-
1
-
-
0035777024
-
Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes
-
DOI 10.1146/annurev.genom.2.1.153
-
Nicholls RD, Knepper JL (2001) Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes. Annu Rev Genomics Hum Genet 2:153-175. (Pubitemid 35265004)
-
(2001)
Annual Review of Genomics and Human Genetics
, vol.2
, pp. 153-175
-
-
Nicholls, R.D.1
Knepper, J.L.2
-
2
-
-
77955888515
-
Prader-Willi syndrome and Angelman syndrome
-
Buiting K (2010) Prader-Willi syndrome and Angelman syndrome. Am J Med Genet C Semin Med Genet 154C:365-376.
-
(2010)
Am J Med Genet C Semin Med Genet
, vol.154 C
, pp. 365-376
-
-
Buiting, K.1
-
4
-
-
0031747932
-
A mouse model for Prader-Willi syndrome imprinting-centre mutations
-
DOI 10.1038/ng0598-25
-
Yang T, et al. (1998) A mouse model for Prader-Willi syndrome imprinting-centre mutations. Nat Genet 19:25-31. (Pubitemid 28242018)
-
(1998)
Nature Genetics
, vol.19
, Issue.1
, 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
-
5
-
-
80051692364
-
A new deletion refines the boundaries of the murine Prader-Willi syndrome imprinting center
-
Dubose AJ, Smith EY, Yang TP, Johnstone KA, Resnick JL (2011) A new deletion refines the boundaries of the murine Prader-Willi syndrome imprinting center. Hum Mol Genet 20:3461-3466.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 3461-3466
-
-
Dubose, A.J.1
Smith, E.Y.2
Yang, T.P.3
Johnstone, K.A.4
Resnick, J.L.5
-
6
-
-
0027730805
-
Functional imprinting and epigenetic modification of the human SNRPN gene
-
Glenn CC, Porter KA, Jong MT, Nicholls RD, Driscoll DJ (1993) Functional imprinting and epigenetic modification of the human SNRPN gene. Hum Mol Genet 2: 2001-2005. (Pubitemid 24003390)
-
(1993)
Human Molecular Genetics
, vol.2
, Issue.12
, pp. 2001-2005
-
-
Glenn, C.C.1
Porter, K.A.2
Jong, M.T.C.3
Nicholls, R.D.4
Driscoll, D.J.5
-
7
-
-
0030886796
-
Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern
-
DOI 10.1073/pnas.94.19.10267
-
Shemer R, Birger Y, Riggs AD, Razin A (1997) Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern. Proc Natl Acad Sci USA 94:10267-10272. (Pubitemid 27407030)
-
(1997)
Proceedings of the National Academy of Sciences of the United States of America
, vol.94
, Issue.19
, pp. 10267-10272
-
-
Shemer, R.1
Birger, Y.2
Riggs, A.D.3
Razin, A.4
-
8
-
-
0031051145
-
Imprinted segments in the human genome: Different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method
-
DOI 10.1093/hmg/6.3.387
-
Zeschnigk M, et al. (1997) Imprinted segments in the human genome: Different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method. Hum Mol Genet 6:387-395. (Pubitemid 27116458)
-
(1997)
Human Molecular Genetics
, vol.6
, Issue.3
, pp. 387-395
-
-
Zeschnigk, M.1
Schmitz, B.2
Dittrich, B.3
Buiting, K.4
Horsthemke, B.5
Doerfler, W.6
-
9
-
-
0036768615
-
Epigenetic reprogramming in mouse primordial germ cells
-
DOI 10.1016/S0925-4773(02)00181-8, PII S0925477302001818
-
Hajkova P, et al. (2002) Epigenetic reprogramming in mouse primordial germ cells. Mech Dev 117:15-23. (Pubitemid 36158711)
-
(2002)
Mechanisms of Development
, vol.117
, Issue.1-2
, 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
-
10
-
-
0028133293
-
Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region
-
DOI 10.1038/ng0994-52
-
Sutcliffe JS, et al. (1994) Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region. Nat Genet 8:52-58. (Pubitemid 24274060)
-
(1994)
Nature Genetics
, vol.8
, Issue.1
, pp. 52-58
-
-
Sutcliffe, J.S.1
Nakao, M.2
Christian, S.3
Orstavik, K.H.4
Tommerup, N.5
Ledbetter, D.H.6
Beaudet, A.L.7
-
11
-
-
0034103656
-
De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch
-
DOI 10.1038/75629
-
Bielinska B, et al. (2000) De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch. Nat Genet 25:74-78. (Pubitemid 30257040)
-
(2000)
Nature Genetics
, vol.25
, Issue.1
, pp. 74-78
-
-
Bielinska, B.1
Blaydes, S.M.2
Buiting, K.3
Yang, T.4
Krajewska-Walasek, M.5
Horsthemke, B.6
Brannan, C.I.7
-
12
-
-
0029566108
-
A cre-transgenic mouse strain for the ubiquitous deletion of loxP-flanked gene segments including deletion in germ cells
-
Schwenk F, Baron U, Rajewsky K (1995) A cre-transgenic mouse strain for the ubiquitous deletion of loxP-flanked gene segments including deletion in germ cells. Nucleic Acids Res 23:5080-5081. (Pubitemid 26012492)
-
(1995)
Nucleic Acids Research
, vol.23
, Issue.24
, pp. 5080-5081
-
-
Schwenk, F.1
Baron, U.2
Rajewsky, K.3
-
13
-
-
0032842478
-
Disruption of the glucocorticoid receptor gene in the nervous system results in reduced anxiety
-
DOI 10.1038/12703
-
Tronche F, et al. (1999) Disruption of the glucocorticoid receptor gene in the nervous system results in reduced anxiety. Nat Genet 23:99-103. (Pubitemid 29418797)
-
(1999)
Nature Genetics
, vol.23
, Issue.1
, pp. 99-103
-
-
Tronche, F.1
Kellendonk, C.2
Kretz, O.3
Gass, P.4
Anlag, K.5
Orban, P.C.6
Bock, R.7
Klein, R.8
Schutz, G.9
-
14
-
-
17944373768
-
Beta1-Class integrins regulate the development of laminae and folia in the cerebral and cerebellar cortex
-
DOI 10.1016/S0896-6273(01)00374-9
-
Graus-Porta D, et al. (2001) Beta1-class integrins regulate the development of laminae and folia in the cerebral and cerebellar cortex. Neuron 31:367-379. (Pubitemid 32778557)
-
(2001)
Neuron
, vol.31
, Issue.3
, pp. 367-379
-
-
Graus-Porta, D.1
Blaess, S.2
Senften, M.3
Littlewood-Evans, A.4
Damsky, C.5
Huang, Z.6
Orban, P.7
Klein, R.8
Schittny, J.C.9
Muller, U.10
-
15
-
-
3042821931
-
Regulation of the large (∼1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn
-
DOI 10.1093/nar/gkh670
-
Landers M, et al. (2004) Regulation of the large (∼1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf. Snrpn. Nucleic Acids Res 32:3480-3492. (Pubitemid 39117465)
-
(2004)
Nucleic Acids Research
, vol.32
, Issue.11
, pp. 3480-3492
-
-
Landers, M.1
Bancescu, D.L.2
Le, M.E.3
Rougeulle, C.4
Glatt-Deeley, H.5
Brannan, C.6
Muscatelli, F.7
Lalande, M.8
-
16
-
-
26644449673
-
Dynamic developmental regulation of the large non-coding RNA associated with the mouse 7C imprinted chromosomal region
-
DOI 10.1016/j.ydbio.2005.07.030, PII S0012160605005105
-
Le Meur E, et al. (2005) Dynamic developmental regulation of the large non-coding RNA associated with the mouse 7C imprinted chromosomal region. Dev Biol 286: 587-600. (Pubitemid 41443295)
-
(2005)
Developmental Biology
, vol.286
, Issue.2
, pp. 587-600
-
-
Le, M.E.1
Watrin, F.2
Landers, M.3
Sturny, R.4
Lalande, M.5
Muscatelli, F.6
-
17
-
-
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, et al. (2001) The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A. Hum Mol Genet 10: 2687-2700. (Pubitemid 33133410)
-
(2001)
Human Molecular Genetics
, vol.10
, Issue.23
, pp. 2687-2700
-
-
Runte, M.1
Huttenhofer, A.2
Gross, S.3
Kiefmann, M.4
Horsthemke, B.5
Buiting, K.6
-
18
-
-
0034931032
-
The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice
-
DOI 10.1038/90067
-
Bressler J, et al. (2001) The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice. Nat Genet 28:232-240. (Pubitemid 32626025)
-
(2001)
Nature Genetics
, vol.28
, Issue.3
, pp. 232-240
-
-
Bressler, J.1
Tsai, T.-F.2
Wu, M.-Y.3
Tsai, S.-F.4
Ramirez, M.A.5
Armstrong, D.6
Beaudet, A.L.7
-
19
-
-
0032067559
-
An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript
-
Rougeulle C, Cardoso C, Fontés M, Colleaux L, Lalande M (1998) An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript. Nat Genet 19:15-16.
