior. Brain Res. Dev. Brain Res. 157, 150-161 (2005).
-
(2005)
Brain Res. Dev. Brain Res.
, vol.157
, pp. 150-161
-
-
Liljelund, P.1
Handforth, A.2
Homanics, G.E.3
Olsen, R.W.4
-
113
-
-
70350674351
-
Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size
-
Leung KN, Vallero RO, DuBose AJ, Resnick JL, LaSalle JM: Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size. Hum. Mol. Genet. 18, 4227-4238 (2009).
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 4227-4238
-
-
Leung, K.N.1
Vallero, R.O.2
Dubose, A.J.3
Resnick, J.L.4
Lasalle, J.M.5
-
114
-
-
34548268591
-
DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency
-
Schule B, Li HH, Fisch-Kohl C, Purmann C, Francke U: DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency. Am. J. Hum. Genet. 81, 492-506 (2007).
-
(2007)
Am. J. Hum. Genet.
, vol.81
, pp. 492-506
-
-
Schule, B.1
Li, H.H.2
Fisch-Kohl, C.3
Purmann, C.4
Francke, U.5
-
115
-
-
49549096037
-
DLX5 expression is monoallelic and Dlx5 is up-regulated in the Mecp2-null frontal cortex
-
Miyano M, Horike S, Cai S, Oshimura M, Kohwi-Shigematsu T: DLX5 expression is monoallelic and Dlx5 is up-regulated in the Mecp2-null frontal cortex. J. Cell. Mol. Med. 12, 1188-1191 (2008).
-
(2008)
J. Cell. Mol. Med.
, vol.12
, pp. 1188-1191
-
-
Miyano, M.1
Horike, S.2
Cai, S.3
Oshimura, M.4
Kohwi-Shigematsu, T.5
-
116
-
-
23044463888
-
Chromosome loops, insulators, and histone methylation: New insights into regulation of imprinting in clusters
-
Reik W, Murrell A, Lewis A et al.: Chromosome loops, insulators, and histone methylation: new insights into regulation of imprinting in clusters. Cold Spring Harb. Symp. Quant. Biol. 69, 29-37 (2004).
-
(2004)
Cold Spring Harb. Symp. Quant. Biol.
, vol.69
, pp. 29-37
-
-
Reik, W.1
Murrell, A.2
Lewis, A.3
-
117
-
-
33750470266
-
Zac1 regulates an imprinted gene network critically involved in the control of embryonic growth
-
Varrault A, Gueydan C, Delalbre A et al.: Zac1 regulates an imprinted gene network critically involved in the control of embryonic growth. Dev. Cell 11, 711-722 (2006).
-
(2006)
Dev. Cell
, vol.11
, pp. 711-722
-
-
Varrault, A.1
Gueydan, C.2
Delalbre, A.3
-
118
-
-
50649122364
-
An imprinted gene network that controls mammalian somatic growth is down-regulated during postnatal growth deceleration in multiple organs
-
Lui JC, Finkielstain GP, Barnes KM, Baron J: An imprinted gene network that controls mammalian somatic growth is down-regulated during postnatal growth deceleration in multiple organs. Am. J. Physiol. Regul. Integr. Comp. Physiol. 295, R189-R196 (2008).
-
(2008)
Am. J. Physiol. Regul. Integr. Comp. Physiol.
, vol.295
-
-
Lui, J.C.1
Finkielstain, G.P.2
Barnes, K.M.3
Baron, J.4
-
119
-
-
77951257526
-
Temporal and spatial expression of a growth-regulated network of imprinted genes in growth plate
-
Andrade AC, Lui JC, Nilsson O: Temporal and spatial expression of a growth-regulated network of imprinted genes in growth plate. Pediatr. Nephrol. 25, 617-623 (2010).
-
(2010)
Pediatr. Nephrol.
, vol.25
, pp. 617-623
-
-
Andrade, A.C.1
Lui, J.C.2
Nilsson, O.3
-
120
-
-
33645814398
-
CTCF mediates interchromosomal colocalization between Igf2/H19 and Wsb1/Nf1
-
Ling JQ, Li T, Hu JF et al.: CTCF mediates interchromosomal colocalization between Igf2/H19 and Wsb1/Nf1. Science 312, 269-272 (2006).
-
(2006)
Science
, vol.312
, pp. 269-272
-
-
Ling, J.Q.1
Li, T.2
Hu, J.F.3
-
121
-
-
72749105143
-
Nonallelic transvection of multiple imprinted loci is organized by the H19 imprinting control region during germline development
-
Sandhu KS, Shi C, Sjolinder M et al.: Nonallelic transvection of multiple imprinted loci is organized by the H19 imprinting control region during germline development. Genes Dev. 23, 2598-2603 (2009).
-
(2009)
Genes Dev.
, vol.23
, pp. 2598-2603
-
-
Sandhu, K.S.1
Shi, C.2
Sjolinder, M.3
-
122
-
-
70350138340
-
H19 acts as a trans regulator of the imprinted gene network controlling growth in mice
-
Gabory A, Ripoche MA, Le Digarcher A et al.: H19 acts as a trans regulator of the imprinted gene network controlling growth in mice. Development 136, 3413-3421 (2009).
-
(2009)
Development
, vol.136
, pp. 3413-3421
-
-
Gabory, A.1
Ripoche, M.A.2
Le Digarcher, A.3
-
123
-
-
0027476242
-
Prader-Willi syndrome: Consensus diagnostic criteria
-
Holm VA, Cassidy SB, Butler MG et al.: Prader-Willi syndrome: consensus diagnostic criteria. Pediatrics 91, 398-402 (1993).
-
(1993)
Pediatrics
, vol.91
, pp. 398-402
-
-
Holm, V.A.1
Cassidy, S.B.2
Butler, M.G.3
-
124
-
-
0035515362
-
The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria
-
Gunay-Aygun M, Schwartz S, Heeger S, O'Riordan MA, Cassidy SB: The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria. Pediatrics 108, E92 (2001).
-
(2001)
Pediatrics
, vol.108
-
-
Gunay-Aygun, M.1
Schwartz, S.2
Heeger, S.3
O'Riordan, M.A.4
Cassidy, S.B.5
-
125
-
-
72949087949
-
Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndrome
-
Relkovic D, Doe CM, Humby T et al.: Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndrome. Eur. J. Neurosci. 31, 156-164 (2010).
-
(2010)
Eur. J. Neurosci.
, vol.31
, pp. 156-164
-
-
Relkovic, D.1
Doe, C.M.2
Humby, T.3
-
126
-
-
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: 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, 2687-2700 (2001).
-
(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
-
127
-
-
0034687740
-
Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization
-
Cavaille J, Buiting K, Kiefmann M et al.: Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization. Proc. Natl Acad. Sci. USA 97, 14311-14316 (2000).
-
(2000)
Proc. Natl Acad. Sci. USA
, vol.97
, pp. 14311-14316
-
-
Cavaille, J.1
Buiting, K.2
Kiefmann, M.3
-
128
-
-
0034931032
-
The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/ Angelman domain in mice
-
Bressler J, Tsai TF, Wu MY et al.: The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/ Angelman domain in mice. Nat. Genet. 28, 232-240 (2001).
-
(2001)
Nat. Genet.
, vol.28
, pp. 232-240
-
-
Bressler, J.1
Tsai, T.F.2
Wu, M.Y.3
-
129
-
-
0031747932
-
A mouse model for Prader-Willi syndrome imprinting-centre mutations
-
Yang T, Adamson TE, Resnick JL et al.: A mouse model for Prader-Willi syndrome imprinting-centre mutations. Nat. Genet. 19, 25-31 (1998).
-
(1998)
Nat. Genet.
, vol.19
, pp. 25-31
-
-
Yang, T.1
Adamson, T.E.2
Resnick, J.L.3
-
130
-
-
14644391578
-
Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth
-
Lee S, Walker CL, Karten B et al.: Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth. Hum. Mol. Genet. 14, 627-637 (2005).
