sebastien_vigneau's Lobanenkov:V [42 articles] Export

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	Conditional expression of the CTCF-paralogous transcriptional factor BORIS in normal cells results in demethylation and derepression of MAGE-A1 and reactivation of other cancer-testis genes. [My Copy] Cancer research, Vol. 65, No. 17. (1 September 2005), pp. 7751-7762. by S. Vatolin, Z. Abdullaev, S. D. Pack, et al.P. T. Flanagan, M. Custer, D. I. Loukinov, E. Pugacheva, J. A. Hong, H. Morse, D. S. Schrump, J. I. Risinger, J. C. Barrett, V. V. Lobanenkov posted to boris cancer ctcf mage-a1 by sebastien_vigneau on 2009-07-14 17:58:22 as along with 1 group CTCF
	Reciprocal binding of CTCF and BORIS to the NY-ESO-1 promoter coincides with derepression of this cancer-testis gene in lung cancer cells. [My Copy] Cancer research, Vol. 65, No. 17. (1 September 2005), pp. 7763-7774. by J. A. Hong, Y. Kang, Z. Abdullaev, et al.P. T. Flanagan, S. D. Pack, M. R. Fischette, M. T. Adnani, D. I. Loukinov, S. Vatolin, J. I. Risinger, M. Custer, G. A. Chen, M. Zhao, D. M. Nguyen, J. C. Barrett, V. V. Lobanenkov, D. S. Schrump posted to boris ctcf lung-cancer ny-eso-1 x-chromosome xci by sebastien_vigneau on 2009-07-14 16:10:05 as along with 2 groups X-chromosome inactivation CTCF
	CTCF binds the proximal exonic region of hTERT and inhibits its transcription. [My Copy] Nucleic acids research, Vol. 33, No. 21. (2005), pp. 6850-6860. by S. Renaud, D. Loukinov, F. T. Bosman, V. Lobanenkov, J. Benhattar posted to ctcf htert by sebastien_vigneau on 2009-07-13 23:41:10 as along with 1 group CTCF
	Transcriptional regulator CTCF controls human interleukin 1 receptor-associated kinase 2 promoter. [My Copy] Journal of molecular biology, Vol. 346, No. 2. (18 February 2005), pp. 411-422. by I. Kuzmin, L. Geil, L. Gibson, et al.T. Cavinato, D. Loukinov, V. Lobanenkov, M. I. Lerman posted to ctcf interleukin irak by sebastien_vigneau on 2009-07-13 23:29:58 as along with 1 group CTCF
	CTCF is a uniquely versatile transcription regulator linked to epigenetics and disease. [My Copy] Trends in genetics : TIG, Vol. 17, No. 9. (September 2001), pp. 520-527. by R. Ohlsson, R. Renkawitz, V. Lobanenkov posted to ctcf by sebastien_vigneau on 2009-07-09 16:02:00 as along with 1 person and 1 group absterga CTCF
	Chromatin architecture near a potential 3' end of the igh locus involves modular regulation of histone modifications during B-Cell development and in vivo occupancy at CTCF sites. [My Copy] Molecular and cellular biology, Vol. 25, No. 4. (February 2005), pp. 1511-1525. by F. E. Garrett, A. V. Emelyanov, M. A. Sepulveda, et al.P. Flanagan, S. Volpi, F. Li, D. Loukinov, L. A. Eckhardt, V. V. Lobanenkov, B. K. Birshtein posted to b-cell ctcf igh orientation-dependant by sebastien_vigneau on 2009-07-07 20:34:46 as along with 1 group CTCF
	Negative protein 1, which is required for function of the chicken lysozyme gene silencer in conjunction with hormone receptors, is identical to the multivalent zinc finger repressor CTCF. [My Copy] Molecular and cellular biology, Vol. 17, No. 3. (March 1997), pp. 1281-1288. by M. Burcin, R. Arnold, M. Lutz, et al.B. Kaiser, D. Runge, F. Lottspeich, G. N. Filippova, V. V. Lobanenkov, R. Renkawitz posted to ctcf lysozyme nep1 represor by sebastien_vigneau on 2009-07-06 19:45:12 as along with 1 group CTCF
	An exceptionally conserved transcriptional repressor, CTCF, employs different combinations of zinc fingers to bind diverged promoter sequences of avian and mammalian c-myc oncogenes [My Copy] Mol. Cell. Biol., Vol. 16, No. 6. (1 June 1996), pp. 2802-2813. by G. N. Filippova, S. Fagerlie, E. M. Klenova, et al.C. Myers, Y. Dehner, G. Goodwin, P. E. Neiman, S. J. Collins, V. V. Lobanenkov posted to c-myc ctcf zinc-finger by sebastien_vigneau on 2009-07-06 19:03:39 as along with 1 person and 1 group absterga CTCF
	A novel sequence-specific DNA binding protein which interacts with three regularly spaced direct repeats of the CCCTC-motif in the 5'-flanking sequence of the chicken c-myc gene. [My Copy] Oncogene, Vol. 5, No. 12. (December 1990), pp. 1743-1753. by V. V. Lobanenkov, R. H. Nicolas, V. V. Adler, et al.H. Paterson, E. M. Klenova, A. V. Polotskaja, G. H. Goodwin posted to c-myc ctcf represor by sebastien_vigneau on 2009-07-06 18:55:43 as along with 2 people and 1 group absterga drestion CTCF
