Loss of DNMT1o Disrupts Imprinted X Chromosome Inactivation and Accentuates Placental Defects in Females

Generalized disruption of inherited genomic imprints leads to wide-ranging placental defects and dysregulated fetal growth

(2012) K.P. Himes et al.   DEVELOPMENTAL BIOLOGY

Lineage-specific function of the noncoding Tsix RNA for Xist repression and Xi reactivation in mice

(2011) T. Ohhata et al.   GENES & DEVELOPMENT

LINE-1 Activity in Facultative Heterochromatin Formation during X Chromosome Inactivation

(2010) Jennifer C. Chow et al.   CELL

Two-Step Imprinted X Inactivation: Repeat versus Genic Silencing in the Mouse

(2010) S. H. Namekawa et al.   MOLECULAR AND CELLULAR BIOLOGY

Imprinted genes and the epigenetic regulation of placental phenotype

(2010) A.L. Fowden et al.   PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY

Identification of a region of the DNMT1 methyltransferase that regulates the maintenance of genomic imprints

(2009) E. Borowczyk et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Preimplantation expression of the somatic form of Dnmt1 suggests a role in the inheritance of genomic imprints

(2008) M Cecilia Cirio et al.   BMC DEVELOPMENTAL BIOLOGY

DNA methyltransferase 1o functions during preimplantation development to preclude a profound level of epigenetic variation

(2008) M. Cecilia Cirio et al.   DEVELOPMENTAL BIOLOGY

Profound phenotypic variation among mice deficient in the maintenance of genomic imprints

(2008) Marc Toppings et al.   HUMAN REPRODUCTION

Maintenance of genomic methylation patterns during preimplantation development requires the somatic form of DNA methyltransferase 1

(2007) Yukiko Kurihara et al.   DEVELOPMENTAL BIOLOGY