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 627-637
-
-
Lee, S.1
Walker, C.L.2
Karten, B.3
-
131
-
-
21244450398
-
Developmental abnormalities of neuronal structure and function in prenatal mice lacking the Prader-Willi syndrome gene necdin
-
Pagliardini S, Ren J, Wevrick R, Greer JJ: Developmental abnormalities of neuronal structure and function in prenatal mice lacking the Prader-Willi syndrome gene necdin. Am. J. Pathol. 167, 175-191 (2005).
-
(2005)
Am. J. Pathol.
, vol.167
, pp. 175-191
-
-
Pagliardini, S.1
Ren, J.2
Wevrick, R.3
Greer, J.J.4
-
132
-
-
46949100270
-
Loss of the Prader-Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons
-
Tennese AA, Gee CB, Wevrick R: Loss of the Prader-Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons. Dev. Dyn. 237, 1935-1943 (2008).
-
(2008)
Dev. Dyn.
, vol.237
, pp. 1935-1943
-
-
Tennese, A.A.1
Gee, C.B.2
Wevrick, R.3
-
133
-
-
23044445639
-
Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival
-
Kuwako K, Hosokawa A, Nishimura I et al.: Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival. J. Neurosci. 25, 7090-7099 (2005).
-
(2005)
J. Neurosci.
, vol.25
, pp. 7090-7099
-
-
Kuwako, K.1
Hosokawa, A.2
Nishimura, I.3
-
134
-
-
33751581604
-
Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death
-
Andrieu D, Meziane H, Marly F, Angelats C, Fernandez PA, Muscatelli F: Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death. BMC Dev. Biol. 6, 56 (2006).
-
(2006)
BMC Dev. Biol.
, vol.6
, pp. 56
-
-
Andrieu, D.1
Meziane, H.2
Marly, F.3
Angelats, C.4
Fernandez, P.A.5
Muscatelli, F.6
-
135
-
-
70449518013
-
Necdin and TrkA contribute to modulation by p75NTR of resistance to oxidant stress
-
Ingraham CA, Schor NF: Necdin and TrkA contribute to modulation by p75NTR of resistance to oxidant stress. Exp. Cell Res. 315, 3532-3542 (2009).
-
(2009)
Exp. Cell Res.
, vol.315
, pp. 3532-3542
-
-
Ingraham, C.A.1
Schor, N.F.2
-
136
-
-
33751081032
-
Necdin downregulates CDC2 expression to attenuate neuronal apoptosis
-
Kurita M, Kuwajima T, Nishimura I, Yoshikawa K: Necdin downregulates CDC2 expression to attenuate neuronal apoptosis. J. Neurosci. 26, 12003-12013 (2006).
-
(2006)
J. Neurosci.
, vol.26
, pp. 12003-12013
-
-
Kurita, M.1
Kuwajima, T.2
Nishimura, I.3
Yoshikawa, K.4
-
137
-
-
33744996959
-
Necdin promotes GABAergic neuron differentiation in cooperation with Dlx homeodomain proteins
-
Kuwajima T, Nishimura I, Yoshikawa K: Necdin promotes GABAergic neuron differentiation in cooperation with Dlx homeodomain proteins. J. Neurosci. 26, 5383-5392 (2006).
-
(2006)
J. Neurosci.
, vol.26
, pp. 5383-5392
-
-
Kuwajima, T.1
Nishimura, I.2
Yoshikawa, K.3
-
138
-
-
20444417035
-
Prediction of preadipocyte differentiation by gene expression reveals role of insulin receptor substrates and necdin
-
Tseng YH, Butte AJ, Kokkotou E et al.: Prediction of preadipocyte differentiation by gene expression reveals role of insulin receptor substrates and necdin. Nat. Cell Biol. 7, 601-611 (2005).
-
(2005)
Nat. Cell Biol.
, vol.7
, pp. 601-611
-
-
Tseng, Y.H.1
Butte, A.J.2
Kokkotou, E.3
-
139
-
-
35548982597
-
Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome
-
Bischof JM, Stewart CL, Wevrick R: Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome. Hum. Mol. Genet. 16, 2713-2719 (2007).
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 2713-2719
-
-
Bischof, J.M.1
Stewart, C.L.2
Wevrick, R.3
-
140
-
-
37749004050
-
Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation
-
Skryabin BV, Gubar LV, Seeger B et al.: Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation. PLoS Genet. 3, E235 (2007).
-
(2007)
PLoS Genet.
, vol.3
-
-
Skryabin, B.V.1
Gubar, L.V.2
Seeger, B.3
-
141
-
-
45849144806
-
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
-
Ding F, Li HH, Zhang S et al.: SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice. PLoS One 3, E1709 (2008).
-
(2008)
PLoS One
, vol.3
-
-
Ding, F.1
Li, H.H.2
Zhang, S.3
-
142
-
-
44349191455
-
Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster
-
Sahoo T, del Gaudio D, German JR et al.: Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster. Nat. Genet. 40, 719-721 (2008).
-
(2008)
Nat. Genet.
, vol.40
, pp. 719-721
-
-
Sahoo, T.1
Del Gaudio, D.2
German, J.R.3
-
143
-
-
68749097161
-
A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism
-
de Smith AJ, Purmann C, Walters RG et al.: A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism. Hum. Mol. Genet. 18, 3257-3265 (2009).
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 3257-3265
-
-
De Smith, A.J.1
Purmann, C.2
Walters, R.G.3
-
144
-
-
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: 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, 1067-1082 (2000).
-
(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
-
145
-
-
0030771087
-
Small nucleolar RNAs direct site-specific synthesis of pseudouridine in ribosomal RNA
-
Ni J, Tien AL, Fournier MJ: Small nucleolar RNAs direct site-specific synthesis of pseudouridine in ribosomal RNA. Cell 89, 565-573 (1997).
-
(1997)
Cell
, vol.89
, pp. 565-573
-
-
Ni, J.1
Tien, A.L.2
Fournier, M.J.3
-
146
-
-
0031942702
-
The U14 snoRNA is required for 2-O-methylation of the pre-18S rRNA in Xenopus oocytes
-
Dunbar DA, Baserga SJ: The U14 snoRNA is required for 2-O-methylation of the pre-18S rRNA in Xenopus oocytes. RNA 4, 195-204 (1998).
-
(1998)
RNA
, vol.4
, pp. 195-204
-
-
Dunbar, D.A.1
Baserga, S.J.2
-
147
-
-
0031012849
-
UBE3A/E6-AP mutations cause Angelman syndrome
-
Kishino T, Lalande M, Wagstaff J: UBE3A/E6-AP mutations cause Angelman syndrome. Nat. Genet. 15, 70-73 (1997).
-
(1997)
Nat. Genet.
, vol.15
, pp. 70-73
-
-
Kishino, T.1
Lalande, M.2
Wagstaff, J.3
-
148
-
-
0031031570
-
De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome
-
Matsuura T, Sutcliffe JS, Fang P et al.: De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome. Nat. Genet. 15, 74-77 (1997).
-
(1997)
Nat. Genet.
, vol.15
, pp. 74-77
-
-
Matsuura, T.1
Sutcliffe, J.S.2
Fang, P.3
-
150
-
-
18244383565
-
Distinct phenotypes distinguish the molecular classes of Angelman syndrome
-
Lossie AC, Whitney MM, Amidon D et al.: Distinct phenotypes distinguish the molecular classes of Angelman syndrome. J. Med. Genet. 38, 834-845 (2001).
-
(2001)
J. Med. Genet.
, vol.38
, pp. 834-845
-
-
Lossie, A.C.1
Whitney, M.M.2
Amidon, D.3
-
151
-
-
33644865491
-
Angelman syndrome 2005: Updated consensus for diagnostic criteria
-
Williams CA, Beaudet AL, Clayton-Smith J et al.: Angelman syndrome 2005: updated consensus for diagnostic criteria. Am. J. Med. Genet. A 140, 413-418 (2006).
-
(2006)
Am. J. Med. Genet. A
, vol.140
, pp. 413-418
-
-
Williams, C.A.1
Beaudet, A.L.2
Clayton-Smith, J.3
-
152
-
-
70350349099
-
Angelman syndrome: Current understanding and research prospects
-
Dan B: Angelman syndrome: current understanding and research prospects. Epilepsia 50, 2331-2339 (2009).
