-
1
-
-
80052413403
-
Necdin protects embryonic motoneurons from programmed cell death
-
21912643 10.1371/journal.pone.0023764 1:CAS:528:DC%2BC3MXht1WrtbfI
-
Aebischer J, Sturny R, Andrieu D, Rieusset A, Schaller F, Geib S, Raoul C, Muscatelli F (2011) Necdin protects embryonic motoneurons from programmed cell death. PLoS One 6:e23764
-
(2011)
PLoS One
, vol.6
, pp. 23764
-
-
Aebischer, J.1
Sturny, R.2
Andrieu, D.3
Rieusset, A.4
Schaller, F.5
Geib, S.6
Raoul, C.7
Muscatelli, F.8
-
2
-
-
33751581604
-
Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death
-
17116257 10.1186/1471-213X-6-56
-
Andrieu D, Meziane H, Marly F, Angelats C, Fernandez PA, Muscatelli F (2006) 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)
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
-
3
-
-
0034103656
-
De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch
-
10802660 10.1038/75629 1:CAS:528:DC%2BD3cXjtFSltrY%3D
-
Bielinska B, Blaydes SM, Buiting K, Yang T, Krajewska-Walasek M, Horsthemke B, Brannan CI (2000) De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch. Nature Genetics 25:74-78
-
(2000)
Nature Genetics
, vol.25
, 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
-
4
-
-
35548982597
-
Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome
-
17728320 10.1093/hmg/ddm225 1:CAS:528:DC%2BD2sXht1aksbjK
-
Bischof JM, Stewart CL, Wevrick R (2007) Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome. Hum Mol Genet 16:2713-2719
-
(2007)
Hum Mol Genet
, vol.16
, pp. 2713-2719
-
-
Bischof, J.M.1
Stewart, C.L.2
Wevrick, R.3
-
5
-
-
33847417017
-
Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome
-
17036336
-
Bittel DC, Kibiryeva N, McNulty SG, Driscoll DJ, Butler MG, White RA (2007) Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome. Am J Med Genet A 143:422-429
-
(2007)
Am J Med Genet A
, vol.143
, pp. 422-429
-
-
Bittel, D.C.1
Kibiryeva, N.2
McNulty, S.G.3
Driscoll, D.J.4
Butler, M.G.5
White, R.A.6
-
6
-
-
0032811481
-
Analysis of murine Snrpn and human SNRPN gene imprinting in transgenic mice
-
10341083 10.1007/s003359901042 1:CAS:528:DyaK1MXkt1Olt7k%3D
-
Blaydes SM, Elmore M, Yang T, Brannan CI (1999) Analysis of murine Snrpn and human SNRPN gene imprinting in transgenic mice. Mammalian Genome 10:549-555
-
(1999)
Mammalian Genome
, vol.10
, pp. 549-555
-
-
Blaydes, S.M.1
Elmore, M.2
Yang, T.3
Brannan, C.I.4
-
7
-
-
0032714383
-
The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region
-
10556298 10.1093/hmg/8.13.2497 1:CAS:528:DyaK1MXnvFKrurs%3D
-
Boccaccio I, Glatt-Deeley H, Watrin F, Roeckel N, Lalande M, Muscatelli F (1999) The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region. Hum Mol Genet 8:2497-2505
-
(1999)
Hum Mol Genet
, vol.8
, pp. 2497-2505
-
-
Boccaccio, I.1
Glatt-Deeley, H.2
Watrin, F.3
Roeckel, N.4
Lalande, M.5
Muscatelli, F.6
-
8
-
-
84864917692
-
The SNORD115 (H/MBII-52) and SNORD116 (H/MBII-85) gene clusters at the imprinted Prader-Willi locus generate canonical box C/D snoRNAs
-
22495932 10.1093/nar/gks321 1:CAS:528:DC%2BC38XhtF2rsLjJ
-
Bortolin-Cavaille ML, Cavaille J (2012) The SNORD115 (H/MBII-52) and SNORD116 (H/MBII-85) gene clusters at the imprinted Prader-Willi locus generate canonical box C/D snoRNAs. Nucleic Acids Res 40:6800-6807
-
(2012)
Nucleic Acids Res
, vol.40
, pp. 6800-6807
-
-
Bortolin-Cavaille, M.L.1
Cavaille, J.2
-
9
-
-
0034931032
-
The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice
-
11431693 10.1038/90067 1:CAS:528:DC%2BD3MXltFSnurk%3D
-
Bressler J, Tsai TF, Wu MY, Tsai SF, Ramirez MA, Armstrong D, Beaudet AL (2001) The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice. Nat Genet 28:232-240
-
(2001)
Nat Genet
, vol.28
, pp. 232-240
-
-
Bressler, J.1
Tsai, T.F.2
Wu, M.Y.3
Tsai, S.F.4
Ramirez, M.A.5
Armstrong, D.6
Beaudet, A.L.7
-
10
-
-
0026450607
-
The mouse pink-eyed dilution locus: A model for aspects of Prader-Willi syndrome, Angelman syndrome, and a form of hypomelanosis of Ito
-
1611213 10.1007/BF00355717 1:CAS:528:DyaK38Xlt1Glurk%3D
-
Brilliant MH (1992) The mouse pink-eyed dilution locus: a model for aspects of Prader-Willi syndrome, Angelman syndrome, and a form of hypomelanosis of Ito. Mamm Genome 3:187-191
-
(1992)
Mamm Genome
, vol.3
, pp. 187-191
-
-
Brilliant, M.H.1
-
11
-
-
77955888515
-
Prader-Willi syndrome and Angelman syndrome
-
20803659 10.1002/ajmg.c.30273 1:CAS:528:DC%2BC3cXhtFKqsr7L
-
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
, pp. 365-376
-
-
Buiting, K.1
-
12
-
-
77957363111
-
Loss of Necdin impairs myosin activation and delays cell polarization
-
Bush JR, Wevrick R (2010) Loss of Necdin impairs myosin activation and delays cell polarization. Genesis 48:540-553
-
(2010)
Genesis
, vol.48
, pp. 540-553
-
-
Bush, J.R.1
Wevrick, R.2
-
13
-
-
84857797436
-
Loss of the Prader-Willi obesity syndrome protein necdin promotes adipogenesis
-
22305984 10.1016/j.gene.2012.01.027 1:CAS:528:DC%2BC38XitFyisr4%3D
-
Bush JR, Wevrick R (2012) Loss of the Prader-Willi obesity syndrome protein necdin promotes adipogenesis. Gene 497:45-51
-
(2012)
Gene
, vol.497
, pp. 45-51
-
-
Bush, J.R.1
Wevrick, R.2
-
15
-
-
0027017879
-
A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression
-
1303278 10.1038/ng1292-270 1:CAS:528:DyaK3sXpvFOhsw%3D%3D
-
Cattanach BM, Barr JA, Evans EP, Burtenshaw M, Beechey CV, Leff SE, Brannan CI, Copeland NG, Jenkins NA, Jones J (1992) A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression. Nat Genet 2:270-274
-
(1992)
Nat Genet
, vol.2
, pp. 270-274
-
-
Cattanach, B.M.1
Barr, J.A.2
Evans, E.P.3
Burtenshaw, M.4
Beechey, C.V.5
Leff, S.E.6
Brannan, C.I.7
Copeland, N.G.8
Jenkins, N.A.9
Jones, J.10
-
16
-
-
