prof. dr. Kris Vleminckx
- ORCID iD
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0000-0002-9666-4105
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Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder
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CRISPR/Cas9 mediated disruption of an evolutionary conserved putative enhancer in the mab21l2 locus induces developmental eye anomalies in Xenopus tropicalis
(2024) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 32(Supplement 1). p.247-247 -
- Journal Article
- A1
- open access
Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development
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- Journal Article
- A1
- open access
Evolutionary origin of Hoxc13-dependent skin appendages in amphibians
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Regulation of non-canonical expression of ABCA4 by an RPE-specific enhancer with implications in ABCA4-associated disease
(2024) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 32(Supplement 1). p.39-40 -
Dual molecular effects of constitutional SF3B2 variants cause a novel dominant spliceosomopathy displaying retinitis pigmentosa or developmental skeletal anomalies
(2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.71-71 -
- Journal Article
- A1
- open access
Mutations in the histone methyltransferase Ezh2 drive context-dependent leukemia in Xenopus tropicalis
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- Journal Article
- A1
- open access
Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy
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Identifying and characterizing EZH2 as a druggable dependency factor for desmoid tumors in a genetic Xenopus tropicalis model for Gardner's Syndrome
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- Journal Article
- A1
- open access
Engraftment of allotransplanted tumor cells in adult rag2 mutant Xenopus tropicalis