-
(2009)
Epilepsia
, vol.50
, pp. 2331-2339
-
-
Dan, B.1
-
153
-
-
0030879482
-
Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons
-
Albrecht U, Sutcliffe JS, Cattanach BM et al.: Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons. Nat. Genet. 17, 75-78 (1997).
-
(1997)
Nat. Genet.
, vol.17
, pp. 75-78
-
-
Albrecht, U.1
Sutcliffe, J.S.2
Cattanach, B.M.3
-
154
-
-
37549057995
-
The Angelman syndrome ubiquitin ligase localizes to the synapse and nucleus, and maternal deficiency results in abnormal dendritic spine morphology
-
Dindot SV, Antalffy BA, Bhattacharjee MB, Beaudet AL: The Angelman syndrome ubiquitin ligase localizes to the synapse and nucleus, and maternal deficiency results in abnormal dendritic spine morphology. Hum. Mol. Genet. 17, 111-118 (2008).
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 111-118
-
-
Dindot, S.V.1
Antalffy, B.A.2
Bhattacharjee, M.B.3
Beaudet, A.L.4
-
155
-
-
0242432463
-
Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a
-
Yamasaki K, Joh K, Ohta T et al.: Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a. Hum. Mol. Genet. 12, 837-847 (2003).
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 837-847
-
-
Yamasaki, K.1
Joh, K.2
Ohta, T.3
-
156
-
-
77954957575
-
Tissue-specific variation of Ube3a protein expression in rodents and in a mouse model of Angelman syndrome
-
Gustin RM, Bichell TJ, Bubser M et al.: Tissue-specific variation of Ube3a protein expression in rodents and in a mouse model of Angelman syndrome. Neurobiol. Dis. 39(3), 283-291 (2010).
-
(2010)
Neurobiol. Dis.
, vol.39
, Issue.3
, pp. 283-291
-
-
Gustin, R.M.1
Bichell, T.J.2
Bubser, M.3
-
157
-
-
3042821931
-
Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn
-
Landers M, Bancescu DL, Le Meur E et al.: Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn. Nucleic Acids Res. 32, 3480-3492 (2004).
-
(2004)
Nucleic Acids Res.
, vol.32
, pp. 3480-3492
-
-
Landers, M.1
Bancescu, D.L.2
Le Meur, E.3
-
158
-
-
0032067559
-
An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript
-
Rougeulle C, Cardoso C, Fontes M, Colleaux L, Lalande M: An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript. Nat. Genet. 19, 15-16 (1998).
-
(1998)
Nat. Genet.
, vol.19
, pp. 15-16
-
-
Rougeulle, C.1
Cardoso, C.2
Fontes, M.3
Colleaux, L.4
Lalande, M.5
-
159
-
-
67349182343
-
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
-
Glessner JT, Wang K, Cai G et al.: Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature 459, 569-573 (2009).
-
(2009)
Nature
, vol.459
, pp. 569-573
-
-
Glessner, J.T.1
Wang, K.2
Cai, G.3
-
160
-
-
14044252235
-
Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3
-
Samaco RC, Hogart A, LaSalle JM: Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. Hum. Mol. Genet. 14, 483-492 (2005).
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 483-492
-
-
Samaco, R.C.1
Hogart, A.2
Lasalle, J.M.3
-
161
-
-
17744380972
-
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression
-
Makedonski K, Abuhatzira L, Kaufman Y, Razin A, Shemer R: MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression. Hum. Mol. Genet. 14, 1049-1058 (2005).
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 1049-1058
-
-
Makedonski, K.1
Abuhatzira, L.2
Kaufman, Y.3
Razin, A.4
Shemer, R.5
-
162
-
-
35548945717
-
The overlapping spectrum of Rett and Angelman syndromes: A clinical review
-
Jedele KB: The overlapping spectrum of Rett and Angelman syndromes: a clinical review. Semin. Pediatr. Neurol. 14, 108-117 (2007).
-
(2007)
Semin. Pediatr. Neurol.
, vol.14
, pp. 108-117
-
-
Jedele, K.B.1
-
163
-
-
0032192481
-
Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation
-
Jiang YH, Armstrong D, Albrecht U et al.: Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation. Neuron 21, 799-811 (1998).
-
(1998)
Neuron
, vol.21
, pp. 799-811
-
-
Jiang, Y.H.1
Armstrong, D.2
Albrecht, U.3
-
164
-
-
0036197031
-
Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice
-
Miura K, Kishino T, Li E et al.: Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice. Neurobiol. Dis. 9, 149-159 (2002).
-
(2002)
Neurobiol. Dis.
, vol.9
, pp. 149-159
-
-
Miura, K.1
Kishino, T.2
Li, E.3
-
165
-
-
67349178189
-
Ube3a is required for experience-dependent maturation of the neocortex
-
Yashiro K, Riday TT, Condon KH et al.: Ube3a is required for experience-dependent maturation of the neocortex. Nat. Neurosci. 12, 777-783 (2009).
-
(2009)
Nat. Neurosci.
, vol.12
, pp. 777-783
-
-
Yashiro, K.1
Riday, T.T.2
Condon, K.H.3
-
166
-
-
77950386683
-
Genomic imprinting of experience-dependent cortical plasticity by the ubiquitin ligase gene Ube3a
-
Sato M, Stryker MP: Genomic imprinting of experience-dependent cortical plasticity by the ubiquitin ligase gene Ube3a. Proc. Natl Acad. Sci. USA 107, 5611-5616 (2010).
-
(2010)
Proc. Natl Acad. Sci. USA
, vol.107
, pp. 5611-5616
-
-
Sato, M.1
Stryker, M.P.2
-
167
-
-
0345701252
-
Derangements of hippocampal calcium/ calmodulin-dependent protein kinase II in a mouse model for Angelman mental retardation syndrome
-
Weeber EJ, Jiang YH, Elgersma Y et al.: Derangements of hippocampal calcium/ calmodulin-dependent protein kinase II in a mouse model for Angelman mental retardation syndrome. J. Neurosci. 23, 2634-2644 (2003).
-
(2003)
J. Neurosci.
, vol.23
, pp. 2634-2644
-
-
Weeber, E.J.1
Jiang, Y.H.2
Elgersma, Y.3
-
168
-
-
0033603339
-
Identification of HHR23A as a substrate for E6-associated protein-mediated ubiquitination
-
Kumar S, Talis AL, Howley PM: Identification of HHR23A as a substrate for E6-associated protein-mediated ubiquitination. J. Biol. Chem. 274, 18785-18792 (1999).
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 18785-18792
-
-
Kumar, S.1
Talis, A.L.2
Howley, P.M.3
-
169
-
-
33748751286
-
Expression of the Rho-GEF Pbl/ECT2 is regulated by the UBE3A E3 ubiquitin ligase
-
Reiter LT, Seagroves TN, Bowers M, Bier E: Expression of the Rho-GEF Pbl/ECT2 is regulated by the UBE3A E3 ubiquitin ligase. Hum. Mol. Genet. 15, 2825-2835 (2006).
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 2825-2835
-
-
Reiter, L.T.1
Seagroves, T.N.2
Bowers, M.3
Bier, E.4
-
171
-
-
77649083119
-
The Angelman syndrome protein Ube3A regulates synapse development by ubiquitinating arc
-
Greer PL, Hanayama R, Bloodgood BL et al.: The Angelman syndrome protein Ube3A regulates synapse development by ubiquitinating arc. Cell 140, 704-716.
-
Cell
, vol.140
, pp. 704-716
-
-
Greer, P.L.1
Hanayama, R.2
Bloodgood, B.L.3
-
172
-
-
0142215375
-
Dosage-sensitive X-linked locus influences the development of amygdala and orbitofrontal cortex, and fear recognition in humans
-
Good CD, Lawrence K, Thomas NS et al.: Dosage-sensitive X-linked locus influences the development of amygdala and orbitofrontal cortex, and fear recognition in humans. Brain 126, 2431-2446 (2003).
