Papers associated with tail (and h4c4)

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	FoxD1 protein interacts with Wnt and BMP signaling to differentially pattern mesoderm and neural tissue., Polevoy H., Int J Dev Biol. January 1, 2017; 61 (3-4-5): 293-302.
	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.
	Characterization of Xenopus tissue inhibitor of metalloproteinases-2: a role in regulating matrix metalloproteinase activity during development., Fu L., PLoS One. January 1, 2012; 7 (5): e36707.
	EBF factors drive expression of multiple classes of target genes governing neuronal development., Green YS., Neural Dev. April 30, 2011; 6 19.
	HDAC activity is required during Xenopus tail regeneration., Tseng AS., PLoS One. January 1, 2011; 6 (10): e26382.
	Nucleosome interactions and stability in an ordered nucleosome array model system., Blacketer MJ., J Biol Chem. November 5, 2010; 285 (45): 34597-607.
	Structure of RCC1 chromatin factor bound to the nucleosome core particle., Makde RD., Nature. September 30, 2010; 467 (7315): 562-6.
	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.
	The Gcn5 bromodomain of the SAGA complex facilitates cooperative and cross-tail acetylation of nucleosomes., Li S., J Biol Chem. April 3, 2009; 284 (14): 9411-7.
	Analysis of histones in Xenopus laevis. II. mass spectrometry reveals an index of cell type-specific modifications on H3 and H4., Nicklay JJ., J Biol Chem. January 9, 2009; 284 (2): 1075-85.
	A role of D domain-related proteins in differentiation and migration of embryonic cells in Xenopus laevis., Shibata T., Mech Dev. January 1, 2008; 125 (3-4): 284-98.
	Structural basis for the histone chaperone activity of Asf1., English CM., Cell. November 3, 2006; 127 (3): 495-508.
	Chromatin fiber folding: requirement for the histone H4 N-terminal tail., Dorigo B., J Mol Biol. March 14, 2003; 327 (1): 85-96.
	foxD5a, a Xenopus winged helix gene, maintains an immature neural ectoderm via transcriptional repression that is dependent on the C-terminal domain., Sullivan SA., Dev Biol. April 15, 2001; 232 (2): 439-57.
	The histone H4 acetyltransferase MOF uses a C2HC zinc finger for substrate recognition., Akhtar A., EMBO Rep. February 1, 2001; 2 (2): 113-8.
	Critical role for the histone H4 N terminus in nucleosome remodeling by ISWI., Clapier CR., Mol Cell Biol. February 1, 2001; 21 (3): 875-83.
	The pitx2 homeobox protein is required early for endoderm formation and nodal signaling. ., Faucourt M., Dev Biol. January 15, 2001; 229 (2): 287-306.
	Functional analysis of the SIN3-histone deacetylase RPD3-RbAp48-histone H4 connection in the Xenopus oocyte., Vermaak D., Mol Cell Biol. September 1, 1999; 19 (9): 5847-60.
	Xenopus Zic-related-1 and Sox-2, two factors induced by chordin, have distinct activities in the initiation of neural induction., Mizuseki K., Development. February 1, 1998; 125 (4): 579-87.
	A role for Xenopus Gli-type zinc finger proteins in the early embryonic patterning of mesoderm and neuroectoderm., Marine JC., Mech Dev. May 1, 1997; 63 (2): 211-25.
	Anterior neurectoderm is progressively induced during gastrulation: the role of the Xenopus homeobox gene orthodenticle., Blitz IL., Development. April 1, 1995; 121 (4): 993-1004.

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