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Found 6 results
Filters: Keyword is Dosage Compensation, Genetic  [Clear All Filters]
2006
Garrick D, Sharpe JA, Arkell R, Dobbie L, Smith AG, Wood WG, Higgs DR, Gibbons RJ.  2006.  Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues.PLoS Genet. 2(4):e58.
2005
Kunath T, Arnaud D, Uy GD, Okamoto I, Chureau C, Yamanaka Y, Heard E, Gardner RL, Avner P, Rossant J.  2005.  Imprinted X-inactivation in extra-embryonic endoderm cell lines from mouse blastocysts.Development. 132(7):1649-61.
Caballero IMartín, Hendrich B.  2005.  MeCP2 in neurons: closing in on the causes of Rett syndrome.Hum Mol Genet. 14 Spec No 1:R19-26.
2002
Peters AHFM, Mermoud JE, O'Carroll D, Pagani M, Schweizer D, Brockdorff N, Jenuwein T.  2002.  Histone H3 lysine 9 methylation is an epigenetic imprint of facultative heterochromatin.Nat Genet. 30(1):77-80.
1997
Buehr M.  1997.  The primordial germ cells of mammals: some current perspectives.Exp Cell Res. 232(2):194-207.
1993
Samuel K, Clarke AR, Ansell JD, Hooper ML.  1993.  Age-dependent selection against hypoxanthine phosphoribosyl transferase-deficient cells in mouse haematopoiesis.Development. 118(3):859-63.