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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.