-
1
-
-
0035852733
-
Conserved interaction between distinct Krüppel-associated box domains and the transcriptional intermediary factor 1 β
-
Abrink M, Ortiz JA, Mark C, Sanchez C, Looman C, Hellman L, Chambon P, Losson R. 2001. Conserved interaction between distinct Krüppel-associated box domains and the transcriptional intermediary factor 1 β. Proc Natl Acad Sci 98: 1422-1426.
-
(2001)
Proc Natl Acad Sci
, vol.98
, pp. 1422-1426
-
-
Abrink, M.1
Ortiz, J.A.2
Mark, C.3
Sanchez, C.4
Looman, C.5
Hellman, L.6
Chambon, P.7
Losson, R.8
-
2
-
-
42049087364
-
The genetic aetiology of Silver-Russell syndrome
-
Abu-Amero S, Monk D, Frost J, Preece M, Stanier P, Moore GE. 2008. The genetic aetiology of Silver-Russell syndrome. J Med Genet 45: 193-199.
-
(2008)
J Med Genet
, vol.45
, pp. 193-199
-
-
Abu-Amero, S.1
Monk, D.2
Frost, J.3
Preece, M.4
Stanier, P.5
Moore, G.E.6
-
3
-
-
56349112904
-
Global survey of genomic imprinting by transcriptome sequencing
-
Babak T, Deveale B, Armour C, Raymond C, Cleary MA, van der Kooy D, Johnson JM, Lim LP. 2008. Global survey of genomic imprinting by transcriptome sequencing. Curr Biol 18: 1735-1741.
-
(2008)
Curr Biol
, vol.18
, pp. 1735-1741
-
-
Babak, T.1
Deveale, B.2
Armour, C.3
Raymond, C.4
Cleary, M.A.5
van der Kooy, D.6
Johnson, J.M.7
Lim, L.P.8
-
4
-
-
0026098090
-
The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus
-
Barlow DP, Stoger R, Herrmann BG, Saito K, Schweifer N. 1991. The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus. Nature 349: 84-87.
-
(1991)
Nature
, vol.349
, pp. 84-87
-
-
Barlow, D.P.1
Stoger, R.2
Herrmann, B.G.3
Saito, K.4
Schweifer, N.5
-
5
-
-
0025809321
-
Parental imprinting of the mouse H19 gene
-
Bartolomei MS, Zemel S, Tilghman SM. 1991. Parental imprinting of the mouse H19 gene. Nature 351: 153-155.
-
(1991)
Nature
, vol.351
, pp. 153-155
-
-
Bartolomei, M.S.1
Zemel, S.2
Tilghman, S.M.3
-
6
-
-
0034713375
-
Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene
-
Bell AC, Felsenfeld G. 2000. Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene. Nature 405: 482-485.
-
(2000)
Nature
, vol.405
, pp. 482-485
-
-
Bell, A.C.1
Felsenfeld, G.2
-
7
-
-
0036144048
-
DNA methylation patterns and epigenetic memory
-
Bird A. 2002. DNA methylation patterns and epigenetic memory. Genes Dev 16: 6-21.
-
(2002)
Genes Dev
, vol.16
, pp. 6-21
-
-
Bird, A.1
-
8
-
-
4544223707
-
Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L
-
Bourc'his D, Bestor TH. 2004. Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L. Nature 431: 96-99.
-
(2004)
Nature
, vol.431
, pp. 96-99
-
-
Bourc'his, D.1
Bestor, T.H.2
-
9
-
-
0035930660
-
Dnmt3L and the establishment of maternal genomic imprints
-
Bourc'his D, Xu GL, Lin CS, Bollman B, Bestor TH. 2001. Dnmt3L and the establishment of maternal genomic imprints. Science 294: 2536-2539.
-
(2001)
Science
, vol.294
, pp. 2536-2539
-
-
Bourc'his, D.1
Xu, G.L.2
Lin, C.S.3
Bollman, B.4
Bestor, T.H.5
-
10
-
-
0242553863
-
Non-disjunction tests with Robertsonian translocations
-
Cattanach BM. 1982. Non-disjunction tests with Robertsonian translocations. Mouse News Lett 66: 62-63.
-
(1982)
Mouse News Lett
, vol.66
, pp. 62-63
-
-
Cattanach, B.M.1
-
11
-
-
0023003125
-
Parental origin effects in mice
-
Cattanach BM. 1986. Parental origin effects in mice. J Embrol Exp Morph Suppl 97: 137-150.
-
(1986)
J Embrol Exp Morph Suppl
, vol.97
, pp. 137-150
-
-
Cattanach, B.M.1
-
12
-
-
0022391691
-
Differential activity of maternally and paternally derived chromosome reigons in mice
-
Cattanach BM, Kirk M. 1985. Differential activity of maternally and paternally derived chromosome reigons in mice. Nature 315: 496-498.
-
(1985)
Nature
, vol.315
, pp. 496-498
-
-
Cattanach, B.M.1
Kirk, M.2
-
13
-
-
66049136160
-
Central nervous system imprinting of the G protein G(s)α and its role in metabolic regulation
-
Chen M, Wang J, Dickerson KE, Kelleher J, Xie T, Gupta D, Lai EW, Pacak K, Gavrilova O, Weinstein LS. 2009. Central nervous system imprinting of the G protein G(s)α and its role in metabolic regulation. Cell Metab 9: 548-555.
-
(2009)
Cell Metab
, vol.9
, pp. 548-555
-
-
Chen, M.1
Wang, J.2
Dickerson, K.E.3
Kelleher, J.4
Xie, T.5
Gupta, D.6
Lai, E.W.7
Pacak, K.8
Gavrilova, O.9
Weinstein, L.S.10
-
14
-
-
58149506281
-
Transcription is required for establishment of germline methylation marks at imprinted genes
-
Chotalia M, Smallwood SA, Ruf N, Dawson C, Lucifero D, Frontera M, James K, Dean W, Kelsey G. 2009. Transcription is required for establishment of germline methylation marks at imprinted genes. Genes Dev 23: 105-117.
