Gabriele Deidda - Publications

Affiliations: 
University of Malta 
Area:
development, visual system, epilepsy, Down syndrome

14/21 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Deidda G, Pierucci M, Crunelli V, Di Giovanni G. 5-HT/GABA interaction in neurodevelopment and plasticity. Progress in Brain Research. 259: 287-317. PMID 33541680 DOI: 10.1016/bs.pbr.2021.01.009  1
2021 Deidda G, Crunelli V, Di Giovanni G. 5-HT/GABA interaction in epilepsy. Progress in Brain Research. 259: 265-286. PMID 33541679 DOI: 10.1016/bs.pbr.2021.01.008  1
2020 Casarrubea M, Davies C, Pierucci M, Colangeli R, Deidda G, Santangelo A, Aiello S, Crescimanno G, Di Giovanni G. The impact of chronic daily nicotine exposure and its overnight withdrawal on the structure of anxiety-related behaviors in rats: Role of the lateral Habenula. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 110131. PMID 33039434 DOI: 10.1016/j.pnpbp.2020.110131  1
2020 Bombardi C, Delicata F, Tagliavia C, Pierucci M, Deidda G, Casarrubea M, De Deurwaerdère P, Di Giovanni G. Acute and Chronic Nicotine Exposures Differentially Affect Central Serotonin 2A Receptor Function: Focus on the Lateral Habenula. International Journal of Molecular Sciences. 21. PMID 32182934 DOI: 10.3390/ijms21051873  1
2019 De Deurwaerdère P, Ramos M, Bharatiya R, Puginier E, Chagraoui A, Manem J, Cuboni E, Pierucci M, Deidda G, Casarrubea M, Di Giovanni G. Lorcaserin bidirectionally regulates dopaminergic function site-dependently and disrupts dopamine brain area correlations in rats. Neuropharmacology. 107915. PMID 31862271 DOI: 10.1016/j.neuropharm.2019.107915  1
2019 Casarrubea M, Pierucci M, Aiello S, Cassar D, Deidda G, Crescimanno G, Di Giovanni G. Effects of chronic nicotine on the temporal structure of anxiety-related behavior in rats tested in hole-board. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 109731. PMID 31394140 DOI: 10.1016/j.pnpbp.2019.109731  1
2019 Colangeli R, Di Maio R, Pierucci M, Deidda G, Casarrubea M, Di Giovanni G. Synergistic action of CB and 5-HT receptors in preventing pilocarpine-induced status epilepticus in rats. Neurobiology of Disease. 125: 135-145. PMID 30716469 DOI: 10.1016/j.nbd.2019.01.026  1
2017 Parrini M, Ghezzi D, Deidda G, Medrihan L, Castroflorio E, Alberti M, Baldelli P, Cancedda L, Contestabile A. Aerobic exercise and a BDNF-mimetic therapy rescue learning and memory in a mouse model of Down syndrome. Scientific Reports. 7: 16825. PMID 29203796 DOI: 10.1038/S41598-017-17201-8  0.84
2016 Baroncelli L, Cenni MC, Melani R, Deidda G, Landi S, Narducci R, Cancedda L, Maffei L, Berardi N. Early IGF-1 Primes Visual Cortex Maturation And Accelerates Developmental Switch Between NKCC1 and KCC2 Chloride Transporters in Enriched Animals. Neuropharmacology. PMID 26924708 DOI: 10.1016/J.Neuropharm.2016.02.034  0.84
2015 Deidda G, Parrini M, Naskar S, Bozarth IF, Contestabile A, Cancedda L. Excitatory GABAergic transmission impairs synaptic plasticity and memory in Down syndrome. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 47: 36. PMID 26531425 DOI: 10.1016/J.Ijdevneu.2015.04.104  0.84
