Genomic Imprinting
Causes and Consequences
Herausgeber: Ohlsson, R.; Ritzen, M.; Hall, K.
Hinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.
Contributors; Part I. Genomic Imprinting in Mammals: 1. The role of
imprinting in early mammalian development A. Gilligan, and D. Solter; 2.
The evolution of parental imprinting: a review of hypotheses D. Haig and R.
Trivers; 3. Genetic variations in parental imprinting on mouse chromosome
17 J. Forejt, S. Gregorovà, M. Landíková, J. Capková and L. M. Silver; Part
II. Chromatin Structure and DNA Modifications: 4. Epigenetic inheritance:
the chromatin connection A. P. Wolffe; 5. Chromobox genes and the molecular
mechanisms of cellular determination P. B. Singh and T. C. James; 6. The
biochemical basis of allele-specific gene expression in genomic imprinting
and X inactivation T. H. Bestor; 7. DNA methylation and mammalian
development R. Jaenisch, C. Beard and E. Li; Part III. Mechanisms of
Imprinting: 8. X chromosome inactivation and imprinting M. F. Lyon; 9.
Imprinting of H19 and Xist in uniparental embryos M. A. Surani, A. C.
Ferguson-Smith, H. Sasaki and S. C. Barton; 10. Imprinted genes, allelic
methylation, and imprinted modifiers of methylation W. Reik, R. Feil, N. D.
Allen, T. F. Moore and J. Walter; 11. Genomic imprinting of the H19 and
Igf2 genes in the mouse S. M. Tilgham, M. S. Bartolomei, A. L. Webber, M.
E. Brunkow, J. Saam, P. A. Leighton and K. Pfeifer; 12. Plasticity of
imprinting R. Ohlsson, T. Ekström, G. Franklin, S. Pfeifer-Ohlsson, H. Cui,
S. Miller, R. Fisher and C. Walsh; 13. Regional regulation of
allele-specific gene expression I. Simon and H. Cedar; Part IV. Genomic
Imprinting in Embryonal Tumors and Overgrowth Disorders: 14. Genomic
imprinting in embryonal tumors and overgrowth disorders A. E. Reeve; 15.
Tracking imprinting: the Beckwith-Wiedemann syndrome M. Mannens; 16.
Genomic imprinting in Beckwith-Wiedemann syndrome R. Weksberg and J.
Squire; 17. Mitotic crossing over and the disruption of genomic imprinting
G. B. Côté; 18. Evaluating H19 as an imprinted tumor suppressor gene B.
Tycko; 19. A domain of abnormal imprinting in human cancer A. P. Feinberg;
Part V. Genomic Imprinting and the Prader-Willi Syndrome: 20.
Parent-of-origin-specific DNA methylation and imprinting mutations on human
chromosome 15 B. Horsthemke, B. Dittrich and K. Buiting; 21. The SNRPN gene
and Prader-Willi syndrome U. Francke, J. A. Kerns and J. Giacalone; Part
VI. Imprinting: A Search for New Genes and Unifying Principles: 22. Use of
chromosome rearrangements for investigations into imprinting in the mouse
B. M. Cattanach, J. Barr and J. Jones; 23. A new imprinted gene,
U2af-related sequence, isolated by a methylation-sensitive genome scanning
method T. Mukai, I. Hatada, T. Yamaoka, K. Kitagawa, X.-D. Wang, T. Sugama,
J. Masuda and J. Ogata; 24. The mouse Igf2/MPR gene: a model for all
gametic imprinted genes? D. P. Barlow; Index.
