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Marie De Borre

Showing results (1-10 of 6) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|August 22, 2020
Oxidative Bisulfite Sequencing: An Experimental and Computational ProtocolMarie De Borre, Miguel R Branco
Prenatal Diagnosis|December 4, 2023
Cell-free DNA methylation-based preeclampsia prediction: A journey to improve maternal healthMio Aerden, Marie De Borre, Bernard Thienpont
Nature Medicine|August 28, 2023
Cell-free DNA methylome analysis for early preeclampsia predictionMarie De Borre, Huiwen Che, Qian Yu, et al.
Nature Communications|March 13, 2024
Cell type signatures in cell-free DNA fragmentation profiles reveal disease biologyKate E Stanley, Tatjana Jatsenko, Stefania Tuveri, et al.
Genome Biology|July 29, 2020
DNA methylation repels binding of hypoxia-inducible transcription factors to maintain tumor immunotoleranceFlora D'Anna, Laurien Van Dyck, Jieyi Xiong, et al.
European Journal of Human Genetics : EJHG|October 7, 2018
Heterozygous loss-of-function variants of MEIS2 cause a triad of palatal defects, congenital heart defects, and intellectual disabilityRosalind Verheije, Gabriel S Kupchik, Bertrand Isidor, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Methods in Molecular Biology (Clifton, N.J.)|August 22, 2020
Oxidative Bisulfite Sequencing: An Experimental and Computational ProtocolMarie De Borre, Miguel R Branco
Prenatal Diagnosis|December 4, 2023
Cell-free DNA methylation-based preeclampsia prediction: A journey to improve maternal healthMio Aerden, Marie De Borre, Bernard Thienpont
Nature Medicine|August 28, 2023
Cell-free DNA methylome analysis for early preeclampsia predictionMarie De Borre, Huiwen Che, Qian Yu, et al.
Nature Communications|March 13, 2024
Cell type signatures in cell-free DNA fragmentation profiles reveal disease biologyKate E Stanley, Tatjana Jatsenko, Stefania Tuveri, et al.
Genome Biology|July 29, 2020
DNA methylation repels binding of hypoxia-inducible transcription factors to maintain tumor immunotoleranceFlora D'Anna, Laurien Van Dyck, Jieyi Xiong, et al.
European Journal of Human Genetics : EJHG|October 7, 2018
Heterozygous loss-of-function variants of MEIS2 cause a triad of palatal defects, congenital heart defects, and intellectual disabilityRosalind Verheije, Gabriel S Kupchik, Bertrand Isidor, et al.
Pageof 1