	CTCF, a conserved nuclear factor required for optimal transcriptional activity of the chicken c-myc gene, is an 11-Zn-finger protein differentially expressed in multiple forms. [My Copy] Mol. Cell. Biol., Vol. 13, No. 12. (1 December 1993), pp. 7612-7624. by E. M. Klenova, R. H. Nicolas, H. F. Paterson, et al.A. F. Carne, C. M. Heath, G. H. Goodwin, P. E. Neiman, V. V. Lobanenkov posted to activator c-myc ctcf by sebastien_vigneau on 2009-07-06 18:50:51 as along with 1 person and 1 group absterga CTCF
	Negative transcriptional regulation mediated by thyroid hormone response element 144 requires binding of the multivalent factor CTCF to a novel target DNA sequence. [My Copy] The Journal of biological chemistry, Vol. 274, No. 38. (17 September 1999), pp. 27092-27098. by T. A. Awad, J. Bigler, J. E. Ulmer, et al.Y. J. Hu, J. M. Moore, M. Lutz, P. E. Neiman, S. J. Collins, R. Renkawitz, V. V. Lobanenkov, G. N. Filippova posted to ctcf thyroid-hormone thyroid-hormone-response-element tr tre tre-144 by sebastien_vigneau on 2009-06-23 20:27:14 as along with 1 group CTCF
	CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locus. [My Copy] Nature genetics, Vol. 28, No. 4. (August 2001), pp. 335-343. by G. N. Filippova, C. P. Thienes, B. H. Penn, et al.D. H. Cho, Y. J. Hu, J. M. Moore, T. R. Klesert, V. V. Lobanenkov, S. J. Tapscott posted to cag ctcf ctg dm1 repeat by sebastien_vigneau on 2009-06-23 00:45:16 as along with 1 group CTCF
	Thyroid hormone-regulated enhancer blocking: cooperation of CTCF and thyroid hormone receptor. [My Copy] The EMBO journal, Vol. 22, No. 7. (1 April 2003), pp. 1579-1587. by M. Lutz, L. J. Burke, P. LeFevre, et al.F. A. Myers, A. W. Thorne, C. Crane-Robinson, C. Bonifer, G. N. Filippova, V. Lobanenkov, R. Renkawitz posted to acetylation ctcf h4ac insulator lysosyme thyroid-hormone-response-element tre by sebastien_vigneau on 2009-06-19 19:59:43 as along with 1 group CTCF
	Physical and functional interaction between two pluripotent proteins, the Y-box DNA/RNA-binding factor, YB-1, and the multivalent zinc finger factor, CTCF. [My Copy] The Journal of biological chemistry, Vol. 275, No. 38. (22 September 2000), pp. 29915-29921. by I. V. Chernukhin, S. Shamsuddin, A. F. Robinson, et al.A. F. Carne, A. Paul, A. I. El-Kady, V. V. Lobanenkov, E. M. Klenova posted to c-myc ctcf gene-repression repression y-box yb-1 zinc-finger by sebastien_vigneau on 2009-06-18 21:16:11 as along with 1 group CTCF
	Transcriptional repression by the insulator protein CTCF involves histone deacetylases. [My Copy] Nucleic acids research, Vol. 28, No. 8. (15 April 2000), pp. 1707-1713. by M. Lutz, L. J. Burke, G. Barreto, et al.F. Goeman, H. Greb, R. Arnold, H. Schultheiss, A. Brehm, T. Kouzarides, V. Lobanenkov, R. Renkawitz posted to acetylation assymetry c-terminal ctcf deacetylase gene-repression histone-deacetylase n-terminal sin3a by sebastien_vigneau on 2009-06-18 18:52:55 as along with 1 group CTCF
	Functional phosphorylation sites in the C-terminal region of the multivalent multifunctional transcriptional factor CTCF. [My Copy] Molecular and cellular biology, Vol. 21, No. 6. (March 2001), pp. 2221-2234. by E. M. Klenova, I. V. Chernukhin, A. El-Kady, et al.R. E. Lee, E. M. Pugacheva, D. I. Loukinov, G. H. Goodwin, D. Delgado, G. N. Filippova, J. León, H. C. Morse, P. E. Neiman, V. V. Lobanenkov posted to assymetry c-terminal ck2 ctcf protein-kinase by sebastien_vigneau on 2009-06-18 17:21:05 as
	Histone modifications at human enhancers reflect global cell-type-specific gene expression. [My Copy] Nature, Vol. 459, No. 7243. (7 May 2009), pp. 108-112. by Nathaniel D. Heintzman, Gary C. Hon, R. David Hawkins, et al.Pouya Kheradpour, Alexander Stark, Lindsey F. Harp, Zhen Ye, Leonard K. Lee, Rhona K. Stuart, Christina W. Ching, Keith A. Ching, Jessica E. Antosiewicz-Bourget, Hui Liu, Xinmin Zhang, Roland D. Green, Victor V. Lobanenkov, Ron Stewart, James A. Thomson, Gregory E. Crawford, Manolis Kellis, Bing Ren posted to binding cell-type ctcf enhancer genome-wide insulator by sebastien_vigneau on 2009-03-23 14:23:48 as along with 15 people and 2 groups suizifish RyuOgawa inesdesantiago gdb djkt tonamswish t08681mn akundaje leliavski scjparker fenghezi TRHvidsten humburg frohike idonaldson Epigenetics CTCF
