Recent insights into the regulation of X-chromosome inactivation
作者： Anton Wutz , Karmele Valencia
DOI: 10.2147/AGG.S60399
关键词: Genetics 、 X-inactivation 、 Biology
摘要:
sci-hub.se 参考文章(118)
S Safavi, E Forestier, I Golovleva, G Barbany, K H Nord, A V Moorman, C J Harrison, B Johansson, K Paulsson, Loss of chromosomes is the primary event in near-haploid and low hypodiploid acute lymphoblastic leukemia. Leukemia. ,vol. 27, pp. 248- 250 ,(2013) , 10.1038/LEU.2012.227
Mario Cazzola, Alison May, Gaetano Bergamaschi, Paola Cerani, Vittorio Rosti, David F. Bishop, Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females. Blood. ,vol. 96, pp. 4363- 4365 ,(2000) , 10.1182/BLOOD.V96.13.4363
P. Koivisto, T. Visakorpi, C. Palmberg, O. P. Kallioniemi, E. Hyytinen, T. Tammela, J. Isola, Analysis of genetic changes underlying local recurrence of prostate carcinoma during androgen deprivation therapy. American Journal of Pathology. ,vol. 147, pp. 1608- 1614 ,(1995)
A. J. M. H. Verkerk, R. J. H. L. M. Van Gurp, L. H. J. Looijenga, A. J. M. Gillis, J. W. Oosterhuis, X inactivation in human testicular tumors. XIST expression and androgen receptor methylation status. American Journal of Pathology. ,vol. 151, pp. 581- 590 ,(1997)
Bruce G. Bender, Mary C. Linden, Arthur Robinson, Sex chromosome tetrasomy and pentasomy. Pediatrics. ,vol. 96, pp. 672- 682 ,(1995)
Céline Vallot, Christophe Huret, Yann Lesecque, Alissa Resch, Noufϊssa Oudrhiri, Annelise Bennaceur, Laurent Duret, Claire Rougeulle, XACT, a long non-coding transcript coating the active X chromosome in human pluripotent cells. Epigenetics & Chromatin. ,vol. 6, pp. 1- 1 ,(2013) , 10.1186/1756-8935-6-S1-O33
Philip Avner, Edith Heard, X-chromosome inactivation: counting, choice and initiation Nature Reviews Genetics. ,vol. 2, pp. 59- 67 ,(2001) , 10.1038/35047580
Jeannie Lee, Lance S Davidow, David Warshawsky, Tsix, a gene antisense to Xist at the X-inactivation centre Nature Genetics. ,vol. 21, pp. 400- 404 ,(1999) , 10.1038/7734
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
Györgyi Csankovszki, Barbara Panning, Brian Bates, John R. Pehrson, Rudolf Jaenisch, Conditional deletion of Xist disrupts histone macroH2A localization but not maintenance of X inactivation. Nature Genetics. ,vol. 22, pp. 323- 324 ,(1999) , 10.1038/11887