John W.R. Schwabe

John W.R. Schwabe

Department of Biochemistry, University of Leicester

Affiliated withUniversity of Leicester

Research Area

Biography

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JoVE Journal Publications

ArticleTotal : 1
Year
Recombinant Protein Expression for Structural Biology in HEK 293F Suspension Cells: A Novel and Accessible Approach
Publication title

Cited by 70

2014

Other Publications

Article
Year
The structural basis for the specificity of retinoid-X receptor-selective agonists: new insights into the role of helix H12.

The Journal of biological chemistry| PubMed ID: 11782480

2002
2003
2003
2003
2004
Nuclear receptors: the evolution of diversity.

Science's STKE : signal transduction knowledge environment| PubMed ID: 14747695

2004
Mechanism of the nuclear receptor molecular switch.

Trends in biochemical sciences| PubMed ID: 15276186

2004
2004
Structural insights into the interaction and activation of histone deacetylase 3 by nuclear receptor corepressors.

Proceedings of the National Academy of Sciences of the United States of America| PubMed ID: 15837933

2005
Structural basis for the activation of PPARgamma by oxidized fatty acids.

Nature structural & molecular biology| PubMed ID: 19172745

2008
2009
Negative regulation by nuclear receptors: a plethora of mechanisms.

Trends in endocrinology and metabolism: TEM| PubMed ID: 21196123

2011
2011
2011
Nuclear hormone receptor co-repressors: structure and function.

Molecular and cellular endocrinology| PubMed ID: 21925568

2012
FERM-dependent E3 ligase recognition is a conserved mechanism for targeted degradation of lipoprotein receptors.

Proceedings of the National Academy of Sciences of the United States of America| PubMed ID: 22109552

2011
A mutation in the thyroid hormone receptor alpha gene.

The New England journal of medicine| PubMed ID: 22168587

2012
2012
2012
2013
2013
An evolving understanding of nuclear receptor coregulator proteins.

Journal of molecular endocrinology| PubMed ID: 24203923

2013
2014
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 of the United States of America| PubMed ID: 24958871

2014