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Endocrine Disrupting Chemicals Targeting Estrogen Receptor Signaling: Identification and Mechanisms of Action

Chemical research in toxicology, 2011-01, Vol.24 (1), p.6-19

2011

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The Taf14 YEATS domain is a reader of histone crotonylation

Nature chemical biology, 2016-06, Vol.12 (6), p.396

2016

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Selectively targeting estrogen receptors for cancer treatment

Advanced drug delivery reviews, 2010-10, Vol.62 (13), p.1265-1276

2010

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An Interactive Database for the Assessment of Histone Antibody Specificity

Molecular cell, 2015-08, Vol.59 (3), p.502-511

2015

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Product Binding Enforces the Genomic Specificity of a Yeast Polycomb Repressive Complex

Cell, 2015-01, Vol.160 (1-2), p.204-218

2015

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HDAC inhibition results in widespread alteration of the histone acetylation landscape and BRD4 targeting to gene bodies

Cell reports (Cambridge), 2021-01, Vol.34 (3), p.108638-108638, Article 108638

2021

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Histone peptide microarray screen of chromo and Tudor domains defines new histone lysine methylation interactions

Epigenetics & chromatin, 2017-03, Vol.10 (1), p.12-12, Article 12

2017

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Generation of stable reporter breast cancer cell lines for the identification of ER subtype selective ligands

Biochemical pharmacology, 2011-12, Vol.82 (12), p.1940-1949

2011

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The essential role of acetyllysine binding by the YEATS domain in transcriptional regulation

Transcription, 2016-01, Vol.7 (1), p.14-20

2016

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Differential action of monohydroxylated polycyclic aromatic hydrocarbons with estrogen receptors α and β

Toxicological sciences, 2013-04, Vol.132 (2), p.359-367

2013

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Yeast-based screening of cancer mutations in the DNA damage response protein Mre11 demonstrates importance of conserved capping domain residues

Molecular biology reports, 2021-05, Vol.48 (5), p.4107-4119

2021

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Multivalent Histone and DNA Engagement by a PHD/BRD/PWWP Triple Reader Cassette Recruits ZMYND8 to K14ac-Rich Chromatin

Cell reports (Cambridge), 2016-12, Vol.17 (10), p.2724-2737

2016

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Research Resource: Global Identification of Estrogen Receptor β Target Genes in Triple Negative Breast Cancer Cells

Molecular endocrinology (Baltimore, Md.), 2013-10, Vol.27 (10), p.1762-1775

2013

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PBRM1 bromodomains variably influence nucleosome interactions and cellular function

The Journal of biological chemistry, 2018-08, Vol.293 (35), p.13592-13603

2018

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Association of Taf14 with acetylated histone H3 directs gene transcription and the DNA damage response

Genes & development, 2015-09, Vol.29 (17), p.1795-1800

2015

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A Student-Focused Lab Module To Investigate Single-Nucleotide Polymorphisms of Common Heritable Traits

Journal of microbiology & biology education, 2020-11, Vol.21 (3)

2020

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A course‐based undergraduate research experience investigating p300 bromodomain mutations

Biochemistry and molecular biology education, 2016-01, Vol.44 (1), p.68-74

2016

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Chromatin biochemistry enters the next generation of code 'seq-ing'

Nature methods, 2014-08, Vol.11 (8), p.799

2014

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Prognostic significance of full-length estrogen receptor beta expression in stage I-III triple negative breast cancer

American journal of translational research, 2015-01, Vol.7 (7), p.1246-1259

2015

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Cancer mutations inhibit the coactivator activity of p300 core

The FASEB journal, 2020-04, Vol.34 (S1), p.1-1

2020

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A Student-Focused Lab Module To Investigate Single-Nucleotide Polymorphisms of Common Heritable Traits xref ref-type="fn" rid="fn1-jmbe-21-70">† /xref

Journal of microbiology & biology education, 2020-01, Vol.21 (3)

2020

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Using S. cerevisiae to screen cancer mutations in the DNA damage response pathway

The FASEB journal, 2020-04, Vol.34 (S1), p.1-1

2020

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Selectively targeting estrogen receptors for cancer treatment: Development of Novel Therapeutic Strategy by Regulating the Nuclear Hormone Receptors

Advanced drug delivery reviews, 2010, Vol.62 (13), p.1265-1276

2010

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Understanding the role of estrogen receptor beta in triple negative breast cancers

Shanle, Erin K

2013

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Endocrine Disrupting Chemicals Targeting Estrogen Receptor Signaling: Identification and Mechanisms of Action

The Taf14 YEATS domain is a reader of histone crotonylation

Selectively targeting estrogen receptors for cancer treatment

An Interactive Database for the Assessment of Histone Antibody Specificity

Product Binding Enforces the Genomic Specificity of a Yeast Polycomb Repressive Complex

HDAC inhibition results in widespread alteration of the histone acetylation landscape and BRD4 targeting to gene bodies

Histone peptide microarray screen of chromo and Tudor domains defines new histone lysine methylation interactions

Generation of stable reporter breast cancer cell lines for the identification of ER subtype selective ligands

The essential role of acetyllysine binding by the YEATS domain in transcriptional regulation

Differential action of monohydroxylated polycyclic aromatic hydrocarbons with estrogen receptors α and β

Yeast-based screening of cancer mutations in the DNA damage response protein Mre11 demonstrates importance of conserved capping domain residues

Multivalent Histone and DNA Engagement by a PHD/BRD/PWWP Triple Reader Cassette Recruits ZMYND8 to K14ac-Rich Chromatin

Research Resource: Global Identification of Estrogen Receptor β Target Genes in Triple Negative Breast Cancer Cells

PBRM1 bromodomains variably influence nucleosome interactions and cellular function

Association of Taf14 with acetylated histone H3 directs gene transcription and the DNA damage response

A Student-Focused Lab Module To Investigate Single-Nucleotide Polymorphisms of Common Heritable Traits

A course‐based undergraduate research experience investigating p300 bromodomain mutations

Chromatin biochemistry enters the next generation of code 'seq-ing'

Prognostic significance of full-length estrogen receptor beta expression in stage I-III triple negative breast cancer

Cancer mutations inhibit the coactivator activity of p300 core

A Student-Focused Lab Module To Investigate Single-Nucleotide Polymorphisms of Common Heritable Traits xref ref-type="fn" rid="fn1-jmbe-21-70">† /xref

Using S. cerevisiae to screen cancer mutations in the DNA damage response pathway

Selectively targeting estrogen receptors for cancer treatment: Development of Novel Therapeutic Strategy by Regulating the Nuclear Hormone Receptors

Understanding the role of estrogen receptor beta in triple negative breast cancers

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