The role of genomic imprinting in biology and disease: an expanding view
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics,Molecular Biology
Link
http://www.nature.com/articles/nrg3766.pdf
Reference153 articles.
1. McGrath, J. & Solter, D. Completion of mouse embryogenesis requires both the maternal and paternal genomes. Cell 37, 179–183 (1984).
2. Surani, M. A., Barton, S. C. & Norris, M. L. Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis. Nature 308, 548–550 (1984). References 1 and 2 provide the first recognition of imprinting and show that both the maternal and the paternal genome are needed for normal development of mouse embryos to term.
3. Cattanach, B. M. & Kirk, M. Differential activity of maternally and paternally derived chromosome regions in mice. Nature 315, 496–498 (1985). This paper shows that imprinting is restricted to some regions of the genome (which implies that genes are involved in the process) and that defects in imprinting could be an important cause of human disease.
4. Searle, A. G. & Beechey, C. V. Complementation studies with mouse translocations. Cytogenet. Cell Genet. 20, 282–303 (1978).
5. Snell, G. D. An analysis of translocations in the mouse. Genetics 31, 157–180 (1946).
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