	Genome wide ChIP-chip analyses reveal important roles for CTCF in Drosophila genome organization. [My Copy] Developmental biology (8 January 2009) by Sheryl T T. Smith, Priyankara Wickramasinghe, Andrew Olson, et al.Dmitri Loukinov, Lan Lin, Joy Deng, Yanping Xiong, John Rux, Ravi Sachidanandam, Hao Sun, Victor Lobanenkov, Jumin Zhou posted to chip-chip ctcf insulator by sebastien_vigneau on 2009-03-03 19:05:31 as along with 1 person and 2 groups cisevol CTCF JLab
	Tumor-associated zinc finger mutations in the CTCF transcription factor selectively alter tts DNA-binding specificity. [My Copy] Cancer research, Vol. 62, No. 1. (1 January 2002), pp. 48-52. by G. N. Filippova, C. F. Qi, J. E. Ulmer, et al.J. M. Moore, M. D. Ward, Y. J. Hu, D. I. Loukinov, E. M. Pugacheva, E. M. Klenova, P. E. Grundy, A. P. Feinberg, A. M. Cleton-Jansen, E. W. Moerland, C. J. Cornelisse, H. Suzuki, A. Komiya, A. Lindblom, F. Dorion-Bonnet, P. E. Neiman, H. C. Morse, S. J. Collins, V. V. Lobanenkov posted to arf ctcf h19 igf2 myc pim1 plk tumor zinc-finger by sebastien_vigneau on 2008-11-15 00:10:30 as
	Cell growth inhibition by the multifunctional multivalent zinc-finger factor CTCF. [My Copy] Cancer research, Vol. 61, No. 16. (15 August 2001), pp. 6002-6007. by J. E. Rasko, E. M. Klenova, J. Leon, et al.G. N. Filippova, D. I. Loukinov, S. Vatolin, A. F. Robinson, Y. J. Hu, J. Ulmer, M. D. Ward, E. M. Pugacheva, P. E. Neiman, H. C. Morse, S. J. Collins, V. V. Lobanenkov posted to cell-cycle cell-growth ctcf myc p19arf by sebastien_vigneau on 2008-11-15 00:04:14 as
	Heightened expression of CTCF in breast cancer cells is associated with resistance to apoptosis. [My Copy] Cancer research, Vol. 65, No. 12. (15 June 2005), pp. 5112-5122. by F. Docquier, D. Farrar, V. D'Arcy, et al.I. Chernukhin, A. F. Robinson, D. Loukinov, S. Vatolin, S. Pack, A. Mackay, R. A. Harris, H. Dorricott, M. J. O'Hare, V. Lobanenkov, E. Klenova posted to apoptosis breast cancer ctcf proliferation sodium_butyrate by sebastien_vigneau on 2008-11-06 18:27:50 as
	Maternal depletion of CTCF reveals multiple functions during oocyte and preimplantation embryo development. [My Copy] Development (Cambridge, England) (9 July 2008) by Le-Ben B. Wan, Hua Pan, Sridhar Hannenhalli, et al.Yong Cheng, Jun Ma, Andrew Fedoriw, Victor Lobanenkov, Keith E E. Latham, Richard M M. Schultz, Marisa S S. Bartolomei posted to ctcf imprinting oocyte zygote by sebastien_vigneau on 2008-07-14 13:13:51 as along with 2 people rschulz aprickett
	The nucleotides responsible for the direct physical contact between the chromatin insulator protein CTCF and the H19 imprinting control region manifest parent of origin-specific long-distance insulation and methylation-free domains [My Copy] Genes Dev., Vol. 17, No. 5. (1 March 2003), pp. 586-590. by Vinod Pant, Piero Mariano, Chandrasekhar Kanduri, et al.Anita Mattsson, Victor Lobanenkov, Rainer Heuchel, Rolf Ohlsson posted to boris ctcf h19 nuclear-localization pairing by sebastien_vigneau on 2008-04-16 20:48:02 as along with 1 person olympos
	Expression of the CTCF-paralogous cancer-testis gene, brother of the regulator of imprinted sites (BORIS), is regulated by three alternative promoters modulated by CpG methylation and by CTCF and p53 transcription factors. [My Copy] Nucleic acids research, Vol. 35, No. 21. (2007), pp. 7372-7388. by S. Renaud, E. M. Pugacheva, M. D. Delgado, et al.R. Braunschweig, Z. Abdullaev, D. Loukinov, J. Benhattar, V. Lobanenkov posted to boris cpg ctcf methylation p53 by sebastien_vigneau on 2008-04-16 20:42:10 as
	BORIS, a novel male germ-line-specific protein associated with epigenetic reprogramming events, shares the same 11-zinc-finger domain with CTCF, the insulator protein involved in reading imprinting marks in the soma. [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 99, No. 10. (14 May 2002), pp. 6806-6811. by D. I. Loukinov, E. Pugacheva, S. Vatolin, et al.S. D. Pack, H. Moon, I. Chernukhin, P. Mannan, E. Larsson, C. Kanduri, A. A. Vostrov, H. Cui, E. L. Niemitz, J. E. Rasko, F. M. Docquier, M. Kistler, J. J. Breen, Z. Zhuang, W. W. Quitschke, R. Renkawitz, E. M. Klenova, A. P. Feinberg, R. Ohlsson, H. C. Morse, V. V. Lobanenkov posted to boris ctcf imprinting by sebastien_vigneau on 2008-04-16 20:14:38 as along with 1 person tonamswish
