Imprinted methylation profiles for proximal mouse chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysis

Proximal mouse Chromosome (Chr) 11 shares regions of orthology with the candidate gene region for the imprinting growth disorder Silver-Russell syndrome (SRS) on human Chr 7p. It has previously been shown that mice with two maternal or two paternal copies (duplications, Dp) of proximal Chr 11 exhibi...

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Veröffentlicht in:	Mammalian genome 2003-12, Vol.14 (12), p.805-816
Hauptverfasser:	Monk, David, Smith, Rachel, Arnaud, Philippe, Preece, Michael A, Stanier, Philip, Beechey, Colin V, Peters, Jo, Kelsey, Gavin, Moore, Gudrun E
Format:	Artikel
Sprache:	eng
Schlagworte:	Aneuploidy Animals Biochemistry, Molecular Biology Blotting, Southern Cancer Chromosome Mapping Chromosomes, Mammalian Chromosomes, Mammalian - genetics Crosses, Genetic Databases, Genetic Disease Models, Animal DNA Methylation Gene Components Genetic Testing Genomic Imprinting Genomic Imprinting - genetics Genomics GRB10 Adaptor Protein Growth Disorders Growth Disorders - genetics Humans Kruppel-Like Transcription Factors Life Sciences Meg1 gene Mice Mice, Mutant Strains Molecular biology Molecular Networks Mutagenesis Protein Kinases Proteins Proteins - genetics Restriction Mapping Sequence Analysis, DNA Sequence Analysis, DNA - methods Silver-Russell syndrome Sulfites Transcription Factors
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