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Giovanni Neri

Showing results (241-250 of 255) with videos related to

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Science Translational Medicine|January 7, 2011
Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056Sébastien Jacquemont, Aurore Curie, Vincent des Portes, et al.
Human Molecular Genetics|August 13, 2003
A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24Xavier J de Mollerat, Fiorella Gurrieri, Chad T Morgan, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 6, 2026
Switching to aflibercept 8 mg in neovascular age-related macular degeneration: real-world outcomes according to switch indicationDaniele Veritti, Valentina Sarao, Marco Lupidi, et al.
Human Molecular Genetics|June 10, 2015
ZC4H2, an XLID gene, is required for the generation of a specific subset of CNS interneuronsMelanie May, Kyu-Seok Hwang, Judith Miles, et al.
EMBO Molecular Medicine|October 5, 2013
The fragile X protein binds mRNAs involved in cancer progression and modulates metastasis formationRossella Lucá, Michele Averna, Francesca Zalfa, et al.
Oncotarget|October 28, 2015
Involvement of MBD4 inactivation in mismatch repair-deficient tumorigenesisRossella Tricarico, Salvatore Cortellino, Antonio Riccio, et al.
Schizophrenia Bulletin|May 22, 2015
Feasibility and Effectiveness of a Multi-Element Psychosocial Intervention for First-Episode Psychosis: Results From the Cluster-Randomized Controlled GET UP PIANO Trial in a Catchment Area of 10 Million InhabitantsMirella Ruggeri, Chiara Bonetto, Antonio Lasalvia, et al.
Human Mutation|March 10, 2011
SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlationsFrancesca Lepri, Alessandro De Luca, Lorenzo Stella, et al.
American Journal of Medical Genetics. Part A|November 21, 2025
9q34.11 Microduplications Encompassing SET Gene Are Associated With Neurodevelopmental Disorder and Recurrent DysmorphismsAlessandro De Falco, Marie Vincent, Gaëlle Vieville, et al.
Human Mutation|May 5, 2006
The spectrum of WRN mutations in Werner syndrome patientsShurong Huang, Lin Lee, Nancy B Hanson, et al.
Pageof 26

Showing results (241-250 of 255) with videos related to

Sort By:
Pageof 26
Science Translational Medicine|January 7, 2011
Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056Sébastien Jacquemont, Aurore Curie, Vincent des Portes, et al.
Human Molecular Genetics|August 13, 2003
A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24Xavier J de Mollerat, Fiorella Gurrieri, Chad T Morgan, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 6, 2026
Switching to aflibercept 8 mg in neovascular age-related macular degeneration: real-world outcomes according to switch indicationDaniele Veritti, Valentina Sarao, Marco Lupidi, et al.
Human Molecular Genetics|June 10, 2015
ZC4H2, an XLID gene, is required for the generation of a specific subset of CNS interneuronsMelanie May, Kyu-Seok Hwang, Judith Miles, et al.
EMBO Molecular Medicine|October 5, 2013
The fragile X protein binds mRNAs involved in cancer progression and modulates metastasis formationRossella Lucá, Michele Averna, Francesca Zalfa, et al.
Oncotarget|October 28, 2015
Involvement of MBD4 inactivation in mismatch repair-deficient tumorigenesisRossella Tricarico, Salvatore Cortellino, Antonio Riccio, et al.
Schizophrenia Bulletin|May 22, 2015
Feasibility and Effectiveness of a Multi-Element Psychosocial Intervention for First-Episode Psychosis: Results From the Cluster-Randomized Controlled GET UP PIANO Trial in a Catchment Area of 10 Million InhabitantsMirella Ruggeri, Chiara Bonetto, Antonio Lasalvia, et al.
Human Mutation|March 10, 2011
SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlationsFrancesca Lepri, Alessandro De Luca, Lorenzo Stella, et al.
American Journal of Medical Genetics. Part A|November 21, 2025
9q34.11 Microduplications Encompassing SET Gene Are Associated With Neurodevelopmental Disorder and Recurrent DysmorphismsAlessandro De Falco, Marie Vincent, Gaëlle Vieville, et al.
Human Mutation|May 5, 2006
The spectrum of WRN mutations in Werner syndrome patientsShurong Huang, Lin Lee, Nancy B Hanson, et al.
Pageof 26