Articoli con mandati relativi all'accesso pubblico - Bernard ThienpontUlteriori informazioni
TotaleFWOEuropean CommissionNIHWellcomeNIHRDFGCancer Research UKCIHRDFFBHFNHMRCMRCFWFNSFCSwedish Research CouncilGovernment of SpainKWFSusan G. KomenA*StarBBSRCRCNHSFAcademy of FinlandINSERMBreast Cancer Now, UKMichael J Fox FoundationLeducq Foundation, USASNSFGenome CanadaNSERCHelmholtzDNATFVillum FoundationVersus Arthritis, UKYorkshire Cancer Research, UKSCLNMRCUK Research & InnovationAXA Research Fund, FranceHFSPBELSPOCZI
Non disponibili pubblicamente: 7
The role of fatty acid β-oxidation in lymphangiogenesis
BW Wong, X Wang, A Zecchin, B Thienpont, I Cornelissen, J Kalucka, ...
Nature 542 (7639), 49-54, 2017
Mandati: Research Foundation (Flanders), German Research Foundation, European …
IGF1R is an entry receptor for respiratory syncytial virus
CD Griffiths, LM Bilawchuk, JE McDonough, KC Jamieson, F Elawar, ...
Nature 583 (7817), 615-619, 2020
Mandati: Canadian Institutes of Health Research
Deletions in the VPS13B (COH1) gene as a cause of Cohen syndrome
I Balikova, AE Lehesjoki, TJL De Ravel, B Thienpont, KE Chandler, ...
Human mutation 30 (9), E845-E854, 2009
Mandati: US National Institutes of Health, Research Foundation (Flanders)
Epigenetics in the heart: the role of histone modifications in cardiac remodelling
A Tingare, B Thienpont, HL Roderick
Biochemical Society Transactions 41 (3), 789-796, 2013
Mandati: UK Biotechnology and Biological Sciences Research Council, British Heart …
Cell-free DNA methylome analysis for early preeclampsia prediction
M De Borre, H Che, Q Yu, L Lannoo, K De Ridder, L Vancoillie, ...
Nature Medicine 29 (9), 2206-2215, 2023
Mandati: Research Foundation (Flanders)
High frequency of submicroscopic chromosomal deletions in patients with idiopathic congenital eye malformations
I Balikova, T de Ravel, C Ayuso, B Thienpont, I Casteels, C Villaverde, ...
American journal of ophthalmology 151 (6), 1087-1094. e45, 2011
Mandati: Research Foundation (Flanders), Government of Spain
TET enzymes as oxygen-dependent tumor suppressors: exciting new avenues for cancer management
B Thienpont, E Galle, D Lambrechts
Epigenomics 8 (11), 1445-1448, 2016
Mandati: Research Foundation (Flanders), European Commission
Disponibili pubblicamente: 66
Phenotype molding of stromal cells in the lung tumor microenvironment
D Lambrechts, E Wauters, B Boeckx, S Aibar, D Nittner, O Burton, ...
Nature medicine 24 (8), 1277-1289, 2018
Mandati: Austrian Science Fund
Single-Cell Transcriptome Atlas of Murine Endothelial Cells
J Kalucka, LPMH de Rooij, J Goveia, K Rohlenova, SJ Dumas, E Meta, ...
Cell 180 (4), 764-779. e20, 2020
Mandati: Research Foundation (Flanders), National Natural Science Foundation of China …
A single-cell transcriptome atlas of the aging Drosophila brain
K Davie, J Janssens, D Koldere, M De Waegeneer, U Pech, Ł Kreft, ...
Cell 174 (4), 982-998. e20, 2018
Mandati: Research Foundation (Flanders), German Research Foundation, European Commission
Tumour hypoxia causes DNA hypermethylation by reducing TET activity
B Thienpont, J Steinbacher, H Zhao, F D’Anna, A Kuchnio, A Ploumakis, ...
Nature 537 (7618), 63-68, 2016
Mandati: Research Foundation (Flanders), German Research Foundation, UK Biotechnology …
Inhibition of the glycolytic activator PFKFB3 in endothelium induces tumor vessel normalization, impairs metastasis, and improves chemotherapy
AR Cantelmo, LC Conradi, A Brajic, J Goveia, J Kalucka, A Pircher, ...
Cancer cell 30 (6), 968-985, 2016
Mandati: US National Institutes of Health, Austrian Science Fund, Research Foundation …
A pan-cancer blueprint of the heterogeneous tumor microenvironment revealed by single-cell profiling
J Qian, S Olbrecht, B Boeckx, H Vos, D Laoui, E Etlioglu, E Wauters, ...
Cell research 30 (9), 745-762, 2020
Mandati: Research Foundation (Flanders), European Commission
Methods and applications for single-cell and spatial multi-omics
K Vandereyken, A Sifrim, B Thienpont, T Voet
Nature Reviews Genetics, 1-22, 2023
Mandati: Research Foundation (Flanders), Michael J Fox Foundation, Chan Zuckerberg …
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing
A Sifrim, MP Hitz, A Wilsdon, J Breckpot, SH Al Turki, B Thienpont, ...
Nature genetics 48 (9), 1060-1065, 2016
Mandati: US National Institutes of Health, Canadian Institutes of Health Research …
An Integrated Gene Expression Landscape Profiling Approach to Identify Lung Tumor Endothelial Cell Heterogeneity and Angiogenic Candidates
J Goveia, K Rohlenova, F Taverna, L Treps, LC Conradi, A Pircher, ...
Cancer Cell 37 (1), 21-36. e13, 2020
Mandati: Austrian Science Fund, Research Foundation (Flanders), National Natural …
Quiescent endothelial cells upregulate fatty acid β-oxidation for vasculoprotection via redox homeostasis
J Kalucka, L Bierhansl, NV Conchinha, R Missiaen, I Elia, U Brüning, ...
Cell metabolism 28 (6), 881-894. e13, 2018
Mandati: Swiss National Science Foundation, Research Foundation (Flanders), National …
Single-Cell RNA Sequencing Maps Endothelial Metabolic Plasticity in Pathological Angiogenesis
K Rohlenova, J Goveia, M García-Caballero, A Subramanian, J Kalucka, ...
Cell Metabolism 31 (4), 862-877. e14, 2020
Mandati: Austrian Science Fund, Research Foundation (Flanders), National Natural …
Lipid availability determines fate of skeletal progenitor cells via SOX9
N van Gastel, S Stegen, G Eelen, S Schoors, A Carlier, VW Daniëls, ...
Nature 579 (7797), 111-117, 2020
Mandati: US National Institutes of Health, Research Foundation (Flanders), European …
Rare variants in NR2F2 cause congenital heart defects in humans
S Al Turki, AK Manickaraj, CL Mercer, SS Gerety, MP Hitz, S Lindsay, ...
The American Journal of Human Genetics 94 (4), 574-585, 2014
Mandati: US National Institutes of Health, Heart and Stroke Foundation of Canada …
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