-
(1998)
Nat Genet
, vol.19
, pp. 15-16
-
-
Rougeulle, C.1
Cardoso, C.2
Fontés, M.3
Colleaux, L.4
Lalande, M.5
-
20
-
-
0035336299
-
The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a
-
DOI 10.1006/geno.2001.6543
-
Chamberlain SJ, Brannan CI (2001) The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a. Genomics 73:316-322. (Pubitemid 32463727)
-
(2001)
Genomics
, vol.73
, Issue.3
, pp. 316-322
-
-
Chamberlain, S.J.1
Brannan, C.I.2
-
21
-
-
31544446862
-
A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects
-
DOI 10.1093/hmg/ddi456
-
Johnstone KA, et al. (2006) A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects. Hum Mol Genet 15:393-404. (Pubitemid 43159892)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.3
, pp. 393-404
-
-
Johnstone, K.A.1
DuBose, A.J.2
Futtner, C.R.3
Elmore, M.D.4
Brannan, C.I.5
Resnick, J.L.6
-
22
-
-
0035102797
-
Establishment and maintenance of DNA methylation patterns in mouse Ndn: Implications for maintenance of imprinting in target genes of the imprinting center
-
DOI 10.1128/MCB.21.7.2384-2392.2001
-
Hanel ML, Wevrick R (2001) Establishment and maintenance of DNA methylation patterns in mouse Ndn: implications for maintenance of imprinting in target genes of the imprinting center. Mol Cell Biol 21:2384-2392. (Pubitemid 32222091)
-
(2001)
Molecular and Cellular Biology
, vol.21
, Issue.7
, pp. 2384-2392
-
-
Hanel, M.L.1
Wevrick, R.2
-
23
-
-
0032896919
-
A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region
-
Jong MT, et al. (1999) A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region. Hum Mol Genet 8:783-793. (Pubitemid 29189045)
-
(1999)
Human Molecular Genetics
, vol.8
, Issue.5
, pp. 783-793
-
-
Jong, M.T.C.1
Gray, T.A.2
Ji, Y.3
Glenn, C.C.4
Saitoh, S.5
Driscoll, D.J.6
Nicholls, R.D.7
-
24
-
-
38349100549
-
Epigenetic events in mammalian germ-cell development: Reprogramming and beyond
-
Sasaki H, Matsui Y (2008) Epigenetic events in mammalian germ-cell development: Reprogramming and beyond. Nat Rev Genet 9:129-140.
-
(2008)
Nat Rev Genet
, vol.9
, pp. 129-140
-
-
Sasaki, H.1
Matsui, Y.2
-
25
-
-
77953429462
-
Brain function and chromatin plasticity
-
Dulac C (2010) Brain function and chromatin plasticity. Nature 465:728-735.
-
(2010)
Nature
, vol.465
, pp. 728-735
-
-
Dulac, C.1
-
26
-
-
77950187447
-
Dnmt1 and Dnmt3a maintain DNA methylation and regulate synaptic function in adult forebrain neurons
-
Feng J, et al. (2010) Dnmt1 and Dnmt3a maintain DNA methylation and regulate synaptic function in adult forebrain neurons. Nat Neurosci 13:423-430.
