Projects per year
Personal profile
Areas of expertise
Diplomas
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
Education/Academic qualification
Doctor of Science, Université Catholique de Louvain
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Dive into the research topics where Olivier De Backer is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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FSR: Caractérisation du déficit apoptotiques observés dans des souris déficientes en Maged1.
3/07/05 → …
Project: Research
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Etude de la fonction de Maged 2 IN VIVO. Analyse de souris knock-out Maged d2
De Backer, O. & DOMBRET, C.
1/01/04 → …
Project: PHD
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Association of Variants in TMEM45A With Keratoglobus
Weiner, C., Hecht, I., Kotlyar, A., Shoshany, N., Zadok, D., Elbaz, U., Segev, F., Maytal, A., Hachmo, Y., Michiels, C., De Backer, O., Shomron, N., Einan-Lifshitz, A. & Pras, E., Oct 2021, In: JAMA ophthalmology. 139, 10, p. 1089-1095 7 p.Research output: Contribution to journal › Article › peer-review
File12 Downloads (Pure) -
Deletion of TNFAIP6 gene in human keratinocytes by CRISPR/Cas9 edition demonstrates a role for TSG-6 to retain hyaluronan inside epidermis
EVRARD, CELINE., Faway, E., De Vuyst, E., Svensek, O., DE BACKER, O., FLAMION, B., Lambert De Rouvroit, C. & Poumay, Y., 20 Apr 2021, p. S20.Research output: Contribution to conference › Abstract › peer-review
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Deletion of TNFAIP6 gene in human keratinocytes demonstrates a role for TSG-6 to retain hyaluronan inside epidermis
Evrard, C., Faway, E., De Vuyst, E., Svensek, O., De Glas, V., Bergerat, D., Salmon, M., De Backer, O., Flamion, B., Le-Buanec, H., Lambert De Rouvroit, C. & Poumay, Y., 24 Sept 2021, In: JID Innovations. 1, 4, 100054.Research output: Contribution to journal › Article › peer-review
Open Access -
A homozygous stop gain mutation in BOD1 gene in a Lebanese patient with syndromic intellectual disability
Hamdan, N., Mehawej, C., Sebaaly, G., Jalkh, N., Corbani, S., Abou-Ghoch, J., De Backer, O. & Chouery, E., 1 Sept 2020, In: Clinical genetics. 98, 3, p. 288-292 5 p.Research output: Contribution to journal › Article › peer-review
Open AccessFile21 Downloads (Pure) -
Deletion of Maged1 in mice abolishes locomotor and reinforcing effects of cocaine
De Backer, J-F., Monlezun, S., Detraux, B., Gazan, A., Vanopdenbosch, L., Cheron, J., Cannazza, G., Valverde, S., Cantacorps, L., Nassar, M., Venance, L., Valverde, O., Faure, P., Zoli, M., De Backer, O., Gall, D., Schiffmann, S. N. & de Kerchove d'Exaerde, A., 1 Sept 2018, In: EMBO J.. 19, 9, e45089.Research output: Contribution to journal › Article › peer-review
Open AccessFile35 Downloads (Pure)