Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

Publications

A Chemical Probe For Tudor Domain Protein Spindlin1 to Investigate Chromatin Functions

Fagan V. et al, (2019)

AKR1D1 regulates glucocorticoid availability and glucocorticoid receptor activation in human hepatoma cells.

Nikolaou N. et al, (2019), J steroid biochem mol biol, 189, 218 - 227

Bromodomain inhibition of the coactivators CBP/EP300 facilitate cellular reprogramming.

Ebrahimi A. et al, (2019), Nat chem biol, 15, 519 - 528

Identification of the 2-Benzoxazol-2-yl-phenol Scaffold as New Hit for JMJD3 Inhibition.

Giordano A. et al, (2019), Acs med chem lett, 10, 601 - 605

A Parsimonious Mechanism of Sugar Dehydration by Human GDP-Mannose-4,6-dehydratase.

Pfeiffer M. et al, (2019), Acs catal, 9, 2962 - 2968

Role of protein structure in variant annotation: structural insight of mutations causing 6-pyruvoyl-tetrahydropterin synthase deficiency.

Muniz JRC. et al, (2019), Pathology, 51, 274 - 280

Divergent roles of prostacyclin and PGE2 in human tendinopathy.

Bergqvist F. et al, (2019), Arthritis res ther, 21

Presence of Amine Oxidase 3 and its Role in Peritoneal Endometriosis Lesions.

De Leo B. et al, (2019), Reproductive sciences, 26, 130A - 130A

Alternative Angiogenesis Mechanisms in Uterine Fibroids Related to Heavy Menstrual Bleeding.

Subramaniam KS. et al, (2019), Reproductive sciences, 26, 226A - 227A

Selective Inhibitors of a Human Prolyl Hydroxylase (OGFOD1) Involved in Ribosomal Decoding.

Thinnes CC. et al, (2019), Chemistry, 25, 2019 - 2024

Design, Synthesis and Characterization of Covalent KDM5 Inhibitors.

Vazquez-Rodriguez S. et al, (2019), Angew chem int ed engl, 58, 515 - 519

Immunophenotypic expression of UCP1 in hibernoma and other adipose/non adipose soft tissue tumours.

Malzahn J. et al, (2019), Clin sarcoma res, 9

Structural insight into the human mitochondrial tRNA purine N1-methyltransferase and ribonuclease P complexes.

Oerum S. et al, (2018), J biol chem, 293, 12862 - 12876

A novel INS mutation in a family with maturity-onset diabetes of the young: Variable insulin secretion and putative mechanisms.

Johnson SR. et al, (2018), Pediatr diabetes, 19, 905 - 909

Investigations on small molecule inhibitors targeting the histone H3K4 tri-methyllysine binding PHD-finger of JmjC histone demethylases.

Bhushan B. et al, (2018), Bioorg med chem, 26, 2984 - 2991

Virtual Fragment Screening Identification of a Quinoline-5,8-dicarboxylic Acid Derivative as a Selective JMJD3 Inhibitor.

Giordano A. et al, (2018), Chemmedchem, 13, 1160 - 1164

Discovery of Orally Bioavailable, Quinoline-Based Aldehyde Dehydrogenase 1A1 (ALDH1A1) Inhibitors with Potent Cellular Activity.

Yang S-M. et al, (2018), J med chem, 61, 4883 - 4903

Non-competitive cyclic peptides for targeting enzyme-substrate complexes.

McAllister TE. et al, (2018), Chem sci, 9, 4569 - 4578

Epigenetic Compound Screening Reveals New Therapeutic Targets for Chordoma

Cottone L. et al, (2018), Journal of pathology, 245, S18 - S18

BROMODOMAIN INHIBITORS ARE POTENT EPIGENETIC REGULATORS OF CATABOLIC GENE EXPRESSION IN HUMAN OSTEOARTHRITIC CHONDROCYTES

de Andres MC. et al, (2018), Osteoarthritis and cartilage, 26, S154 - S154

Load More

Include forthcoming?