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 *

276 related articles for article (PubMed ID: 10915770)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome region.
    Watrin F; Roëckel N; Lacroix L; Mignon C; Mattei MG; Disteche C; Muscatelli F
    Eur J Hum Genet; 1997; 5(5):324-32. PubMed ID: 9412790
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome.
    Bischof JM; Stewart CL; Wevrick R
    Hum Mol Genet; 2007 Nov; 16(22):2713-9. PubMed ID: 17728320
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Truncating Mutations of MAGEL2, a Gene within the Prader-Willi Locus, Are Responsible for Severe Arthrogryposis.
    Mejlachowicz D; Nolent F; Maluenda J; Ranjatoelina-Randrianaivo H; Giuliano F; Gut I; Sternberg D; Laquerrière A; Melki J
    Am J Hum Genet; 2015 Oct; 97(4):616-20. PubMed ID: 26365340
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Schaaf-Yang syndrome shows a Prader-Willi syndrome-like phenotype during infancy.
    Negishi Y; Ieda D; Hori I; Nozaki Y; Yamagata T; Komaki H; Tohyama J; Nagasaki K; Tada H; Saitoh S
    Orphanet J Rare Dis; 2019 Dec; 14(1):277. PubMed ID: 31791363
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Two mouse models carrying truncating mutations in Magel2 show distinct phenotypes.
    Ieda D; Negishi Y; Miyamoto T; Johmura Y; Kumamoto N; Kato K; Miyoshi I; Nakanishi M; Ugawa S; Oishi H; Saitoh S
    PLoS One; 2020; 15(8):e0237814. PubMed ID: 32804975
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Evaluation of Prader-Willi Syndrome gene MAGEL2 in severe childhood-onset obesity.
    O'Neill MA; Farooqi IS; Wevrick R
    Obes Res; 2005 Oct; 13(10):1841-2. PubMed ID: 16286533
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Magel2 knockout mice manifest altered social phenotypes and a deficit in preference for social novelty.
    Fountain MD; Tao H; Chen CA; Yin J; Schaaf CP
    Genes Brain Behav; 2017 Jul; 16(6):592-600. PubMed ID: 28296079
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of a novel paternally expressed gene in the Prader-Willi syndrome region.
    Wevrick R; Kerns JA; Francke U
    Hum Mol Genet; 1994 Oct; 3(10):1877-82. PubMed ID: 7849716
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Progressive postnatal decline in leptin sensitivity of arcuate hypothalamic neurons in the Magel2-null mouse model of Prader-Willi syndrome.
    Pravdivyi I; Ballanyi K; Colmers WF; Wevrick R
    Hum Mol Genet; 2015 Aug; 24(15):4276-83. PubMed ID: 25926624
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.