-
(2003)
Brain
, vol.126
, pp. 2431-2446
-
-
Good, C.D.1
Lawrence, K.2
Thomas, N.S.3
-
173
-
-
0036185877
-
Turners syndrome in adulthood
-
Elsheikh M, Dunger DB, Conway GS, Wass JA: Turners syndrome in adulthood. Endocr. Rev. 23, 120-140 (2002).
-
(2002)
Endocr. Rev.
, vol.23
, pp. 120-140
-
-
Elsheikh, M.1
Dunger, D.B.2
Conway, G.S.3
Wass, J.A.4
-
174
-
-
0023322047
-
The Turner syndrome: Cognitive deficits, affective discrimination, and behavior problems
-
McCauley E, Kay T, Ito J, Treder R: The Turner syndrome: cognitive deficits, affective discrimination, and behavior problems. Child Dev. 58, 464-473 (1987).
-
(1987)
Child Dev.
, vol.58
, pp. 464-473
-
-
McCauley, E.1
Kay, T.2
Ito, J.3
Treder, R.4
-
175
-
-
0035676457
-
Psychosocial development in adolescents with Turner syndrome
-
McCauley E, Feuillan P, Kushner H, Ross JL: Psychosocial development in adolescents with Turner syndrome. J. Dev. Behav. Pediatr. 22, 360-365 (2001).
-
(2001)
J. Dev. Behav. Pediatr.
, vol.22
, pp. 360-365
-
-
McCauley, E.1
Feuillan, P.2
Kushner, H.3
Ross, J.L.4
-
176
-
-
0033963348
-
Use of estrogen in young girls with Turner syndrome: Effects on memory
-
Ross JL, Roeltgen D, Feuillan P, Kushner H, Cutler GB Jr: Use of estrogen in young girls with Turner syndrome: effects on memory. Neurology 54, 164-170 (2000).
-
(2000)
Neurology
, vol.54
, pp. 164-170
-
-
Ross, J.L.1
Roeltgen, D.2
Feuillan, P.3
Kushner, H.4
Cutler Jr., G.B.5
-
177
-
-
16944366964
-
Evidence from Turners syndrome of an imprinted X-linked locus affecting cognitive function
-
Skuse DH, James RS, Bishop DV et al.: Evidence from Turners syndrome of an imprinted X-linked locus affecting cognitive function. Nature 387, 705-708 (1997).
-
(1997)
Nature
, vol.387
, pp. 705-708
-
-
Skuse, D.H.1
James, R.S.2
Bishop, D.V.3
-
178
-
-
0033981995
-
Distinctive patterns of memory function in subgroups of females with Turner syndrome: Evidence for imprinted loci on the X-chromosome affecting neurodevelopment
-
Bishop DV, Canning E, Elgar K, Morris E, Jacobs PA, Skuse DH: Distinctive patterns of memory function in subgroups of females with Turner syndrome: evidence for imprinted loci on the X-chromosome affecting neurodevelopment. Neuropsychologia 38, 712-721 (2000).
-
(2000)
Neuropsychologia
, vol.38
, pp. 712-721
-
-
Bishop, D.V.1
Canning, E.2
Elgar, K.3
Morris, E.4
Jacobs, P.A.5
Skuse, D.H.6
-
179
-
-
0034640697
-
Female with autistic disorder and monosomy X (Turner syndrome): Parent-of-origin effect of the X chromosome
-
Donnelly SL, Wolpert CM, Menold MM et al.: Female with autistic disorder and monosomy X (Turner syndrome): parent-of-origin effect of the X chromosome. Am. J. Med. Genet. 96, 312-316 (2000).
-
(2000)
Am. J. Med. Genet.
, vol.96
, pp. 312-316
-
-
Donnelly, S.L.1
Wolpert, C.M.2
Menold, M.M.3
-
180
-
-
0027384938
-
X-chromosome effects on female brain: A magnetic resonance imaging study of Turners syndrome
-
Murphy DG, DeCarli C, Daly E et al.: X-chromosome effects on female brain: a magnetic resonance imaging study of Turners syndrome. Lancet 342, 1197-1200 (1993).
-
(1993)
Lancet
, vol.342
, pp. 1197-1200
-
-
Murphy, D.G.1
Decarli, C.2
Daly, E.3
-
181
-
-
0028843730
-
Neurodevelopmental effects of X monosomy: A volumetric imaging study
-
Reiss AL, Mazzocco MM, Greenlaw R, Freund LS, Ross JL: Neurodevelopmental effects of X monosomy: a volumetric imaging study. Ann. Neurol. 38, 731-738 (1995).
-
(1995)
Ann. Neurol.
, vol.38
, pp. 731-738
-
-
Reiss, A.L.1
Mazzocco, M.M.2
Greenlaw, R.3
Freund, L.S.4
Ross, J.L.5
-
182
-
-
4544226673
-
Amygdala and hippocampal volumes in Turner syndrome: A high-resolution MRI study of X-monosomy
-
Kesler SR, Garrett A, Bender B, Yankowitz J, Zeng SM, Reiss AL: Amygdala and hippocampal volumes in Turner syndrome: a high-resolution MRI study of X-monosomy. Neuropsychologia 42, 1971-1978 (2004).
-
(2004)
Neuropsychologia
, vol.42
, pp. 1971-1978
-
-
Kesler, S.R.1
Garrett, A.2
Bender, B.3
Yankowitz, J.4
Zeng, S.M.5
Reiss, A.L.6
-
183
-
-
0242348826
-
Effects of X-monosomy and X-linked imprinting on superior temporal gyrus morphology in Turner syndrome
-
Kesler SR, Blasey CM, Brown WE et al.: Effects of X-monosomy and X-linked imprinting on superior temporal gyrus morphology in Turner syndrome. Biol. Psychiatry 54, 636-646 (2003).
-
(2003)
Biol. Psychiatry
, vol.54
, pp. 636-646
-
-
Kesler, S.R.1
Blasey, C.M.2
Brown, W.E.3
-
184
-
-
33947730075
-
The 39,XO mouse as a model for the neurobiology of Turner syndrome and sex-biased neuropsychiatric disorders
-
Lynn PM, Davies W: The 39,XO mouse as a model for the neurobiology of Turner syndrome and sex-biased neuropsychiatric disorders. Behav. Brain Res. 179, 173-182 (2007).
-
(2007)
Behav. Brain Res.
, vol.179
, pp. 173-182
-
-
Lynn, P.M.1
Davies, W.2
-
185
-
-
20044387409
-
Identification of a cluster of X-linked imprinted genes in mice
-
Raefski AS, ONeill MJ: Identification of a cluster of X-linked imprinted genes in mice. Nat. Genet. 37, 620-624 (2005).
-
(2005)
Nat. Genet.
, vol.37
, pp. 620-624
-
-
Raefski, A.S.1
Oneill, M.J.2
-
186
-
-
20044386140
-
Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice
-
Davies W, Isles A, Smith R et al.: Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice. Nat. Genet. 37, 625-629 (2005).
-
(2005)
Nat. Genet.
, vol.37
, pp. 625-629
-
-
Davies, W.1
Isles, A.2
Smith, R.3
-
187
-
-
0032939266
-
High level expression of the Xlr nuclear protein in immature thymocytes and colocalization with the matrix-associated region-binding SATB1 protein
-
Escalier D, Allenet B, Badrichani A, Garchon HJ: High level expression of the Xlr nuclear protein in immature thymocytes and colocalization with the matrix-associated region-binding SATB1 protein. J. Immunol. 162, 292-298 (1999).
-
(1999)
J. Immunol.
, vol.162
, pp. 292-298
-
-
Escalier, D.1
Allenet, B.2
Badrichani, A.3
Garchon, H.J.4
-
188
-
-
0036731651
-
A new gene family (FAM9) of low-copy repeats in Xp22.3 expressed exclusively in testis: Implications for recombinations in this region
-
Martinez-Garay I, Jablonka S, Sutajova M, Steuernagel P, Gal A, Kutsche K: A new gene family (FAM9) of low-copy repeats in Xp22.3 expressed exclusively in testis: implications for recombinations in this region. Genomics 80, 259-267 (2002).
