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Valter Tucci

Showing results (41-50 of 56) with videos related to

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Human Molecular Genetics|May 20, 2020
Loss of Snord116 alters cortical neuronal activity in mice: a preclinical investigation of Prader-Willi syndromeMarta Pace, Ilaria Colombi, Matteo Falappa, et al.
JCI Insight|May 5, 2020
Loss of Snord116 impacts lateral hypothalamus, sleep, and food-related behaviorsMarta Pace, Matteo Falappa, Andrea Freschi, et al.
Mechanisms of Ageing and Development|July 25, 2016
With mouse age comes wisdom: A review and suggestions of relevant mouse models for age-related conditionsSusanne Drechsler, Marina A Lynch, Susana Novella, et al.
Scientific Reports|December 21, 2017
The after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasisSilvia Maggi, Edoardo Balzani, Glenda Lassi, et al.
Sleep|October 9, 2015
Deletion of the Snord116/SNORD116 Alters Sleep in Mice and Patients with Prader-Willi SyndromeGlenda Lassi, Lorenzo Priano, Silvia Maggi, et al.
Plos One|February 18, 2010
ENU mutagenesis reveals a novel phenotype of reduced limb strength in mice lacking fibrillin 2Gaynor Miller, Monica Neilan, Ruth Chia, et al.
Science Advances|March 1, 2024
Early IGF-1 receptor inhibition in mice mimics preterm human brain disorders and reveals a therapeutic targetAlberto Potenzieri, Sara Uccella, Deborah Preiti, et al.
Cell Reports. Medicine|May 13, 2026
Traumatic life experiences during critical periods lead to diverse developmental trajectoriesGiovanni Morelli, Greta Visintin, Elisa Gelli, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|March 10, 2015
TAAR1 Modulates Cortical Glutamate NMDA Receptor FunctionStefano Espinoza, Gabriele Lignani, Lucia Caffino, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 13, 2021
<i>Dlk1</i> dosage regulates hippocampal neurogenesis and cognitionRaquel Montalbán-Loro, Glenda Lassi, Anna Lozano-Ureña, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|May 20, 2020
Loss of Snord116 alters cortical neuronal activity in mice: a preclinical investigation of Prader-Willi syndromeMarta Pace, Ilaria Colombi, Matteo Falappa, et al.
JCI Insight|May 5, 2020
Loss of Snord116 impacts lateral hypothalamus, sleep, and food-related behaviorsMarta Pace, Matteo Falappa, Andrea Freschi, et al.
Mechanisms of Ageing and Development|July 25, 2016
With mouse age comes wisdom: A review and suggestions of relevant mouse models for age-related conditionsSusanne Drechsler, Marina A Lynch, Susana Novella, et al.
Scientific Reports|December 21, 2017
The after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasisSilvia Maggi, Edoardo Balzani, Glenda Lassi, et al.
Sleep|October 9, 2015
Deletion of the Snord116/SNORD116 Alters Sleep in Mice and Patients with Prader-Willi SyndromeGlenda Lassi, Lorenzo Priano, Silvia Maggi, et al.
Plos One|February 18, 2010
ENU mutagenesis reveals a novel phenotype of reduced limb strength in mice lacking fibrillin 2Gaynor Miller, Monica Neilan, Ruth Chia, et al.
Science Advances|March 1, 2024
Early IGF-1 receptor inhibition in mice mimics preterm human brain disorders and reveals a therapeutic targetAlberto Potenzieri, Sara Uccella, Deborah Preiti, et al.
Cell Reports. Medicine|May 13, 2026
Traumatic life experiences during critical periods lead to diverse developmental trajectoriesGiovanni Morelli, Greta Visintin, Elisa Gelli, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|March 10, 2015
TAAR1 Modulates Cortical Glutamate NMDA Receptor FunctionStefano Espinoza, Gabriele Lignani, Lucia Caffino, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 13, 2021
<i>Dlk1</i> dosage regulates hippocampal neurogenesis and cognitionRaquel Montalbán-Loro, Glenda Lassi, Anna Lozano-Ureña, et al.
Pageof 6