scispace - formally typeset
T

Trent C. Bjorndahl

Researcher at University of Alberta

Publications -  27
Citations -  4491

Trent C. Bjorndahl is an academic researcher from University of Alberta. The author has contributed to research in topics: Docking (molecular) & Metabolome. The author has an hindex of 15, co-authored 27 publications receiving 3934 citations. Previous affiliations of Trent C. Bjorndahl include International Agency for Research on Cancer.

Papers
More filters
Journal ArticleDOI

HMDB 3.0—The Human Metabolome Database in 2013

TL;DR: New database visualization tools and new data content have been added or enhanced to the HMDB, which includes better spectral viewing tools, more powerful chemical substructure searches, an improved chemical taxonomy and better, more interactive pathway maps.
Journal ArticleDOI

The Human Urine Metabolome

TL;DR: A comprehensive, quantitative, metabolome-wide characterization of human urine and the identification and annotation of several previously unknown urine metabolites and to substantially enhance the level of metabolome coverage are undertaken.
Journal ArticleDOI

Metabolomic Fingerprint of Heart Failure with Preserved Ejection Fraction

TL;DR: A unique metabolomic fingerprint was identified of HFpEF that is distinct from that of HFrEF that will help understand its pathophysiology and assist in establishing new biomarkers for its diagnosis.
Journal ArticleDOI

Probing the Structural Determinants of Type II‘ β-Turn Formation in Peptides and Proteins

TL;DR: The structural determinants of type II' beta-turns were probed through a comprehensive CD, NMR, and molecular dynamics analysis of 10 specially designed beta-hairpin peptides and it is demonstrated that backbone heterochirality, which determines equatorial and axial side-chain orientation at the i+1 and i+2 residues oftype II' turns, may account for up to 60% ofType II' Beta-turn stabilization.
Journal ArticleDOI

Detailed Biophysical Characterization of the Acid-Induced PrPc to PrPβ Conversion Process

TL;DR: It is found that acid-induced PrP(β) oligomers could be converted to fibrils without the use of chaotropic denaturants, and this finding represents one of the first examples wherein physiologically accessible conditions were used to achieve PrP conversion and fibril formation.