Papers associated with h2bc21

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	Purification of yeast histones competent for nucleosome assembly in vitro., Fukuma M, Hiraoka Y, Sakurai H, Fukasawa T., Yeast. March 1, 1994; 10 (3): 319-31.
	A role for histones H2A/H2B in chromatin folding and transcriptional repression., Hansen JC, Wolffe AP., Proc Natl Acad Sci U S A. March 15, 1994; 91 (6): 2339-43.
	Remodeling of sperm chromatin induced in egg extracts of amphibians., Katagiri C, Ohsumi K., Int J Dev Biol. June 1, 1994; 38 (2): 209-16.
	Contacts of the globular domain of histone H5 and core histones with DNA in a "chromatosome"., Hayes JJ, Pruss D, Wolffe AP., Proc Natl Acad Sci U S A. August 2, 1994; 91 (16): 7817-21.
	High mobility group proteins 14 and 17 can space nucleosomal particles deficient in histones H2A and H2B creating a template that is transcriptionally active., Tremethick DJ., J Biol Chem. November 11, 1994; 269 (45): 28436-42.
	Oncogenic ras stimulates a 96-kDa histone H2b kinase activity in activated Xenopus egg extracts. Correlation with the suppression of p34cdc2 kinase., Chen CT, Pan BT., J Biol Chem. November 11, 1994; 269 (45): 28034-43.
	Interaction of the CCAAT displacement protein with shared regulatory elements required for transcription of paired histone genes., el-Hodiri HM, Perry M., Mol Cell Biol. July 1, 1995; 15 (7): 3587-96.
	Isolation of Xenopus laevis TFIID subunit p22 reveals two distinct structural regions., Hasegawa S, Choi BI, Horikoshi M., Gene. March 9, 1996; 169 (2): 285-6.
	High mobility group protein 14 and 17 can prevent the close packing of nucleosomes by increasing the strength of protein contacts in the linker DNA., Tremethick DJ, Hyman L., J Biol Chem. May 17, 1996; 271 (20): 12009-16.
	The five cleavage-stage (CS) histones of the sea urchin are encoded by a maternally expressed family of replacement histone genes: functional equivalence of the CS H1 and frog H1M (B4) proteins., Mandl B, Brandt WF, Superti-Furga G, Graninger PG, Birnstiel ML, Busslinger M., Mol Cell Biol. March 1, 1997; 17 (3): 1189-200.
	The 96 kDa protein kinase activated by oncogenic Ras in Xenopus egg extracts is also activated by constitutively active Mek: activation requires serine/threonine phosphorylation., Pan BT, Zhang Y, Brott B, Chen DH., Oncogene. April 10, 1997; 14 (14): 1653-60.
	Isolation and amino acid sequence analysis reveal an ancient evolutionary origin of the cleavage stage (CS) histones of the sea urchin., Brandt WF, Schwager SU, Rodrigues JA, Busslinger M., Eur J Biochem. August 1, 1997; 247 (3): 784-91.
	Characterization of nucleosome core particles containing histone proteins made in bacteria., Luger K, Rechsteiner TJ, Flaus AJ, Waye MM, Richmond TJ., J Mol Biol. September 26, 1997; 272 (3): 301-11.
	Nucleosome binding by the polymerase I transactivator upstream binding factor displaces linker histone H1., Kermekchiev M, Workman JL, Pikaard CS., Mol Cell Biol. October 1, 1997; 17 (10): 5833-42.
	Sin mutations of histone H3: influence on nucleosome core structure and function., Kurumizaka H, Wolffe AP., Mol Cell Biol. December 1, 1997; 17 (12): 6953-69.
	Asymmetric linker histone association directs the asymmetric rearrangement of core histone interactions in a positioned nucleosome containing a thyroid hormone response element., Guschin D, Chandler S, Wolffe AP., Biochemistry. June 16, 1998; 37 (24): 8629-36.
	Characterization of p96h2bk: immunoreaction with an anti-Erk(extracellular-signal-regulated kinase) peptide antibody and activity in Xenopus oocytes and eggs., Chen DH, Chen CT, Zhang Y, Liu MA, Campos-Gonzalez R, Pan BT., Biochem J. October 1, 1998; 335 ( Pt 1) 43-50.