-
(2002)
Genomics
, vol.80
, pp. 259-267
-
-
Martinez-Garay, I.1
Jablonka, S.2
Sutajova, M.3
Steuernagel, P.4
Gal, A.5
Kutsche, K.6
-
189
-
-
77953251284
-
Cux1 and Cux2 regulate dendritic branching, spine morphology, and synapses of the upper layer neurons of the cortex
-
Cubelos B, Sebastian-Serrano A, Beccari L et al.: Cux1 and Cux2 regulate dendritic branching, spine morphology, and synapses of the upper layer neurons of the cortex. Neuron 66, 523-535 (2010).
-
(2010)
Neuron
, vol.66
, pp. 523-535
-
-
Cubelos, B.1
Sebastian-Serrano, A.2
Beccari, L.3
-
190
-
-
0032971826
-
Xp deletions associated with autism in three females
-
Thomas NS, Sharp AJ, Browne CE, Skuse D, Hardie C, Dennis NR: Xp deletions associated with autism in three females. Hum. Genet. 104, 43-48 (1999).
-
(1999)
Hum. Genet.
, vol.104
, pp. 43-48
-
-
Thomas, N.S.1
Sharp, A.J.2
Browne, C.E.3
Skuse, D.4
Hardie, C.5
Dennis, N.R.6
-
191
-
-
0032768870
-
Schizophrenia susceptibility gene locus at Xp22.3
-
Milunsky J, Huang XL, Wyandt HE, Milunsky A: Schizophrenia susceptibility gene locus at Xp22.3. Clin. Genet. 55, 455-460 (1999).
-
(1999)
Clin. Genet.
, vol.55
, pp. 455-460
-
-
Milunsky, J.1
Huang, X.L.2
Wyandt, H.E.3
Milunsky, A.4
-
192
-
-
0028076305
-
Synaptonemal complex proteins: Occurrence, epitope mapping and chromosome disjunction
-
Dobson MJ, Pearlman RE, Karaiskakis A, Spyropoulos B, Moens PB: Synaptonemal complex proteins: occurrence, epitope mapping and chromosome disjunction. J. Cell Sci. 107(Pt. 10), 2749-2760 (1994).
-
(1994)
J. Cell Sci.
, vol.107
, Issue.PART 10
, pp. 2749-2760
-
-
Dobson, M.J.1
Pearlman, R.E.2
Karaiskakis, A.3
Spyropoulos, B.4
Moens, P.B.5
-
193
-
-
0035072804
-
Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations
-
Shahbazian MD, Zoghbi HY: Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations. Curr. Opin. Neurol. 14, 171-176 (2001).
-
(2001)
Curr. Opin. Neurol.
, vol.14
, pp. 171-176
-
-
Shahbazian, M.D.1
Zoghbi, H.Y.2
-
195
-
-
0032830639
-
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
-
Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY: Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat. Genet. 23, 185-188 (1999).
-
(1999)
Nat. Genet.
, vol.23
, pp. 185-188
-
-
Amir, R.E.1
Van Den Veyver, I.B.2
Wan, M.3
Tran, C.Q.4
Francke, U.5
Zoghbi, H.Y.6
-
196
-
-
0026747761
-
Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA
-
Lewis JD, Meehan RR, Henzel WJ et al.: Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA. Cell 69, 905-914 (1992).
-
(1992)
Cell
, vol.69
, pp. 905-914
-
-
Lewis, J.D.1
Meehan, R.R.2
Henzel, W.J.3
-
197
-
-
0026658662
-
Characterization of MeCP2, a vertebrate DNA binding protein with affinity for methylated DNA
-
Meehan RR, Lewis JD, Bird AP: Characterization of MeCP2, a vertebrate DNA binding protein with affinity for methylated DNA. Nucleic Acids Res. 20, 5085-5092 (1992).
-
(1992)
Nucleic Acids Res.
, vol.20
, pp. 5085-5092
-
-
Meehan, R.R.1
Lewis, J.D.2
Bird, A.P.3
-
198
-
-
7244243971
-
MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions
-
Kishi N, Macklis JD: MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions. Mol. Cell Neurosci. 27, 306-321 (2004).
-
(2004)
Mol. Cell Neurosci.
, vol.27
, pp. 306-321
-
-
Kishi, N.1
MacKlis, J.D.2
-
199
-
-
0037280319
-
Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation
-
Balmer D, Goldstine J, Rao YM, LaSalle JM: Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation. J. Mol. Med. 81, 61-68 (2003).
-
(2003)
J. Mol. Med.
, vol.81
, pp. 61-68
-
-
Balmer, D.1
Goldstine, J.2
Rao, Y.M.3
Lasalle, J.M.4
-
200
-
-
0032574977
-
Transcriptional repression by the methyl- CpG-binding protein MeCP2 involves a histone deacetylase complex
-
Nan X, Ng HH, Johnson CA et al.: Transcriptional repression by the methyl- CpG-binding protein MeCP2 involves a histone deacetylase complex. Nature 393, 386-389 (1998).
-
(1998)
Nature
, vol.393
, pp. 386-389
-
-
Nan, X.1
Ng, H.H.2
Johnson, C.A.3
-
201
-
-
34547118571
-
Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets
-
Jordan C, Li HH, Kwan HC, Francke U: Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets. BMC Med. Genet. 8, 36 (2007).
-
(2007)
BMC Med. Genet.
, vol.8
, pp. 36
-
-
Jordan, C.1
Li, H.H.2
Kwan, H.C.3
Francke, U.4
-
202
-
-
26444516160
-
Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome
-
Nuber UA, Kriaucionis S, Roloff TC et al.: Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome. Hum. Mol. Genet. 14, 2247-2256 (2005).
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 2247-2256
-
-
Nuber, U.A.1
Kriaucionis, S.2
Roloff, T.C.3
-
203
-
-
0037180492
-
Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain
-
Tudor M, Akbarian S, Chen RZ, Jaenisch R: Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain. Proc. Natl Acad. Sci. USA 99, 15536-15541 (2002).
-
(2002)
Proc. Natl Acad. Sci. USA
, vol.99
, pp. 15536-15541
-
-
Tudor, M.1
Akbarian, S.2
Chen, R.Z.3
Jaenisch, R.4
-
204
-
-
56649107908
-
Mecp2-null mice provide new neuronal targets for Rett syndrome
-
Urdinguio RG, Lopez-Serra L, Lopez-Nieva P et al.: Mecp2-null mice provide new neuronal targets for Rett syndrome. PLoS One 3, E3669 (2008).
-
(2008)
PLoS One
, vol.3
-
-
Urdinguio, R.G.1
Lopez-Serra, L.2
Lopez-Nieva, P.3
-
205
-
-
29144447632
-
Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2
-
Young JI, Hong EP, Castle JC et al.: Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2. Proc. Natl Acad. Sci. USA 102, 17551-17558 (2005).
-
(2005)
Proc. Natl Acad. Sci. USA
, vol.102
, pp. 17551-17558
-
-
Young, J.I.1
Hong, E.P.2
Castle, J.C.3
-
206
-
-
76849094693
-
Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state
-
Skene PJ, Illingworth RS, Webb S et al.: Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state. Mol. Cell 37, 457-468 (2010).
-
(2010)
Mol. Cell
, vol.37
, pp. 457-468
-
-
Skene, P.J.1
Illingworth, R.S.2
Webb, S.3
-
207
-
-
0035093830
-
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
-
Chen RZ, Akbarian S, Tudor M, Jaenisch R: Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice. Nat. Genet. 27, 327-331 (2001).
-
(2001)
Nat. Genet.
, vol.27
, pp. 327-331
-
-
Chen, R.Z.1
Akbarian, S.2
Tudor, M.3
Jaenisch, R.4
-
208
-
-
0035094767
-
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
-
Guy J, Hendrich B, Holmes M, Martin JE, Bird A: A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome. Nat. Genet. 27, 322-326 (2001).
-
(2001)
Nat. Genet.
