Papers associated with blastema (and h2bc21)

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	Inversion of Sonic hedgehog action on its canonical pathway by electrical activity., Belgacem YH., Proc Natl Acad Sci U S A. March 31, 2015; 112 (13): 4140-5.
	A distinct switch in interactions of the histone H4 tail domain upon salt-dependent folding of nucleosome arrays., Pepenella S., J Biol Chem. September 26, 2014; 289 (39): 27342-27351.
	BRCA1 is a histone-H2A-specific ubiquitin ligase., Kalb R., Cell Rep. August 21, 2014; 8 (4): 999-1005.
	Prolonged in vivo imaging of Xenopus laevis., Hamilton PW., Dev Dyn. August 1, 2014; 243 (8): 1011-9.
	Transgenic Xenopus laevis for live imaging in cell and developmental biology., Takagi C., Dev Growth Differ. May 1, 2013; 55 (4): 422-33.
	Pax3 and Zic1 drive induction and differentiation of multipotent, migratory, and functional neural crest in Xenopus embryos., Milet C., Proc Natl Acad Sci U S A. April 2, 2013; 110 (14): 5528-33.
	ASH2L regulates ubiquitylation signaling to MLL: trans-regulation of H3 K4 methylation in higher eukaryotes., Wu L., Mol Cell. March 28, 2013; 49 (6): 1108-20.
	Structure of the arginine methyltransferase PRMT5-MEP50 reveals a mechanism for substrate specificity., Ho MC., PLoS One. January 1, 2013; 8 (2): e57008.
	Chromatin modification by PSC occurs at one PSC per nucleosome and does not require the acidic patch of histone H2A., Lo SM., PLoS One. January 1, 2012; 7 (10): e47162.
	Origin and segregation of cranial placodes in Xenopus laevis., Pieper M., Dev Biol. December 15, 2011; 360 (2): 257-75.
	Histone H3 tail acetylation modulates ATP-dependent remodeling through multiple mechanisms., Chatterjee N., Nucleic Acids Res. October 1, 2011; 39 (19): 8378-91.
	Crystal structure and function of human nucleoplasmin (npm2): a histone chaperone in oocytes and embryos., Platonova O., Biochemistry. September 20, 2011; 50 (37): 8078-89.
	The RING finger protein MSL2 in the MOF complex is an E3 ubiquitin ligase for H2B K34 and is involved in crosstalk with H3 K4 and K79 methylation., Wu L., Mol Cell. July 8, 2011; 43 (1): 132-44.
	Mitotic progression becomes irreversible in prometaphase and collapses when Wee1 and Cdc25 are inhibited., Potapova TA., Mol Biol Cell. April 15, 2011; 22 (8): 1191-206.
	Perturbations in nucleosome structure from heavy metal association., Mohideen K., Nucleic Acids Res. October 1, 2010; 38 (18): 6301-11.
	Structure of RCC1 chromatin factor bound to the nucleosome core particle., Makde RD., Nature. September 30, 2010; 467 (7315): 562-6.
	Oriented cell motility and division underlie early limb bud morphogenesis., Wyngaarden LA., Development. August 1, 2010; 137 (15): 2551-8.
	A random cell motility gradient downstream of FGF controls elongation of an amniote embryo., Bénazéraf B., Nature. July 8, 2010; 466 (7303): 248-52.
	Role of direct interactions between the histone H4 Tail and the H2A core in long range nucleosome contacts., Sinha D., J Biol Chem. May 28, 2010; 285 (22): 16572-81.
	Functional dissection of XDppa2/4 structural domains in Xenopus development., Siegel D., Mech Dev. December 1, 2009; 126 (11-12): 974-89.
	A mechanism for histone chaperoning activity of nucleoplasmin: thermodynamic and structural models., Taneva SG., J Mol Biol. October 23, 2009; 393 (2): 448-63.
	Histone N-terminal tails interfere with nucleosome traversal by RNA polymerase II., Ujvári A., J Biol Chem. November 21, 2008; 283 (47): 32236-43.
	A thermodynamic model for Nap1-histone interactions., Andrews AJ., J Biol Chem. November 21, 2008; 283 (47): 32412-8.
	Structure of the Drosophila nucleosome core particle highlights evolutionary constraints on the H2A-H2B histone dimer., Clapier CR., Proteins. April 1, 2008; 71 (1): 1-7.
	Developmental regulation of central spindle assembly and cytokinesis during vertebrate embryogenesis., Kieserman EK., Curr Biol. January 22, 2008; 18 (2): 116-23.
	Acetylation mimics within individual core histone tail domains indicate distinct roles in regulating the stability of higher-order chromatin structure., Wang X., Mol Cell Biol. January 1, 2008; 28 (1): 227-36.
	Site-specific binding affinities within the H2B tail domain indicate specific effects of lysine acetylation., Wang X., J Biol Chem. November 9, 2007; 282 (45): 32867-76.
	Nucleosome recognition by the Piccolo NuA4 histone acetyltransferase complex., Berndsen CE., Biochemistry. February 27, 2007; 46 (8): 2091-9.
	Formation of the ascidian epidermal sensory neurons: insights into the origin of the chordate peripheral nervous system., Pasini A., PLoS Biol. July 1, 2006; 4 (7): e225.
	The NH2 tail of the novel histone variant H2BFWT exhibits properties distinct from conventional H2B with respect to the assembly of mitotic chromosomes., Boulard M., Mol Cell Biol. February 1, 2006; 26 (4): 1518-26.
	The histone fold subunits of Drosophila CHRAC facilitate nucleosome sliding through dynamic DNA interactions., Hartlepp KF., Mol Cell Biol. November 1, 2005; 25 (22): 9886-96.
	The core histone N-terminal tail domains function independently and additively during salt-dependent oligomerization of nucleosomal arrays., Gordon F., J Biol Chem. October 7, 2005; 280 (40): 33701-6.
	Alteration of the nucleosomal DNA path in the crystal structure of a human nucleosome core particle., Tsunaka Y., Nucleic Acids Res. June 10, 2005; 33 (10): 3424-34.
	A Xenopus tribbles orthologue is required for the progression of mitosis and for development of the nervous system., Saka Y., Dev Biol. September 15, 2004; 273 (2): 210-25.
	Intra- and inter-nucleosomal protein-DNA interactions of the core histone tail domains in a model system., Zheng C., J Biol Chem. June 27, 2003; 278 (26): 24217-24.
	Direct association of p300 with unmodified H3 and H4 N termini modulates p300-dependent acetylation and transcription of nucleosomal templates., An W., J Biol Chem. January 17, 2003; 278 (3): 1504-10.
	The N-terminal tails of the H2A-H2B histones affect dimer structure and stability., Placek BJ., Biochemistry. December 17, 2002; 41 (50): 14960-8.
	The N-terminus of histone H2B, but not that of histone H3 or its phosphorylation, is essential for chromosome condensation., de la Barre AE., EMBO J. November 15, 2001; 20 (22): 6383-93.
	The H3-H4 N-terminal tail domains are the primary mediators of transcription factor IIIA access to 5S DNA within a nucleosome., Vitolo JM., Mol Cell Biol. March 1, 2000; 20 (6): 2167-75.
	hSWI/SNF disrupts interactions between the H2A N-terminal tail and nucleosomal DNA., Lee KM., Biochemistry. June 29, 1999; 38 (26): 8423-9.

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