0034687740
-
Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization
-
11106375 10.1073/pnas.250426397
-
Cavaillé J, Buiting K, Kiefmann M, Lalande M, Brannan CI, Horsthemke B, Bachellerie JP, Brosius J, Huttenhofer A (2000) Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization. Proc Natl Acad Sci USA 97:14311-14316
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 14311-14316
-
-
Cavaillé, 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
-
17
-
-
0034749783
-
Retrotransposed genes such as Frat3 in the mouse Chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion site
-
11845283 10.1007/s00335-001-2083-1 1:CAS:528:DC%2BD3MXnvFOlt7c%3D
-
Chai JH, Locke DP, Ohta T, Greally JM, Nicholls RD (2001) Retrotransposed genes such as Frat3 in the mouse Chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion site. Mamm Genome 12:813-821
-
(2001)
Mamm Genome
, vol.12
, pp. 813-821
-
-
Chai, J.H.1
Locke, D.P.2
Ohta, T.3
Greally, J.M.4
Nicholls, R.D.5
-
18
-
-
0035336299
-
The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a
-
11350123 10.1006/geno.2001.6543 1:CAS:528:DC%2BD3MXjtlGgsb4%3D
-
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
-
(2001)
Genomics
, vol.73
, pp. 316-322
-
-
Chamberlain, S.J.1
Brannan, C.I.2
-
19
-
-
78049303170
-
Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes
-
20876107 10.1073/pnas.1004487107 1:CAS:528:DC%2BC3cXhtlamtbjE
-
Chamberlain SJ, Chen PF, Ng KY, Bourgois-Rocha F, Lemtiri-Chlieh F, Levine ES, Lalande M (2010) Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes. Proc Natl Acad Sci USA 107:17668-17673
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, pp. 17668-17673
-
-
Chamberlain, S.J.1
Chen, P.F.2
Ng, K.Y.3
Bourgois-Rocha, F.4
Lemtiri-Chlieh, F.5
Levine, E.S.6
Lalande, M.7
-
20
-
-
9744241653
-
Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice
-
15459179 10.1093/hmg/ddh314 1:CAS:528:DC%2BD2cXhtVSkt7bK
-
Chamberlain SJ, Johnstone KA, DuBose AJ, Simon TA, Bartolomei MS, Resnick JL, Brannan CI (2004) Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice. Hum Mol Genet 13:2971-2977
-
(2004)
Hum Mol Genet
, vol.13
, 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
-
21
-
-
77952885487
-
Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11-q13
-
20304067 10.1016/j.nbd.2010.03.011 1:CAS:528:DC%2BC3cXmtFahtL4%3D
-
Chamberlain SJ, Lalande M (2010) Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11-q13. Neurobiol Dis 39:13-20
-
(2010)
Neurobiol Dis
, vol.39
, pp. 13-20
-
-
Chamberlain, S.J.1
Lalande, M.2
-
22
-
-
79956205399
-
Impact of induced pluripotent stem cells on the study of central nervous system disease
-
21277194 10.1016/j.gde.2011.01.008 1:CAS:528:DC%2BC3MXmvVanu7o%3D
-
Cundiff PE, Anderson SA (2011) Impact of induced pluripotent stem cells on the study of central nervous system disease. Curr Opin Genet Dev 21:354-361
-
(2011)
Curr Opin Genet Dev
, vol.21
, pp. 354-361
-
-
Cundiff, P.E.1
Anderson, S.A.2
-
23
-
-
35549005030
-
Necdin mediates skeletal muscle regeneration by promoting myoblast survival and differentiation
-
17954612 10.1083/jcb.200701027 1:CAS:528:DC%2BD2sXht1ekurbO
-
Deponti D, Francois S, Baesso S, Sciorati C, Innocenzi A, Broccoli V, Muscatelli F, Meneveri R, Clementi E, Cossu G, Brunelli S (2007) Necdin mediates skeletal muscle regeneration by promoting myoblast survival and differentiation. J Cell Biol 179:305-319
-
(2007)
J Cell Biol
, vol.179
, pp. 305-319
-
-
Deponti, D.1
Francois, S.2
Baesso, S.3
Sciorati, C.4
Innocenzi, A.5
Broccoli, V.6
Muscatelli, F.7
Meneveri, R.8
Clementi, E.9
Cossu, G.10
Brunelli, S.11
-
24
-
-
77949752708
-
Neonatal maternal deprivation response and developmental changes in gene expression revealed by hypothalamic gene expression profiling in mice
-
20195375 10.1371/journal.pone.0009402
-
Ding F, Li HH, Li J, Myers RM, Francke U (2010) Neonatal maternal deprivation response and developmental changes in gene expression revealed by hypothalamic gene expression profiling in mice. PLoS One 5:e9402
-
(2010)
PLoS One
, vol.5
, pp. 9402
-
-
Ding, F.1
Li, H.H.2
Li, J.3
Myers, R.M.4
Francke, U.5
-
25
-
-
45849144806
-
SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice
-
18320030 10.1371/journal.pone.0001709
-
Ding F, Li HH, Zhang S, Solomon NM, Camper SA, Cohen P, Francke U (2008) SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice. PLoS One 3:e1709
-
(2008)
PLoS One
, vol.3
, pp. 1709
-
-
Ding, F.1
Li, H.H.2
Zhang, S.3
Solomon, N.M.4
Camper, S.A.5
Cohen, P.6
Francke, U.7
-
26
-
-
27644455834
-
Lack of Pwcr1/MBII-85 snoRNA is critical for neonatal lethality in Prader-Willi syndrome mouse models
-
16075369 10.1007/s00335-005-2460-2 1:CAS:528:DC%2BD2MXmvFSlsrk%3D
-
Ding F, Prints Y, Dhar MS, Johnson DK, Garnacho-Montero C, Nicholls RD, Francke U (2005) Lack of Pwcr1/MBII-85 snoRNA is critical for neonatal lethality in Prader-Willi syndrome mouse models. Mamm Genome 16:424-431
-
(2005)
Mamm Genome
, vol.16
, pp. 424-431
-
-
Ding, F.1
Prints, Y.2
Dhar, M.S.3
Johnson, D.K.4
Garnacho-Montero, C.5
Nicholls, R.D.6
Francke, U.7
-
27
-
-
66149158193
-
Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviour
-
19304781 10.1093/hmg/ddp137 1:CAS:528:DC%2BD1MXmtlWnt7k%3D
-
Doe CM, Relkovic D, Garfield AS, Dalley JW, Theobald DE, Humby T, Wilkinson LS, Isles AR (2009) Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviour. Hum Mol Genet 18:2140-2148
-
(2009)
Hum Mol Genet
, vol.18
, pp. 2140-2148
-
-
Doe, C.M.1
Relkovic, D.2
Garfield, A.S.3
Dalley, J.W.4
Theobald, D.E.5
Humby, T.6
Wilkinson, L.S.7
Isles, A.R.8
-
28
-
-
77954657726
-
Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-IC
-