-
(2010)
Nat Neurosci
, vol.13
, pp. 423-430
-
-
Feng, J.1
-
27
-
-
0034658545
-
H19 and Igf2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream of H19
-
Srivastava M, et al. (2000) H19 and Igf2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream of H19. Genes Dev 14: 1186-1195. (Pubitemid 30327500)
-
(2000)
Genes and Development
, vol.14
, Issue.10
, pp. 1186-1195
-
-
Srivastava, M.1
Hsieh, S.2
Grinberg, A.3
Williams-Simons, L.4
Huang, S.-P.5
Pfeifer, K.6
-
28
-
-
32044441436
-
Developmental profile of H19 differentially methylated domain (DMD) deletion alleles reveals multiple roles of the DMD in regulating allelic expression and DNA methylation at the imprinted H19/Igf2 locus
-
DOI 10.1128/MCB.26.4.1245-1258.2006
-
Thorvaldsen JL, Fedoriw AM, Nguyen S, Bartolomei MS (2006) Developmental profile of H19 differentially methylated domain (DMD) deletion alleles reveals multiple roles of the DMD in regulating allelic expression and DNA methylation at the imprinted H19/Igf2 locus. Mol Cell Biol 26:1245-1258. (Pubitemid 43202553)
-
(2006)
Molecular and Cellular Biology
, vol.26
, Issue.4
, pp. 1245-1258
-
-
Thorvaldsen, J.L.1
Fedoriw, A.M.2
Nguyen, S.3
Bartolomei, M.S.4
-
29
-
-
33845456113
-
Timing and sequence requirements defined for embryonic maintenance of imprinted DNA methylation at Rasgrf1
-
DOI 10.1128/MCB.00058-06
-
Holmes R, Chang Y, Soloway PD (2006) Timing and sequence requirements defined for embryonic maintenance of imprinted DNA methylation at Rasgrf1. Mol Cell Biol 26:9564-9570. (Pubitemid 44904447)
-
(2006)
Molecular and Cellular Biology
, vol.26
, Issue.24
, pp. 9564-9570
-
-
Holmes, R.1
Chang, Y.2
Soloway, P.D.3
-
30
-
-
0034687740
-
Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization
-
DOI 10.1073/pnas.250426397
-
Cavaillé J, et al. (2000) Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization. Proc Natl Acad Sci USA 97: 14311-14316. (Pubitemid 32016572)
-
(2000)
Proceedings of the National Academy of Sciences of the United States of America
, vol.97
, Issue.26
, pp. 14311-14316
-
-
Cavaille, J.1
Buiting, K.2
Kiefmann, M.3
Lalande, M.4
Brannan, C.I.5
Horsthemke, B.6
Bachellerie, J.-P.7
Brosius, J.8
Huttenhofer, A.9
-
31
-
-
0033754151
-
Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brain
-
de los Santos T, Schweizer J, Rees CA, Francke U (2000) Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brain. Am J Hum Genet 67:1067-1082.
-
(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
-
32
-
-
0031040496
-
An imprinted mouse transcript homglogous to the human imprinted in Prader-Willi syndrome (IPW) gene
-
DOI 10.1093/hmg/6.2.325
-
Wevrick R, Francke U (1997) An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) gene. Hum Mol Genet 6:325-332. (Pubitemid 27078090)
-
(1997)
Human Molecular Genetics
, vol.6
, Issue.2
, pp. 325-332
-
-
Wevrick, R.1
Francke, U.2
-
33
-
-
9744241653
-
Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice
-
DOI 10.1093/hmg/ddh314
-
Chamberlain SJ, et al. (2004) Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice. Hum Mol Genet 13:2971-2977. (Pubitemid 39585229)
-
(2004)
Human Molecular Genetics
, vol.13
, Issue.23
, pp. 2971-2977
-
-
Chamberlain, S.J.1
Johnstone, K.A.2
DuBose, A.J.3
Simon, T.A.4
Bartolomei, M.S.5
Resnick, J.L.6
Brannan, C.I.7
-
34
-
-
0032837539
-
Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome
-
DOI 10.1093/hmg/8.8.1357
-
Tsai TF, Jiang YH, Bressler J, Armstrong D, Beaudet AL (1999) Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome. Hum Mol Genet 8:1357-1364. (Pubitemid 29374068)
-
(1999)
Human Molecular Genetics
, vol.8
, Issue.8
, pp. 1357-1364
-
-
Tsai, T.-F.1
Jiang, Y.-H.2
Bressler, J.3
Armstrong, D.4
Beaudet, A.L.5
-
35
-
-
45849144806
-
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
-
Ding F, et al. (2008) SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice. PLoS ONE 3:e1709.
-
(2008)
PLoS ONE
, vol.3
-
-
Ding, F.1
-
36
-
-
37749004050
-
Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation
-
Skryabin BV, et al. (2007) Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation. PLoS Genet 3:e235.
-
(2007)
PLoS Genet
, vol.3
-
-
Skryabin, B.V.1
|