Marco Benevento
Affiliations: | 2011-2016 | CNS | Radboud university medical centre |
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Sign in to add mentor| Nael Nadif Kasri | grad student | 2011-2016 | Radboud university medical centre |
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Publications
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| Iacono G, Benevento M, Dubos A, et al. (2017) Integrated transcriptional analysis unveils the dynamics of cellular differentiation in the developing mouse hippocampus. Scientific Reports. 7: 18073 |
| Bart Martens M, Frega M, Classen J, et al. (2016) Euchromatin histone methyltransferase 1 regulates cortical neuronal network development. Scientific Reports. 6: 35756 |
| Benevento M, Iacono G, Selten M, et al. (2016) Histone Methylation by the Kleefstra Syndrome Protein EHMT1 Mediates Homeostatic Synaptic Scaling. Neuron |
| Ba W, Selten MM, van der Raadt J, et al. (2016) ARHGAP12 Functions as a Developmental Brake on Excitatory Synapse Function. Cell Reports |
| Benevento M, van de Molengraft M, van Westen R, et al. (2015) The role of chromatin repressive marks in cognition and disease: A focus on the repressive complex GLP/G9a. Neurobiology of Learning and Memory. 124: 88-96 |
| Iqbal Z, Willemsen MH, Papon MA, et al. (2015) Homozygous SLC6A17 mutations cause autosomal-recessive intellectual disability with progressive tremor, speech impairment, and behavioral problems. American Journal of Human Genetics. 96: 386-96 |
| Balemans MC, Ansar M, Oudakker AR, et al. (2014) Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice. Developmental Biology. 386: 395-407 |
| Balemans MC, Kasri NN, Kopanitsa MV, et al. (2013) Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndrome. Human Molecular Genetics. 22: 852-66 |