Federico Tinarelli
Affiliations: | Dundee University |
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| Tinarelli F, Ivanova E, Colombi I, et al. (2021) Cell-cell coupling and DNA methylation abnormal phenotypes in the after-hours mice. Epigenetics & Chromatin. 14: 1 |
| Maggi S, Balzani E, Lassi G, et al. (2017) The after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasis. Scientific Reports. 7: 17765 |
| Barini E, Miccoli A, Tinarelli F, et al. (2017) The Anthelmintic Drug Niclosamide and its Analogues Activate the Parkinson's Disease Associated Protein Kinase PINK1. Chembiochem : a European Journal of Chemical Biology |
| Banks G, Lassi G, Hoerder-Suabedissen A, et al. (2017) A missense mutation in Katnal1 underlies behavioural, neurological and ciliary anomalies. Molecular Psychiatry |
| Colombi I, Tinarelli F, Pasquale V, et al. (2016) Corrigendum: A Simplified In vitro Experimental Model Encompasses the Essential Features of Sleep. Frontiers in Neuroscience. 10: 409 |
| Colombi I, Tinarelli F, Pasquale V, et al. (2016) A Simplified In vitro Experimental Model Encompasses the Essential Features of Sleep. Frontiers in Neuroscience. 10: 315 |
| Lassi G, Priano L, Maggi S, et al. (2016) Deletion of the Snor D116/S no RD116 alters sleep in mice and patients with Prader-Willi syndrome Sleep. 39: 637-644 |
| Lassi G, Priano L, Maggi S, et al. (2015) Deletion of the Snord116/SNORD116 Alters Sleep in Mice and Patients with Prader-Willi Syndrome. Sleep |
| Tucci V, Kleefstra T, Hardy A, et al. (2014) Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features. The Journal of Clinical Investigation. 124: 1468-82 |
| Tinarelli F, Garcia-Garcia C, Nicassio F, et al. (2014) Parent-of-origin genetic background affects the transcriptional levels of circadian and neuronal plasticity genes following sleep loss. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 369: 20120471 |