-
(2009)
Genes Dev
, vol.23
, pp. 105-117
-
-
Chotalia, M.1
Smallwood, S.A.2
Ruf, N.3
Dawson, C.4
Lucifero, D.5
Frontera, M.6
James, K.7
Dean, W.8
Kelsey, G.9
-
15
-
-
56049114840
-
DNA methyltransferase 1o functions during preimplantation development to preclude a profound level of epigenetic variation
-
Cirio MC, Martel J, Mann M, Toppings M, Bartolomei M, Trasler J, Chaillet JR. 2008. DNA methyltransferase 1o functions during preimplantation development to preclude a profound level of epigenetic variation. Dev Biol 324: 139-150.
-
(2008)
Dev Biol
, vol.324
, pp. 139-150
-
-
Cirio, M.C.1
Martel, J.2
Mann, M.3
Toppings, M.4
Bartolomei, M.5
Trasler, J.6
Chaillet, J.R.7
-
18
-
-
0015246689
-
Phosphoglycerate kinase polymorphism in kangaroos provides further evidence for paternal X inactivation
-
Cooper DW, VandeBerg JL, Sharman GB, Poole WE. 1971. Phosphoglycerate kinase polymorphism in kangaroos provides further evidence for paternal X inactivation. Nature New Biology 230: 155-157.
-
(1971)
Nature New Biology
, vol.230
, pp. 155-157
-
-
Cooper, D.W.1
VandeBerg, J.L.2
Sharman, G.B.3
Poole, W.E.4
-
19
-
-
44149101388
-
Genomic imprinting at the mammalian Dlk1-Dio3 domain
-
da Rocha ST, Edwards CA, Ito M, Ogata T, Ferguson-Smith AC. 2008. Genomic imprinting at the mammalian Dlk1-Dio3 domain. Trends Genet 24: 306-316.
-
(2008)
Trends Genet
, vol.24
, pp. 306-316
-
-
da Rocha, S.T.1
Edwards, C.A.2
Ito, M.3
Ogata, T.4
Ferguson-Smith, A.C.5
-
20
-
-
61449215237
-
Gene dosage effects of the imprinted Delta-like homologue 1 (Dlk1/Pref1) in development: Implications for the evolution of imprinting
-
da Rocha S, Charalambous M, Lin SP, Gutteridge I, Ito Y, Gray D, DeanW, Ferguson-Smith AC. 2009. Gene dosage effects of the imprinted Delta-like homologue 1 (Dlk1/Pref1) in development: Implications for the evolution of imprinting. PLoS Genet 5: e1000392.
-
(2009)
PLoS Genet
, vol.5
-
-
da Rocha, S.1
Charalambous, M.2
Lin, S.P.3
Gutteridge, I.4
Ito, Y.5
Gray, D.6
Dean, W.7
Ferguson-Smith, A.C.8
-
21
-
-
0033562954
-
Acquisition of the H19 methylation imprint occurs differentially on the parental alleles during spermatogenesis
-
Davis TL, Trasler JM, Moss SB, Yang GJ, Bartolomei MS. 1999. Acquisition of the H19 methylation imprint occurs differentially on the parental alleles during spermatogenesis. Genomics 58: 18-28.
-
(1999)
Genomics
, vol.58
, pp. 18-28
-
-
Davis, T.L.1
Trasler, J.M.2
Moss, S.B.3
Yang, G.J.4
Bartolomei, M.S.5
-
22
-
-
0025967857
-
Parental imprinting of the mouse insulin-like growth factor II gene
-
DeChiara TM, Robertson EJ, Efstratiadis A. 1991. Parental imprinting of the mouse insulin-like growth factor II gene. Cell 64: 849-859.
-
(1991)
Cell
, vol.64
, pp. 849-859
-
-
DeChiara, T.M.1
Robertson, E.J.2
Efstratiadis, A.3
-
23
-
-
45849118721
-
The evolution of the DLK1-DIO3 imprinted domain in mammals
-
Edwards CA, Mungall AJ, Matthews L, Ryder E, Gray DJ, Pask AJ, Shaw G, Graves JA, Rogers J, Dunham I, et al. 2008. The evolution of the DLK1-DIO3 imprinted domain in mammals. PLoS Biol 6: e135.
-
(2008)
PLoS Biol
, vol.6
-
-
Edwards, C.A.1
Mungall, A.J.2
Matthews, L.3
Ryder, E.4
Gray, D.J.5
Pask, A.J.6
Shaw, G.7
Graves, J.A.8
Rogers, J.9
Dunham, I.10
-
24
-
-
52949088690
-
Three-dimensional conformation at the H19/Igf2 locus supports a model of enhancer tracking
-
Engel N, Raval AK, Thorvaldsen JL, Bartolomei MS. 2008. Three-dimensional conformation at the H19/Igf2 locus supports a model of enhancer tracking. Hum Mol Genet 17: 3021-3029.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 3021-3029
-
-
Engel, N.1
Raval, A.K.2
Thorvaldsen, J.L.3
Bartolomei, M.S.4
-
25
-
-
34047093266
-
Convergent evolution of genomic imprinting in plants and mammals
-
Feil R, Berger F. 2007. Convergent evolution of genomic imprinting in plants and mammals. Trends Genet 23: 192-199.
-
(2007)
Trends Genet
, vol.23
, pp. 192-199
-
-
Feil, R.1
Berger, F.2
-
26
-
-
34548633129
-
Epigenetics: Perceptive enzymes
-
Ferguson-Smith AC, Greally JM. 2007. Epigenetics: Perceptive enzymes. Nature 449: 148-149.
-
(2007)
Nature
, vol.449
, pp. 148-149
-
-
Ferguson-Smith, A.C.1
Greally, J.M.2
-
27
-
-
0026428611
-
Embryological and molecular investigations of parental imprinting on mouse chromosome 7
-
Ferguson-Smith AC, Cattanach BM, Barton SC, BeecheyCV, Surani MA. 1991. Embryological and molecular investigations of parental imprinting on mouse chromosome 7. Nature 351: 667-670.
-
(1991)
Nature
, vol.351
, pp. 667-670
-
-
Ferguson-Smith, A.C.1
Cattanach, B.M.2
Barton, S.C.3
Beechey, C.V.4
Surani, M.A.5
-
28
-
-
0036831864
-
Regional loss of imprinting and growth deficiency in mice with a targeted deleion of KvDMR1
-
Fitzpatrick GV, Soloway PD, Higgins MJ. 2002. Regional loss of imprinting and growth deficiency in mice with a targeted deleion of KvDMR1. Nat Genet 32: 426-431.
