메뉴 건너뛰기




Volumn 24, Issue 5-6, 2013, Pages 165-178

Recommendations for the investigation of animal models of Prader-Willi syndrome

Author keywords

[No Author keywords available]

Indexed keywords

SMALL NUCLEOLAR RNA;

EID: 84879555953     PISSN: 09388990     EISSN: 14321777     Source Type: Journal    
DOI: 10.1007/s00335-013-9454-2     Document Type: Review
Times cited : (35)

References (97)
  • 2
    • 33751581604 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 17
    • 0034749783 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 21
    • 77952885487 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 24
    • 77949752708 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 32
    • 84856085058 scopus 로고    scopus 로고
    • 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
  • 34
    • 0037032614 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 37
    • 0033545993 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 44
    • 73349092431 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 63
    • 0034642301 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 71
    • 0037335439 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 76
    • 84855273820 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 88
    • 0028124726 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 95
    • 38449111010 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.