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  1. 1.   The imprinted gene Magel2 regulates normal circadian output
  2. Kozlov, S. V.; Bogenpohl, J. W.; Howell, M. P.; Wevrick, R.; Panda, S.; Hogenesch, J. B.; Muglia, L. J.; Van Gelder, R. N.; Herzog, E. D.; Stewart, C. L.
  3. Nature Genetics. 2007, Oct; 39(10): 1266-1272.
  1. 2.   DNA demethylation reactivates a subset of imprinted genes in uniparental mouse embryonic fibroblasts
  2. El Kharroubi, A.; Piras, G.; Stewart, C. L.
  3. Journal of Biological Chemistry. 2001 276(12): 8674-8680.
  1. 3.   Expression and imprinting of MAGEL2 suggest a role in Prader-Willi syndrome and the homologous murine imprinting phenotype
  2. Lee, S.; Kozlov, S.; Hernandez, L.; Chamberlain, S. J.; Brannan, C. I.; Stewart, C. L.; Wevrick, R.
  3. Human Molecular Genetics. 2000 9(12): 1813-1819.
  1. 4.   Disruption of the mouse necdin gene results in early post-natal lethality
  2. Gerard, M.; Hernandez, L.; Wevrick, R.; Stewart, C. L.
  3. Nature Genetics. 1999 23(2): 199-202.
  1. 5.   A Mouse Model For Prader-Willi Syndrome Imprinting-Centre Mutations
  2. Yang, T.; Adamson, T. E.; Resnick, J. L.; Leff, S.; Wevrick, R.; Francke, U.; Jenkins, N. A.; Copeland, N. G.; Brannan, C. I.
  3. Nature Genetics. 1998 19(1): 25-31.
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