19894069 10.1007/s10048-009-0226-9 1:CAS:528:DC%2BC3cXkvVynuro%3D
-
DuBose AJ, Johnstone KA, Smith EY, Hallett RA, Resnick JL (2010) Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-IC. Neurogenetics 11:145-151
-
(2010)
Neurogenetics
, vol.11
, pp. 145-151
-
-
Dubose, A.J.1
Johnstone, K.A.2
Smith, E.Y.3
Hallett, R.A.4
Resnick, J.L.5
-
29
-
-
84857737967
-
Temporal and developmental requirements for the Prader-Willi imprinting center
-
22331910 10.1073/pnas.1115057109 1:CAS:528:DC%2BC38XksVyhtLk%3D
-
DuBose AJ, Smith EY, Johnstone KA, Resnick JL (2012) Temporal and developmental requirements for the Prader-Willi imprinting center. Proc Natl Acad Sci USA 109:3446-3450
-
(2012)
Proc Natl Acad Sci USA
, vol.109
, pp. 3446-3450
-
-
Dubose, A.J.1
Smith, E.Y.2
Johnstone, K.A.3
Resnick, J.L.4
-
30
-
-
80051692364
-
A new deletion refines the boundaries of the murine Prader-Willi syndrome imprinting center
-
21659337 10.1093/hmg/ddr262 1:CAS:528:DC%2BC3MXhtVWmtr%2FE
-
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
-
31
-
-
0035090961
-
Maternal methylation imprints on human chromosome 15 are established during or after fertilization
-
11242121 10.1038/85927 1:CAS:528:DC%2BD3MXhslOitr0%3D
-
El-Maarri O, Buiting K, Peery EG, Kroisel PM, Balaban B, Wagner K, Urman B, Heyd J, Lich C, Brannan CI, Walter J, Horsthemke B (2001) Maternal methylation imprints on human chromosome 15 are established during or after fertilization. Nat Genet 27:341-344
-
(2001)
Nat Genet
, vol.27
, pp. 341-344
-
-
El-Maarri, O.1
Buiting, K.2
Peery, E.G.3
Kroisel, P.M.4
Balaban, B.5
Wagner, K.6
Urman, B.7
Heyd, J.8
Lich, C.9
Brannan, C.I.10
Walter, J.11
Horsthemke, B.12
-
32
-
-
84856085058
-
Necdin controls proliferation of white adipocyte progenitor cells
-
22292082 10.1371/journal.pone.0030948 1:CAS:528:DC%2BC38XitFemtLw%3D
-
Fujiwara K, Hasegawa K, Ohkumo T, Miyoshi H, Tseng YH, Yoshikawa K (2012) Necdin controls proliferation of white adipocyte progenitor cells. PLoS One 7:e30948
-
(2012)
PLoS One
, vol.7
, pp. 30948
-
-
Fujiwara, K.1
Hasegawa, K.2
Ohkumo, T.3
Miyoshi, H.4
Tseng, Y.H.5
Yoshikawa, K.6
-
33
-
-
0033529801
-
A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes
-
10430930 10.1073/pnas.96.16.9258 1:CAS:528:DyaK1MXltVequ7w%3D
-
Gabriel JM, Merchant M, Ohta T, Ji Y, Caldwell RG, Ramsey MJ, Tucker JD, Longnecker R, Nicholls RD (1999) A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes. Proc Natl Acad Sci USA 96:9258-9263
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 9258-9263
-
-
Gabriel, J.M.1
Merchant, M.2
Ohta, T.3
Ji, Y.4
Caldwell, R.G.5
Ramsey, M.J.6
Tucker, J.D.7
Longnecker, R.8
Nicholls, R.D.9
-
34
-
-
0037032614
-
Anorexigenic melanocortin signaling in the hypothalamus is augmented in association with failure-to-thrive in a transgenic mouse model for Prader-Willi syndrome
-
12443978 10.1016/S0006-8993(02)03583-7 1:CAS:528:DC%2BD38Xoslamsr8%3D
-
Ge Y, Ohta T, Driscoll DJ, Nicholls RD, Kalra SP (2002) Anorexigenic melanocortin signaling in the hypothalamus is augmented in association with failure-to-thrive in a transgenic mouse model for Prader-Willi syndrome. Brain Res 957:42-45
-
(2002)
Brain Res
, vol.957
, pp. 42-45
-
-
Ge, Y.1
Ohta, T.2
Driscoll, D.J.3
Nicholls, R.D.4
Kalra, S.P.5
-
35
-
-
0345062183
-
Disruption of the mouse necdin gene results in early post-natal lethality
-
10508517 10.1038/13828 1:CAS:528:DyaK1MXmtlOhtbk%3D
-
Gerard M, Hernandez L, Wevrick R, Stewart CL (1999) Disruption of the mouse necdin gene results in early post-natal lethality. Nat Genet 23:199-202
-
(1999)
Nat Genet
, vol.23
, pp. 199-202
-
-
Gerard, M.1
Hernandez, L.2
Wevrick, R.3
Stewart, C.L.4
-
36
-
-
57349156874
-
Recommendations for the diagnosis and management of Prader-Willi syndrome
-
18697869 10.1210/jc.2008-0649 1:CAS:528:DC%2BD1cXhtlyqs7jN
-
Goldstone AP, Holland AJ, Hauffa BP, Hokken-Koelega AC, Tauber M (2008) Recommendations for the diagnosis and management of Prader-Willi syndrome. J Clin Endocrinol Metab 93:4183-4197
-
(2008)
J Clin Endocrinol Metab
, vol.93
, pp. 4183-4197
-
-
Goldstone, A.P.1
Holland, A.J.2
Hauffa, B.P.3
Hokken-Koelega, A.C.4
Tauber, M.5
-
37
-
-
0033545993
-
An imprinted, mammalian bicistronic transcript encodes two independent proteins
-
10318933 10.1073/pnas.96.10.5616 1:CAS:528:DyaK1MXjtFCnt7g%3D
-
Gray TA, Saitoh S, Nicholls RD (1999) An imprinted, mammalian bicistronic transcript encodes two independent proteins. Proc Natl Acad Sci USA 96:5616-5621
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 5616-5621
-
-
Gray, T.A.1
Saitoh, S.2
Nicholls, R.D.3
-
38
-
-
52049096152
-
Necdin regulates p53 acetylation via Sirtuin1 to modulate DNA damage response in cortical neurons
-
18753379 10.1523/JNEUROSCI.3052-08.2008 1:CAS:528:DC%2BD1cXhtVyksL3F
-
Hasegawa K, Yoshikawa K (2008) Necdin regulates p53 acetylation via Sirtuin1 to modulate DNA damage response in cortical neurons. J Neurosci 28:8772-8784
-
(2008)
J Neurosci
, vol.28
, pp. 8772-8784
-
-
Hasegawa, K.1
Yoshikawa, K.2
-
39
-
-
31544446862
-
A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects
-
16368707 10.1093/hmg/ddi456 1:CAS:528:DC%2BD28XmsFOhsA%3D%3D
-
Johnstone KA, DuBose AJ, Futtner CR, Elmore MD, Brannan CI, Resnick JL (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
-
(2006)
Hum Mol Genet
, vol.15
, 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
-
40
-
-
0032896919
-
A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region
-
10196367 10.1093/hmg/8.5.783 1:CAS:528:DyaK1MXivFamsbg%3D
-
Jong MT, Gray TA, Ji Y, Glenn CC, Saitoh S, Driscoll DJ, Nicholls RD (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
-
(1999)
Hum Mol Genet
, vol.8
, pp. 783-793
-