2015 Deidda G, Parrini M, Naskar S, Bozarth IF, Contestabile A, Cancedda L. Reversing excitatory GABAAR signaling restores synaptic plasticity and memory in a mouse model of Down syndrome. Nature Medicine. 21: 318-26. PMID 25774849 DOI: 10.1038/Nm.3827  0.84
2015 Deidda G, Allegra M, Cerri C, Naskar S, Bony G, Zunino G, Bozzi Y, Caleo M, Cancedda L. Early depolarizing GABA controls critical-period plasticity in the rat visual cortex. Nature Neuroscience. 18: 87-96. PMID 25485756 DOI: 10.1038/Nn.3890  0.84
2014 Deidda G, Bozarth IF, Cancedda L. Modulation of GABAergic transmission in development and neurodevelopmental disorders: investigating physiology and pathology to gain therapeutic perspectives. Frontiers in Cellular Neuroscience. 8: 119. PMID 24904277 DOI: 10.3389/Fncel.2014.00119  0.84
2012 dal Maschio M, Ghezzi D, Bony G, Alabastri A, Deidda G, Brondi M, Sato SS, Zaccaria RP, Di Fabrizio E, Ratto GM, Cancedda L. High-performance and site-directed in utero electroporation by a triple-electrode probe. Nature Communications. 3: 960. PMID 22805567 DOI: 10.1038/Ncomms1961  0.84
Low-probability matches
2018 Wang B, Deidda G, Mitraki A, MacLeod KT, Terracciano CM. P5718Self-assembling arginine-glycine-aspartic acid-containing peptides abbreviate human cardiomyocyte calcium transients and increase sarcoplasmic reticulum contribution to excitation-contraction coupling European Heart Journal. 39. DOI: 10.1093/eurheartj/ehy566.p5718  0.01
2004 Rijkers T, Deidda G, van Koningsbruggen S, van Geel M, Lemmers RJ, van Deutekom JC, Figlewicz D, Hewitt JE, Padberg GW, Frants RR, van der Maarel SM. FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients. Journal of Medical Genetics. 41: 826-36. PMID 15520407 DOI: 10.1136/jmg.2004.019364  0.01
2001 van Overveld PG, Lemmers RJ, Deidda G, Sandkuijl L, Padberg GW, Frants RR, van der Maarel SM. Interchromosomal repeat array interactions between chromosomes 4 and 10: a model for subtelomeric plasticity. Human Molecular Genetics. 9: 2879-84. PMID 11092764 DOI: 10.1093/HMG/9.19.2879  0.01
2000 van der Maarel SM, Deidda G, Lemmers RJ, van Overveld PG, van der Wielen M, Hewitt JE, Sandkuijl L, Bakker B, van Ommen GJ, Padberg GW, Frants RR. De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10. American Journal of Human Genetics. 66: 26-35. PMID 10631134 DOI: 10.1086/302730  0.01
1999 Galluzzi G, Deidda G, Cacurri S, Colantoni L, Piazzo N, Vigneti E, Ricci E, Servidei S, Merico B, Pachì A, Brambati B, Mangiola F, Tonali P, Felicetti L. Molecular analysis of 4q35 rearrangements in fascioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease. Neuromuscular Disorders : Nmd. 9: 190-8. PMID 10382915 DOI: 10.1016/S0960-8966(98)00116-3  0.01
1998 Lemmers RJ, van der Maarel SM, van Deutekom JC, van der Wielen MJ, Deidda G, Dauwerse HG, Hewitt J, Hofker M, Bakker E, Padberg GW, Frants RR. Inter- and intrachromosomal sub-telomeric rearrangements on 4q35: implications for facioscapulohumeral muscular dystrophy (FSHD) aetiology and diagnosis. Human Molecular Genetics. 7: 1207-14. PMID 9668160 DOI: 10.1093/HMG/7.8.1207  0.01
1994 Deidda GC, Cacurri S, La Cesa I, Scoppetta C, Felicetti L. 4q35 molecular probes for the diagnosis and genetic counseling of facioscapulohumeral muscular dystrophy. Annals of Neurology. 36: 117-8. PMID 8024254 DOI: 10.1002/ANA.410360128  0.01
Hide low-probability matches.