-
(2002)
Nat Genet
, vol.32
, pp. 426-431
-
-
Fitzpatrick, G.V.1
Soloway, P.D.2
Higgins, M.J.3
-
29
-
-
0029858585
-
KAP-1, a novel corepressor for the highly conserved KRAB repression domain
-
Friedman JR, Fredericks WJ, Jensen DE, Speicher DW, Huang XP, Neilson EG, Rauscher FJ III. 1996. KAP-1, a novel corepressor for the highly conserved KRAB repression domain. Genes Dev 10: 2067-2078.
-
(1996)
Genes Dev
, vol.10
, pp. 2067-2078
-
-
Friedman, J.R.1
Fredericks, W.J.2
Jensen, D.E.3
Speicher, D.W.4
Huang, X.P.5
Neilson, E.G.6
Rauscher III, F.J.7
-
30
-
-
15744401773
-
Eukaryotic cytosine methyltransferases
-
Goll MG, Bestor TH. 2005. Eukaryotic cytosine methyltransferases. Annu Rev Biochem 74: 481-514.
-
(2005)
Annu Rev Biochem
, vol.74
, pp. 481-514
-
-
Goll, M.G.1
Bestor, T.H.2
-
31
-
-
0028815477
-
Genomic imprinting ofMash-2, a mouse gene required for trophoblast development
-
Guillemot F, Caspary T, Tilghman SM, Copeland NG, Gilbery DJ, Jenkins NA, Anderson DJ, Joyner AL, Rossant J, Nagy A. 1995. Genomic imprinting ofMash-2, a mouse gene required for trophoblast development. Nature Genet 9: 235-241.
-
(1995)
Nature Genet
, vol.9
, pp. 235-241
-
-
Guillemot, F.1
Caspary, T.2
Tilghman, S.M.3
Copeland, N.G.4
Gilbery, D.J.5
Jenkins, N.A.6
Anderson, D.J.7
Joyner, A.L.8
Rossant, J.9
Nagy, A.10
-
32
-
-
42249094716
-
Chromatin dynamics during epigenetic reprogramming in the mouse germ line
-
Hajkova P, Ancelin K, Waldmann T, Lacoste N, Lange UC, Cesari F, Lee C, Almouzni G, Schneider R, Surani MA. 2008. Chromatin dynamics during epigenetic reprogramming in the mouse germ line. Nature 452: 877-881.
-
(2008)
Nature
, vol.452
, pp. 877-881
-
-
Hajkova, P.1
Ancelin, K.2
Waldmann, T.3
Lacoste, N.4
Lange, U.C.5
Cesari, F.6
Lee, C.7
Almouzni, G.8
Schneider, R.9
Surani, M.A.10
-
33
-
-
0036768615
-
Epigenetic reprogramming in mouse primordial germ cells
-
Hajkova P, Erhardt S, Lane N, Haaf T, El-Maarri O, ReikW, Walter J, Surani MA. 2002. Epigenetic reprogramming in mouse primordial germ cells. Mech Dev 117: 15-23.
-
(2002)
Mech Dev
, vol.117
, pp. 15-23
-
-
Hajkova, P.1
Erhardt, S.2
Lane, N.3
Haaf, T.4
El-Maarri, O.5
Reik, W.6
Walter, J.7
Surani, M.A.8
-
34
-
-
0034713275
-
CTCF mediates methylationsensitive enhancer-blocking activity at the H19/Igf2 locus
-
Hark AT, Schoenherr CJ, Katz DJ, Ingram RS, Levorse JM, Tilghman SM. 2000. CTCF mediates methylationsensitive enhancer-blocking activity at the H19/Igf2 locus. Nature 405: 486-489.
-
(2000)
Nature
, vol.405
, pp. 486-489
-
-
Hark, A.T.1
Schoenherr, C.J.2
Katz, D.J.3
Ingram, R.S.4
Levorse, J.M.5
Tilghman, S.M.6
-
35
-
-
0036333103
-
Dnmt3L cooperates with the Dnmt3 family of de novo DNA methyltransferases to establish maternal imprints in mice
-
Hata K, Okano M, Lei H, Li E. 2002. Dnmt3L cooperates with the Dnmt3 family of de novo DNA methyltransferases to establish maternal imprints in mice. Development 129: 1983-1993.
-
(2002)
Development
, vol.129
, pp. 1983-1993
-
-
Hata, K.1
Okano, M.2
Lei, H.3
Li, E.4
-
36
-
-
45349108598
-
Maternal and zygotic Dnmt1 are necessary and sufficient for the maintenance of DNA methylation imprints during preimplantation development
-
Hirasawa R, Chiba H, Kaneda M, Tajima S, Li E, Jaenisch R, Sasaki H. 2008. Maternal and zygotic Dnmt1 are necessary and sufficient for the maintenance of DNA methylation imprints during preimplantation development. Genes Dev 22: 1607-1616.
-
(2008)
Genes Dev
, vol.22
, pp. 1607-1616
-
-
Hirasawa, R.1
Chiba, H.2
Kaneda, M.3
Tajima, S.4
Li, E.5
Jaenisch, R.6
Sasaki, H.7
-
37
-
-
33645455075
-
Imprinting defects on human chromosome 15
-
Horsthemke B, Buiting K. 2006. Imprinting defects on human chromosome 15. Cytogenet Genome Res 113: 292-299.
-
(2006)
Cytogenet Genome Res
, vol.113
, pp. 292-299
-
-
Horsthemke, B.1
Buiting, K.2
-
38
-
-
49449111926
-
Mechanisms of imprinting of the Prader-Willi/Angelman region
-
Horsthemke B, Wagstaff J. 2008. Mechanisms of imprinting of the Prader-Willi/Angelman region. AmJMed Genet A 146A: 2041-2052.
-
(2008)
Am J Med Genet A
, vol.146 A
, pp. 2041-2052
-
-
Horsthemke, B.1
Wagstaff, J.2
-
39
-
-
0035937404
-
Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene
-
Howell CY, Bestor TH, Ding F, Latham KE, Mertineit C, Trasler JM, Chaillet JR. 2001. Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene. Cell 104: 829-838.