, vol.27
, pp. 322-326
-
-
Guy, J.1
Hendrich, B.2
Holmes, M.3
Martin, J.E.4
Bird, A.5
-
209
-
-
0037130455
-
Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3
-
Shahbazian M, Young J, Yuva-Paylor L et al.: Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3. Neuron 35, 243-254 (2002).
-
(2002)
Neuron
, vol.35
, pp. 243-254
-
-
Shahbazian, M.1
Young, J.2
Yuva-Paylor, L.3
-
210
-
-
1942533500
-
Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice
-
Luikenhuis S, Giacometti E, Beard CF, Jaenisch R: Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice. Proc. Natl Acad. Sci. USA 101, 6033-6038 (2004).
-
(2004)
Proc. Natl Acad. Sci. USA
, vol.101
, pp. 6033-6038
-
-
Luikenhuis, S.1
Giacometti, E.2
Beard, C.F.3
Jaenisch, R.4
-
211
-
-
33846924001
-
Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2
-
Giacometti E, Luikenhuis S, Beard C, Jaenisch R: Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2. Proc. Natl Acad. Sci. USA 104, 1931-1936 (2007).
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 1931-1936
-
-
Giacometti, E.1
Luikenhuis, S.2
Beard, C.3
Jaenisch, R.4
-
212
-
-
60549115413
-
Partial reversal of Rett syndrome-like symptoms in MeCP2 mutant mice
-
Tropea D, Giacometti E, Wilson NR et al.: Partial reversal of Rett syndrome-like symptoms in MeCP2 mutant mice. Proc. Natl Acad. Sci. USA 106, 2029-2034 (2009).
-
(2009)
Proc. Natl Acad. Sci. USA
, vol.106
, pp. 2029-2034
-
-
Tropea, D.1
Giacometti, E.2
Wilson, N.R.3
-
213
-
-
33847266846
-
Reversal of neurological defects in a mouse model of Rett syndrome
-
Guy J, Gan J, Selfridge J, Cobb S, Bird A: Reversal of neurological defects in a mouse model of Rett syndrome. Science 315, 1143-1147 (2007).
-
(2007)
Science
, vol.315
, pp. 1143-1147
-
-
Guy, J.1
Gan, J.2
Selfridge, J.3
Cobb, S.4
Bird, A.5
-
214
-
-
34249711442
-
The odyssey of MeCP2 and parental imprinting
-
LaSalle JM: The odyssey of MeCP2 and parental imprinting. Epigenetics 2, 5-10 (2007).
-
(2007)
Epigenetics
, vol.2
, pp. 5-10
-
-
Lasalle, J.M.1
-
215
-
-
33745610875
-
Ube3a expression is not altered in Mecp2 mutant mice
-
Jordan C, Francke U: Ube3a expression is not altered in Mecp2 mutant mice. Hum. Mol. Genet. 15, 2210-2215 (2006).
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 2210-2215
-
-
Jordan, C.1
Francke, U.2
-
216
-
-
0030745624
-
Chicken MAR-binding protein ARBP is homologous to rat methyl-CpG-binding protein MeCP2
-
Weitzel JM, Buhrmester H, Stratling WH: Chicken MAR-binding protein ARBP is homologous to rat methyl-CpG-binding protein MeCP2. Mol. Cell. Biol. 17, 5656-5666 (1997).
-
(1997)
Mol. Cell. Biol.
, vol.17
, pp. 5656-5666
-
-
Weitzel, J.M.1
Buhrmester, H.2
Stratling, W.H.3
-
217
-
-
0342316480
-
Origin and roles of nuclear matrix proteins. Specific functions of the MAR-binding protein MeCP2/ARBP
-
Stratling WH, Yu F: Origin and roles of nuclear matrix proteins. Specific functions of the MAR-binding protein MeCP2/ARBP. Crit. Rev. Eukaryot. Gene Expr. 9, 311-318 (1999).
-
(1999)
Crit. Rev. Eukaryot. Gene Expr.
, vol.9
, pp. 311-318
-
-
Stratling, W.H.1
Yu, F.2
-
218
-
-
41849119117
-
MeCP2-dependent repression of an imprinted miR-184 released by depolarization
-
Nomura T, Kimura M, Horii T et al.: MeCP2-dependent repression of an imprinted miR-184 released by depolarization. Hum. Mol. Genet. 17, 1192-1199 (2008).
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 1192-1199
-
-
Nomura, T.1
Kimura, M.2
Horii, T.3
-
219
-
-
0037423186
-
The methyl-CpG-binding protein MeCP2 links DNA methylation to histone methylation
-
Fuks F, Hurd PJ, Wolf D, Nan X, Bird AP, Kouzarides T: The methyl-CpG-binding protein MeCP2 links DNA methylation to histone methylation. J. Biol. Chem. 278, 4035-4040 (2003).
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 4035-4040
-
-
Fuks, F.1
Hurd, P.J.2
Wolf, D.3
Nan, X.4
Bird, A.P.5
Kouzarides, T.6
-
220
-
-
0036493248
-
Methylation-dependent silencing at the H19 imprinting control region by MeCP2
-
Drewell RA, Goddard CJ, Thomas JO, Surani MA: Methylation-dependent silencing at the H19 imprinting control region by MeCP2. Nucleic Acids Res. 30, 1139-1144 (2002).
-
(2002)
Nucleic Acids Res.
, vol.30
, pp. 1139-1144
-
-
Drewell, R.A.1
Goddard, C.J.2
Thomas, J.O.3
Surani, M.A.4
-
221
-
-
33847282970
-
Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation
-
Nan X, Hou J, Maclean A et al.: Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation. Proc. Natl Acad. Sci. USA 104, 2709-2714 (2007).
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 2709-2714
-
-
Nan, X.1
Hou, J.2
MacLean, A.3
-
222
-
-
0034069652
-
Mutations in ATRX, encoding a SWI/ SNF-like protein, cause diverse changes in the pattern of DNA methylation
-
Gibbons RJ, McDowell TL, Raman S et al.: Mutations in ATRX, encoding a SWI/ SNF-like protein, cause diverse changes in the pattern of DNA methylation. Nat. Genet. 24, 368-371 (2000).
-
(2000)
Nat. Genet.
, vol.24
, pp. 368-371
-
-
Gibbons, R.J.1
McDowell, T.L.2
Raman, S.3
-
223
-
-
0029827343
-
ATRX encodes a novel member of the SNF2 family of proteins: Mutations point to a common mechanism underlying the ATR-X syndrome
-
Picketts DJ, Higgs DR, Bachoo S, Blake DJ, Quarrell OW, Gibbons RJ: ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome. Hum. Mol. Genet. 5, 1899-1907 (1996).
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1899-1907
-
-
Picketts, D.J.1
Higgs, D.R.2
Bachoo, S.3
Blake, D.J.4
Quarrell, O.W.5
Gibbons, R.J.6
-
224
-
-
58149391969
-
Neuronal death resulting from targeted disruption of the Snf2 protein ATRX is mediated by p53
-
Seah C, Levy MA, Jiang Y et al.: Neuronal death resulting from targeted disruption of the Snf2 protein ATRX is mediated by p53. J. Neurosci. 28, 12570-12580 (2008).
-
(2008)
J. Neurosci.
, vol.28
, pp. 12570-12580
-
-
Seah, C.1
Levy, M.A.2
Jiang, Y.3
-
225
-
-
13544277156
-
Mutation in the 5 alternatively spliced region of the XNP/ATR-X gene causes Chudley-Lowry syndrome
-
Abidi FE, Cardoso C, Lossi AM et al.: Mutation in the 5 alternatively spliced region of the XNP/ATR-X gene causes Chudley-Lowry syndrome. Eur J. Hum. Genet. 13, 176-183 (2005).
-
(2005)
Eur J. Hum. Genet.
, vol.13
, pp. 176-183
-
-
Abidi, F.E.1
Cardoso, C.2
Lossi, A.M.3
-
226
-
-
38749117849
-
Loss of ATRX leads to chromosome cohesion and congression defects
-
Ritchie K, Seah C, Moulin J, Isaac C, Dick F, Berube NG: Loss of ATRX leads to chromosome cohesion and congression defects. J. Cell. Biol. 180, 315-324 (2008).
