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Luca Colantoni

Showing results (1-10 of 17) with videos related to

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Muscle & Nerve|October 9, 2009
Facioscapulohumeral muscular dystrophy: do neurotrophins play a role?Francesco Angelucci, Luca Colantoni
BMC Medical Genetics|March 6, 2007
The Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressureMonica Rossi, Enzo Ricci, Luca Colantoni, et al.
Electrophoresis|August 11, 2023
Epigenetic profiling of the D4Z4 locus: Optimization of the protocol for studying DNA methylation at single CpG site levelDomenica Megalizzi, Giulia Trastulli, Valerio Caputo, et al.
Cells|September 9, 2022
Update on the Molecular Aspects and Methods Underlying the Complex Architecture of FSHDValerio Caputo, Domenica Megalizzi, Carlo Fabrizio, et al.
International Journal of Molecular Sciences|October 26, 2024
Deciphering the Complexity of FSHD: A Multimodal Approach as a Model for Rare DisordersDomenica Megalizzi, Giulia Trastulli, Luca Colantoni, et al.
Genes|August 26, 2022
Relationship between Nutrition, Lifestyle, and Neurodegenerative Disease: Lessons from <i>ADH1B</i>, <i>CYP1A2</i> and <i>MTHFR</i>Shila Barati, Carlo Fabrizio, Claudia Strafella, et al.
Current Alzheimer Research|March 9, 2010
Alzheimer's disease (AD) and Mild Cognitive Impairment (MCI) patients are characterized by increased BDNF serum levelsFrancesco Angelucci, Gianfranco Spalletta, Fulvia di Iulio, et al.
Proteomics|October 3, 2006
Parallel protein and transcript profiles of FSHD patient muscles correlate to the D4Z4 arrangement and reveal a common impairment of slow to fast fibre differentiation and a general deregulation of MyoD-dependent genesBarbara Celegato, Daniele Capitanio, Mario Pescatori, et al.
Frontiers in Genetics|September 7, 2023
Whole exome sequencing highlights rare variants in <i>CTCF</i>, <i>DNMT1</i>, <i>DNMT3A</i>, <i>EZH2</i> and <i>SUV39H1</i> as associated with FSHDClaudia Strafella, Valerio Caputo, Sara Bortolani, et al.
Neurogenetics|March 27, 2019
Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS eraStefania Zampatti, Luca Colantoni, Claudia Strafella, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Muscle & Nerve|October 9, 2009
Facioscapulohumeral muscular dystrophy: do neurotrophins play a role?Francesco Angelucci, Luca Colantoni
BMC Medical Genetics|March 6, 2007
The Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressureMonica Rossi, Enzo Ricci, Luca Colantoni, et al.
Electrophoresis|August 11, 2023
Epigenetic profiling of the D4Z4 locus: Optimization of the protocol for studying DNA methylation at single CpG site levelDomenica Megalizzi, Giulia Trastulli, Valerio Caputo, et al.
Cells|September 9, 2022
Update on the Molecular Aspects and Methods Underlying the Complex Architecture of FSHDValerio Caputo, Domenica Megalizzi, Carlo Fabrizio, et al.
International Journal of Molecular Sciences|October 26, 2024
Deciphering the Complexity of FSHD: A Multimodal Approach as a Model for Rare DisordersDomenica Megalizzi, Giulia Trastulli, Luca Colantoni, et al.
Genes|August 26, 2022
Relationship between Nutrition, Lifestyle, and Neurodegenerative Disease: Lessons from <i>ADH1B</i>, <i>CYP1A2</i> and <i>MTHFR</i>Shila Barati, Carlo Fabrizio, Claudia Strafella, et al.
Current Alzheimer Research|March 9, 2010
Alzheimer's disease (AD) and Mild Cognitive Impairment (MCI) patients are characterized by increased BDNF serum levelsFrancesco Angelucci, Gianfranco Spalletta, Fulvia di Iulio, et al.
Proteomics|October 3, 2006
Parallel protein and transcript profiles of FSHD patient muscles correlate to the D4Z4 arrangement and reveal a common impairment of slow to fast fibre differentiation and a general deregulation of MyoD-dependent genesBarbara Celegato, Daniele Capitanio, Mario Pescatori, et al.
Frontiers in Genetics|September 7, 2023
Whole exome sequencing highlights rare variants in <i>CTCF</i>, <i>DNMT1</i>, <i>DNMT3A</i>, <i>EZH2</i> and <i>SUV39H1</i> as associated with FSHDClaudia Strafella, Valerio Caputo, Sara Bortolani, et al.
Neurogenetics|March 27, 2019
Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS eraStefania Zampatti, Luca Colantoni, Claudia Strafella, et al.
Pageof 2