The epigenetic regulation of RIZ1 in human leukemia

作者: Erika Lauren Dawn Beaton-Brown

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参考文章(174)
Michael Alderson, The Epidemiology Of Leukemia Advances in Cancer Research. ,vol. 31, pp. 1- 76 ,(1980) , 10.1016/S0065-230X(08)60656-9
G F Saunders, D E Anderson, H Tsihira, M Genuardi, Distal deletion of chromosome Ip in ductal carcinoma of the breast. American Journal of Human Genetics. ,vol. 45, pp. 73- 82 ,(1989)
Christina M Grozinger, Stuart L Schreiber, Deacetylase Enzymes: Biological Functions and the Use of Small-Molecule Inhibitors Chemistry & Biology. ,vol. 9, pp. 3- 16 ,(2002) , 10.1016/S1074-5521(02)00092-3
Elizabeth E. Cameron, Kurtis E. Bachman, Sanna Myöhänen, James G. Herman, Stephen B. Baylin, Synergy of demethylation and histone deacetylase inhibition in the re-expression of genes silenced in cancer Nature Genetics. ,vol. 21, pp. 103- 107 ,(1999) , 10.1038/5047
James G Herman, Jin Jen, Adrian Merlo, Stephen B Baylin, None, Hypermethylation-associated inactivation indicates a tumor suppressor role for p15INK4B Cancer Research. ,vol. 56, pp. 722- 727 ,(1996)
Ina Rhee, Kam-Wing Jair, Ray-Whay Chiu Yen, Christoph Lengauer, James G. Herman, Kenneth W. Kinzler, Bert Vogelstein, Stephen B. Baylin, Kornel E. Schuebel, CpG methylation is maintained in human cancer cells lacking DNMT1 Nature. ,vol. 404, pp. 1003- 1007 ,(2000) , 10.1038/35010000
Colum P. Walsh, J. Richard Chaillet, Timothy H. Bestor, Transcription of IAP endogenous retroviruses is constrained by cytosine methylation Nature Genetics. ,vol. 20, pp. 116- 117 ,(1998) , 10.1038/2413
Hisashi Tamaru, Eric U. Selker, A Histone H3 Methyltransferase Controls DNA Methylation in Neurospora Crassa Nature. ,vol. 414, pp. 277- 283 ,(2001) , 10.1038/35104508
Richard J. Lin, Laszlo Nagy, Satoshi Inoue, Wenlin Shao, Wilson H. Miller, Ronald M. Evans, Role of the histone deacetylase complex in acute promyelocytic leukaemia Nature. ,vol. 391, pp. 811- 814 ,(1998) , 10.1038/35895
Ruthie E. Amir, Ignatia B. Van den Veyver, Mimi Wan, Charles Q. Tran, Uta Francke, Huda Y. Zoghbi, Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nature Genetics. ,vol. 23, pp. 185- 188 ,(1999) , 10.1038/13810