-
(2008)
J. Cell. Biol.
, vol.180
, pp. 315-324
-
-
Ritchie, K.1
Seah, C.2
Moulin, J.3
Isaac, C.4
Dick, F.5
Berube, N.G.6
-
227
-
-
3042780173
-
ATRX, a member of the SNF2 family of helicase/ATPases, is required for chromosome alignment and meiotic spindle organization in metaphase II stage mouse oocytes
-
De La Fuente R, Viveiros MM, Wigglesworth K, Eppig JJ: ATRX, a member of the SNF2 family of helicase/ATPases, is required for chromosome alignment and meiotic spindle organization in metaphase II stage mouse oocytes. Dev. Biol. 272, 1-14 (2004).
-
(2004)
Dev. Biol.
, vol.272
, pp. 1-14
-
-
De La Fuente, R.1
Viveiros, M.M.2
Wigglesworth, K.3
Eppig, J.J.4
-
228
-
-
13044252871
-
Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes
-
McDowell TL, Gibbons RJ, Sutherland H et al.: Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes. Proc. Natl Acad. Sci. USA 96, 13983-13988 (1999).
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
, pp. 13983-13988
-
-
McDowell, T.L.1
Gibbons, R.J.2
Sutherland, H.3
-
229
-
-
0342514792
-
Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association
-
Berube NG, Smeenk CA, Picketts DJ: Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association. Hum. Mol. Genet. 9, 539-547 (2000).
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 539-547
-
-
Berube, N.G.1
Smeenk, C.A.2
Picketts, D.J.3
-
230
-
-
33646473832
-
Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues
-
Garrick D, Sharpe JA, Arkell R et al.: Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues. PLoS Genet. 2, E58 (2006).
-
(2006)
PLoS Genet.
, vol.2
-
-
Garrick, D.1
Sharpe, J.A.2
Arkell, R.3
-
231
-
-
14944359718
-
The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis
-
Berube NG, Mangelsdorf M, Jagla M et al.: The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis. J. Clin. Invest. 115, 258-267 (2005).
-
(2005)
J. Clin. Invest.
, vol.115
, pp. 258-267
-
-
Berube, N.G.1
Mangelsdorf, M.2
Jagla, M.3
-
232
-
-
55449131886
-
The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome
-
Levy MA, Fernandes AD, Tremblay DC, Seah C, Berube NG: The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome. BMC Genomics 9, 468 (2008).
-
(2008)
BMC Genomics
, vol.9
, pp. 468
-
-
Levy, M.A.1
Fernandes, A.D.2
Tremblay, D.C.3
Seah, C.4
Berube, N.G.5
-
233
-
-
4243158485
-
Haplotype analysis of SNAP-25 suggests a role in the aetiology of ADHD
-
Mill J, Richards S, Knight J, Curran S, Taylor E, Asherson P: Haplotype analysis of SNAP-25 suggests a role in the aetiology of ADHD. Mol. Psychiatry 9, 801-810 (2004).
-
(2004)
Mol. Psychiatry
, vol.9
, pp. 801-810
-
-
Mill, J.1
Richards, S.2
Knight, J.3
Curran, S.4
Taylor, E.5
Asherson, P.6
-
234
-
-
0038513591
-
Biased paternal transmission of SNAP-25 risk alleles in attention-deficit hyperactivity disorder
-
Kustanovich V, Merriman B, McGough J, McCracken JT, Smalley SL, Nelson SF: Biased paternal transmission of SNAP-25 risk alleles in attention-deficit hyperactivity disorder. Mol. Psychiatry 8, 309-315 (2003).
-
(2003)
Mol. Psychiatry
, vol.8
, pp. 309-315
-
-
Kustanovich, V.1
Merriman, B.2
McGough, J.3
McCracken, J.T.4
Smalley, S.L.5
Nelson, S.F.6
-
235
-
-
27144502791
-
Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD
-
Kent L, Green E, Hawi Z et al.: Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD. Mol. Psychiatry 10, 939-943 (2005).
-
(2005)
Mol. Psychiatry
, vol.10
, pp. 939-943
-
-
Kent, L.1
Green, E.2
Hawi, Z.3
-
236
-
-
27144480407
-
Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD
-
Sheehan K, Lowe N, Kirley A et al.: Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD. Mol. Psychiatry 10, 944-949 (2005).
-
(2005)
Mol. Psychiatry
, vol.10
, pp. 944-949
-
-
Sheehan, K.1
Lowe, N.2
Kirley, A.3
-
237
-
-
12244292661
-
The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder
-
Quist JF, Barr CL, Schachar R et al.: The serotonin 5-HT1B receptor gene and attention deficit hyperactivity disorder. Mol. Psychiatry 8, 98-102 (2003).
-
(2003)
Mol. Psychiatry
, vol.8
, pp. 98-102
-
-
Quist, J.F.1
Barr, C.L.2
Schachar, R.3
-
238
-
-
0037041326
-
Transmission disequilibrium studies of the serotonin 5-HT2A receptor gene (HTR2A) in autism
-
Veenstra-VanderWeele J, Kim SJ, Lord C et al.: Transmission disequilibrium studies of the serotonin 5-HT2A receptor gene (HTR2A) in autism. Am. J. Med. Genet. 114, 277-283 (2002).
-
(2002)
Am. J. Med. Genet.
, vol.114
, pp. 277-283
-
-
Veenstra-Vanderweele, J.1
Kim, S.J.2
Lord, C.3
-
239
-
-
85047695028
-
Linkage and association of the glutamate receptor 6 gene with autism
-
Jamain S, Bncur C, Quach H et al.: Linkage and association of the glutamate receptor 6 gene with autism. Mol. Psychiatry 7, 302-310 (2002).
-
(2002)
Mol. Psychiatry
, vol.7
, pp. 302-310
-
-
Jamain, S.1
Bncur, C.2
Quach, H.3
-
240
-
-
0042824074
-
Possible parent-of-origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder
-
Borglum AD, Kirov G, Craddock N et al.: Possible parent-of-origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder. Am. J. Med. Genet. B Neuropsychiatr Genet 117B, 18-22 (2003).
-
(2003)
Am. J. Med. Genet. B Neuropsychiatr Genet 117B
, pp. 18-22
-
-
Borglum, A.D.1
Kirov, G.2
Craddock, N.3
-
241
-
-
0036382921
-
Dopamine D4 receptor and tyrosine hydroxylase genes in bipolar disorder: Evidence for a role of DRD4
-
Muglia P, Petronis A, Mundo E, Lander S, Cate T, Kennedy JL: Dopamine D4 receptor and tyrosine hydroxylase genes in bipolar disorder: evidence for a role of DRD4. Mol. Psychiatry 7, 860-866 (2002).
-
(2002)
Mol. Psychiatry
, vol.7
, pp. 860-866
-
-
Muglia, P.1
Petronis, A.2
Mundo, E.3
Lander, S.4
Cate, T.5
Kennedy, J.L.6
-
242
-
-
0038777244
-
Family-based association study of the serotonin-2A receptor gene (5-HT2A) and bipolar disorder
-
Ni X, Trakalo JM, Mundo E, Lee L, Parikh S, Kennedy JL: Family-based association study of the serotonin-2A receptor gene (5-HT2A) and bipolar disorder. Neuromolecular Med. 2, 251-259 (2002).
-
(2002)
Neuromolecular Med.
, vol.2
, pp. 251-259
-
-
Ni, X.1
Trakalo, J.M.2
Mundo, E.3
Lee, L.4
Parikh, S.5
Kennedy, J.L.6
-
243
-
-
2642710063
-
Investigation of the candidate genes ACTHR and golf for bipolar illness by the transmission/disequilibrium test
-
Bickeboller H, Kistler M, Scholz M: Investigation of the candidate genes ACTHR and golf for bipolar illness by the transmission/disequilibrium test. Genet Epidemiol 14, 575-580 (1997).
