Heritable Imprinting Defect Caused by Epigenetic Abnormalities in Mouse Spermatogonial Stem Cells1

Author:

Lee Jiyoung,Kanatsu-Shinohara Mito,Ogonuki Narumi,Miki Hiromi,Inoue Kimiko,Morimoto Takeshi,Morimoto Hiroko,Ogura Atsuo,Shinohara Takashi

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,General Medicine,Reproductive Medicine

Reference58 articles.

1. Genomic imprinting in mammals.,2007

2. Extensive and orderly reprogramming of genome-wide chromatin modifications associated with specification and early development of germ cells in mice.;Dev Biol,2004

3. Acquisition of the H19 methylation imprint occurs differentially on the parental alleles during spermatogenesis.;Genomics,1999

4. The H19 methylation imprint is erased and re-established differentially on the parental alleles during male germ cell development.;Hum Mol Genet,2000

5. Methylation dynamics of repetitive DNA elements in the mouse germ cell lineage.;Genomics,2003

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