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Mita Chotalia et al.
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Paternal deletion of Meg1/Grb10 DMR causes maternalization of the Meg1/Grb10 cluster in mouse proximal Chromosome 11 leading to severe pre- and postnatal growth retardation
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A mono-allelic bivalent chromatin domain controls tissue-specific imprinting at Grb10
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EMBO JOURNAL (2008)
Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing
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Grb10/Nedd4-mediated multiubiquitination of the insulin-like growth factor receptor regulates receptor internalization
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Combinatorial patterns of histone acetylations and methylations in the human genome
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Evolution of genomic imprinting with biparental care: Implications for Prader-Willi and Angelman syndromes
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The genetic aetiology of Silver-Russell syndrome
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JOURNAL OF MEDICAL GENETICS (2008)
Ring1-mediated ubiquitination of H2A restrains poised RNA polymerase II at bivalent genes in mouse ES cells
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High histone acetylation and decreased polycomb repressive complex 2 member levels regulate gene specific transcriptional changes during early embryonic stem cell differentiation induced by retinoic acid
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Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight
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JOURNAL OF MOLECULAR MEDICINE-JMM (2007)
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
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CELL (2006)
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CYTOGENETIC AND GENOME RESEARCH (2006)
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NATURE GENETICS (2005)
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TRENDS IN GENETICS (2005)
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark
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HUMAN MOLECULAR GENETICS (2003)
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NUCLEIC ACIDS RESEARCH (2003)
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SCIENCE (2001)
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BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2001)
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MOLECULAR AND CELLULAR BIOLOGY (2001)
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JOURNAL OF MEDICAL GENETICS (2001)
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EUROPEAN JOURNAL OF HUMAN GENETICS (2001)
Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion
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