Double duty: ZMYND8 in the DNA damage response and cancer.

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Double duty: ZMYND8 in the DNA damage response and cancer.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Double duty: ZMYND8 in the DNA damage response and cancer.

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Double duty: ZMYND8 in the DNA damage response and cancer.

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Double duty: ZMYND8 in the DNA damage response and cancer.

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Double duty: ZMYND8 in the DNA damage response and cancer.

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Double duty: ZMYND8 in the DNA damage response and cancer.

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Double duty: ZMYND8 in the DNA damage response and cancer.

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P1476

Double duty: ZMYND8 in the DNA damage response and cancer.

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P2093

Fade Gong

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Regulation of DNA-damage responses and cell-cycle progression by the chromatin remodelling factor CHD4

MDC1 directly binds phosphorylated histone H2AX to regulate cellular responses to DNA double-strand breaks

Selective inhibition of BET bromodomains

Histone recognition and large-scale structural analysis of the human bromodomain family

ATM-dependent chromatin changes silence transcription in cis to DNA double-strand breaks

The DNA-damage response in human biology and disease

Dynamics of DNA damage response proteins at DNA breaks: a focus on protein modifications

Structural basis for the methylation state-specific recognition of histone H4-K20 by 53BP1 and Crb2 in DNA repair

Set9, a novel histone H3 methyltransferase that facilitates transcription by precluding histone tail modifications required for heterochromatin formation.

Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukaemia

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414-420

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scholarly article

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10.1080/15384101.2017.1376150

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Kyle M Miller

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2018-02-02T00:00:00Z

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29393731

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5927707

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