-
(2001)
Cell
, vol.104
, pp. 829-838
-
-
Howell, C.Y.1
Bestor, T.H.2
Ding, F.3
Latham, K.E.4
Mertineit, C.5
Trasler, J.M.6
Chaillet, J.R.7
-
40
-
-
34548603504
-
Structure of Dnmt3a bound to Dnmt3L suggests a model for de novo DNA methylation
-
Jia D, Jurkowska RZ, Zhang X, Jeltsch A, Cheng X. 2007a. Structure of Dnmt3a bound to Dnmt3L suggests a model for de novo DNA methylation. Nature 449: 248-251.
-
(2007)
Nature
, vol.449
, pp. 248-251
-
-
Jia, D.1
Jurkowska, R.Z.2
Zhang, X.3
Jeltsch, A.4
Cheng, X.5
-
41
-
-
35148838929
-
The Notch signaling pathway controls the size of the ocular lens by directly suppressing p57Kip2 expression
-
Jia J, Lin M, Zhang L, York JP, Zhang P. 2007b. The Notch signaling pathway controls the size of the ocular lens by directly suppressing p57Kip2 expression. Mol Cell Biol 27: 7236-7247.
-
(2007)
Mol Cell Biol
, vol.27
, pp. 7236-7247
-
-
Jia, J.1
Lin, M.2
Zhang, L.3
York, J.P.4
Zhang, P.5
-
42
-
-
0016137486
-
Hairpin-tail: A case of post-reductional gene action in the mouse egg
-
Johnson DR. 1974. Hairpin-tail: A case of post-reductional gene action in the mouse egg. Genetics 76: 795-805.
-
(1974)
Genetics
, vol.76
, pp. 795-805
-
-
Johnson, D.R.1
-
43
-
-
3042584653
-
Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting
-
Kaneda M, Okano M, Hata K, Sado T, Tsujimoto N, Li E, Sasaki H. 2004. Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting. Nature 429: 900-903.
-
(2004)
Nature
, vol.429
, pp. 900-903
-
-
Kaneda, M.1
Okano, M.2
Hata, K.3
Sado, T.4
Tsujimoto, N.5
Li, E.6
Sasaki, H.7
-
44
-
-
33645455938
-
Complementation hypothesis: The necessity of a monoallelic gene expression mechanism in mammalian development
-
Kaneko-Ishino T, Kohda T, Ono R, Ishino F. 2006. Complementation hypothesis: The necessity of a monoallelic gene expression mechanism in mammalian development. Cytogenet Genome Res 113: 24-30.
-
(2006)
Cytogenet Genome Res
, vol.113
, pp. 24-30
-
-
Kaneko-Ishino, T.1
Kohda, T.2
Ono, R.3
Ishino, F.4
-
45
-
-
0029114716
-
Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization
-
Kaneko-Ishino T, Kuroiwa Y, Miyoshi N, Kohda T, Suzuki R, Yokoyama M, Viville S, Barton SC, Ishino F, Surani MA. 1995. Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization. Nat Genet 11: 52-59.
-
(1995)
Nat Genet
, vol.11
, pp. 52-59
-
-
Kaneko-Ishino, T.1
Kuroiwa, Y.2
Miyoshi, N.3
Kohda, T.4
Suzuki, R.5
Yokoyama, M.6
Viville, S.7
Barton, S.C.8
Ishino, F.9
Surani, M.A.10
-
46
-
-
34948834096
-
High-frequency generation of viable mice from engineered bi-maternal embryos
-
Kawahara M, Wu Q, Takahashi N, Morita S, Yamada K, Ito M, Ferguson-Smith AC, Kono T. 2007. High-frequency generation of viable mice from engineered bi-maternal embryos. Nat Biotechnol 25: 1045-1050.
-
(2007)
Nat Biotechnol
, vol.25
, pp. 1045-1050
-
-
Kawahara, M.1
Wu, Q.2
Takahashi, N.3
Morita, S.4
Yamada, K.5
Ito, M.6
Ferguson-Smith, A.C.7
Kono, T.8
-
47
-
-
54549093572
-
Genomic imprinting: A balance between antagonistic roles of parental chromosomes
-
Kinoshita T, Ikeda Y, Ishikawa R. 2008. Genomic imprinting: A balance between antagonistic roles of parental chromosomes. Semin Cell Dev Biol 19: 574-579.
-
(2008)
Semin Cell Dev Biol
, vol.19
, pp. 574-579
-
-
Kinoshita, T.1
Ikeda, Y.2
Ishikawa, R.3
-
48
-
-
0024619007
-
Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion
-
Knoll JHM, Nicholls RD, Magenis RE, Graham JMJ, Lalande M, Latt SA. 1989. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion. Am J Med Genet 32: 285-290.
-
(1989)
Am J Med Genet
, vol.32
, pp. 285-290
-
-
Knoll, J.H.M.1
Nicholls, R.D.2
Magenis, R.E.3
Graham, J.M.J.4
Lalande, M.5
Latt, S.A.6
-
50
-
-
1942531259
-
Birth of parthenogenetic mice that can develop to adulthood
-
Kono T, Obata Y, Wu Q, Niwa K, Ono Y, Yamamoto Y, Park ES, Seo JS, Ogawa H. 2004. Birth of parthenogenetic mice that can develop to adulthood. Nature 428: 860-864.
-
(2004)
Nature
, vol.428
, pp. 860-864
-
-
Kono, T.1
Obata, Y.2
Wu, Q.3
Niwa, K.4
Ono, Y.5
Yamamoto, Y.6
Park, E.S.7
Seo, J.S.8
Ogawa, H.9
-
51
-
-
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, Pugacheva E, Murrell A, Zhao Z, Lobanenkov V, Reik W, Ohlsson R. 2006. CTCF binding at the H19 imprinting control region mediates maternally inherited higher-order chromatin conformation to restrict enhancer access to Igf2. Proc Natl Acad Sci 103: 10684-10689.
-
(2006)
Proc Natl Acad Sci
, vol.103
, pp. 10684-10689
-
-
Kurukuti, S.1
Tiwari, V.K.2
Tavoosidana, G.3
Pugacheva, E.4
Murrell, A.5
Zhao, Z.6
Lobanenkov, V.7
Reik, W.8
Ohlsson, R.9
-
52
-
-
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. 1998. Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest. Nat Genet 20: 163-169.
