Mouse/Human Sequence Divergence in a Region with a Paternal-Specific Methylation Imprint at the Human H19 Locus

By Jinno Yoshihiro   Sengoku Kazuo   Nakao Mitsuyoshi   Tamate Kenichi   Miyamoto Toshinobu   Matsuzaka Tetsuo   Sutcliffe James S.   Anan Tadashi   Takuma Naoyuki   Nishiwaki Kunihiko   Ikeda Yuichiro   Ishimaru Tadayuki   Ishikawa Mutsuo   Niikawa Norio  

Human Molecular Genetics, Vol. 5, Iss. 8, 1996-01 ,pp. : 1155-1161

Oxford University Press

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A human H19 transgene exhibits impaired paternal-specific imprint acquisition and maintenance in mice

By Jones B.K.   Levorse J.   Tilghman S.M.  

Human Molecular Genetics, Vol. 11, Iss. 4, 2002-02 ,pp. : 411-418

Oxford University Press

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The H19 methylation imprint is erased and re‐established differentially on the parental alleles during male germ cell development

By Davis Tamara L.   Yang Grace J.   McCarrey JohnR.   Bartolomei MarisaS.  

Human Molecular Genetics, Vol. 9, Iss. 19, 2000-11 ,pp. : 2885-2894

Oxford University Press

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Human PEG1/MEST , an Imprinted Gene on Chromosome 7

By Kobayashi Shin  

Human Molecular Genetics, Vol. 6, Iss. 5, 1997-05 ,pp. : 781-786

Oxford University Press

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Paternal monoallelic expression of PEG3 in the human placenta

By Hiby S.E.  

Human Molecular Genetics, Vol. 10, Iss. 10, 2001-05 ,pp. : 1093-1100

Oxford University Press

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