Zhou, Huiqing

Epigenetic Regulation of Learning and Memory by Drosophila EHMT/G9a

Kramer, J. M., Kochinke, K., Oortveld, M. A. W., Marks, H., Kramer, D., de Jong, E. K., Asztalos, Z., Westwood, J. T., Stunnenberg, H. G., Sokolowski, M. B., et al. (2011) · PLoS Biology

Neurobiology and Insect Physiology ResearchEpigenetics and DNA Methylation

Cited by 204

Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling

Frega, M., Linda, K., Keller, J. M., Gümüş-Akay, G., Mossink, B., van Rhijn, J.-R., Negwer, M., Klein Gunnewiek, T., Foreman, K., Kompier, N., et al. (2019) · Nature Communications

Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

Cited by 137

Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesis

Ockeloen, C. W., Khandelwal, K. D., Dreesen, K., Ludwig, K. U., Sullivan, R., van Rooij, I. A. L. M., Thonissen, M., Swinnen, S., Phan, M., Conte, F., et al. (2016) · Genetics in Medicine

dental development and anomaliesCleft Lip and Palate Research

Cited by 78

Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice

Balemans, M. C. M., Ansar, M., Oudakker, A. R., van Caam, A. P. M., Bakker, B., Vitters, E. L., van der Kraan, P. M., de Bruijn, D. R. H., Janssen, S. M., Kuipers, A. J., et al. (2014) · Developmental Biology

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 72

Modeling of Aniridia-Related Keratopathy by CRISPR/Cas9 Genome Editing of Human Limbal Epithelial Cells and Rescue by Recombinant PAX6 Protein

Roux, L. N., Petit, I., Domart, R., Concordet, J.-P., Qu, J., Zhou, H., Joliot, A., Ferrigno, O., & Aberdam, D. (2018) · Stem Cells

Corneal Surgery and TreatmentsOcular Disorders and Treatments

Cited by 56