-
Jong, M.T.1
Gray, T.A.2
Ji, Y.3
Glenn, C.C.4
Saitoh, S.5
Driscoll, D.J.6
Nicholls, R.D.7
-
41
-
-
85041813459
-
Improving bioscience research reporting: The ARRIVE guidelines for reporting animal research
-
20613859 10.1371/journal.pbio.1000412
-
Kilkenny C, Browne WJ, Cuthill IC, Emerson M, Altman DG (2010) Improving bioscience research reporting: the ARRIVE guidelines for reporting animal research. PLoS Biol 8:e1000412
-
(2010)
PLoS Biol
, vol.8
, pp. 1000412
-
-
Kilkenny, C.1
Browne, W.J.2
Cuthill, I.C.3
Emerson, M.4
Altman, D.G.5
-
42
-
-
77952473473
-
The snoRNA MBII-52 (SNORD 115) is processed into smaller RNAs and regulates alternative splicing
-
20053671 10.1093/hmg/ddp585 1:CAS:528:DC%2BC3cXjs1Glur4%3D
-
Kishore S, Khanna A, Zhang Z, Hui J, Balwierz PJ, Stefan M, Beach C, Nicholls RD, Zavolan M, Stamm S (2010) The snoRNA MBII-52 (SNORD 115) is processed into smaller RNAs and regulates alternative splicing. Hum Mol Genet 19:1153-1164
-
(2010)
Hum Mol Genet
, vol.19
, pp. 1153-1164
-
-
Kishore, S.1
Khanna, A.2
Zhang, Z.3
Hui, J.4
Balwierz, P.J.5
Stefan, M.6
Beach, C.7
Nicholls, R.D.8
Zavolan, M.9
Stamm, S.10
-
43
-
-
34748925845
-
The imprinted gene Magel2 regulates normal circadian output
-
17893678 10.1038/ng2114 1:CAS:528:DC%2BD2sXhtV2isL%2FM
-
Kozlov SV, Bogenpohl JW, Howell MP, Wevrick R, Panda S, Hogenesch JB, Muglia LJ, Van Gelder RN, Herzog ED, Stewart CL (2007) The imprinted gene Magel2 regulates normal circadian output. Nat Genet 39:1266-1272
-
(2007)
Nat Genet
, vol.39
, pp. 1266-1272
-
-
Kozlov, S.V.1
Bogenpohl, J.W.2
Howell, M.P.3
Wevrick, R.4
Panda, S.5
Hogenesch, J.B.6
Muglia, L.J.7
Van Gelder, R.N.8
Herzog, E.D.9
Stewart, C.L.10
-
44
-
-
73349092431
-
Necdin restricts proliferation of hematopoietic stem cells during hematopoietic regeneration
-
19770359 10.1182/blood-2009-07-230292 1:CAS:528:DC%2BD1MXhsVGrsLvP
-
Kubota Y, Osawa M, Jakt LM, Yoshikawa K, Nishikawa S (2009) Necdin restricts proliferation of hematopoietic stem cells during hematopoietic regeneration. Blood 114:4383-4392
-
(2009)
Blood
, vol.114
, pp. 4383-4392
-
-
Kubota, Y.1
Osawa, M.2
Jakt, L.M.3
Yoshikawa, K.4
Nishikawa, S.5
-
45
-
-
33751081032
-
Necdin downregulates CDC2 expression to attenuate neuronal apoptosis
-
17108174 10.1523/JNEUROSCI.3002-06.2006 1:CAS:528:DC%2BD28Xht1ylu7fI
-
Kurita M, Kuwajima T, Nishimura I, Yoshikawa K (2006) Necdin downregulates CDC2 expression to attenuate neuronal apoptosis. J Neurosci 26:12003-12013
-
(2006)
J Neurosci
, vol.26
, pp. 12003-12013
-
-
Kurita, M.1
Kuwajima, T.2
Nishimura, I.3
Yoshikawa, K.4
-
46
-
-
77949342623
-
Necdin promotes tangential migration of neocortical interneurons from basal forebrain
-
20220004 10.1523/JNEUROSCI.5797-09.2010 1:CAS:528:DC%2BC3cXlvVKnurc%3D
-
Kuwajima T, Hasegawa K, Yoshikawa K (2010) Necdin promotes tangential migration of neocortical interneurons from basal forebrain. J Neurosci 30:3709-3714
-
(2010)
J Neurosci
, vol.30
, pp. 3709-3714
-
-
Kuwajima, T.1
Hasegawa, K.2
Yoshikawa, K.3
-
47
-
-
33744996959
-
Necdin promotes GABAergic neuron differentiation in cooperation with Dlx homeodomain proteins
-
16707790 10.1523/JNEUROSCI.1262-06.2006 1:CAS:528:DC%2BD28XlsVOhsb8%3D
-
Kuwajima T, Nishimura I, Yoshikawa K (2006) Necdin promotes GABAergic neuron differentiation in cooperation with Dlx homeodomain proteins. J Neurosci 26:5383-5392
-
(2006)
J Neurosci
, vol.26
, pp. 5383-5392
-
-
Kuwajima, T.1
Nishimura, I.2
Yoshikawa, K.3
-
48
-
-
23044445639
-
Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival
-
16049186 10.1523/JNEUROSCI.2083-05.2005 1:CAS:528:DC%2BD2MXntVantLY%3D
-
Kuwako K, Hosokawa A, Nishimura I, Uetsuki T, Yamada M, Nada S, Okada M, Yoshikawa K (2005) Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival. J Neurosci 25:7090-7099
-
(2005)
J Neurosci
, vol.25
, pp. 7090-7099
-
-
Kuwako, K.1
Hosokawa, A.2
Nishimura, I.3
Uetsuki, T.4
Yamada, M.5
Nada, S.6
Okada, M.7
Yoshikawa, K.8
-
49
-
-
3042821931
-
Regulation of the large (~1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn
-
15226413 10.1093/nar/gkh670 1:CAS:528:DC%2BD2cXltlyis74%3D
-
Landers M, Bancescu DL, Le Meur E, Rougeulle C, Glatt-Deeley H, Brannan C, Muscatelli F, Lalande M (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
-
(2004)
Nucleic Acids Res
, vol.32
, pp. 3480-3492
-
-
Landers, M.1
Bancescu, D.L.2
Le Meur, E.3
Rougeulle, C.4
Glatt-Deeley, H.5
Brannan, C.6
Muscatelli, F.7
Lalande, M.8
-
50
-
-
0033852735
-
Expression and imprinting of MAGEL2 suggest a role in Prader-Willi syndrome and the homologous murine imprinting phenotype
-
10915770 10.1093/hmg/9.12.1813 1:CAS:528:DC%2BD3cXlsFOqu78%3D
-
Lee S, Kozlov S, Hernandez L, Chamberlain SJ, Brannan CI, Stewart CL, Wevrick R (2000) Expression and imprinting of MAGEL2 suggest a role in Prader-Willi syndrome and the homologous murine imprinting phenotype. Hum Mol Genet 9:1813-1819
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1813-1819
-
-
Lee, S.1
Kozlov, S.2
Hernandez, L.3
Chamberlain, S.J.4
Brannan, C.I.5
Stewart, C.L.6
Wevrick, R.7
-
51
-
-
14644391578
-
Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth
-
15649943 10.1093/hmg/ddi059 1:CAS:528:DC%2BD2MXhsFSgs7c%3D
-
Lee S, Walker CL, Karten B, Kuny SL, Tennese AA, O'Neill MA, Wevrick R (2005) Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth. Hum Mol Genet 14:627-637
-
(2005)
Hum Mol Genet
, vol.14
, pp. 627-637
-
-
Lee, S.1
Walker, C.L.2
Karten, B.3
Kuny, S.L.4
Tennese, A.A.5
O'Neill, M.A.6
Wevrick, R.7
-
52
-
-
0042786856
-
Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain
-
12971993 10.1016/S1567-133X(03)00113-3 1:CAS:528:DC%2BD3sXntVGiuro%3D
-