	Cloning and characterization of zebrafish CTCF: Developmental expression patterns, regulation of the promoter region, and evolutionary aspects of gene organization. [My Copy] Gene, Vol. 375 (21 June 2006), pp. 26-36. by E. M. Pugacheva, Y. W. Kwon, N. A. Hukriede, et al. Pack, P. T. Flanagan, J. C. Ahn, J. A. Park, K. S. Choi, K. W. Kim, D. Loukinov, I. B. Dawid, V. V. Lobanenkov posted to ctcf evolution zebrafish by sebastien_vigneau on 2008-04-16 20:12:31 as
	Characterization of the chicken CTCF genomic locus, and initial study of the cell cycle-regulated promoter of the gene. [My Copy] The Journal of biological chemistry, Vol. 273, No. 41. (9 October 1998), pp. 26571-26579. by E. M. Klenova, S. Fagerlie, G. N. Filippova, et al.L. Kretzner, G. H. Goodwin, G. Loring, P. E. Neiman, V. V. Lobanenkov posted to chicken ctcf by sebastien_vigneau on 2008-04-16 19:59:06 as
	CTCF interacts with and recruits the largest subunit of RNA polymerase II to CTCF target sites genome-wide. [My Copy] Molecular and cellular biology, Vol. 27, No. 5. (1 March 2007), pp. 1631-1648. by I. Chernukhin, S. Shamsuddin, S. Y. Kang, et al.R. Bergström, Y. W. Kwon, W. Yu, J. Whitehead, R. Mukhopadhyay, F. Docquier, D. Farrar, I. Morrison, M. Vigneron, S. Y. Wu, C. M. Chiang, D. Loukinov, V. Lobanenkov, R. Ohlsson, E. Klenova posted to assymetry c-terminal chip-chip ctcf polii by sebastien_vigneau on 2008-01-17 16:51:25 as along with 2 people and 1 group kengg clearbluespring Plantandetc
	CTCF is conserved from Drosophila to humans and confers enhancer blocking of the Fab-8 insulator [My Copy] EMBO Reports, Vol. aop, No. current. (21 January 2005) by Hanlim Moon, Galina Filippova, Dmitry Loukinov, et al.Elena Pugacheva, Qi Chen, Sheryl T. Smith, Adam Munhall, Britta Grewe, Marek Bartkuhn, Rudiger Arnold, Les J. Burke, Renate Renkawitz-Pohl, Rolf Ohlsson, Jumin Zhou, Rainer Renkawitz, Victor Lobanenkov posted to ctcf drosophila evolution fab-8 insulator by sebastien_vigneau on 2007-10-29 14:45:55 as along with 1 person JeffR100
	Dynamic association of the mammalian insulator protein CTCF with centrosomes and the midbody. [My Copy] Exp Cell Res, Vol. 294, No. 1. (10 March 2004), pp. 86-93. by R. Zhang, L. J. Burke, J. E. Rasko, V. Lobanenkov, R. Renkawitz posted to centrosome ctcf localization nucleolus by sebastien_vigneau on 2007-10-19 18:56:48 as
	Allele-specific binding of CTCF to the multipartite imprinting control region KvDMR1. [My Copy] Mol Cell Biol, Vol. 27, No. 7. (April 2007), pp. 2636-2647. by G. V. Fitzpatrick, E. M. Pugacheva, J. Y. Shin, et al.Z. Abdullaev, Y. Yang, K. Khatod, V. V. Lobanenkov, M. J. Higgins posted to icr imprinting kcnq1ot1 kvdmr1 by sebastien_vigneau on 2007-10-19 13:25:02 as
	Poly(ADP-ribosyl)ation regulates CTCF-dependent chromatin insulation [My Copy] Nat Genet, Vol. 36, No. 10. (October 2004), pp. 1105-1110. by Wenqiang Yu, Vasudeva Ginjala, Vinod Pant, et al.Igor Chernukhin, Joanne Whitehead, France Docquier, Dawn Farrar, Gholamreza Tavoosidana, Rituparna Mukhopadhyay, Chandrasekhar Kanduri, Mitsuo Oshimura, Andrew P. Feinberg, Victor Lobanenkov, Elena Klenova, Rolf Ohlsson posted to adp assymetry ctcf n-terminal nucleolus parp polyadpribosylation ribosylation by sebastien_vigneau on 2007-10-10 13:15:35 as along with 1 person olympos
	The novel BORIS + CTCF gene family is uniquely involved in the epigenetics of normal biology and cancer. [My Copy] Semin Cancer Biol, Vol. 12, No. 5. (October 2002), pp. 399-414. by E. M. Klenova, H. C. Morse, R. Ohlsson, V. V. Lobanenkov posted to boris cancer ctcf by sebastien_vigneau on 2007-09-03 22:19:05 as
	CTCF is a uniquely versatile transcription regulator linked to epigenetics and disease [My Copy] Trends in Genetics, Vol. 17, No. 9. (1 September 2001), pp. 520-527. by Rolf Ohlsson, Rainer Renkawitz, Victor Lobanenkov posted to ctcf disease epigenetics by sebastien_vigneau on 2007-08-07 14:21:56 as
	Rasgrf1 imprinting is regulated by a CTCF-dependent methylation-sensitive enhancer blocker. [My Copy] Mol Cell Biol, Vol. 25, No. 24. (December 2005), pp. 11184-11190. by B. Yoon, H. Herman, B. Hu, et al.Y. J. Park, A. Lindroth, A. Bell, A. G. West, Y. Chang, A. Stablewski, J. C. Piel, D. I. Loukinov, V. V. Lobanenkov, P. D. Soloway posted to ctcf icr imprinting rasgrf1 by sebastien_vigneau on 2007-08-07 13:53:07 as
	A differentially methylated imprinting control region within the Kcnq1 locus harbors a methylation-sensitive chromatin insulator. [My Copy] J Biol Chem, Vol. 277, No. 20. (17 May 2002), pp. 18106-18110. by C. Kanduri, G. Fitzpatrick, R. Mukhopadhyay, et al.M. Kanduri, V. Lobanenkov, M. Higgins, R. Ohlsson posted to ctcf icr imprinting kcnq1 by sebastien_vigneau on 2007-08-07 13:26:04 as
	The Binding Sites for the Chromatin Insulator Protein CTCF Map to DNA Methylation-Free Domains Genome-Wide [My Copy] Genome Res., Vol. 14, No. 8. (1 August 2004), pp. 1594-1602. by Rituparna Mukhopadhyay, Wenqiang Yu, Joanne Whitehead, et al.Junwang Xu, Magda Lezcano, Svetlana Pack, Chandrasekhar Kanduri, Meena Kanduri, Vasudeva Ginjala, Alexander Vostrov, Wolfgang Quitschke, Igor Chernukhin, Elena Klenova, Victor Lobanenkov, Rolf Ohlsson posted to chip-chip ctcf genome-wide insulator mbd2 methylation by sebastien_vigneau on 2007-07-24 13:55:46 as along with 2 people olympos clearbluespring
	Analysis of the Vertebrate Insulator Protein CTCF-Binding Sites in the Human Genome [My Copy] Cell, Vol. 128, No. 6. (23 March 2007), pp. 1231-1245. by T. Kim, Z. Abdullaev, A. Smith, et al.K. Ching, D. Loukinov, R. Green, M. Zhang, V. Lobanenkov, B. Ren posted to ctcf genome-wide insulator map by sebastien_vigneau on 2007-07-24 11:05:22 as along with 6 people lusk suizifish clearbluespring caseybrown rschulz xingxu
	Familial cases of point mutations in the XIST promoter reveal a correlation between CTCF binding and pre-emptive choices of X chromosome inactivation [My Copy] Hum Mol Genet, Vol. 14, No. 7. (Apr 2005), pp. 953-65. by Elena M. Pugacheva, Vijay K. Tiwari, Ziedulla Abdullaev, et al.Alexander A. Vostrov, Patrick T. Flanagan, Wolfgang W. Quitschke, Dmitri I. Loukinov, Rolf Ohlsson, Victor V. Lobanenkov posted to choice ctcf inactivation promoter x-chromosome xist by sebastien_vigneau on 2007-07-11 14:09:14 as
	CTCF binding at the H19 imprinting control region mediates maternally inherited higher-order chromatin conformation to restrict enhancer access to Igf2 [My Copy] Proc Natl Acad Sci U S A, Vol. 103, No. 28. (Jul 2006), pp. 10684-9. by Sreenivasulu Kurukuti, Vijay K. Tiwari, Gholamreza Tavoosidana, et al.Elena Pugacheva, Adele Murrell, Zhihu Zhao, Victor Lobanenkov, Wolf Reik, Rolf Ohlsson posted to ctcf h19 icr imprinting network by sebastien_vigneau on 2007-07-11 14:02:32 as
	Functional association of CTCF with the insulator upstream of the H19 gene is parent of origin-specific and methylation-sensitive. [My Copy] Curr Biol, Vol. 10, No. 14. (Jul 2000), pp. 853-6. by C. Kanduri, V. Pant, D. Loukinov, et al.E. Pugacheva, C. F. Qi, A. Wolffe, R. Ohlsson, V. V. Lobanenkov posted to inactivation x-chromosome by sebastien_vigneau on 2007-07-11 14:02:32 as
	CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locus. [My Copy] Nat Genet, Vol. 28, No. 4. (Aug 2001), pp. 335-43. by G. N. Filippova, C. P. Thienes, B. H. Penn, et al.D. H. Cho, Y. J. Hu, J. M. Moore, T. R. Klesert, V. V. Lobanenkov, S. J. Tapscott posted to inactivation x-chromosome by sebastien_vigneau on 2007-07-11 14:01:28 as

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x-chromosome	634
inactivation	590
ctcf	156
imprinting	102
evolution	85
methylation	77
xist	63
stemness	61
chromatin	57
h19	53
rna	50
mirna	47
transcription	46
nucleus	45
epigenetics	44
genome-wide	41
insulator	37
replication	36
tsix	35
histone	34
igf2	34
pcr	34
germline	32
network	32
bioinformatics	30
heterochromatin	30
technology	30
es	28
nucleolus	28
cancer	27
promoter	27
reprogramming	27
brain	26
icr	26
sirna	25
rnai	24
software	24
cpg	23
development	22
meiosis	22
splicing	22
oocyte	21
xci	21
drosophila	20
enhancer	20
nuclear-localization	20
review	19
sex	19
imprint	18
polycomb	18
small-rna	18
cohesin	17
expression	17
imaging	17
nuclear-organization	17
polii	17
snp	17
marsupial	16
microarray	16
antisense	15
brca1	15
esc	15
localization	15
oct4	15
recombination	15
technique	15
yy1	15
assymetry	14
c-myc	14
disease	14
dmr	14
pgc	14
chip-chip	13
mrna	13
repeat	13
sox2	13
x-inactivation	13
early-mouse-embryo	12
human	12
nuclear-envelope	12
nucleosome	12
transcription-factor	12
centromere	11
chip	11
mecp2	11
pluripotency	11
protocol	11
real-time-pcr	11
regulator	11
xic	11
3d	10
acetylation	10
dmd	10
embryo	10
loop	10
nuclear-architecture	10
polymorphism	10
boris	9
chip-seq	9
dnmt1	9
dxpas34	9
exon	9
fish	9
h3k27me3	9
hox	9
kcnq1ot1	9
klf4	9
mir	9
neuron	9
recombineering	9
translation	9
x-chromosome-inactivation	9
break	8
choice	8
chromosome	8
dicer	8
euchromatin	8
gtl2	8
intron	8
kcnq1	8
microrna	8
mitosis	8
ncrna	8
oct	8
rett	8
sequencing	8
sperm	8
territory	8
transposon	8
algorithm	7
beta-globin	7
cell-cycle	7
c-terminal	7
eed	7
genome	7
h3k4me3	7
h3k9me2	7
hp1	7
microscopy	7
mirtron	7
mutagenesis	7
pericentric	7
piwi	7
polymerase	7
reactivation	7
spermatogenesis	7
zinc-finger	7
affymetrix	6
binding-site	6
chromatin-ip	6
city	6
cre	6
differentiation	6
dlk1	6
dna	6
dna-methylation	6
dsb	6
extra-embryonic	6
h3k9	6
interaction	6
knock-out	6
kshv	6
monoallelic	6
monotreme	6
nanog	6
n-terminal	6
oct34	6
parp	6
pcna	6
peg3	6
pirna	6
probe	6
stain	6
translocation	6
y-chromosome	6
adp-ribose	5
ageing	5
argonaute	5
assay	5
binding	5
blastocyst	5
cloning	5
compartment	5
dosage	5
efficiency	5
enhancer-blocking	5
gc	5
genotyping	5
h3	5
h3k36me3	5
h3k4me2	5
high-throughput	5
multiple-probe	5
myc	5
nuclear-pore	5
nucleosome-positioning	5
p53	5
pairing	5
pcg	5
prc1	5
prc2	5
preimplantation	5
regulation	5
ribosylation	5
screen	5
society	5
sociology	5
suv39h	5
trophoblast	5
3c	4
adp-ribosylation	4
afm	4
axis	4
caenorhabditis	4
centrosome	4
communication	4
condensin	4
counting	4
database	4
exosome	4
facultative-heterochromatin	4
fgf	4
gene	4
gene-repression	4
h3k9me	4
heatmap	4
ips	4
mbd	4
methylome	4
model	4
msl	4
mutation	4
nmd	4
nucleophosmin	4
parp1	4
phosphorylation	4
platypus	4
qpcr	4
rasgrf1	4
repair	4
rest	4
rett-syndrome	4
structure	4
virus	4
xce	4
aging	3
allele-specific	3
allele-specific-expression	3
arf	3
atomic-force-microscopy	3
behavior	3
bibliography	3
boundary	3
breast	3
cdx2	3
cenp-a	3
ciliates	3
cluster	3
clustering	3
competition	3
constitutive-heterochromatin	3
ctcfl	3
ctg	3
dapi	3
duplication	3
enu	3
epiblast	3
epigenome	3
er	3
escape	3
ezh2	3
factory	3
fusion	3
gaba	3
gene-activation	3
genome-browser	3
gnas	3
grb10	3
h3k27	3
h3k27me	3
h3k9me3	3
hematopoiesis	3
herpesvirus	3
histone-code	3
hs	3
icm	3
internet	3
lacz	3
lamina	3
lana	3
lcr	3
line	3
lineage	3
lit1	3
lna	3
lysozyme	3
map	3
memory	3
minisatellite	3
motif	3
music	3
noise	3
nuclear-transfer	3
olfactory-receptor	3
pausing	3
pho	3
plutipotency	3
politics	3
proliferation	3
pseudogene	3
psychology	3
rdrp	3
rearrangement	3
remodelling	3
retrotransposon	3
ribosome	3
ring1b	3
sense	3
sequence	3
sex-determination	3
sex-ratio	3
snf2	3
sox	3
specificity	3
spermatocyte	3
spreading	3
sumo	3
tcr	3
tilling-array	3
to-pro-3	3
transcriptome	3
trans-splicing	3
tre	3
tss	3
tumor	3
word	3
xi	3
xite	3
zebrafish	3
zp3	3
zygote	3
2-cell	2
4c	2
activator	2
ago	2
ago1	2
air	2
akt	2
alignment	2
allelic	2
alpha-satellite	2
apbbeta	2
apoptosis	2
arabidopsis	2
architecture	2
assembly	2
autosome	2
bac	2
barrier	2
b-cell	2
bias	2
binding-motif	2
biological-theme	2
b-lymphocyte	2
bmp4	2
bovine	2
cdkn1c	2
centriole	2
chromatin-barrier	2
chromocenter	2
ck2	2
cmyc	2
codon-bias	2
coevolution	2
cohesion	2
cow	2
cp190	2
cpg-methylation	2
data-mining	2
degradation	2
deletion	2
division	2
dm1	2
dnmt3l	2
dosage-compensation	2
drosha	2
ebv	2
elongation	2
encode	2
endoderm	2
ensembl	2
enx1	2
epidemiology	2
epimutation	2
erk	2
fab-8	2
fertilization	2
g9a	2
gamete	2
gametogenesis	2
gene-body	2
gene-expression	2
genetics	2
gro-seq	2
h1	2
h2a	2
h2aub	2
h2ax	2
h3k4	2
h3k4me	2
hesc	2
histone-deacetylase	2
history	2
hiv	2
hla-dqa1	2
hla-drb1	2
how	2
ig	2
igf	2
igf2r	2
igh	2
immunoglobulin	2
immunology	2
inhibition	2
ink4a	2
kaiso	2
knock-down	2
lab-on-a-chip	2
lamin	2
learning	2
locked-nucleic-acid	2
long-ncrna	2
loxp	2
maize	2
major-histocompatibilit-complex	2
mar	2
matrix	2
mbd2	2
meg3	2
mh2a	2
micro-rna	2
migration	2
mir292	2
momme	2
mommed1	2
morula	2
nep1	2
nodal	2
normalization	2
nucleocytoplasmic-transport	2
nucleoporin	2
oogenesis	2
or	2
orientation	2
orientation-dependant	2
orientation-dependent	2
p19arf	2
pachytene	2
par	2
pattern	2
phenotype	2
phylogeny	2
pic	2
placenta	2
pleiohomeotic	2
plk	2
polya	2
polyadenylation	2
prc	2
pre	2
primer	2
primitive-endoderm	2
progenitor	2
protein	2
protein-kinase	2
quantitative	2
rad21	2
real-time	2
receptor	2
reparation	2
replication-origin	2
represor	2
repression	2
retinoic-acid	2
ring1a	2
risc	2
rt-pcr	2
satellite	2
screening	2
senescence	2
shadow-enhancer	2
shrna	2
silencer	2
silencing	2
sine	2
skewing	2
smc1	2
snorna	2
snrpn	2
spermatid	2
srna	2
stability	2
stabilization	2
stem	2
stem-cell	2
stress	2
substitution	2
suz12	2
swisnf	2
t-cell	2
testis	2
tf	2
therapy	2
thyroid-hormone	2
thyroid-hormone-response-element	2
tip60	2
tr	2
transcript	2
trithorax	2
trophectoderm	2
trxg	2
urbanism	2
variegation	2
x	2
xenopus	2
xl9	2
x-ray	2
yeast	2
zfp57	2
3	1
4d	1
96-well-plate	1
ablation	1
acethylation	1
acetyltransferase	1
activin	1
adhesion	1
adp	1
affinity	1
ago2	1
agouti	1
aids	1
alflatoxin	1
allelic-assay	1
alternative_splicing	1
alu	1
aml	1
amplification	1
amyloid-beta-protein-precursor	1
amyloid-precursor-protein	1
analysis	1
androgen	1
aneuploidy	1
apob	1
apolipoprotein-b	1
a-repeat	1
ascl2	1
ase	1
astrocyte	1
asymetries	1
at	1
atomic_force_microscopy	1
atp	1
atr	1
at-rich	1
attp	1
aurkb	1
aurora	1
autism	1
b23	1
bacillus	1
bag-1	1
band	1
bat3	1
batman	1
bayesian	1
bc1	1
bead-1	1
beaf	1
beat	1
beckwith-wiedemann	1
bent-dna	1
betaglobin	1
beta-satellite	1
bicoid	1
binding-motid	1
bioconductor	1
biography	1
biology	1
bionformatics	1
biophysics	1
bivalent	1
bkm	1
blimp1	1
blood-pressure	1
bmp	1
bpx	1
brc-1	1
bromodomain	1
brpf1	1
brx	1
cag	1
cajal-body	1
cajal-retzius	1
calorie-restriction	1
camp	1
cap	1
cbp	1
ccctc	1
ccf	1
cd4	1
cell	1
cell-autonomous	1
cell-cyle	1
cell-growth	1
cell-lineage	1
cell-nonautonomous	1
cell-type	1
centrality	1
centric	1
cerebelum	1
cftr	1
cg	1
chd8	1
chicken	1
chimpanzee	1
chorion	1
chp1	1
chromatid	1
chromosomal-domain	1
ciita	1
clcn4	1
cleavage	1
climate	1
clock	1
clot	1
clr4	1
cnp1	1
cns	1
coactivator	1
cobra	1
code	1
codon	1
co-expression	1
compaction	1
comparison	1
compensation	1
computer	1
connectivity	1
consensus	1
conservation	1
conserved-non-coding-sequence	1
contraction	1
control-gene	1
cooperation	1
co-regulation	1
correlation	1
cortex	1
creb	1
crm	1
crossover	1
cross-over	1
csc	1
csf2	1
ct	1
ctd	1
cyp2a13	1
cytogenetics	1
cytometry	1
cytoskeleton	1
dad1	1
damage	1
dart	1
dbhs	1
dcl3	1
deacetylase	1
decay	1
deconvolution	1
demethylase	1
dendrite	1
diabetes	1
differenciation	1
diffraction	1
directionality	1
dissection	1
dna-fish	1
dnmt	1
dnmt3b	1
dnmto	1
dominance	1
dorsal	1
dot1l	1
double-strand-break	1
downbeat	1
dsif	1
dsrna	1
dual-core-binding	1
dxz4	1
dye	1
e2f	1
e5	1
e6	1
e65	1
e7	1
e95	1
ecology	1
economy	1
editing	1
education	1
eg	1
egc	1
eif2s3	1
eif2s3x	1
electricity	1
embryoid-body	1
endonuclease	1
endoplasmic-reticulum	1
endo-sirna	1
energy	1
enhancer-blocker	1
enrichment	1
envelope	1
epi	1
epiallele	1
epigenomics	1
episome	1
epistasis	1
epistemology	1
epitope	1
epstein-barr-virus	1
erythrocyte	1
est	1
establishment	1
estrogen	1
eutheria	1
evoultion	1
exit	1
export	1
exportin-5	1
extraembryonic	1
fab	1
fact	1
false-positive	1
fate	1
fertilisation	1
fgf4	1
fibrin	1
fixation	1
flexibility	1
fluorescence	1
fmri	1
fmrp	1
foci	1
fossile	1
fractal	1
fractionation	1
fragile-x	1
fret	1
fxyd5-cox7a1	1
g1	1
g6pd	1
gain-of-function	1
galk	1
gammaherpesvirus	1
gastrulation	1
gata	1
gata4	1
gata6	1
g-banding	1
gdf-9	1
gene-cluster	1
gene-regulation	1
gene-rich	1
gene-targeting	1
genetic-circuit	1
genetic-code	1
genetic-drift	1
germ-cell	1
germinal-vesicle	1
gfap	1
gfp	1
gh4	1
giemsa	1
gli1	1
globin	1
glucocorticoid-receptor	1
gm-csf	1
gonad	1
gr	1
gradient	1
gsk3	1
h2az	1
h2bk5	1
h2s10	1
h33	1
h33k4	1
h3ac	1
h3h4	1
h3k14ac	1
h3k20me2	1
h3k20me3	1
h3k3me2	1
h3k4e3	1
h3k79	1
h3k79me	1
h3k79me2	1
h3k9ac	1
h3k9me1	1
h3t11	1
h4ac	1
h4k16	1
h4k20	1
hacns1	1
haplotype	1
hcg	1
hdac	1
health	1
heart	1
hen	1
heritability	1
heterocaryon	1
hfgf	1
hh	1
him-14	1
hips	1
histone-positioning-code	1
histone-variant	1
hmg	1
hnrnp	1
homie	1
homologous-recombination	1
hotspot	1
hprna	1
hprt	1
hs2	1
hs4	1
hssea4	1
htert	1
hub	1
huntington	1
hybridization	1
hypersensitivity	1
iab-4	1
iab4as	1
iab-8	1
iap	1
ifn-gamma	1
igf-1	1
il-13	1
il-3	1
il-4	1
il-5	1
immunoprecipitation	1
impact	1
impact-factor	1
implantation	1
in-degree	1
informatics	1
initiation	1
in-situ-hybridization	1
interferon	1
interleukin	1
interleukin-3	1
interphase	1
interview	1
intrisically-bent-dna	1
inversion	1
irak	1
ires	1
isochore	1
jarid	1
jazf1	1
jil-1	1
jljd2c	1
jmjc	1
jmjd1a	1
jmjd2c	1
k14	1
k18	1
k27me3	1
kap1	1
kaposi	1
kdm2b	1
kid	1
kinase	1
kinetic	1
klinefelter	1
kvdmr1	1
k-word	1
l1	1
lamin-b-receptor	1
laminopathy	1
lana-1	1
lana-body	1
landscape	1
lanscape	1
lap2beta	1
lbr	1
lebrasseur	1
lif	1
life-span	1
lightcycler	1
limb	1
lin28	1
line-1	1
logical-circuit	1
loi	1
long-non-coding-rna	1
loss-of-imprinting	1
lox	1
lsh	1
lung	1
lung-cancer	1
lymphocyte	1
lysosyme	1
m3g-cap	1
macaque	1
macrosatellite	1
mage-a1	1
magnetic-tweezer	1
maintenance	1
major-satellite	1
malaria	1
maldi-tof	1
malware	1
mammals	1
man	1
man1	1
mar4	1
mbd3	1
mct	1
mdm2	1
medip	1
medip-seq	1
mef	1
meg1	1
meisis	1
mest	1
metabolomics	1
methodology	1
mhc	1
microdeletion	1
microencephalopathy	1
microsatellite	1
microtubule	1
midblastula	1
mime	1
minichromosome	1
minor-satellite	1
mir-145	1
mirn	1
mknr3	1
mll	1
mobility	1
mod1	1
module	1
monocarboxylate	1
monodelphis	1
morphogen	1
morphology	1
mouse	1
moz	1
mri	1
mrna-processing	1
mrnp	1
ms	1
msh4	1
msl2	1
msuc	1
msx2	1
mucleolus	1
muscle	1
myo7a	1
myod	1
myosin	1
myst3	1
nanos	1
nanotube	1
naonog	1
nap1l2	1
ndc1	1
ndy1	1
neat1	1
neighborhood-disease	1
nelf	1
nervous-system	1
nestin	1
neurulation	1
nf1	1
nono	1
nonsense	1
nor	1
northern	1
northern-blot	1
npm2	1
nre	1
nuclear-matrix	1
nuclease	1
nucleoplasmin	1
nucleoprotein-hairpin	1
nucleosole	1
ny-eso-1	1
oct3	1
odn	1
oil	1
oleic-acid	1
oligo	1
oligodeoxynucleotide	1
olive	1
omics	1
ontogeny	1
ontology	1
openid	1
open-source	1
operion	1
opinion	1
optical-tweezer	1
orc1	1
orf	1
orf71	1
orf72	1
orf73	1
orf74	1
ortholog	1
outron	1
overhang	1
ovulation	1
p16ink4a	1
p21	1
p21cdkn1a	1
p27	1
p300	1
p54nrb	1
pairwise	1
pallium	1
paramutation	1
paraspeckle	1
parkinson	1
pathway	1
pax6	1
p-body	1
pc	1
pcbp2	1
pcl	1
pcp	1
pe	1
peg1	1
p-element	1
periimplantation	1
peri-implantation	1
periodicity	1
persistence	1
pev	1
pgk1	1
phic31	1
phol	1
pi3k	1
pi3-k	1
pim1	1
pleiohomeotic-like	1
plolii	1
pmsg	1
pna	1
poised	1
polarity	1
poliii	1
polo	1
polyadpribosylation	1
polycistronic	1
polycomblike	1
polynerase	1
polyploidy	1
polysome	1
polytene	1
pom121	1
pore	1
positional-weight-matrix	1
position-effect-variegation	1
poster	1
post-transcription	1
prdm1	1
prdm14	1
pre-mirna	1
pre-t	1
primordial-follicle	1
privacy	1
prk1	1
prmt7	1
prob	1
processing	1
profiling	1
prompt	1
prophase	1
proteomics	1
psd-95	1
psf	1
pspc1	1
ptc	1
pubmed	1
pwm	1
pwwp	1
pyramidal-neurone	1
quantitative-epigenetics	1
quest	1
r	1
rad-51	1
rad54p	1
ras	1
rasirna	1
rat	1
rb1	1
r-band	1
rbp1	1
rbpl10	1
rdr2	1
recessive	1
recessivity	1
reciprocity	1
recognition	1
recombinant	1
recruiter	1
recursive	1
regulon	1
remembering	1
remodeling	1
renin	1
replicaton	1
reproduction	1
researcherid	1
restriction	1
reticulum	1
reviw	1
rflp	1
rfx5	1
rhythm	1
rhythmic-cycle	1
rice	1
rna-binding	1
rna-dependent-rna-polymerase	1
rna-duplex	1
rnf2	1
rox	1
rpb3	1
rpb4	1
rpii	1
rpl10	1
rrna	1
rtt	1
rumpelstiltskin	1
sage	1
sarcoma	1
sca7	1
sdmr	1
segmentation	1
self-cleaving-peptide	1
separase	1
ser-2	1
ser-5	1
set1a	1
set2	1
set7	1
sex-chromosome	1
sex-ration	1
sexuality	1
sfpq	1
sg	1
signature	1
simulation	1
sin3a	1
single-cell	1
single-molecule	1
single-molecule-fluorescence-spectroscopy	1
sir2p	1
sir3p	1
sir4p	1
sirt	1
sisirna	1
sister-chromatid	1
six5	1
smad1	1
small-regulatory-rna	1
smc	1
smchd1	1
smcx	1
smg	1
smg1	1
smi	1
snrna	1
snrnp	1
sodium_butyrate	1
solexa	1
sono-seq	1
sp1	1
specke	1
s-phase	1
spinocerebellar-ataxia-type-7	1
spo-11	1
sry	1
stage	1
staging	1
stalled-polii	1
star	1
stemnes	1
stereocilia	1
stochasticity	1
strand	1
stress-granule	1
subclass	1
subpallium	1
suhw	1
superovulation	1
suv39	1
suv39h1	1
suvar	1
switch	1
sybr	1
sybr-green	1
synapse	1
synapsis	1
syp-2	1
t3	1
targeting	1
tata	1
tbp	1
tcfcp2l1	1
tcl1	1
te	1
testes	1
tethered-particle-motion	1
tetraploid	1
text-mining	1
th2	1
three-prime-expression-array	1
titration	1
tools	1
topoii	1
transcription-factory	1
transcriptomics	1
trans-effect	1
transgene	1
transitivity	1
transporter	1
travel	1
tre-144	1
triplet	1
triplex	1
trna	1
ts	1
tsx	1
turnover	1
ubiquitin	1
ubx	1
uh2a	1
untranscribed	1
upf1	1
usf	1
usp21	1
uterus	1
utx	1
valproic-acid	1
vcyclin	1
vflip	1
vgpcr	1
visualization	1
vmirna	1
vole	1
vpa	1
web20	1
werner	1
wifi	1
wilms-tumor	1
window	1
woman	1
wsb1	1
xen	1
xol	1
xse	1
yb-1	1
y-box	1
yolk-sac	1
zac1	1
zfy	1
zim1	1
zing-finger	1

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