-
(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
-
53
-
-
0027378582
-
Role for DNA methylation in genomic imprinting
-
Li E, Beard C, Jaenisch R. 1993. Role for DNA methylation in genomic imprinting. Nature 366: 362-365.
-
(1993)
Nature
, vol.366
, pp. 362-365
-
-
Li, E.1
Beard, C.2
Jaenisch, R.3
-
54
-
-
33644534493
-
L3mbtl, the mouse orthologue of the imprinted L3MBTL, displays a complex pattern of alternative splicing and escapes genomic imprinting
-
Li J, Bench AJ, Piltz S, Vassiliou G, Baxter EJ, Ferguson-Smith AC, Green AR. 2005. L3mbtl, the mouse orthologue of the imprinted L3MBTL, displays a complex pattern of alternative splicing and escapes genomic imprinting. Genomics 86: 489-494.
-
(2005)
Genomics
, vol.86
, pp. 489-494
-
-
Li, J.1
Bench, A.J.2
Piltz, S.3
Vassiliou, G.4
Baxter, E.J.5
Ferguson-Smith, A.C.6
Green, A.R.7
-
55
-
-
2442544539
-
Imprinting of the human L3MBTL gene, a polycomb family member located in a region of chromosome 20 deleted in humanmyeloid malignancies
-
Li J, Bench AJ, Vassiliou GS, Fourouclas N, Ferguson-Smith AC, Green AR. 2004a. Imprinting of the human L3MBTL gene, a polycomb family member located in a region of chromosome 20 deleted in humanmyeloid malignancies. Proc Natl Acad Sci 101: 7341-7346.
-
(2004)
Proc Natl Acad Sci
, vol.101
, pp. 7341-7346
-
-
Li, J.1
Bench, A.J.2
Vassiliou, G.S.3
Fourouclas, N.4
Ferguson-Smith, A.C.5
Green, A.R.6
-
56
-
-
7944221225
-
Timing of establishment of paternal methylation imprints in the mouse
-
Li JY, Lees-Murdock DJ, Xu GL, Walsh CP. 2004b. Timing of establishment of paternal methylation imprints in the mouse. Genomics 84: 952-960.
-
(2004)
Genomics
, vol.84
, pp. 952-960
-
-
Li, J.Y.1
Lees-Murdock, D.J.2
Xu, G.L.3
Walsh, C.P.4
-
57
-
-
53249098795
-
A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints
-
Li X, Ito M, Zhou F, Youngson N, Zuo X, Leder P, Ferguson-Smith AC. 2008. A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints. Dev Cell 15: 547-557.
-
(2008)
Dev Cell
, vol.15
, pp. 547-557
-
-
Li, X.1
Ito, M.2
Zhou, F.3
Youngson, N.4
Zuo, X.5
Leder, P.6
Ferguson-Smith, A.C.7
-
58
-
-
0033537716
-
Regulation of maternal behavior and offspring growth by paternally expressed Peg3
-
Li L, Keverne EB, Aparicio SA, Ishino F, Barton SC, Surani MA. 1999. Regulation of maternal behavior and offspring growth by paternally expressed Peg3. Science 284: 330-333.
-
(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
-
59
-
-
0042856381
-
Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12
-
Lin SP, Youngson N, Takada S, Seitz H, Reik W, Paulsen M, Cavaille J, Ferguson-Smith AC. 2003. Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12. Nat Genet 35: 97-102.
-
(2003)
Nat Genet
, vol.35
, pp. 97-102
-
-
Lin, S.P.1
Youngson, N.2
Takada, S.3
Seitz, H.4
Reik, W.5
Paulsen, M.6
Cavaille, J.7
Ferguson-Smith, A.C.8
-
60
-
-
0036205914
-
Methylation dynamics of imprinted genes in mouse germ cells
-
Lucifero D, Mertineit C, Clarke HJ, Bestor TH, Trasler JM. 2002. Methylation dynamics of imprinted genes in mouse germ cells. Genomics 79: 530-538.
-
(2002)
Genomics
, vol.79
, pp. 530-538
-
-
Lucifero, D.1
Mertineit, C.2
Clarke, H.J.3
Bestor, T.H.4
Trasler, J.M.5
-
61
-
-
0034118382
-
The imprinted antisense RNA at the Igf2r locus overlaps but does not imprint Mas1
-
Lyle R, Watanabe D, te Vruchte D, LerchnerW, Smrzka OW, Wutz A, Schageman J, Hahner L, Davies C, Barlow DP. 2000. The imprinted antisense RNA at the Igf2r locus overlaps but does not imprint Mas1. Nat Genet 25: 19-21.
-
(2000)
Nat Genet
, vol.25
, pp. 19-21
-
-
Lyle, R.1
Watanabe, D.2
te Vruchte, D.3
Lerchner, W.4
Smrzka, O.W.5
Wutz, A.6
Schageman, J.7
Hahner, L.8
Davies, C.9
Barlow, D.P.10
-
62
-
-
48349092985
-
Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57
-
Mackay DJ, Callaway JL, Marks SM, White HE, Acerini CL, Boonen SE, Dayanikli P, FirthHV, Goodship JA, Haemers AP, et al. 2008. Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57. Nat Genet 40: 949-951.
-
(2008)
Nat Genet
, vol.40
, pp. 949-951
-
-
Mackay, D.J.1
Callaway, J.L.2
Marks, S.M.3
White, H.E.4
Acerini, C.L.5
Boonen, S.E.6
Dayanikli, P.7
Firth, H.V.8
Goodship, J.A.9
Haemers, A.P.10
-
63
-
-
0020852953
-
Nuclear transplantation in mouse embryos
-
McGrath J, Solter D. 1983. Nuclear transplantation in mouse embryos. J Exp Zool 228: 355-362.
-
(1983)
J Exp Zool
, vol.228
, pp. 355-362
-
-
McGrath, J.1
Solter, D.2
-
64
-
-
0021139084
-
Completion of mouse embryogenesis requires both the maternal and paternal genomes
-
McGrath J, Solter D. 1984. Completion of mouse embryogenesis requires both the maternal and paternal genomes. Cell 37: 179-183.
