Papers associated with tail region (and h2bc21)

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	Caged Dexamethasone to Photo-control the Development of Embryos through Activation of the Glucocorticoid Receptor., Mandal M., Chemistry. February 13, 2024; e202400579.
	Ash2l, an obligatory component of H3K4 methylation complexes, regulates neural crest development., Mohammadparast S., Dev Biol. December 1, 2022; 492 14-24.
	FGF-mediated establishment of left-right asymmetry requires Rab7 function in the dorsal mesoderm in Xenopus., Kreis J., Front Cell Dev Biol. January 1, 2022; 10 981762.
	Binding of regulatory proteins to nucleosomes is modulated by dynamic histone tails., Peng Y., Nat Commun. September 6, 2021; 12 (1): 5280.
	Rab7 is required for mesoderm patterning and gastrulation in Xenopus., Kreis J., Biol Open. July 15, 2021; 10 (7):
	Furry is required for cell movements during gastrulation and functionally interacts with NDR1., Cervino AS., Sci Rep. March 23, 2021; 11 (1): 6607.
	Nucleosome Core Particles Lacking H2B or H3 Tails Are Altered Structurally and Have Differential Base Excision Repair Fingerprints., Caffrey PJ., Biochemistry. January 26, 2021; 60 (3): 210-218.
	JARID2 and AEBP2 regulate PRC2 in the presence of H2AK119ub1 and other histone modifications., Kasinath V., Science. January 22, 2021; 371 (6527):
	Structural basis for PRC2 decoding of active histone methylation marks H3K36me2/3., Finogenova K., Elife. November 19, 2020; 9
	Nucleosome-CHD4 chromatin remodeler structure maps human disease mutations., Farnung L., Elife. June 16, 2020; 9
	Structure of SWI/SNF chromatin remodeller RSC bound to a nucleosome., Wagner FR., Nature. March 1, 2020; 579 (7799): 448-451.
	Dynamics of the nucleosomal histone H3 N-terminal tail revealed by high precision single-molecule FRET., Lehmann K., Nucleic Acids Res. February 20, 2020; 48 (3): 1551-1571.
	Mechanism of Cross-talk between H2B Ubiquitination and H3 Methylation by Dot1L., Worden EJ., Cell. March 7, 2019; 176 (6): 1490-1501.e12.
	The structural basis of human Spt16 N-terminal domain interaction with histone (H3-H4)2 tetramer., Jiang H., Biochem Biophys Res Commun. January 15, 2019; 508 (3): 864-870.
	Structure of the chromatin remodelling enzyme Chd1 bound to a ubiquitinylated nucleosome., Sundaramoorthy R., Elife. August 6, 2018; 7
	NMDA Receptor Signaling Is Important for Neural Tube Formation and for Preventing Antiepileptic Drug-Induced Neural Tube Defects., Sequerra EB., J Neurosci. May 16, 2018; 38 (20): 4762-4773.
	An interaction between myosin-10 and the cell cycle regulator Wee1 links spindle dynamics to mitotic progression in epithelia., Sandquist JC., J Cell Biol. March 5, 2018; 217 (3): 849-859.
	Dynamic intramolecular regulation of the histone chaperone nucleoplasmin controls histone binding and release., Warren C., Nat Commun. December 20, 2017; 8 (1): 2215.
	PFKFB4 control of AKT signaling is essential for premigratory and migratory neural crest formation., Figueiredo AL., Development. November 15, 2017; 144 (22): 4183-4194.
	Smarcal1-Mediated Fork Reversal Triggers Mre11-Dependent Degradation of Nascent DNA in the Absence of Brca2 and Stable Rad51 Nucleofilaments., Kolinjivadi AM., Mol Cell. September 7, 2017; 67 (5): 867-881.e7.
	The Chd1 chromatin remodeler shifts hexasomes unidirectionally., Levendosky RF., Elife. December 29, 2016; 5
	A Quantitative Characterization of Nucleoplasmin/Histone Complexes Reveals Chaperone Versatility., Fernández-Rivero N., Sci Rep. August 25, 2016; 6 32114.
	The Influence of Ionic Environment and Histone Tails on Columnar Order of Nucleosome Core Particles., Berezhnoy NV., Biophys J. April 26, 2016; 110 (8): 1720-1731.
	T-type Calcium Channel Regulation of Neural Tube Closure and EphrinA/EPHA Expression., Abdul-Wajid S., Cell Rep. October 27, 2015; 13 (4): 829-839.
	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.
	Transgenic Xenopus laevis for live imaging in cell and developmental biology., Takagi C., Dev Growth Differ. May 1, 2013; 55 (4): 422-33.
	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.
	Eps15R is required for bone morphogenetic protein signalling and differentially compartmentalizes with Smad proteins., Callery EM., Open Biol. April 1, 2012; 2 (4): 120060.
	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.
	Caldesmon regulates actin dynamics to influence cranial neural crest migration in Xenopus., Nie S., Mol Biol Cell. September 1, 2011; 22 (18): 3355-65.
	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.
	Unfertilized Xenopus eggs die by Bad-dependent apoptosis under the control of Cdk1 and JNK., Du Pasquier D., PLoS One. January 1, 2011; 6 (8): e23672.
	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.

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