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The highly conserved N-terminal domains of histones H3 and H4 are required for normal cell cycle progression.

Data up to Jan 2025

Published1991
Citations47
References35

Total Citations Per Year

Abstract

References (35)

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1988 • 441 citations

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1987 • 164 citations

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1990 • 133 citations

Nucleosome linking number change controlled by acetylation of histones H3 and H4.

1990 • 132 citations

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1988 • 123 citations

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1978 • 120 citations

Localization of the sites along nucleosome DNA which interact with NH2-terminal histone regions.

1977 • 119 citations

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1990 • 118 citations

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1990 • 108 citations

Yeast histone H2A and H2B amino termini have interchangeable functions

1986 • 88 citations

Yeast H3 and H4 histone messenger RNAs are transcribed from two non-allelic gene sets

1983 • 86 citations

Foot-and-mouth disease virus protease 3C inhibits cellular transcription and mediates cleavage of histone H3

1990 • 80 citations

Chromatin core particle unfolding induced by tryptic cleavage of histones

1977 • 75 citations

Yeast histone H2B containing large amino terminus deletions can function in vivo

1983 • 73 citations

Isolation and characterization of acetylated histones H3 and H4 and their assembly into nucleosomes.

1990 • 71 citations

Histone H3 and H4 gene deletions in Saccharomyces cerevisiae.

1988 • 52 citations

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The highly conserved N-terminal domains of histones H3 and H4 are required for normal… (1991) – Molecular and Cellular Biology | Metascience Observatory Explorer