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. 1985 Jul;37(4):827–829.

Chromosomal imprinting and the parent transmission specific variation in expressivity of Huntington disease.

R P Erickson
PMCID: PMC1684611  PMID: 9556671

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Chandra H. S., Brown S. W. Chromosome imprinting and the mammalian X chromosome. Nature. 1975 Jan 17;253(5488):165–168. doi: 10.1038/253165a0. [DOI] [PubMed] [Google Scholar]
  2. Crouse H V. The Controlling Element in Sex Chromosome Behavior in Sciara. Genetics. 1960 Oct;45(10):1429–1443. doi: 10.1093/genetics/45.10.1429. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Erickson R. P. Glucose-6-phosphate dehydrogenase activity changes during spermatogenesis: possible relevance to X-chromosome inactivation. Dev Biol. 1976 Oct 1;53(1):134–137. doi: 10.1016/0012-1606(76)90216-5. [DOI] [PubMed] [Google Scholar]
  4. Falconer D. S., Isaacson J. H., Gauld I. K. Non-random X-chromosome inactivation in the mouse: difference of reaction to imprinting. Genet Res. 1982 Jun;39(3):237–259. doi: 10.1017/s0016672300020930. [DOI] [PubMed] [Google Scholar]
  5. Gusella J. F., Wexler N. S., Conneally P. M., Naylor S. L., Anderson M. A., Tanzi R. E., Watkins P. C., Ottina K., Wallace M. R., Sakaguchi A. Y. A polymorphic DNA marker genetically linked to Huntington's disease. Nature. 1983 Nov 17;306(5940):234–238. doi: 10.1038/306234a0. [DOI] [PubMed] [Google Scholar]
  6. Johnson D. R. Further observations on the haipin-tail (Thp) mutation in the mouse. Genet Res. 1974 Oct;24(2):207–213. doi: 10.1017/s0016672300015226. [DOI] [PubMed] [Google Scholar]
  7. Kratzer P. G., Chapman V. M., Lambert H., Evans R. E., Liskay R. M. Differences in the DNA of the inactive X chromosomes of fetal and extraembryonic tissues of mice. Cell. 1983 May;33(1):37–42. doi: 10.1016/0092-8674(83)90332-x. [DOI] [PubMed] [Google Scholar]
  8. Lifschytz E., Lindsley D. L. The role of X-chromosome inactivation during spermatogenesis (Drosophila-allocycly-chromosome evolution-male sterility-dosage compensation). Proc Natl Acad Sci U S A. 1972 Jan;69(1):182–186. doi: 10.1073/pnas.69.1.182. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Lyon M. F., Rastan S. Parental source of chromosome imprinting and its relevance for X chromosome inactivation. Differentiation. 1984;26(1):63–67. doi: 10.1111/j.1432-0436.1984.tb01375.x. [DOI] [PubMed] [Google Scholar]
  10. Mann J. R., Lovell-Badge R. H. Inviability of parthenogenones is determined by pronuclei, not egg cytoplasm. Nature. 1984 Jul 5;310(5972):66–67. doi: 10.1038/310066a0. [DOI] [PubMed] [Google Scholar]
  11. McGrath J., Solter D. Completion of mouse embryogenesis requires both the maternal and paternal genomes. Cell. 1984 May;37(1):179–183. doi: 10.1016/0092-8674(84)90313-1. [DOI] [PubMed] [Google Scholar]
  12. McGrath J., Solter D. Maternal Thp lethality in the mouse is a nuclear, not cytoplasmic, defect. Nature. 1984 Apr 5;308(5959):550–551. doi: 10.1038/308550a0. [DOI] [PubMed] [Google Scholar]
  13. Myers R. H., Goldman D., Bird E. D., Sax D. S., Merril C. R., Schoenfeld M., Wolf P. A. Maternal transmission in Huntington's disease. Lancet. 1983 Jan 29;1(8318):208–210. doi: 10.1016/s0140-6736(83)92587-4. [DOI] [PubMed] [Google Scholar]
  14. Sanford J., Forrester L., Chapman V., Chandley A., Hastie N. Methylation patterns of repetitive DNA sequences in germ cells of Mus musculus. Nucleic Acids Res. 1984 Mar 26;12(6):2823–2836. doi: 10.1093/nar/12.6.2823. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Surani M. A., Barton S. C., Norris M. L. Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis. Nature. 1984 Apr 5;308(5959):548–550. doi: 10.1038/308548a0. [DOI] [PubMed] [Google Scholar]
  16. Takagi N., Sasaki M. Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse. Nature. 1975 Aug 21;256(5519):640–642. doi: 10.1038/256640a0. [DOI] [PubMed] [Google Scholar]
  17. West J. D., Frels W. I., Chapman V. M., Papaioannou V. E. Preferential expression of the maternally derived X chromosome in the mouse yolk sac. Cell. 1977 Dec;12(4):873–882. doi: 10.1016/0092-8674(77)90151-9. [DOI] [PubMed] [Google Scholar]
  18. Zellweger H., Ionasescu V. Early onset of myotonic dystrophy in infants. Am J Dis Child. 1973 Apr;125(4):601–604. doi: 10.1001/archpedi.1973.04160040097021. [DOI] [PubMed] [Google Scholar]

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