Browsing by Subject "genome imprinting"
Now showing items 1-4 of 4
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Balanced translocations for the analysis of imprinted regions of the mouse genome.
(2001)Experimental studies that investigate the functional and mechanistic properties of an imprinted locus require material in which the two parental chromosome homologs can be easily distinguished. The use of animals with ...
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Parental origin effects in human trisomy for chromosome 14q: Implications for genomic imprinting
(1998)Parental origin specific congenital anomalies have been noted in patients with uniparental disomy of the long arm of human chromosome 14 (UPD14). This suggests the presence of imprinted genes, consistent with observations ...
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Parental origin-specific developmental defects in mice with uniparental disomy for chromosome 12
(2000)Genetic analysis has shown that the distal portion of mouse chromosome 12 is imprinted
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Roles for genomic imprinting and the zygotic genome in placental development
(2001)The placenta contains several types of fetomaternal interfaces where zygote-derived cells interact with maternal cells or maternal blood for the promotion of fetal growth and viability. The genetic factors regulating the ...