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2. Analysis of imprinting in mice with uniparental duplication of proximal chromosomes 7 and 15 by use of a custom oligonucleotide microarray. Buettner VL; Longmate JA; Barish ME; Mann JR; Singer-Sam J Mamm Genome; 2004 Mar; 15(3):199-209. PubMed ID: 15014969 [TBL] [Abstract][Full Text] [Related]
3. The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a. Chamberlain SJ; Brannan CI Genomics; 2001 May; 73(3):316-22. PubMed ID: 11350123 [TBL] [Abstract][Full Text] [Related]
4. The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region. Boccaccio I; Glatt-Deeley H; Watrin F; Roëckel N; Lalande M; Muscatelli F Hum Mol Genet; 1999 Dec; 8(13):2497-505. PubMed ID: 10556298 [TBL] [Abstract][Full Text] [Related]
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6. The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene. Watrin F; Le Meur E; Roeckel N; Ripoche MA; Dandolo L; Muscatelli F BMC Genet; 2005 Jan; 6():1. PubMed ID: 15634360 [TBL] [Abstract][Full Text] [Related]
7. Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype. Lee S; Kozlov S; Hernandez L; Chamberlain SJ; Brannan CI; Stewart CL; Wevrick R Hum Mol Genet; 2000 Jul; 9(12):1813-9. PubMed ID: 10915770 [TBL] [Abstract][Full Text] [Related]
8. 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. Stefan M; Portis T; Longnecker R; Nicholls RD Genomics; 2005 May; 85(5):630-40. PubMed ID: 15820315 [TBL] [Abstract][Full Text] [Related]
9. Genetic differentiation of hypothalamus parentally biased transcripts in populations of the house mouse implicate the Prader-Willi syndrome imprinted region as a possible source of behavioral divergence. Lorenc A; Linnenbrink M; Montero I; Schilhabel MB; Tautz D Mol Biol Evol; 2014 Dec; 31(12):3240-9. PubMed ID: 25172960 [TBL] [Abstract][Full Text] [Related]
10. Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number. Hogart A; Leung KN; Wang NJ; Wu DJ; Driscoll J; Vallero RO; Schanen NC; LaSalle JM J Med Genet; 2009 Feb; 46(2):86-93. PubMed ID: 18835857 [TBL] [Abstract][Full Text] [Related]
11. The imprinting box of the Prader-Willi/Angelman syndrome domain. Shemer R; Hershko AY; Perk J; Mostoslavsky R; Tsuberi B; Cedar H; Buiting K; Razin A Nat Genet; 2000 Dec; 26(4):440-3. PubMed ID: 11101841 [TBL] [Abstract][Full Text] [Related]
12. Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain. Lee S; Walker CL; Wevrick R Gene Expr Patterns; 2003 Oct; 3(5):599-609. PubMed ID: 12971993 [TBL] [Abstract][Full Text] [Related]
13. Deletion analysis of the imprinting center region in patients with Angelman syndrome and Prader-Willi syndrome by real-time quantitative PCR. Raca G; Buiting K; Das S Genet Test; 2004; 8(4):387-94. PubMed ID: 15684868 [TBL] [Abstract][Full Text] [Related]
14. Prader-Willi syndrome and Angelman syndrome. Buiting K Am J Med Genet C Semin Med Genet; 2010 Aug; 154C(3):365-76. PubMed ID: 20803659 [TBL] [Abstract][Full Text] [Related]
15. The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region. Jay P; Rougeulle C; Massacrier A; Moncla A; Mattei MG; Malzac P; Roëckel N; Taviaux S; Lefranc JL; Cau P; Berta P; Lalande M; Muscatelli F Nat Genet; 1997 Nov; 17(3):357-61. PubMed ID: 9354807 [TBL] [Abstract][Full Text] [Related]
16. Paternal expression of a novel imprinted gene, Peg12/Frat3, in the mouse 7C region homologous to the Prader-Willi syndrome region. Kobayashi S; Kohda T; Ichikawa H; Ogura A; Ohki M; Kaneko-Ishino T; Ishino F Biochem Biophys Res Commun; 2002 Jan; 290(1):403-8. PubMed ID: 11779183 [TBL] [Abstract][Full Text] [Related]
17. A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects. Johnstone KA; DuBose AJ; Futtner CR; Elmore MD; Brannan CI; Resnick JL Hum Mol Genet; 2006 Feb; 15(3):393-404. PubMed ID: 16368707 [TBL] [Abstract][Full Text] [Related]
18. Imprinting analysis of the mouse chromosome 7C region in DNMT1-null embryos. Nakagaki A; Osanai H; Kishino T Gene; 2014 Dec; 553(1):63-8. PubMed ID: 25300248 [TBL] [Abstract][Full Text] [Related]
19. Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes. Nicholls RD; Knepper JL Annu Rev Genomics Hum Genet; 2001; 2():153-75. PubMed ID: 11701647 [TBL] [Abstract][Full Text] [Related]
20. Disruption of the mouse necdin gene results in early post-natal lethality. Gérard M; Hernandez L; Wevrick R; Stewart CL Nat Genet; 1999 Oct; 23(2):199-202. PubMed ID: 10508517 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]