Mohanraj Gopalswamy

Duesseldorf, NW, Germany

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 16 publications

A farnesoid X receptor T296I variant disrupts ligand-induced FXR activation and thus bile acid transport in progressive familial intrahepatic cholestasis.

A farnesoid X receptor T296I variant disrupts ligand-induced FXR activation and thus bile acid transport in progressive familial intrahepatic cholestasis.

Journal: The Journal of biological chemistry

Published: April 28, 2025

Identification of non-charged 7.44 analogs interacting with the NHR2 domain of RUNX1-ETO with improved antiproliferative effect in RUNX-ETO positive cells.

Identification of non-charged 7.44 analogs interacting with the NHR2 domain of RUNX1-ETO with improved antiproliferative effect in RUNX-ETO positive cells.

Journal: Scientific reports

Published: January 31, 2025

The mycotoxin Beauvericin is an uncompetitive inhibitor of Cathepsin B.

The mycotoxin Beauvericin is an uncompetitive inhibitor of Cathepsin B.

Journal: Protein science : a publication of the Protein Society

Published: January 18, 2025

Total Synthesis of the Antimycobacterial Natural Product Chlorflavonin and Analogs via a Late-Stage Ruthenium(II)-Catalyzed ortho-C(sp2)-H-Hydroxylation.

Total Synthesis of the Antimycobacterial Natural Product Chlorflavonin and Analogs via a Late-Stage Ruthenium(II)-Catalyzed ortho-C(sp2)-H-Hydroxylation.

Journal: Pharmaceuticals (Basel, Switzerland)

Published: July 08, 2022

Distinct conformational and energetic features define the specific recognition of (di)aromatic peptide motifs by PEX14.

Distinct conformational and energetic features define the specific recognition of (di)aromatic peptide motifs by PEX14.

Journal: Biological chemistry

Published: May 08, 2022

Biophysical and pharmacokinetic characterization of a small-molecule inhibitor of RUNX1/ETO tetramerization with anti-leukemic effects.

Biophysical and pharmacokinetic characterization of a small-molecule inhibitor of RUNX1/ETO tetramerization with anti-leukemic effects.

Journal: Scientific reports

Published: April 19, 2022

Development of a First-in-Class Small-Molecule Inhibitor of the C-Terminal Hsp90 Dimerization.

Development of a First-in-Class Small-Molecule Inhibitor of the C-Terminal Hsp90 Dimerization.

Journal: ACS central science

Published: January 05, 2022

Time-resolved structural analysis of an RNA-cleaving DNA catalyst.

Time-resolved structural analysis of an RNA-cleaving DNA catalyst.

Journal: Nature

Published: May 29, 2021

Membrane Interactions of the Peroxisomal Proteins PEX5 and PEX14.

Membrane Interactions of the Peroxisomal Proteins PEX5 and PEX14.

Journal: Frontiers in cell and developmental biology

Published: January 09, 2021

Small-molecule inhibitors of nisin resistance protein NSR from the human pathogen Streptococcus agalactiae.

Small-molecule inhibitors of nisin resistance protein NSR from the human pathogen Streptococcus agalactiae.

Journal: Bioorganic & medicinal chemistry

Published: May 08, 2019

Phosphorylation-induced unfolding regulates p19INK4d during the human cell cycle.

Phosphorylation-induced unfolding regulates p19INK4d during the human cell cycle.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: March 14, 2018

DNA annealing by Redβ is insufficient for homologous recombination and the additional requirements involve intra- and inter-molecular interactions.

DNA annealing by Redβ is insufficient for homologous recombination and the additional requirements involve intra- and inter-molecular interactions.

Journal: Scientific reports

Published: February 10, 2016

Showing 1-12 of 16

Last Updated: 09/26/2026