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MacroH2A, a core histone containing a large nonhistone region.
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SWI/SNF remodeling and p300-dependent transcription of histone variant H2ABbd nucleosomal arrays.
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macroH2A1 histone variants are depleted on active genes but concentrated on the inactive X chromosome.
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Identification of higher-order functional domains in the human ENCODE regions.
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The DNA binding and catalytic domains of poly(ADP-ribose) polymerase 1 cooperate in the regulation of chromatin structure and transcription.
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H2A.Z: view from the top.
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macroH2A1-dependent silencing of endogenous murine leukemia viruses.
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MACROH2A2, a new member of the MARCOH2A core histone family.
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A short pseudoautosomal region in laboratory mice.
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The essential histone variant H2A.Z regulates the equilibrium between different chromatin conformational states.
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Histone H2A variants H2AX and H2AZ.
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Conserved histone variant H2A.Z protects euchromatin from the ectopic spread of silent heterochromatin.
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H2A.Z has a function reminiscent of an activator required for preferential binding to intergenic DNA.
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Phylogenomics of the nucleosome.
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Histone macroH2A1.2 relocates to the inactive X chromosome after initiation and propagation of X-inactivation.
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Widespread aneuploidy revealed by DNA microarray expression profiling.
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Histone H2A.Z regulats transcription and is partially redundant with nucleosome remodeling complexes.
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Crystal structure of a nucleosome core particle containing the variant histone H2A.Z.
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Higher concentrations of histone macroH2A in the Barr body are correlated with higher nucleosome density.
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Histone variant H2ABbd confers lower stability to the nucleosome.
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RNA interference demonstrates a novel role for H2A.Z in chromosome segregation.
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A histone variant, Htz1p, and a Sir1p-like protein, Esc2p, mediate silencing at HMR.
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Nucleosomes containing the histone variant H2A.Bbd organize only 118 base pairs of DNA.
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Histone macroH2A1 is concentrated in the inactive X chromosome of female mammals.
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