Dominique Schols
Researcher Next ID · RN-035245
Researcher · Biochemistry, Genetics and Molecular Biology
Rega Institute for Medical Research
Leuven, Spain
- Works count
- 883
- Citation count
- 29,760
- H-index
- 85
- i10-index
- 418
Research interests
Publications
A single-dose live-attenuated YF17D-vectored SARS-CoV-2 vaccine candidate
Nature · 2020 · https://doi.org/10.1038/s41586-020-3035-9
STAT2 signaling restricts viral dissemination but drives severe pneumonia in SARS-CoV-2 infected hamsters
Nature Communications · 2020 · 10.1038/s41467-020-19684-y
Chloro-1,4-dimethyl-9H-carbazole Derivatives Displaying Anti-HIV Activity
Molecules · 2018 · 10.3390/molecules23020286
The Viral Polymerase Inhibitor 7-Deaza-2’-C-Methyladenosine Is a Potent Inhibitor of In Vitro Zika Virus Replication and Delays Disease Progression in a Robust Mouse Infection Model
PLoS neglected tropical diseases · 2016 · 10.1371/journal.pntd.0004695
CXCR4 nanobodies (VHH-based single variable domains) potently inhibit chemotaxis and HIV-1 replication and mobilize stem cells
Proceedings of the National Academy of Sciences · 2010 · https://doi.org/10.1073/pnas.1012865107
CXCL12-CXCR4 Axis in Angiogenesis, Metastasis and Stem Cell Mobilization
Current Pharmaceutical Design · 2010 · 10.2174/138161210794455003
Safety, Pharmacokinetics, and Antiviral Activity of AMD3100, a Selective CXCR4 Receptor Inhibitor, in HIV-1 Infection
JAIDS Journal of Acquired Immune Deficiency Syndromes · 2004 · 10.1097/01.qai.0000137371.80695.ef
Chemokine receptor inhibition by AMD3100 is strictly confined to CXCR4
FEBS Letters · 2002 · 10.1016/s0014-5793(02)03143-5
AMD3100, a CxCR4 Antagonist, Attenuates Allergic Lung Inflammation and Airway Hyperreactivity
American Journal Of Pathology · 2002 · 10.1016/s0002-9440(10)62562-x
CXCR4-activated astrocyte glutamate release via TNFα: amplification by microglia triggers neurotoxicity
Nature Neuroscience · 2001 · https://doi.org/10.1038/89490
AMD3100, a Potent and Specific Antagonist of the Stromal Cell-Derived Factor-1 Chemokine Receptor CXCR4, Inhibits Autoimmune Joint Inflammation in IFN-γ Receptor-Deficient Mice
The Journal of Immunology · 2001 · https://doi.org/10.4049/jimmunol.167.8.4686
Macrophage Tropism of Human Immunodeficiency Virus Type 1 Isolates from Brain and Lymphoid Tissues Predicts Neurotropism Independent of Coreceptor Specificity
Journal of Virology · 2001 · https://doi.org/10.1128/jvi.75.21.10073-10089.2001
AMD3100, a small molecule inhibitor of HIV-1 entry via the CXCR4 co-receptor
Nature Medicine · 1998 · https://doi.org/10.1038/nm0198-072
Amino-terminal Truncation of Chemokines by CD26/Dipeptidyl-peptidase IV
Journal of Biological Chemistry · 1998 · https://doi.org/10.1074/jbc.273.13.7222
Bicyclams, a class of potent anti-HIV agents, are targeted at the HIV coreceptor Fusin/CXCR-4
Antiviral Research · 1997 · 10.1016/s0166-3542(97)00025-9
Inhibition of T-tropic HIV Strains by Selective Antagonization of the Chemokine Receptor CXCR4
The Journal of Experimental Medicine · 1997 · https://doi.org/10.1084/jem.186.8.1383
Potent and highly selective human immunodeficiency virus type 1 (HIV-1) inhibition by a series of alpha-anilinophenylacetamide derivatives targeted at HIV-1 reverse transcriptase.
Proceedings of the National Academy of Sciences · 1993 · https://doi.org/10.1073/pnas.90.5.1711
Differential antiherpesvirus and antiretrovirus effects of the (S) and (R) enantiomers of acyclic nucleoside phosphonates: potent and selective in vitro and in vivo antiretrovirus activities of (R)-9-(2-phosphonomethoxypropyl)-2,6-diaminopurine
Antimicrobial Agents and Chemotherapy · 1993 · https://doi.org/10.1128/aac.37.2.332
Potent and selective inhibition of human immunodeficiency virus (HIV)-1 and HIV-2 replication by a class of bicyclams interacting with a viral uncoating event.
Proceedings of the National Academy of Sciences · 1992 · https://doi.org/10.1073/pnas.89.12.5286
The mannose-specific plant lectins from Cymbidium hybrid and Epipactis helleborine and the (N-acetylglucosamine)n-specific plant lectin from Urtica dioica are potent and selective inhibitors of human immunodeficiency virus and cytomegalovirus replication in vitro
Antiviral Research · 1992 · https://doi.org/10.1016/0166-3542(92)90038-7
Alpha-(1-3)- and alpha-(1-6)-D-mannose-specific plant lectins are markedly inhibitory to human immunodeficiency virus and cytomegalovirus infections in vitro
Antimicrobial Agents and Chemotherapy · 1991 · https://doi.org/10.1128/aac.35.3.410
Dextran sulfate and other polyanionic anti-HIV compounds specifically interact with the viral gp120 glycoprotein expressed by T-cells persistently infected with HIV-1
Virology · 1990 · 10.1016/0042-6822(90)90440-3
Potent and selective inhibition of HIV-1 replication in vitro by a novel series of TIBO derivatives
Nature · 1990 · https://doi.org/10.1038/343470a0
Highly specific inhibition of human immunodeficiency virus type 1 by a novel 6-substituted acyclouridine derivative
Biochemical and Biophysical Research Communications · 1989 · https://doi.org/10.1016/0006-291x(89)92756-3
Rapid and automated tetrazolium-based colorimetric assay for the detection of anti-HIV compounds
Journal of Virological Methods · 1988 · https://doi.org/10.1016/0166-0934(88)90134-6
Phosphonylmethoxyethyl purine derivatives, a new class of anti-human immunodeficiency virus agents
Antimicrobial Agents and Chemotherapy · 1988 · https://doi.org/10.1128/aac.32.7.1025
Current projects
No projects listed.