	Nuclear reassembly in vitro is independent of nucleosome/chromatin assembly., Jiang Z, Zhang B, Zhai Z., Sci China C Life Sci. October 1, 1998; 41 (5): 512-9.
	hSWI/SNF disrupts interactions between the H2A N-terminal tail and nucleosomal DNA., Lee KM, Sif S, Kingston RE, Hayes JJ., Biochemistry. June 29, 1999; 38 (26): 8423-9.
	NF-Y associates with H3-H4 tetramers and octamers by multiple mechanisms., Caretti G, Motta MC, Mantovani R., Mol Cell Biol. December 1, 1999; 19 (12): 8591-603.
	Translation of maternal TATA-binding protein mRNA potentiates basal but not activated transcription in Xenopus embryos at the midblastula transition., Veenstra GJ, Destrée OH, Wolffe AP., Mol Cell Biol. December 1, 1999; 19 (12): 7972-82.
	The H3-H4 N-terminal tail domains are the primary mediators of transcription factor IIIA access to 5S DNA within a nucleosome., Vitolo JM, Thiriet C, Hayes JJ., Mol Cell Biol. March 1, 2000; 20 (6): 2167-75.
	Nuclear transport of histone 2b in mammalian cells is signal- and energy-dependent and different from the importin alpha/beta-mediated process., Langer T., Histochem Cell Biol. June 1, 2000; 113 (6): 455-65.
	Core histones of the amitochondriate protist, Giardia lamblia., Wu G, McArthur AG, Fiser A, Sali A, Sogin ML, Mllerm M., Mol Biol Evol. August 1, 2000; 17 (8): 1156-63.
	Crystal structures of recombinant histones HMfA and HMfB from the hyperthermophilic archaeon Methanothermus fervidus., Decanniere K, Babu AM, Sandman K, Reeve JN, Heinemann U., J Mol Biol. October 13, 2000; 303 (1): 35-47.
	Crystal structure of a nucleosome core particle containing the variant histone H2A.Z., Suto RK, Clarkson MJ, Tremethick DJ, Luger K., Nat Struct Biol. December 1, 2000; 7 (12): 1121-4.
	Reconstitution of licensed replication origins on Xenopus sperm nuclei using purified proteins., Gillespie PJ, Li A, Blow JJ., BMC Biochem. January 1, 2001; 2 15.
	Chromatin docking and exchange activity enhancement of RCC1 by histones H2A and H2B., Nemergut ME, Mizzen CA, Stukenberg T, Allis CD, Macara IG., Science. May 25, 2001; 292 (5521): 1540-3.
	Crystal structure of negative cofactor 2 recognizing the TBP-DNA transcription complex., Kamada K, Shu F, Chen H, Malik S, Stelzer G, Roeder RG, Meisterernst M, Burley SK., Cell. July 13, 2001; 106 (1): 71-81.
	Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen., Phiel CJ, Zhang F, Huang EY, Guenther MG, Lazar MA, Klein PS., J Biol Chem. September 28, 2001; 276 (39): 36734-41.
	The N-terminus of histone H2B, but not that of histone H3 or its phosphorylation, is essential for chromosome condensation., de la Barre AE, Angelov D, Molla A, Dimitrov S., EMBO J. November 15, 2001; 20 (22): 6383-93.
	A novel p21-activated kinase binds the actin and microtubule networks and induces microtubule stabilization., Cau J, Faure S, Comps M, Delsert C, Morin N., J Cell Biol. December 10, 2001; 155 (6): 1029-42.
	Nucleosome remodeling by the human SWI/SNF complex requires transient global disruption of histone-DNA interactions., Aoyagi S, Narlikar G, Zheng C, Sif S, Kingston RE, Hayes JJ., Mol Cell Biol. June 1, 2002; 22 (11): 3653-62.
	A role for G1/S cyclin-dependent protein kinases in the apoptotic response to ionizing radiation., Finkielstein CV, Chen LG, Maller JL., J Biol Chem. October 11, 2002; 277 (41): 38476-85.
	Roles of aurora-A kinase in mitotic entry and G2 checkpoint in mammalian cells., Marumoto T, Hirota T, Morisaki T, Kunitoku N, Zhang D, Ichikawa Y, Sasayama T, Kuninaka S, Mimori T, Tamaki N, Kimura M, Okano Y, Saya H., Genes Cells. November 1, 2002; 7 (11): 1173-82.
	The N-terminal tails of the H2A-H2B histones affect dimer structure and stability., Placek BJ, Gloss LM., Biochemistry. December 17, 2002; 41 (50): 14960-8.
	The effect of salts on the stability of the H2A-H2B histone dimer., Gloss LM, Placek BJ., Biochemistry. December 17, 2002; 41 (50): 14951-9.
	Direct association of p300 with unmodified H3 and H4 N termini modulates p300-dependent acetylation and transcription of nucleosomal templates., An W, Roeder RG., J Biol Chem. January 17, 2003; 278 (3): 1504-10.
	A mechanism of coupling RCC1 mobility to RanGTP production on the chromatin in vivo., Li HY, Wirtz D, Zheng Y., J Cell Biol. March 3, 2003; 160 (5): 635-44.
	Intra- and inter-nucleosomal protein-DNA interactions of the core histone tail domains in a model system., Zheng C, Hayes JJ., J Biol Chem. June 27, 2003; 278 (26): 24217-24.
	Interaction of nucleoplasmin with core histones., Arnan C, Saperas N, Prieto C, Chiva M, Ausió J., J Biol Chem. August 15, 2003; 278 (33): 31319-24.
	Facile synthesis of site-specifically acetylated and methylated histone proteins: reagents for evaluation of the histone code hypothesis., He S, Bauman D, Davis JS, Loyola A, Nishioka K, Gronlund JL, Reinberg D, Meng F, Kelleher N, McCafferty DG., Proc Natl Acad Sci U S A. October 14, 2003; 100 (21): 12033-8.
	Preferential binding of the histone (H3-H4)2 tetramer by NAP1 is mediated by the amino-terminal histone tails., McBryant SJ, Park YJ, Abernathy SM, Laybourn PJ, Nyborg JK, Luger K., J Biol Chem. November 7, 2003; 278 (45): 44574-83.
	Histone H2A/H2B dimer exchange by ATP-dependent chromatin remodeling activities., Bruno M, Flaus A, Stockdale C, Rencurel C, Ferreira H, Owen-Hughes T., Mol Cell. December 1, 2003; 12 (6): 1599-606.
	A Xenopus tribbles orthologue is required for the progression of mitosis and for development of the nervous system., Saka Y, Smith JC., Dev Biol. September 15, 2004; 273 (2): 210-25.
	SWI/SNF remodeling and p300-dependent transcription of histone variant H2ABbd nucleosomal arrays., Angelov D, Verdel A, An W, Bondarenko V, Hans F, Doyen CM, Studitsky VM, Hamiche A, Roeder RG, Bouvet P, Dimitrov S., EMBO J. October 1, 2004; 23 (19): 3815-24.
	The structure and function of Xenopus NO38-core, a histone chaperone in the nucleolus., Namboodiri VM, Akey IV, Schmidt-Zachmann MS, Head JF, Akey CW., Structure. December 1, 2004; 12 (12): 2149-60.
	The spindle assembly checkpoint is not essential for CSF arrest of mouse oocytes., Tsurumi C, Hoffmann S, Geley S, Graeser R, Polanski Z., J Cell Biol. December 20, 2004; 167 (6): 1037-50.
	The H2A.Z/H2B dimer is unstable compared to the dimer containing the major H2A isoform., Placek BJ, Harrison LN, Villers BM, Gloss LM., Protein Sci. February 1, 2005; 14 (2): 514-22.
	The hydrophobicity of the H3 histone fold differs from the hydrophobicity of the other three folds., Silverman BD., J Mol Evol. March 1, 2005; 60 (3): 354-64.

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