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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 -
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Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development
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Benchtop mesoSPIM : a next-generation open-source light-sheet microscope for cleared samples
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Reflective multi-immersion microscope objectives inspired by the Schmidt telescope
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Mutations in the histone methyltransferase Ezh2 drive context-dependent leukemia in Xenopus tropicalis
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HNF1B alters an evolutionarily conserved nephrogenic program of target genes
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Genetic variants in ARHGEF6 cause congenital anomalies of the kidneys and urinary tract in humans, mice, and frogs
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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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Deep learning is widely applicable to phenotyping embryonic development and disease