-
(1984)
Cell
, vol.37
, pp. 179-183
-
-
McGrath, J.1
Solter, D.2
-
65
-
-
63449130373
-
Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann syndrome)
-
Meyer E, Lim D, Pasha S, Tee LJ, Rahman F, Yates JR, Woods CG, Reik W, Maher ER. 2009. Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann syndrome). PLoS Genet 5: e1000423.
-
(2009)
PLoS Genet
, vol.5
-
-
Meyer, E.1
Lim, D.2
Pasha, S.3
Tee, L.J.4
Rahman, F.5
Yates, J.R.6
Woods, C.G.7
Reik, W.8
Maher, E.R.9
-
66
-
-
33646265537
-
Limited evolutionary conservation of imprinting in the human placenta
-
Monk D, Arnaud P, Apostolidou S, Hills FA, Kelsey G, Stanier P, Feil R, Moore GE. 2006. Limited evolutionary conservation of imprinting in the human placenta. Proc Natl Acad Sci 103: 6623-6628.
-
(2006)
Proc Natl Acad Sci
, vol.103
, pp. 6623-6628
-
-
Monk, D.1
Arnaud, P.2
Apostolidou, S.3
Hills, F.A.4
Kelsey, G.5
Stanier, P.6
Feil, R.7
Moore, G.E.8
-
67
-
-
0036318227
-
Mice lacking paternally expressed Pref-1/Dlk1 display growth retardation and accelerated adiposity
-
Moon YS, Smas CM, Lee K, Villena JA, Kim KH, Yun EJ, Sul HS. 2002. Mice lacking paternally expressed Pref-1/Dlk1 display growth retardation and accelerated adiposity. Mol Cell Biol 22: 5585-5592.
-
(2002)
Mol Cell Biol
, vol.22
, pp. 5585-5592
-
-
Moon, Y.S.1
Smas, C.M.2
Lee, K.3
Villena, J.A.4
Kim, K.H.5
Yun, E.J.6
Sul, H.S.7
-
68
-
-
17444409344
-
Epigenetic reprogramming in mammals
-
Morgan HD, Santos F, Green K, DeanW, ReikW. 2005. Epigenetic reprogramming in mammals. HumMol Genet 14 Spec No 1: R47-R58.
-
(2005)
HumMol Genet 14 Spec No
, vol.1
-
-
Morgan, H.D.1
Santos, F.2
Green, K.3
Dean, W.4
Reik, W.5
-
69
-
-
33644615366
-
Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans
-
Murdoch S, DjuricU, Mazhar B, Seoud M, Khan R, Kuick R, Bagga R, Kircheisen R, Ao A, Ratti B, et al. 2006. Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans. Nat Genet 38: 300-302.
-
(2006)
Nat Genet
, vol.38
, pp. 300-302
-
-
Murdoch, S.1
Djuric, U.2
Mazhar, B.3
Seoud, M.4
Khan, R.5
Kuick, R.6
Bagga, R.7
Kircheisen, R.8
Ao, A.9
Ratti, B.10
-
70
-
-
3543018516
-
Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loops
-
Murrell A, Heeson S, ReikW. 2004. Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loops. Nat Genet 36: 889-893.
-
(2004)
Nat Genet
, vol.36
, pp. 889-893
-
-
Murrell, A.1
Heeson, S.2
Reik, W.3
-
71
-
-
56549111129
-
The Air noncoding RNA epigenetically silences transcription by targeting G9a to chromatin
-
Nagano T, Mitchell JA, Sanz LA, Pauler FM, Ferguson-Smith AC, Feil R, Fraser P. 2008. The Air noncoding RNA epigenetically silences transcription by targeting G9a to chromatin. Science 322: 1717-1720.
-
(2008)
Science
, vol.322
, pp. 1717-1720
-
-
Nagano, T.1
Mitchell, J.A.2
Sanz, L.A.3
Pauler, F.M.4
Ferguson-Smith, A.C.5
Feil, R.6
Fraser, P.7
-
72
-
-
33845885282
-
PGC7/Stella protects against DNA demethylation in early embryogenesis
-
Nakamura T, Arai Y, Umehara H, Masuhara M, Kimura T, Taniguchi H, Sekimoto T, Ikawa M, Yoneda Y, Okabe M, et al. 2007. PGC7/Stella protects against DNA demethylation in early embryogenesis. Nat Cell Biol 9: 64-71.
-
(2007)
Nat Cell Biol
, vol.9
, pp. 64-71
-
-
Nakamura, T.1
Arai, Y.2
Umehara, H.3
Masuhara, M.4
Kimura, T.5
Taniguchi, H.6
Sekimoto, T.7
Ikawa, M.8
Yoneda, Y.9
Okabe, M.10
-
73
-
-
0035777024
-
Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes
-
Nicholls RD, Knepper JL. 2001. Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes. Annu Rev Genomics Hum Genet 2: 153-175.
-
(2001)
Annu Rev Genomics Hum Genet
, vol.2
, pp. 153-175
-
-
Nicholls, R.D.1
Knepper, J.L.2
-
74
-
-
54949115836
-
Molecular mechanisms regulating phenotypic outcome in paternal and maternal uniparental disomy for chromosome 14
-
Ogata T, Kagami M, Ferguson-Smith AC. 2008. Molecular mechanisms regulating phenotypic outcome in paternal and maternal uniparental disomy for chromosome 14. Epigenetics 3: 181-187.
-
(2008)
Epigenetics
, vol.3
, pp. 181-187
-
-
Ogata, T.1
Kagami, M.2
Ferguson-Smith, A.C.3
-
75
-
-
29444434486
-
Deletion of Peg10, an imprinted gene acquired from a retrotransposon, causes early embryonic lethality
-
Ono R, Nakamura K, Inoue K, Naruse M, Usami T, Wakisaka-Saito N, Hino T, Suzuki-Migishima R, Ogonuki N, Miki H, et al. 2006. Deletion of Peg10, an imprinted gene acquired from a retrotransposon, causes early embryonic lethality. Nat Genet 38: 101-106.