Lee S, Walker CL, Wevrick R (2003) Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain. Gene Expr Patterns 3:599-609
-
(2003)
Gene Expr Patterns
, vol.3
, pp. 599-609
-
-
Lee, S.1
Walker, C.L.2
Wevrick, R.3
-
53
-
-
0027018063
-
Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region
-
1303276 10.1038/ng1292-259 1:CAS:528:DyaK3sXpsFeqtg%3D%3D
-
Leff SE, Brannan CI, Reed ML, Ozcelik T, Francke U, Copeland NG, Jenkins NA (1992) Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region. Nat Genet 2:259-264
-
(1992)
Nat Genet
, vol.2
, pp. 259-264
-
-
Leff, S.E.1
Brannan, C.I.2
Reed, M.L.3
Ozcelik, T.4
Francke, U.5
Copeland, N.G.6
Jenkins, N.A.7
-
54
-
-
70350674351
-
Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size
-
19656775 10.1093/hmg/ddp373 1:CAS:528:DC%2BD1MXhtlWhu7bI
-
Leung KN, Vallero RO, DuBose AJ, Resnick JL, LaSalle JM (2009) Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size. Hum Mol Genet 18:4227-4238
-
(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
-
55
-
-
0030773594
-
The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse
-
9302265 10.1093/hmg/6.11.1873 1:CAS:528:DyaK2sXmslGrtL0%3D
-
MacDonald HR, Wevrick R (1997) The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse. Hum Mol Genet 6:1873-1878
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1873-1878
-
-
Macdonald, H.R.1
Wevrick, R.2
-
56
-
-
0025871554
-
A novel brain-specific mRNA encoding nuclear protein (necdin) expressed in neurally differentiated embryonal carcinoma cells
-
2069569 10.1016/0006-291X(91)91812-Q 1:CAS:528:DyaK38XhsVGisLs%3D
-
Maruyama K, Usami M, Aizawa T, Yoshikawa K (1991) A novel brain-specific mRNA encoding nuclear protein (necdin) expressed in neurally differentiated embryonal carcinoma cells. Biochem Biophys Res Commun 178:291-296
-
(1991)
Biochem Biophys Res Commun
, vol.178
, pp. 291-296
-
-
Maruyama, K.1
Usami, M.2
Aizawa, T.3
Yoshikawa, K.4
-
57
-
-
72049117629
-
Regionally reduced brain volume, altered serotonin neurochemistry, and abnormal behavior in mice null for the circadian rhythm output gene Magel2
-
19199291 10.1002/ajmg.b.30934 1:CAS:528:DC%2BC3cXitlCksA%3D%3D
-
Mercer RE, Kwolek EM, Bischof JM, van Eede M, Henkelman RM, Wevrick R (2009a) Regionally reduced brain volume, altered serotonin neurochemistry, and abnormal behavior in mice null for the circadian rhythm output gene Magel2. Am J Med Genet B Neuropsychiatr Genet 150B:1085-1099
-
(2009)
Am J Med Genet B Neuropsychiatr Genet
, vol.150
, pp. 1085-1099
-
-
Mercer, R.E.1
Kwolek, E.M.2
Bischof, J.M.3
Van Eede, M.4
Henkelman, R.M.5
Wevrick, R.6
-
58
-
-
84873493133
-
Magel2 is required for leptin-mediated depolarization of POMC neurons in the hypothalamic arcuate nucleus in mice
-
23341784 10.1371/journal.pgen.1003207 1:CAS:528:DC%2BC3sXivVehtLo%3D
-
Mercer RE, Michaelson SD, Chee MJ, Atallah TA, Wevrick R, Colmers WF (2013) Magel2 is required for leptin-mediated depolarization of POMC neurons in the hypothalamic arcuate nucleus in mice. PLoS Genet 9:e1003207
-
(2013)
PLoS Genet
, vol.9
, pp. 1003207
-
-
Mercer, R.E.1
Michaelson, S.D.2
Chee, M.J.3
Atallah, T.A.4
Wevrick, R.5
Colmers, W.F.6
-
59
-
-
59349099147
-
Loss of magel2, a candidate gene for features of Prader-Willi syndrome, impairs reproductive function in mice
-
19172181 10.1371/journal.pone.0004291
-
Mercer RE, Wevrick R (2009b) Loss of magel2, a candidate gene for features of Prader-Willi syndrome, impairs reproductive function in mice. PLoS One 4:e4291
-
(2009)
PLoS One
, vol.4
, pp. 4291
-
-
Mercer, R.E.1
Wevrick, R.2
-
60
-
-
84858996228
-
Energy homeostasis in Prader-Willi syndrome: How clinical research informs studies of animal models of genetic obesity: Comment on "nutritional phases in Prader-Willi syndrome", Miller et al., 2011. Am J Med Genet Part A, 155:1040-1049
-
22419655 10.1002/ajmg.a.35249
-
Mercer RE, Wevrick R (2012) Energy homeostasis in Prader-Willi syndrome: how clinical research informs studies of animal models of genetic obesity: comment on "Nutritional phases in Prader-Willi syndrome", Miller et al., 2011. Am J Med Genet Part A, 155:1040-1049. Am J Med Genet A 158A:966-968
-
(2012)
Am J Med Genet A
, vol.158
, pp. 966-968
-
-
Mercer, R.E.1
Wevrick, R.2
-
61
-
-
58049209787
-
Necdin, a Prader-Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development
-
18930956 10.1093/hmg/ddn344 1:CAS:528:DC%2BD1cXhsFagtLfE
-
Miller NL, Wevrick R, Mellon PL (2009) Necdin, a Prader-Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development. Hum Mol Genet 18:248-260
-
(2009)
Hum Mol Genet
, vol.18
, pp. 248-260
-
-
Miller, N.L.1
Wevrick, R.2
Mellon, P.L.3
-
62
-
-
79955038318
-
Nutritional phases in Prader-Willi syndrome
-
21465655
-
Miller JL, Lynn CH, Driscoll DC, Goldstone AP, Gold JA, Kimonis V, Dykens E, Butler MG, Shuster JJ, Driscoll DJ (2011) Nutritional phases in Prader-Willi syndrome. Am J Med Genet A 155A:1040-1049
-
(2011)
Am J Med Genet A
, vol.155
, pp. 1040-1049
-
-
Miller, J.L.1
Lynn, C.H.2
Driscoll, D.C.3
Goldstone, A.P.4
Gold, J.A.5
Kimonis, V.6
Dykens, E.7
Butler, M.G.8
Shuster, J.J.9
Driscoll, D.J.10
-
63
-
-
0034642301
-
Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome
-
11115855 10.1093/hmg/9.20.3101 1:CAS:528:DC%2BD3MXjt1al
-
Muscatelli F, Abrous DN, Massacrier A, Boccaccio I, Le Moal M, Cau P, Cremer H (2000) 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)
Hum Mol Genet
, vol.9
, pp. 3101-3110
-
-
Muscatelli, F.1
Abrous, D.N.2
Massacrier, A.3
Boccaccio, I.4
Le Moal, M.5
Cau, P.6
Cremer, H.7
-
64
-
-
84865780870
-
The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein
-
22694955 10.1093/hmg/dds228 1:CAS:528:DC%2BC38Xht1yntr3F
-
