Squeezing the most from every crystal: the fine details of data collection. Read more about Squeezing the most from every crystal: the fine details of data collection.
Molecular architecture of the ankyrin SOCS box family of Cul5-dependent E3 ubiquitin ligases. Read more about Molecular architecture of the ankyrin SOCS box family of Cul5-dependent E3 ubiquitin ligases.
Substrate Specificity and Oligomerization of Human GMP Synthetase. Read more about Substrate Specificity and Oligomerization of Human GMP Synthetase.
Ionic strength-dependent conformations of a ubiquitin-like small archaeal modifier protein (SAMP2) from Haloferax volcanii. Read more about Ionic strength-dependent conformations of a ubiquitin-like small archaeal modifier protein (SAMP2) from Haloferax volcanii.
Control of the Hippo Pathway by Set7-Dependent Methylation of Yap. Read more about Control of the Hippo Pathway by Set7-Dependent Methylation of Yap.
Topical anti-angiogenic SRPK1 inhibitors reduce choroidal neovascularization in rodent models of exudative-AMD. Read more about Topical anti-angiogenic SRPK1 inhibitors reduce choroidal neovascularization in rodent models of exudative-AMD.
Discovery of a Potent and Selective DDR1 Receptor Tyrosine Kinase Inhibitor. Read more about Discovery of a Potent and Selective DDR1 Receptor Tyrosine Kinase Inhibitor.
Testis specific gene expression drives disease progression and Rituximab resistance in lymphoma. Read more about Testis specific gene expression drives disease progression and Rituximab resistance in lymphoma.
Suppressor of Cytokine Signaling (SOCS) 5 Utilises Distinct Domains for Regulation of JAK1 and Interaction with the Adaptor Protein Shc-1. Read more about Suppressor of Cytokine Signaling (SOCS) 5 Utilises Distinct Domains for Regulation of JAK1 and Interaction with the Adaptor Protein Shc-1.
Synthesis and SAR studies of 5-(pyridin-4-yl)-1,3,4-thiadiazol-2-amine derivatives as potent inhibitors of Bloom helicase. Read more about Synthesis and SAR studies of 5-(pyridin-4-yl)-1,3,4-thiadiazol-2-amine derivatives as potent inhibitors of Bloom helicase.
