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Imprinting defects in mouse embryos: stochastic errors or polymorphic phenotype?Sylvie Croteau; Constantin Polychronakos; Anna K. Naumova · 2001
X Chromosome Inactivation in Carriers of Barth SyndromeKaren Helene Ørstavik; Ragnhild E. Ørstavik; Anna K. Naumova; Patrizia D'Adamo; Agi Gedeon; Pieter A. Bolhuis; Peter G. Barth; Daniela Toniolo · 1998
A longitudinal study of X-inactivation ratio in human femalesIonel Sandovici; Anna K. Naumova; Mark Leppert; Yendi Linares; Carmen Sapienza · 2004
Defective imprint resetting in carriers of Robertsonian translocation Rb (8.12)Aabida Saferali; Soizik Berlivet; John Schimenti; Marisa S. Bartolomei; Teruko Taketo; Anna K. Naumova · 2010
Neuregulin 1-alpha regulates phosphorylation, acetylation, and alternative splicing in lymphoblastoid cells <sup>1</sup>Ghahramani Seno, Mohammad M.; Gwadry, Fuad G.; Hu, Pingzhao; Scherer, Stephen W.; Naumova, Anna K. · Genome · 2013
Oocyte heterogeneity with respect to the meiotic silencing of unsynapsed X chromosomes in the XY female mouseTaketo, Teruko; Naumova, Anna K. · Chromosoma · 2013
Alternative splicing and imprinting control of theMeg3/Gtl2-Dlk1locus in mouse embryosSylvie Croteau; Marie-Claude Charron; Keith E. Latham; Anna K. Naumova · 2003
BioEssays 11/2012BioEssays · 2012
BiotecVisions 2012, October (pages A1-A8)BioEssays · 2012
BioEssays - Next IssueBioEssays · 2012
Men in scienceMoore, Andrew · BioEssays · 2012
In grateful recognition of our Editorial BoardBioEssays · 2012
BioEssays 12/2012BioEssays · 2012