Fluorescence, Biochemistry, Integrase, Molecular biology and Tubulin are his primary areas of study. His Fluorescence study integrates concerns from other disciplines, such as Luminescent Proteins, Photochemistry, Analytical chemistry, Protein structure and Conformational isomerism. His Integrase research includes themes of Nuclear transport, Nuclear localization sequence, Viral replication and Recombinant DNA.
His work in Molecular biology is not limited to one particular discipline; it also encompasses Binding site. His research in Tubulin intersects with topics in Crystallography, Fluorescence anisotropy and Polymerization, Polymer. His work investigates the relationship between Microtubule and topics such as Molecular mass that intersect with problems in Fluorescence correlation spectroscopy.
Yves Engelborghs focuses on Fluorescence, Biochemistry, Biophysics, Crystallography and Tubulin. His work deals with themes such as Tryptophan, Photochemistry and Analytical chemistry, which intersect with Fluorescence. His Tryptophan study incorporates themes from Conformational isomerism and Quenching.
Biochemistry is closely attributed to Molecular biology in his work. His Crystallography research is multidisciplinary, incorporating elements of Protein secondary structure, Nucleation, Molecular dynamics, Dissociation and GTP'. As part of one scientific family, Yves Engelborghs deals mainly with the area of Tubulin, narrowing it down to issues related to the Stereochemistry, and often Protein structure and Reaction rate constant.
His main research concerns Biochemistry, Biophysics, Fluorescence correlation spectroscopy, Cell biology and Fluorescence. Yves Engelborghs interconnects Thapsigargin, Calcium, Cytoplasm and Fluorescence microscope in the investigation of issues within Biophysics. His work carried out in the field of Fluorescence correlation spectroscopy brings together such families of science as Microscope, Vesicle, Calcium flux and Monomer.
His Cell biology research integrates issues from Chromatin, Neuroscience, Alpha-synuclein and Anaphase. The various areas that Yves Engelborghs examines in his Fluorescence study include Side chain and Nanotechnology, Rational design. In Förster resonance energy transfer, he works on issues like Conformational change, which are connected to Protein structure.
His primary areas of investigation include Biochemistry, Fluorescence correlation spectroscopy, Fluorescence recovery after photobleaching, Protein structure and Fluorescence microscope. His research brings together the fields of Calcium and Biochemistry. His Fluorescence correlation spectroscopy research is multidisciplinary, relying on both Wide dynamic range, Laser and Nucleation.
The concepts of his Fluorescence recovery after photobleaching study are interwoven with issues in Binding domain, Chromatin, Transcription factor, Chromatin binding and Integrase. Yves Engelborghs has researched Fluorescence microscope in several fields, including Photochemistry and Fluorescence spectroscopy, Fluorescence cross-correlation spectroscopy. Yves Engelborghs focuses mostly in the field of Fluorescence, narrowing it down to topics relating to Crystallography and, in certain cases, Biophysics.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
HIV-1 integrase forms stable tetramers and associates with LEDGF/p75 protein in human cells
Peter Cherepanov;Goedele Maertens;Paul Proost;Bart Devreese.
Journal of Biological Chemistry (2003)
LEDGF/p75 Is Essential for Nuclear and Chromosomal Targeting of HIV-1 Integrase in Human Cells
Goedele Maertens;Peter Cherepanov;Willem Pluymers;Katrien Busschots.
Journal of Biological Chemistry (2003)
Fluorescence lifetime standards for time and frequency domain fluorescence spectroscopy
Noël Boens;Wenwu Qin;Nikola Basarić;Johan Hofkens.
Analytical Chemistry (2007)
The Endocrine Disruptor Monoethyl-hexyl-phthalate Is a Selective Peroxisome Proliferator-activated Receptor γ Modulator That Promotes Adipogenesis
Jérôme N. Feige;Laurent Gelman;Daniel Rossi;Vincent Zoete.
Journal of Biological Chemistry (2007)
The Correct Use of “Average” Fluorescence Parameters
Alain Sillen;Yves Engelborghs.
Photochemistry and Photobiology (1998)
Stretched exponential decay and correlations in the catalytic activity of fluctuating single lipase molecules
Ophir Flomenbom;Kelly Velonia;Davey Loos;Sadahiro Masuo.
Proceedings of the National Academy of Sciences of the United States of America (2005)
The Interaction of LEDGF/p75 with Integrase Is Lentivirus-specific and Promotes DNA Binding
Katrien Busschots;Jo Vercammen;Stéphane Emiliani;Richard Benarous.
Journal of Biological Chemistry (2005)
Tryptophan fluorescence study of the interaction of penetratin peptides with model membranes.
Bart Christiaens;Sofie Symoens;Stefan Vanderheyden;Yves Engelborghs.
FEBS Journal (2002)
Single-enzyme kinetics of CALB-catalyzed hydrolysis
Kelly Velonia;Ophir Flomenbom;Davey Loos;Sadahiro Masuo.
Angewandte Chemie (2005)
Overexpression of the Lens Epithelium-Derived Growth Factor/p75 Integrase Binding Domain Inhibits Human Immunodeficiency Virus Replication
Jan De Rijck;Linos Vandekerckhove;Rik Gijsbers;Anneleen Hombrouck.
Journal of Virology (2006)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: