These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

210 related articles for article (PubMed ID: 25003016)

  • 1. Natural breaking of the maternal silence at the mouse and human imprinted Prader-Willi locus: A whisper with functional consequences.
    Matarazzo V; Muscatelli F
    Rare Dis; 2013; 1():e27228. PubMed ID: 25003016
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences.
    Rieusset A; Schaller F; Unmehopa U; Matarazzo V; Watrin F; Linke M; Georges B; Bischof J; Dijkstra F; Bloemsma M; Corby S; Michel FJ; Wevrick R; Zechner U; Swaab D; Dudley K; Bezin L; Muscatelli F
    PLoS Genet; 2013; 9(9):e1003752. PubMed ID: 24039599
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse.
    MacDonald HR; Wevrick R
    Hum Mol Genet; 1997 Oct; 6(11):1873-8. PubMed ID: 9302265
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. An unexpected function of the Prader-Willi syndrome imprinting center in maternal imprinting in mice.
    Wu MY; Jiang M; Zhai X; Beaudet AL; Wu RC
    PLoS One; 2012; 7(4):e34348. PubMed ID: 22496793
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Retrotransposed genes such as Frat3 in the mouse Chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion site.
    Chai JH; Locke DP; Ohta T; Greally JM; Nicholls RD
    Mamm Genome; 2001 Nov; 12(11):813-21. PubMed ID: 11845283
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Conservation of Imprinting and Methylation of
    Li J; Chen W; Li D; Gu S; Liu X; Dong Y; Jin L; Zhang C; Li S
    Animals (Basel); 2021 Jul; 11(7):. PubMed ID: 34359112
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Genetics of Prader-Willi syndrome and Prader-Will-Like syndrome.
    Cheon CK
    Ann Pediatr Endocrinol Metab; 2016 Sep; 21(3):126-135. PubMed ID: 27777904
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Regulatory elements associated with paternally-expressed genes in the imprinted murine Angelman/Prader-Willi syndrome domain.
    Rodriguez-Jato S; Shan J; Khadake J; Heggestad AD; Ma X; Johnstone KA; Resnick JL; Yang TP
    PLoS One; 2013; 8(2):e52390. PubMed ID: 23390487
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mechanism of EHMT2-mediated genomic imprinting associated with Prader-Willi syndrome.
    Wang SE; Cheng Y; Lim J; Jang MA; Forrest EN; Kim Y; Donahue M; Qiao SN; Xiong Y; Jin J; Wang S; Jiang YH
    Res Sq; 2024 Jul; ():. PubMed ID: 39011107
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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
    Proc Natl Acad Sci U S A; 2012 May; 109(19):7403-8. PubMed ID: 22529396
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control.
    Lee S; Wevrick R
    Am J Hum Genet; 2000 Mar; 66(3):848-58. PubMed ID: 10712201
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndrome.
    Kanber D; Giltay J; Wieczorek D; Zogel C; Hochstenbach R; Caliebe A; Kuechler A; Horsthemke B; Buiting K
    Eur J Hum Genet; 2009 May; 17(5):582-90. PubMed ID: 19066619
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Angelman syndrome imprinting center encodes a transcriptional promoter.
    Lewis MW; Brant JO; Kramer JM; Moss JI; Yang TP; Hansen PJ; Williams RS; Resnick JL
    Proc Natl Acad Sci U S A; 2015 Jun; 112(22):6871-5. PubMed ID: 25378697
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Why is there no diploid overdose effect in Prader-Willi syndrome due to uniparental disomy?
    Smith A
    Acta Genet Med Gemellol (Roma); 1996; 45(1-2):179-89. PubMed ID: 8872029
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes.
    Glenn CC; Driscoll DJ; Yang TP; Nicholls RD
    Mol Hum Reprod; 1997 Apr; 3(4):321-32. PubMed ID: 9237260
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.