Robert Edward Kingston, Ph.D.
Professor of Genetics, Harvard Medical School
Chief Department of Molecular Biology, Massachusetts General Hospital
Native and recombinant polycomb group complexes establish a selective block to template accessibility to repress transcription in vitro.
Histone methyltransferase activity of a Drosophila Polycomb group repressor complex.
Authors: Authors: Müller J, Hart CM, Francis NJ, Vargas ML, Sengupta A, Wild B, Miller EL, O'Connor MB, Kingston RE, Simon JA.
Cell
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Cell
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The core of the polycomb repressive complex is compositionally and functionally conserved in flies and humans.
Authors: Authors: Levine SS, Weiss A, Erdjument-Bromage H, Shao Z, Tempst P, Kingston RE.
Mol Cell Biol
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Mol Cell Biol
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Nucleosome remodeling by the human SWI/SNF complex requires transient global disruption of histone-DNA interactions.
Authors: Authors: Aoyagi S, Narlikar G, Zheng C, Sif S, Kingston RE, Hayes JJ.
Mol Cell Biol
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Mol Cell Biol
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Cooperation between complexes that regulate chromatin structure and transcription.
Effect of delays in primary care referral on survival of women with epithelial ovarian cancer: retrospective audit.
Authors: Authors: Kirwan JM, Tincello DG, Herod JJ, Frost O, Kingston RE.
BMJ
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BMJ
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Specifying transcription.
Direct imaging of human SWI/SNF-remodeled mono- and polynucleosomes by atomic force microscopy employing carbon nanotube tips.
Authors: Authors: Schnitzler GR, Cheung CL, Hafner JH, Saurin AJ, Kingston RE, Lieber CM.
Mol Cell Biol
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Mol Cell Biol
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Generation and interconversion of multiple distinct nucleosomal states as a mechanism for catalyzing chromatin fluidity.
Functional differences between the human ATP-dependent nucleosome remodeling proteins BRG1 and SNF2H.