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European Journal of Human Genetics : EJHG|January 27, 2025
RNA-sequencing unveils FLT4 splice site variants in variable congenital heart diseaseMaxim Verlee, Erika D'haenens, Laurenz De Cock, et al.
Frontiers in Immunology|June 23, 2023
The Wiskott-Aldrich syndrome protein is required for positive selection during T-cell lineage differentiationMelissa Pille, John Avila, Guillem Sanchez Sanchez, et al.
European Journal of Immunology|September 9, 2024
ThymoSpheres culture: A model to study human polyclonal unconventional T cellsLore Billiet, Hanne Jansen, Melissa Pille, et al.
Cytotherapy|October 26, 2021
Small-scale manufacturing of neoantigen-encoding messenger RNA for early-phase clinical trialsJoline Ingels, Laurenz De Cock, Rupert L Mayer, et al.
Medrxiv : the Preprint Server for Health Sciences|June 9, 2023
A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) geneMaría Del Rocío Pérez Baca, Eva Z Jacobs, Lies Vantomme, et al.
American Journal of Human Genetics|February 27, 2024
Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disabilityMaría Del Rocío Pérez Baca, Eva Z Jacobs, Lies Vantomme, et al.
Cancer Immunology Research|June 14, 2024
Knocking Out CD70 Rescues CD70-Specific NanoCAR T Cells from Antigen-Induced ExhaustionStijn De Munter, Juliane L Buhl, Laurenz De Cock, et al.
The Journal of Experimental Medicine|March 20, 2023
Single-cell profiling identifies a novel human polyclonal unconventional T cell lineageLore Billiet, Laurenz De Cock, Guillem Sanchez Sanchez, et al.
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