Neumann LC, Markaki Y, Mladenov E, Hoffmann D, Buiting K, Horsthemke B (2012) The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein. Hum Mol Genet 21:4038-4048
-
(2012)
Hum Mol Genet
, vol.21
, pp. 4038-4048
-
-
Neumann, L.C.1
Markaki, Y.2
Mladenov, E.3
Hoffmann, D.4
Buiting, K.5
Horsthemke, B.6
-
65
-
-
0035777024
-
Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes
-
11701647 10.1146/annurev.genom.2.1.153 1:CAS:528:DC%2BD3MXos1antb8%3D
-
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
-
66
-
-
0027502537
-
Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse
-
8095339 10.1073/pnas.90.5.2050 1:CAS:528:DyaK3sXit1Ois70%3D
-
Nicholls RD, Gottlieb W, Russell LB, Davda M, Horsthemke B, Rinchik EM (1993) Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse. Proc Natl Acad Sci USA 90:2050-2054
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 2050-2054
-
-
Nicholls, R.D.1
Gottlieb, W.2
Russell, L.B.3
Davda, M.4
Horsthemke, B.5
Rinchik, E.M.6
-
67
-
-
21244450398
-
Developmental abnormalities of neuronal structure and function in prenatal mice lacking the prader-willi syndrome gene necdin
-
15972963 10.1016/S0002-9440(10)62964-1 1:CAS:528:DC%2BD2MXms1eitrk%3D
-
Pagliardini S, Ren J, Wevrick R, Greer JJ (2005) Developmental abnormalities of neuronal structure and function in prenatal mice lacking the prader-willi syndrome gene necdin. Am J Pathol 167:175-191
-
(2005)
Am J Pathol
, vol.167
, pp. 175-191
-
-
Pagliardini, S.1
Ren, J.2
Wevrick, R.3
Greer, J.J.4
-
68
-
-
34250178425
-
A targeted deletion upstream of Snrpn does not result in an imprinting defect
-
17514346 10.1007/s00335-007-9019-3 1:CAS:528:DC%2BD2sXmtlShtrg%3D
-
Peery EG, Elmore MD, Resnick JL, Brannan CI, Johnstone KA (2007) A targeted deletion upstream of Snrpn does not result in an imprinting defect. Mamm Genome 18:255-262
-
(2007)
Mamm Genome
, vol.18
, pp. 255-262
-
-
Peery, E.G.1
Elmore, M.D.2
Resnick, J.L.3
Brannan, C.I.4
Johnstone, K.A.5
-
69
-
-
84860805533
-
Mechanisms of activation of the paternally expressed genes by the Prader-Willi imprinting center in the Prader-Willi/Angelman syndromes domains
-
Rabinovitz S, Kaufman Y, Ludwig G, Razin A, Shemer R (2012) Mechanisms of activation of the paternally expressed genes by the Prader-Willi imprinting center in the Prader-Willi/Angelman syndromes domains. Proc Natl Acad Sci USA 109:7403-7408
-
(2012)
Proc Natl Acad Sci USA
, vol.109
, pp. 7403-7408
-
-
Rabinovitz, S.1
Kaufman, Y.2
Ludwig, G.3
Razin, A.4
Shemer, R.5
-
70
-
-
72949087949
-
Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndrome
-
20092561 10.1111/j.1460-9568.2009.07048.x
-
Relkovic D, Doe CM, Humby T, Johnstone KA, Resnick JL, Holland AJ, Hagan JJ, Wilkinson LS, Isles AR (2010) Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndrome. Eur J Neurosci 31:156-164
-
(2010)
Eur J Neurosci
, vol.31
, pp. 156-164
-
-
Relkovic, D.1
Doe, C.M.2
Humby, T.3
Johnstone, K.A.4
Resnick, J.L.5
Holland, A.J.6
Hagan, J.J.7
Wilkinson, L.S.8
Isles, A.R.9
-
71
-
-
0037335439
-
Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice
-
12629158 1:CAS:528:DC%2BD3sXjtFylt70%3D
-
Ren J, Lee S, Pagliardini S, Gerard M, Stewart CL, Greer JJ, Wevrick R (2003) Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice. J Neurosci 23:1569-1573
-
(2003)
J Neurosci
, vol.23
, pp. 1569-1573
-
-
Ren, J.1
Lee, S.2
Pagliardini, S.3
Gerard, M.4
Stewart, C.L.5
Greer, J.J.6
Wevrick, R.7
-
72
-
-
0028871957
-
Complementation analyses for 45 mutations encompassing the pink-eyed dilution (p) locus of the mouse
-
8601493 1:CAS:528:DyaK28XlvFKktg%3D%3D
-
Russell LB, Montgomery CS, Cacheiro NL, Johnson DK (1995) Complementation analyses for 45 mutations encompassing the pink-eyed dilution (p) locus of the mouse. Genetics 141:1547-1562
-
(1995)
Genetics
, vol.141
, pp. 1547-1562
-
-
Russell, L.B.1
Montgomery, C.S.2
Cacheiro, N.L.3
Johnson, D.K.4
-
73
-
-
78649454993
-
A single postnatal injection of oxytocin rescues the lethal feeding behaviour in mouse newborns deficient for the imprinted Magel2 gene
-
20876615 10.1093/hmg/ddq424 1:CAS:528:DC%2BC3cXhsVyhsrzN
-
Schaller F, Watrin F, Sturny R, Massacrier A, Szepetowski P, Muscatelli F (2010) A single postnatal injection of oxytocin rescues the lethal feeding behaviour in mouse newborns deficient for the imprinted Magel2 gene. Hum Mol Genet 19:4895-4905
-
(2010)
Hum Mol Genet
, vol.19
, pp. 4895-4905
-
-
Schaller, F.1
Watrin, F.2
Sturny, R.3
Massacrier, A.4
Szepetowski, P.5
Muscatelli, F.6
-
74
-
-
66849141985
-
Necdin is expressed in cachectic skeletal muscle to protect fibers from tumor-induced wasting
-
19339547 10.1242/jcs.041665 1:CAS:528:DC%2BD1MXlvFSrt7c%3D
-
Sciorati C, Touvier T, Buono R, Pessina P, Francois S, Perrotta C, Meneveri R, Clementi E, Brunelli S (2009) Necdin is expressed in cachectic skeletal muscle to protect fibers from tumor-induced wasting. J Cell Sci 122:1119-1125
-
(2009)
J Cell Sci
, vol.122
, pp. 1119-1125
-
-
Sciorati, C.1
Touvier, T.2
Buono, R.3
Pessina, P.4
Francois, S.5
Perrotta, C.6
Meneveri, R.7
Clementi, E.8
Brunelli, S.9
-
75
-
-
37749004050
-
Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation
-
18166085 10.1371/journal.pgen.0030235
-
Skryabin BV, Gubar LV, Seeger B, Pfeiffer J, Handel S, Robeck T, Karpova E, Rozhdestvensky TS, Brosius J (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
, pp. 235
-
-
Skryabin, B.V.1
Gubar, L.V.2
Seeger, B.3
Pfeiffer, J.4
Handel, S.5
Robeck, T.6
Karpova, E.7
Rozhdestvensky, T.S.8
Brosius, J.9
-
76
-
-
84855273820
-
Transcription is required to establish maternal imprinting at the Prader-Willi syndrome and Angelman syndrome locus
-
22242001 10.1371/journal.pgen.1002422 1:CAS:528:DC%2BC38Xms1OnsQ%3D%3D
-
Smith EY, Futtner CR, Chamberlain SJ, Johnstone KA, Resnick JL (2011) Transcription is required to establish maternal imprinting at the Prader-Willi syndrome and Angelman syndrome locus. PLoS Genet 7:e1002422
-
(2011)
PLoS Genet
, vol.7
, pp. 1002422
-
-
Smith, E.Y.1
Futtner, C.R.2
Chamberlain, S.J.3
Johnstone, K.A.4
Resnick, J.L.5
-
77
-
-
27944457262
-
Genetic mapping of putative Chrna7 and Luzp2 neuronal transcriptional enhancers due to impact of a transgene-insertion and 6.8 Mb deletion in a mouse model of Prader-Willi and Angelman syndromes
-
16280085 10.1186/1471-2164-6-157
-
Stefan M, Claiborn KC, Stasiek E, Chai JH, Ohta T, Longnecker R, Greally JM, Nicholls RD (2005a) Genetic mapping of putative Chrna7 and Luzp2 neuronal transcriptional enhancers due to impact of a transgene-insertion and 6.8 Mb deletion in a mouse model of Prader-Willi and Angelman syndromes. BMC Genomics 6:157
-
(2005)
BMC Genomics
, vol.6
, pp. 157
-
-
Stefan, M.1
Claiborn, K.C.2
Stasiek, E.3
Chai, J.H.4
Ohta, T.5
Longnecker, R.6
Greally, J.M.7
Nicholls, R.D.8
-
78
-
-
24944441699
-
Hormonal and metabolic defects in a prader-willi syndrome mouse model with neonatal failure to thrive
-
16002520 10.1210/en.2005-0371 1:CAS:528:DC%2BD2MXhtVGmurbE
-
Stefan M, Ji H, Simmons RA, Cummings DE, Ahima RS, Friedman MI, Nicholls RD (2005b) Hormonal and metabolic defects in a prader-willi syndrome mouse model with neonatal failure to thrive. Endocrinology 146:4377-4385
-
(2005)
Endocrinology
, vol.146
, pp. 4377-4385
-
-
Stefan, M.1
Ji, H.2
Simmons, R.A.3
Cummings, D.E.4
Ahima, R.S.5
Friedman, M.I.6
Nicholls, R.D.7
-
79
-
-
16244414335
-
A nonimprinted Prader-Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels
-
15820315 10.1016/j.ygeno.2005.02.004 1:CAS:528:DC%2BD2MXjtVOitbk%3D
-
Stefan M, Portis T, Longnecker R, Nicholls RD (2005c) A nonimprinted Prader-Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels. Genomics 85:630-640
-
(2005)
Genomics
, vol.85
, pp. 630-640
-
-
Stefan, M.1
Portis, T.2
Longnecker, R.3
Nicholls, R.D.4
-
80
-
-
79955554996
-
Global deficits in development, function, and gene expression in the endocrine pancreas in a deletion mouse model of Prader-Willi syndrome
-
21343540 10.1152/ajpendo.00185.2010 1:CAS:528:DC%2BC3MXmsFClsLc%3D
-
Stefan M, Simmons RA, Bertera S, Trucco M, Esni F, Drain P, Nicholls RD (2011) Global deficits in development, function, and gene expression in the endocrine pancreas in a deletion mouse model of Prader-Willi syndrome. Am J Physiol Endocrinol Metab 300:E909-E922
-
(2011)
Am J Physiol Endocrinol Metab
, vol.300
, pp. 909-922
-
-
Stefan, M.1
Simmons, R.A.2
Bertera, S.3
Trucco, M.4
Esni, F.5
Drain, P.6
Nicholls, R.D.7
-
81
-
-
34249908626
-
DNA demethylation reactivation of imprinted genes in cell lines from patients with Prader-Willi syndrome and a mouse model
-
17506103 10.1002/ajmg.a.31765 1:CAS:528:DC%2BD2sXntlOhsrs%3D
-
Takano K, Okajima M, Saitoh S (2007) DNA demethylation reactivation of imprinted genes in cell lines from patients with Prader-Willi syndrome and a mouse model. Am J Med Genet A 143A:1386-1390
-
(2007)
Am J Med Genet A
, vol.143
, pp. 1386-1390
-
-
Takano, K.1
Okajima, M.2
Saitoh, S.3
-
82
-
-
46949100270
-
Loss of the Prader-Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons
-
18570257 10.1002/dvdy.21615
-
Tennese AA, Gee CB, Wevrick R (2008) 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)
Dev Dyn
, vol.237
, pp. 1935-1943
-
-
Tennese, A.A.1
Gee, C.B.2
Wevrick, R.3
-
83
-
-
79951865949
-
Impaired hypothalamic regulation of endocrine function and delayed counterregulatory response to hypoglycemia in Magel2-null mice
-
21248145 10.1210/en.2010-0709 1:CAS:528:DC%2BC3MXktVGrsLc%3D
-
Tennese AA, Wevrick R (2011) Impaired hypothalamic regulation of endocrine function and delayed counterregulatory response to hypoglycemia in Magel2-null mice. Endocrinology 152:967-978
-
(2011)
Endocrinology
, vol.152
, pp. 967-978
-
-
Tennese, A.A.1
Wevrick, R.2
-
84
-
-
0032963667
-
Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome
-
10319852 10.1038/8722 1:CAS:528:DyaK1MXjtVagsrs%3D
-
Tsai TF, Armstrong D, Beaudet AL (1999) Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome. Nat Genet 22:15-16
-
(1999)
Nat Genet
, vol.22
, pp. 15-16
-
-
Tsai, T.F.1
Armstrong, D.2
Beaudet, A.L.3
-
85
-
-
0036647286
-
Evidence for translational regulation of the imprinted Snurf-Snrpn locus in mice
-
12075010 10.1093/hmg/11.14.1659 1:CAS:528:DC%2BD38XlsFCmsrk%3D
-
Tsai TF, Chen KS, Weber JS, Justice MJ, Beaudet AL (2002) Evidence for translational regulation of the imprinted Snurf-Snrpn locus in mice. Hum Mol Genet 11:1659-1668
-
(2002)
Hum Mol Genet
, vol.11
, pp. 1659-1668
-
-
Tsai, T.F.1
Chen, K.S.2
Weber, J.S.3
Justice, M.J.4
Beaudet, A.L.5
-
86
-
-
84856442945
-
A guide to analysis of mouse energy metabolism
-
10.1038/nmeth.1806
-
Tschop MH, Speakman JR, Arch JR, Auwerx J, Bruning JC, Chan L, Eckel RH, Farese RV Jr, Galgani JE, Hambly C, Herman MA, Horvath TL, Kahn BB, Kozma SC, Maratos-Flier E, Muller TD, Munzberg H, Pfluger PT, Plum L, Reitman ML, Rahmouni K, Shulman GI, Thomas G, Kahn CR, Ravussin E (2012) A guide to analysis of mouse energy metabolism. Nat Methods 9:57-63
-
(2012)
Nat Methods
, vol.9
, pp. 57-63
-
-
Tschop, M.H.1
Speakman, J.R.2
Arch, J.R.3
Auwerx, J.4
Bruning, J.C.5
Chan, L.6
Eckel, R.H.7
Farese, Jr.R.V.8
Galgani, J.E.9
Hambly, C.10
Herman, M.A.11
Horvath, T.L.12
Kahn, B.B.13
Kozma, S.C.14
Maratos-Flier, E.15
Muller, T.D.16
Munzberg, H.17
Pfluger, P.T.18
Plum, L.19
Reitman, M.L.20
Rahmouni, K.21
Shulman, G.I.22
Thomas, G.23
Kahn, C.R.24
Ravussin, E.25
more..