-
(2006)
Nat Genet
, vol.38
, pp. 101-106
-
-
Ono, R.1
Nakamura, K.2
Inoue, K.3
Naruse, M.4
Usami, T.5
Wakisaka-Saito, N.6
Hino, T.7
Suzuki-Migishima, R.8
Ogonuki, N.9
Miki, H.10
-
76
-
-
34547725157
-
DNMT3L connects unmethylated lysine 4 of histone H3 to de novo methylation of DNA
-
Ooi SK, Qiu C, Bernstein E, Li K, Jia D, Yang Z, Erdjument-Bromage H, Tempst P, Lin SP, Allis CD, et al. 2007. DNMT3L connects unmethylated lysine 4 of histone H3 to de novo methylation of DNA. Nature 448: 714-717.
-
(2007)
Nature
, vol.448
, pp. 714-717
-
-
Ooi, S.K.1
Qiu, C.2
Bernstein, E.3
Li, K.4
Jia, D.5
Yang, Z.6
Erdjument-Bromage, H.7
Tempst, P.8
Lin, S.P.9
Allis, C.D.10
-
77
-
-
46749142929
-
Dlk1 influences differentiation and function of B lymphocytes
-
Raghunandan R, Ruiz-Hidalgo M, Jia Y, Ettinger R, Rudikoff E, Riggins P, Farnsworth R, Tesfaye A, Laborda J, Bauer SR. 2008. Dlk1 influences differentiation and function of B lymphocytes. Stem Cells Dev 17: 495-507.
-
(2008)
Stem Cells Dev
, vol.17
, pp. 495-507
-
-
Raghunandan, R.1
Ruiz-Hidalgo, M.2
Jia, Y.3
Ettinger, R.4
Rudikoff, E.5
Riggins, P.6
Farnsworth, R.7
Tesfaye, A.8
Laborda, J.9
Bauer, S.R.10
-
79
-
-
0017877927
-
Complementation studies with mouse translocations
-
Searle AG, Beechey CV. 1978. Complementation studies with mouse translocations. Cytogenet Cell Genet 20: 282-303.
-
(1978)
Cytogenet Cell Genet
, vol.20
, pp. 282-303
-
-
Searle, A.G.1
Beechey, C.V.2
-
80
-
-
0025242074
-
Genome imprinting phenomena on mouse chromosome 7
-
Searle AG, Beechey CV. 1990. Genome imprinting phenomena on mouse chromosome 7. Genet Res 56: 237-244.
-
(1990)
Genet Res
, vol.56
, pp. 237-244
-
-
Searle, A.G.1
Beechey, C.V.2
-
81
-
-
38649091005
-
Role of retrotransposon-derived imprinted gene, Rtl1, in the feto-maternal interface of mouse placenta
-
Sekita Y, Wagatsuma H, Nakamura K, Ono R, Kagami M, Wakisaka N, Hino T, Suzuki-Migishima R, Kohda T, Ogura A, et al. 2008. Role of retrotransposon-derived imprinted gene, Rtl1, in the feto-maternal interface of mouse placenta. Nat Genet 40: 243-248.
-
(2008)
Nat Genet
, vol.40
, pp. 243-248
-
-
Sekita, Y.1
Wagatsuma, H.2
Nakamura, K.3
Ono, R.4
Kagami, M.5
Wakisaka, N.6
Hino, T.7
Suzuki-Migishima, R.8
Kohda, T.9
Ogura, A.10
-
82
-
-
2542555066
-
Placental-specific insulin-like growth factor 2 (Igf2) regulates the diffusional exchange characteristics of the mouse placenta
-
Sibley CP, Coan PM, Ferguson-Smith AC, Dean W, Hughes J, Smith P, Reik W, Burton GJ, Fowden AL, Constancia M. 2004. Placental-specific insulin-like growth factor 2 (Igf2) regulates the diffusional exchange characteristics of the mouse placenta. Proc Natl Acad Sci 101: 8204-8208.
-
(2004)
Proc Natl Acad Sci
, vol.101
, pp. 8204-8208
-
-
Sibley, C.P.1
Coan, P.M.2
Ferguson-Smith, A.C.3
Dean, W.4
Hughes, J.5
Smith, P.6
Reik, W.7
Burton, G.J.8
Fowden, A.L.9
Constancia, M.10
-
83
-
-
0037075032
-
The non-coding Air RNA is required for silencing autosomal imprinted genes
-
Sleutels F, Zwart R, Barlow DP. 2002. The non-coding Air RNA is required for silencing autosomal imprinted genes. Nature 415: 810-813.
-
(2002)
Nature
, vol.415
, pp. 810-813
-
-
Sleutels, F.1
Zwart, R.2
Barlow, D.P.3
-
84
-
-
48249141249
-
Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians
-
Smits G, Mungall AJ, Griffiths-Jones S, Smith P, Beury D, Matthews L, Rogers J, Pask AJ, Shaw G, Vandeberg JL, et al. 2008. Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians. Nat Genet 40: 971-976.
-
(2008)
Nat Genet
, vol.40
, pp. 971-976
-
-
Smits, G.1
Mungall, A.J.2
Griffiths-Jones, S.3
Smith, P.4
Beury, D.5
Matthews, L.6
Rogers, J.7
Pask, A.J.8
Shaw, G.9
Vandeberg, J.L.10
-
85
-
-
0027400888
-
Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal
-
Stöger R, Kubicka P, Liu C-G, Kafri T, Razin A, Cedar H, Barlow DP. 1993. Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal. Cell 73: 61-71.
-
(1993)
Cell
, vol.73
, pp. 61-71
-
-
Stöger, R.1
Kubicka, P.2
Liu, C-G.3
Kafri, T.4
Razin, A.5
Cedar, H.6
Barlow, D.P.7
-
86
-
-
0021067190
-
Development of gynogenetic eggs in the mouse: Implications for parthenogenetic embryos
-
Surani MAH, Barton SC. 1983. Development of gynogenetic eggs in the mouse: implications for parthenogenetic embryos. Science 222: 1034-1036.
-
(1983)
Science
, vol.222
, pp. 1034-1036
-
-
Surani, M.A.H.1
Barton, S.C.2
-
87
-
-
0021237658
-
Development of reconstituted mouse eggs suggest imprinting of the genome during gametogenesis
-
Surani MAH, Barton SC, Norris ML. 1984. Development of reconstituted mouse eggs suggest imprinting of the genome during gametogenesis. Nature 308: 548-550.