-
(1997)
Genet Epidemiol
, vol.14
, pp. 575-580
-
-
Bickeboller, H.1
Kistler, M.2
Scholz, M.3
-
244
-
-
4444291477
-
Maternal transmission disequilibrium of the glutamate receptor GRIK2 in schizophrenia
-
Bah J, Quach H, Ebstein RP et al.: Maternal transmission disequilibrium of the glutamate receptor GRIK2 in schizophrenia. Neuroreport 15, 1987-1991 (2004).
-
(2004)
Neuroreport
, vol.15
, pp. 1987-1991
-
-
Bah, J.1
Quach, H.2
Ebstein, R.P.3
-
245
-
-
0037741860
-
Analysis of the linkage of the Taq1A and Taq1B loci of the dopamine D2 receptor gene with schizophrenia in patients and their siblings
-
Golimbet VE, Aksenova MG, Nosikov VV, Orlova VA, Kaleda VG: Analysis of the linkage of the Taq1A and Taq1B loci of the dopamine D2 receptor gene with schizophrenia in patients and their siblings. Neurosci. Behav. Physiol. 33, 223-225 (2003).
-
(2003)
Neurosci. Behav. Physiol.
, vol.33
, pp. 223-225
-
-
Golimbet, V.E.1
Aksenova, M.G.2
Nosikov, V.V.3
Orlova, V.A.4
Kaleda, V.G.5
-
246
-
-
78650051022
-
Induced pluripotent stem cells can be used to model the genomic imprinting disorder Prader- Willi syndrome
-
doi: 10.1074/ jbc.M110.183392 Epub ahead of print
-
Yang J, Cai J, Zhang Y et al.: Induced pluripotent stem cells can be used to model the genomic imprinting disorder Prader- Willi syndrome. J. Biol. Chem. doi: 10.1074/ jbc.M110.183392 (2010) (Epub ahead of print).
-
J. Biol. Chem.
, vol.2010
-
-
Yang, J.1
Cai, J.2
Zhang, Y.3
-
247
-
-
78049303170
-
Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes
-
Chamberlain SJ, Chen PF, Ng KY et al.: Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes. Proc. Natl Acad. Sci. USA 107, 17668-17673 (2010).
-
(2010)
Proc. Natl Acad. Sci. USA
, vol.107
, pp. 17668-17673
-
-
Chamberlain, S.J.1
Chen, P.F.2
Ng, K.Y.3
-
248
-
-
0034931032
-
The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice
-
Bressler J, Tsai TF, Wu MY et al.: The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice. Nat. Genet. 28, 232-240 (2001).
-
(2001)
Nat. Genet.
, vol.28
, pp. 232-240
-
-
Bressler, J.1
Tsai, T.F.2
Wu, M.Y.3
-
249
-
-
0032103697
-
Imprinting in Angelman and Prader-Willi syndromes
-
Jiang Y, Tsai TF, Bressler J, Beaudet AL: Imprinting in Angelman and Prader-Willi syndromes. Curr. Opin. Genet. Dev. 8, 334-342 (1998).
-
(1998)
Curr. Opin. Genet. Dev.
, vol.8
, pp. 334-342
-
-
Jiang, Y.1
Tsai, T.F.2
Bressler, J.3
Beaudet, A.L.4
-
250
-
-
0034642301
-
Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome
-
Muscatelli F, Abrous DN, Massacrier A et al.: Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome. Hum. Mol. Genet. 9, 3101-3110 (2000).
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 3101-3110
-
-
Muscatelli, F.1
Abrous, D.N.2
Massacrier, A.3
-
251
-
-
35548982597
-
Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome
-
Bischof JM, Stewart CL, Wevrick R: Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome. Hum. Mol. Genet. 16, 2713-2719 (2007).
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 2713-2719
-
-
Bischof, J.M.1
Stewart, C.L.2
Wevrick, R.3
-
252
-
-
34748925845
-
The imprinted gene Magel2 regulates normal circadian output
-
Kozlov SV, Bogenpohl JW, Howell MP et al.: The imprinted gene Magel2 regulates normal circadian output. Nat. Genet. 39, 1266-1272 (2007).
-
(2007)
Nat. Genet.
, vol.39
, pp. 1266-1272
-
-
Kozlov, S.V.1
Bogenpohl, J.W.2
Howell, M.P.3
-
253
-
-
59349099147
-
Loss of magel2, a candidate gene for features of Prader-Willi syndrome, impairs reproductive function in mice
-
Mercer RE, Wevrick R: Loss of magel2, a candidate gene for features of Prader-Willi syndrome, impairs reproductive function in mice. PLoS ONE 4, e4291 (2009).
-
(2009)
PLoS ONE
, vol.4
-
-
Mercer, R.E.1
Wevrick, R.2
-
254
-
-
45849144806
-
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
-
Ding F, Li HH, Zhang S et al.: SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice. PLoS ONE 3, e1709 (2008).
-
(2008)
PLoS ONE
, vol.3
-
-
Ding, F.1
Li, H.H.2
Zhang, S.3
-
255
-
-
0025371230
-
Patchy fur (Paf), a semidominant X-linked gene associated with a high level of X-Y nondisjunction in male mice
-
Lane PW, Davisson MT: Patchy fur (Paf), a semidominant X-linked gene associated with a high level of X-Y nondisjunction in male mice. J. Hered. 81, 43-50 (1990).
-
(1990)
J. Hered.
, vol.81
, pp. 43-50
-
-
Lane, P.W.1
Davisson, M.T.2
-
256
-
-
0015838771
-
Reproductive lifespan in irradiated and unirradiated chromosomally XO mice
-
Lyon MF, Hawker SG: Reproductive lifespan in irradiated and unirradiated chromosomally XO mice. Genet. Res. 21, 185-194 (1973).
-
(1973)
Genet. Res.
, vol.21
, pp. 185-194
-
-
Lyon, M.F.1
Hawker, S.G.2
-
257
-
-
0028291185
-
Ear and hearing problems in 44 middle-aged women with Turners syndrome
-
Hultcrantz M, Sylven L, Borg E: Ear and hearing problems in 44 middle-aged women with Turners syndrome. Hear. Res. 76, 127-132 (1994).
-
(1994)
Hear. Res.
, vol.76
, pp. 127-132
-
-
Hultcrantz, M.1
Sylven, L.2
Borg, E.3
-
258
-
-
0019849858
-
Some characteristics of the XO mouse (Mus musculus L.) II. Reproduction: Fertility and gametic segregation
-
Deckers JFM, Kroon PHW, Douglas LT: Some characteristics of the XO mouse (Mus musculus L.) II. Reproduction: fertility and gametic segregation. Genetica 57(1), 3-11 (1981).
-
(1981)
Genetica
, vol.57
, Issue.1
, pp. 3-11
-
-
Jfm, D.1
Phw, K.2
Douglas, L.T.3
-
259
-
-
0027302189
-
A paternally imprinted X chromosome retards the development of the early mouse embryo
-
Thornhill AR, Burgoyne PS: A paternally imprinted X chromosome retards the development of the early mouse embryo. Development 118, 171-174 (1993).
-
(1993)
Development
, vol.118
, pp. 171-174
-
-
Thornhill, A.R.1
Burgoyne, P.S.2
-
260
-
-
0022370034
-
TG: Perinatal oocyte loss in XO mice and its implications for the aetiology of gonadal dysgenesis in XO women
-
Baker
-
Burgoyne PS, Baker TG: Perinatal oocyte loss in XO mice and its implications for the aetiology of gonadal dysgenesis in XO women. J. Reprod. Fertil. 75, 633-645 (1985).
-
(1985)
J. Reprod. Fertil.
, vol.75
, pp. 633-645
-
-
Burgoyne, P.S.1
-
261
-
-
8444253290
-
Mild overexpression of MeCP2 causes a progressive neurological disorder in mice
-
Collins AL, Levenson JM, Vilaythong AP et al.: Mild overexpression of MeCP2 causes a progressive neurological disorder in mice. Hum. Mol. Genet. 13, 2679-2689 (2004)
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 2679-2689
-
-
Collins, A.L.1
Levenson, J.M.2
Vilaythong, A.P.3
|