-
87
-
-
13844292692
-
Frat is dispensable for canonical Wnt signaling in mammals
-
15681612 10.1101/gad.326705
-
van Amerongen R, Nawijn M, Franca-Koh J, Zevenhoven J, van der Gulden H, Jonkers J, Berns A (2005) Frat is dispensable for canonical Wnt signaling in mammals. Genes Dev 19:425-430
-
(2005)
Genes Dev
, vol.19
, pp. 425-430
-
-
Van Amerongen, R.1
Nawijn, M.2
Franca-Koh, J.3
Zevenhoven, J.4
Van Der Gulden, H.5
Jonkers, J.6
Berns, A.7
-
88
-
-
0028124726
-
Identification of a novel paternally expressed gene in the Prader-Willi syndrome region
-
7849716 10.1093/hmg/3.10.1877 1:CAS:528:DyaK2MXhtlOgur4%3D
-
Wevrick R, Kerns JA, Francke U (1994) Identification of a novel paternally expressed gene in the Prader-Willi syndrome region. Hum Mol Genet 3:1877-1882
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1877-1882
-
-
Wevrick, R.1
Kerns, J.A.2
Francke, U.3
-
89
-
-
78049409366
-
Neurobehavioral phenotype in Prader-Willi syndrome
-
20981773 10.1002/ajmg.c.30283
-
Whittington J, Holland A (2010) Neurobehavioral phenotype in Prader-Willi syndrome. Am J Med Genet C Semin Med Genet 154C:438-447
-
(2010)
Am J Med Genet C Semin Med Genet
, vol.154
, pp. 438-447
-
-
Whittington, J.1
Holland, A.2
-
90
-
-
84859332682
-
An unexpected function of the prader-willi syndrome imprinting center in maternal imprinting in mice
-
22496793 10.1371/journal.pone.0034348 1:CAS:528:DC%2BC38Xls1Giu70%3D
-
Wu MY, Jiang M, Zhai X, Beaudet AL, Wu RC (2012) An unexpected function of the prader-willi syndrome imprinting center in maternal imprinting in mice. PLoS One 7:e34348
-
(2012)
PLoS One
, vol.7
, pp. 34348
-
-
Wu, M.Y.1
Jiang, M.2
Zhai, X.3
Beaudet, A.L.4
Wu, R.C.5
-
91
-
-
33751086773
-
Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain
-
17043311 10.1101/gad.1452206 1:CAS:528:DC%2BD28XhtFWqsbfM
-
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
-
92
-
-
0031747932
-
A mouse model for Prader-Willi syndrome imprinting-centre mutations
-
9590284 10.1038/ng0598-25 1:CAS:528:DyaK1cXislWqurg%3D
-
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 imprinting-centre mutations. Nat Genet 19:25-31
-
(1998)
Nat Genet
, vol.19
, pp. 25-31
-
-
Yang, T.1
Adamson, T.E.2
Resnick, J.L.3
Leff, S.4
Wevrick, R.5
Francke, U.6
Jenkins, N.A.7
Copeland, N.G.8
Brannan, C.I.9
-
93
-
-
78650051022
-
Induced pluripotent stem cells can be used to model the genomic imprinting disorder Prader-Willi syndrome
-
20956530 10.1074/jbc.M110.183392 1:CAS:528:DC%2BC3cXhsFChtLrE
-
Yang J, Cai J, Zhang Y, Wang X, Li W, Xu J, Li F, Guo X, Deng K, Zhong M, Chen Y, Lai L, Pei D, Esteban MA (2010) Induced pluripotent stem cells can be used to model the genomic imprinting disorder Prader-Willi syndrome. J Biol Chem 285:40303-40311
-
(2010)
J Biol Chem
, vol.285
, pp. 40303-40311
-
-
Yang, J.1
Cai, J.2
Zhang, Y.3
Wang, X.4
Li, W.5
Xu, J.6
Li, F.7
Guo, X.8
Deng, K.9
Zhong, M.10
Chen, Y.11
Lai, L.12
Pei, D.13
Esteban, M.A.14
-
94
-
-
84868152631
-
Long noncoding RNAs with snoRNA ends
-
22959273 10.1016/j.molcel.2012.07.033 1:CAS:528:DC%2BC38XhtlSktr3L
-
Yin QF, Yang L, Zhang Y, Xiang JF, Wu YW, Carmichael GG, Chen LL (2012) Long noncoding RNAs with snoRNA ends. Mol Cell 48:219-230
-
(2012)
Mol Cell
, vol.48
, pp. 219-230
-
-
Yin, Q.F.1
Yang, L.2
Zhang, Y.3
Xiang, J.F.4
Wu, Y.W.5
Carmichael, G.G.6
Chen, L.L.7
-
95
-
-
38449111010
-
Necdin gene, respiratory disturbances and Prader-Willi syndrome
-
18085265 10.1007/978-0-387-73693-8-28
-
Zanella S, Barthelemy M, Muscatelli F, Hilaire G (2008a) Necdin gene, respiratory disturbances and Prader-Willi syndrome. Adv Exp Med Biol 605:159-164
-
(2008)
Adv Exp Med Biol
, vol.605
, pp. 159-164
-
-
Zanella, S.1
Barthelemy, M.2
Muscatelli, F.3
Hilaire, G.4
-
96
-
-
68949174070
-
Breathing deficits of the Prader-Willi syndrome
-
19712904 10.1016/j.resp.2009.03.010
-
Zanella S, Tauber M, Muscatelli F (2009) Breathing deficits of the Prader-Willi syndrome. Respir Physiol Neurobiol 168:119-124
-
(2009)
Respir Physiol Neurobiol
, vol.168
, pp. 119-124
-
-
Zanella, S.1
Tauber, M.2
Muscatelli, F.3
-
97
-
-
39549109269
-
Necdin plays a role in the serotonergic modulation of the mouse respiratory network: Implication for Prader-Willi syndrome
-
18272695 10.1523/JNEUROSCI.4334-07.2008 1:CAS:528:DC%2BD1cXnvVSrtLw%3D
-
Zanella S, Watrin F, Mebarek S, Marly F, Roussel M, Gire C, Diene G, Tauber M, Muscatelli F, Hilaire G (2008b) Necdin plays a role in the serotonergic modulation of the mouse respiratory network: implication for Prader-Willi syndrome. J Neurosci 28:1745-1755
-
(2008)
J Neurosci
, vol.28
, pp. 1745-1755
-
-
Zanella, S.1
Watrin, F.2
Mebarek, S.3
Marly, F.4
Roussel, M.5
Gire, C.6
Diene, G.7
Tauber, M.8
Muscatelli, F.9
Hilaire, G.10
|