-
(1984)
Nature
, vol.308
, pp. 548-550
-
-
Surani, M.A.H.1
Barton, S.C.2
Norris, M.L.3
-
88
-
-
34250660148
-
Retrotransposon silencing byDNA methylation can drive mammalian genomic imprinting
-
Suzuki S, Ono R, Narita T, Pask AJ, Shaw G, Wang C, Kohda T, Alsop AE, Marshall Graves JA, Kohara Y, et al. 2007. Retrotransposon silencing byDNA methylation can drive mammalian genomic imprinting. PLoS Genet 3: e55.
-
(2007)
PLoS Genet
, vol.3
-
-
Suzuki, S.1
Ono, R.2
Narita, T.3
Pask, A.J.4
Shaw, G.5
Wang, C.6
Kohda, T.7
Alsop, A.E.8
Marshall Graves, J.A.9
Kohara, Y.10
-
89
-
-
38449101833
-
Imprinting in human disease with special reference to transient neonatal diabetes and Beckwith-Wiedemann syndrome
-
Temple IK. 2007. Imprinting in human disease with special reference to transient neonatal diabetes and Beckwith-Wiedemann syndrome. Endocr Dev 12: 113-123.
-
(2007)
Endocr Dev
, vol.12
, pp. 113-123
-
-
Temple, I.K.1
-
90
-
-
0036918736
-
Transient neonatal diabetes, a disorder of imprinting
-
Temple IK, Shield JP. 2002. Transient neonatal diabetes, a disorder of imprinting. J Med Genet 39: 872-875.
-
(2002)
J Med Genet
, vol.39
, pp. 872-875
-
-
Temple, I.K.1
Shield, J.P.2
-
91
-
-
0032419812
-
Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2
-
Thorvaldsen JL, Duran KL, Bartolomei MS. 1998. Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. Genes Dev 12: 3693-3702.
-
(1998)
Genes Dev
, vol.12
, pp. 3693-3702
-
-
Thorvaldsen, J.L.1
Duran, K.L.2
Bartolomei, M.S.3
-
92
-
-
0030802395
-
0 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development
-
0 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development. Mol Cell Biol 17: 4322-4329.
-
(1997)
Mol Cell Biol
, vol.17
, pp. 4322-4329
-
-
Tremblay, K.D.1
Duran, K.L.2
Bartolomei, M.S.3
-
93
-
-
33750470266
-
Zac1 regulates an imprinted gene network critically involved in the control of embryonic growth
-
Varrault A, Gueydan C, Delalbre A, Bellmann A, Houssami S, Aknin C, Severac D, Chotard L, Kahli M, Le Digarcher A, et al. 2006. Zac1 regulates an imprinted gene network critically involved in the control of embryonic growth. Dev Cell 11: 711-722.
-
(2006)
Dev Cell
, vol.11
, pp. 711-722
-
-
Varrault, A.1
Gueydan, C.2
Delalbre, A.3
Bellmann, A.4
Houssami, S.5
Aknin, C.6
Severac, D.7
Chotard, L.8
Kahli, M.9
Le Digarcher, A.10
-
94
-
-
57349168544
-
Transcriptome-wide identification of novel imprinted genes in neonatal mouse brain
-
Wang X, Sun Q, McGrath SD, Mardis ER, Soloway PD, Clark AG. 2008. Transcriptome-wide identification of novel imprinted genes in neonatal mouse brain. PLoS ONE 3: e3839.
-
(2008)
PLoS ONE
, vol.3
-
-
Wang, X.1
Sun, Q.2
McGrath, S.D.3
Mardis, E.R.4
Soloway, P.D.5
Clark, A.G.6
-
96
-
-
35549001312
-
Genomic imprinting effects on brain development and function
-
Wilkinson LS, Davies W, Isles AR. 2007. Genomic imprinting effects on brain development and function. Nat Rev Neurosci 8: 832-843.
-
(2007)
Nat Rev Neurosci
, vol.8
, pp. 832-843
-
-
Wilkinson, L.S.1
Davies, W.2
Isles, A.R.3
-
97
-
-
33644617486
-
Identification of an imprinting control region affecting the expression of all transcripts in the Gnas cluster
-
Williamson CM, Turner MD, Ball ST, Nottingham WT, Glenister P, Fray M, Tymowska-Lalanne Z, Plagge A, Powles-Glover N, Kelsey G, et al. 2006. Identification of an imprinting control region affecting the expression of all transcripts in the Gnas cluster. Nat Genet 38: 350-355.
-
(2006)
Nat Genet
, vol.38
, pp. 350-355
-
-
Williamson, C.M.1
Turner, M.D.2
Ball, S.T.3
Nottingham, W.T.4
Glenister, P.5
Fray, M.6
Tymowska-Lalanne, Z.7
Plagge, A.8
Powles-Glover, N.9
Kelsey, G.10
-
98
-
-
33751086773
-
Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain
-
Wu MY, Tsai TF, Beaudet AL. 2006. Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain. Genes Dev 20: 2859-2870.
-
(2006)
Genes Dev
, vol.20
, pp. 2859-2870
-
-
Wu, M.Y.1
Tsai, T.F.2
Beaudet, A.L.3
-
99
-
-
0030694713
-
Imprinted expression of the Igf2r gene depends on an intronic CpG island
-
Wutz A, Smrzka OW, Schweifer N, Schellander K, Wagner EF, Barlow DP. 1997. Imprinted expression of the Igf2r gene depends on an intronic CpG island. Nature 389: 745-749.
-
(1997)
Nature
, vol.389
, pp. 745-749
-
-
Wutz, A.1
Smrzka, O.W.2
Schweifer, N.3
Schellander, K.4
Wagner, E.F.5
Barlow, D.P.6
-
101
-
-
0031747932
-
A mouse model for Prader-Willi syndrome imprintingcentre mutations
-
Yang T, Adamson TE, Resnick JL, Leff S, Wevrick R, Francke U, Jenkins NA, Copeland NG, Brannan CI. 1998. A mouse model for Prader-Willi syndrome imprintingcentre mutations. Nature Genet 19: 25-31.
-
(1998)
Nature Genet
, vol.19
, pp. 25-31
-
-
Yang, T.1
Adamson, T.E.2
Resnick, J.L.3
Leff, S.4
Wevrick, R.5
Francke, U.6
Jenkins, N.A.7
Copeland, N.G.8
Brannan, C.I.9
|