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Structure of HDAC3 bound to co-repressor and inositol tetraphosphate

Nature (London), 2012-01, Vol.481 (7381), p.335-340

2012

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PROTAC-mediated degradation of class I histone deacetylase enzymes in corepressor complexes

Chemical communications (Cambridge, England), 2020-04, Vol.56 (32), p.4476-4479

2020

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The structure of the core NuRD repression complex provides insights into its interaction with chromatin

eLife, 2016-04, Vol.5, p.e13941-e13941

2016

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A Mutation in the Thyroid Hormone Receptor Alpha Gene

The New England journal of medicine, 2012-01, Vol.366 (3), p.243-249

2012

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In vitro evolution predicts emerging SARS-CoV-2 mutations with high affinity for ACE2 and cross-species binding

PLoS pathogens, 2022-07, Vol.18 (7), p.e1010733

2022

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Towards an understanding of the structure and function of MTA1

Cancer and metastasis reviews, 2014-12, Vol.33 (4), p.857-867

2014

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Negative regulation by nuclear receptors: a plethora of mechanisms

Trends in endocrinology and metabolism, 2011-03, Vol.22 (3), p.87-93

2011

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FERM-dependent E3 ligase recognition is a conserved mechanism for targeted degradation of lipoprotein receptors

Proceedings of the National Academy of Sciences - PNAS, 2011-12, Vol.108 (50), p.20107-20112

2011

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Insights into the activation mechanism of class I HDAC complexes by inositol phosphates

Nature communications, 2016-04, Vol.7 (1), p.11262-11262, Article 11262

2016

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Histone H2B Deacylation Selectivity: Exploring Chromatin’s Dark Matter with an Engineered Sortase

Journal of the American Chemical Society, 2022-03, Vol.144 (8), p.3360-3364

2022

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Cryo-EM structural analysis of FADD:Caspase-8 complexes defines the catalytic dimer architecture for co-ordinated control of cell fate

Nature communications, 2021-02, Vol.12 (1), p.819-17, Article 819

2021

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A potential histone-chaperone activity for the MIER1 histone deacetylase complex

Nucleic acids research, 2023-07, Vol.51 (12), p.6006-6019

2023

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The MiDAC histone deacetylase complex is essential for embryonic development and has a unique multivalent structure

Nature communications, 2020-06, Vol.11 (1), p.3252-3252, Article 3252

2020

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Nuclear hormone receptor co-repressors: Structure and function

Molecular and cellular endocrinology, 2012-01, Vol.348 (2), p.440-449

2012

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The ansamycin antibiotic, rifamycin SV, inhibits BCL6 transcriptional repression and forms a complex with the BCL6-BTB/POZ domain

PloS one, 2014-03, Vol.9 (3), p.e90889

2014

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A variant NuRD complex containing PWWP2A/B excludes MBD2/3 to regulate transcription at active genes

Nature communications, 2018-09, Vol.9 (1), p.3798-14, Article 3798

2018

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Histone deacetylase (HDAC) 1 and 2 are essential for accurate cell division and the pluripotency of embryonic stem cells

Proceedings of the National Academy of Sciences - PNAS, 2014-07, Vol.111 (27), p.9840-9845

2014

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Mutations in TBL1X Are Associated With Central Hypothyroidism

The journal of clinical endocrinology and metabolism, 2016-12, Vol.101 (12), p.4564-4573

2016

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Synthesis of HDAC Substrate Peptidomimetic Inhibitors Using Fmoc Amino Acids Incorporating Zinc-Binding Groups

Organic letters, 2019-05, Vol.21 (9), p.3178-3182

2019

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A Pharmacogenetic Approach to the Treatment of Patients With PPARG Mutations

Diabetes (New York, N.Y.), 2018-06, Vol.67 (6), p.1086-1092

2018

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An evolving understanding of nuclear receptor coregulator proteins

Journal of molecular endocrinology, 2013-12, Vol.51 (3), p.T23-T36

2013

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Structural basis for the assembly of the SMRT/NCoR core transcriptional repression machinery

Nature structural & molecular biology, 2011-02, Vol.18 (2), p.177-184

2011

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A dynamic mechanism of nuclear receptor activation and its perturbation in a human disease

Nature structural & molecular biology, 2003-02, Vol.10 (2), p.136-140

2003

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Structure-Guided Approach to Relieving Transcriptional Repression in Resistance to Thyroid Hormone α

Molecular and cellular biology, 2022-02, Vol.42 (2), p.e0036321-e0036321

2022

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Structural and functional characterization of a cell cycle associated HDAC1/2 complex reveals the structural basis for complex assembly and nucleosome targeting

Nucleic acids research, 2015-02, Vol.43 (4), p.2033-2044

2015

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Structure of HDAC3 bound to co-repressor and inositol tetraphosphate

PROTAC-mediated degradation of class I histone deacetylase enzymes in corepressor complexes

The structure of the core NuRD repression complex provides insights into its interaction with chromatin

A Mutation in the Thyroid Hormone Receptor Alpha Gene

In vitro evolution predicts emerging SARS-CoV-2 mutations with high affinity for ACE2 and cross-species binding

Towards an understanding of the structure and function of MTA1

Negative regulation by nuclear receptors: a plethora of mechanisms

FERM-dependent E3 ligase recognition is a conserved mechanism for targeted degradation of lipoprotein receptors

Insights into the activation mechanism of class I HDAC complexes by inositol phosphates

Histone H2B Deacylation Selectivity: Exploring Chromatin’s Dark Matter with an Engineered Sortase

Cryo-EM structural analysis of FADD:Caspase-8 complexes defines the catalytic dimer architecture for co-ordinated control of cell fate

A potential histone-chaperone activity for the MIER1 histone deacetylase complex

The MiDAC histone deacetylase complex is essential for embryonic development and has a unique multivalent structure

Nuclear hormone receptor co-repressors: Structure and function

The ansamycin antibiotic, rifamycin SV, inhibits BCL6 transcriptional repression and forms a complex with the BCL6-BTB/POZ domain

A variant NuRD complex containing PWWP2A/B excludes MBD2/3 to regulate transcription at active genes

Histone deacetylase (HDAC) 1 and 2 are essential for accurate cell division and the pluripotency of embryonic stem cells

Mutations in TBL1X Are Associated With Central Hypothyroidism

Synthesis of HDAC Substrate Peptidomimetic Inhibitors Using Fmoc Amino Acids Incorporating Zinc-Binding Groups

A Pharmacogenetic Approach to the Treatment of Patients With PPARG Mutations

An evolving understanding of nuclear receptor coregulator proteins

Structural basis for the assembly of the SMRT/NCoR core transcriptional repression machinery

A dynamic mechanism of nuclear receptor activation and its perturbation in a human disease

Structure-Guided Approach to Relieving Transcriptional Repression in Resistance to Thyroid Hormone α

Structural and functional characterization of a cell cycle associated HDAC1/2 complex reveals the structural basis for complex assembly and nucleosome targeting

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