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Frontiers in Cellular Neuroscience|December 6, 2021
Rett Syndrome and Fragile X Syndrome: Different Etiology With Common Molecular DysfunctionsSnow Bach, Stephen Shovlin, Michael Moriarty, et al.Orphanet Journal of Rare Diseases|July 13, 2018
Transcriptome level analysis in Rett syndrome using human samples from different tissuesStephen Shovlin, Daniela TropeaFrontiers in Neuroscience|June 17, 2022
Molecular Signatures of Response to Mecasermin in Children With Rett SyndromeStephen Shovlin, Chloe Delepine, Lindsay Swanson, et al.Orphanet Journal of Rare Diseases|January 30, 2024
Rett syndrome in Ireland: a demographic studyKomal Zade, Ciara Campbell, Snow Bach, et al.Neuroscience Letters|April 16, 2016
Expression of nuclear Methyl-CpG binding protein 2 (Mecp2) is dependent on neuronal stimulation and application of Insulin-like growth factor 1Daniela Tropea, Niall Mortimer, Stefania Bellini, et al.Scientific Reports|December 18, 2020
Methyl-CpG-binding protein 2 mediates overlapping mechanisms across brain disordersSnow Bach, Niamh M Ryan, Paolo Guasoni, et al.Med (New York, N.Y.)|October 12, 2024
Trofinetide treatment for Rett syndrome: Lessons to learnDaniela TropeaEndocrine Reviews|June 20, 2026
DAX-1 in sex determination and gonadal development: revisiting the anti-testis hypothesisBarbara Bardoni, Enzo LalliMolecular Psychiatry|January 8, 2021
Role of phosphodiesterases in the pathophysiology of neurodevelopmental disordersSébastien Delhaye, Barbara BardoniBiochimie|June 24, 2010
The role of G-quadruplex in RNA metabolism: involvement of FMRP and FMR2PMireille Melko, Barbara BardoniPageof 13