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Gianluca Cestra

Showing results (11-20 of 28) with videos related to

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International Journal of Molecular Sciences|February 23, 2020
TUBB Variants Underlying Different Phenotypes Result in Altered Vesicle Trafficking and Microtubule DynamicsAntonella Sferra, Stefania Petrini, Emanuele Bellacchio, et al.
Human Molecular Genetics|August 6, 2009
A conserved role for the mitochondrial citrate transporter Sea/SLC25A1 in the maintenance of chromosome integrityPatrizia Morciano, Chiara Carrisi, Loredana Capobianco, et al.
Nature|November 8, 2002
Recruitment and regulation of phosphatidylinositol phosphate kinase type 1 gamma by the FERM domain of talinGilbert Di Paolo, Lorenzo Pellegrini, Kresimir Letinic, et al.
Cell Death & Disease|April 15, 2025
A variant of the autophagic receptor NDP52 counteracts phospho-TAU accumulation and emerges as a protective factor for Alzheimer's diseaseAnna Mattioni, Claudia Carsetti, Krenare Bruqi, et al.
Disease Models & Mechanisms|April 20, 2026
Distinct cellular effects of myotonic dystrophy type 2 RAN tetrapeptides in Drosophila melanogasterMarta Marzullo, Assia De Simone, Marta Terribili, et al.
Scientific Reports|May 2, 2018
Publisher Correction: Functional interaction between FUS and SMN underlies SMA-like splicing changes in wild-type hFUS miceAlessia Mirra, Simona Rossi, Silvia Scaricamazza, et al.
Scientific Reports|May 19, 2017
Functional interaction between FUS and SMN underlies SMA-like splicing changes in wild-type hFUS miceAlessia Mirra, Simona Rossi, Silvia Scaricamazza, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|November 28, 2019
A Lipophilic 4-Phenylbutyric Acid Derivative That Prevents Aggregation and Retention of Misfolded ProteinsSalome Azoulay-Ginsburg, Laura Trobiani, Andrea Setini, et al.
Neurobiology of Disease|February 7, 2020
UsnRNP trafficking is regulated by stress granules and compromised by mutant ALS proteinsSimona Rossi, Valentina Rompietti, Ylenia Antonucci, et al.
Human Mutation|October 30, 2018
Recessive mutations in the neuronal isoforms of DST, encoding dystonin, lead to abnormal actin cytoskeleton organization and HSAN type VIPaola Fortugno, Francesco Angelucci, Gianluca Cestra, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
International Journal of Molecular Sciences|February 23, 2020
TUBB Variants Underlying Different Phenotypes Result in Altered Vesicle Trafficking and Microtubule DynamicsAntonella Sferra, Stefania Petrini, Emanuele Bellacchio, et al.
Human Molecular Genetics|August 6, 2009
A conserved role for the mitochondrial citrate transporter Sea/SLC25A1 in the maintenance of chromosome integrityPatrizia Morciano, Chiara Carrisi, Loredana Capobianco, et al.
Nature|November 8, 2002
Recruitment and regulation of phosphatidylinositol phosphate kinase type 1 gamma by the FERM domain of talinGilbert Di Paolo, Lorenzo Pellegrini, Kresimir Letinic, et al.
Cell Death & Disease|April 15, 2025
A variant of the autophagic receptor NDP52 counteracts phospho-TAU accumulation and emerges as a protective factor for Alzheimer's diseaseAnna Mattioni, Claudia Carsetti, Krenare Bruqi, et al.
Disease Models & Mechanisms|April 20, 2026
Distinct cellular effects of myotonic dystrophy type 2 RAN tetrapeptides in Drosophila melanogasterMarta Marzullo, Assia De Simone, Marta Terribili, et al.
Scientific Reports|May 2, 2018
Publisher Correction: Functional interaction between FUS and SMN underlies SMA-like splicing changes in wild-type hFUS miceAlessia Mirra, Simona Rossi, Silvia Scaricamazza, et al.
Scientific Reports|May 19, 2017
Functional interaction between FUS and SMN underlies SMA-like splicing changes in wild-type hFUS miceAlessia Mirra, Simona Rossi, Silvia Scaricamazza, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|November 28, 2019
A Lipophilic 4-Phenylbutyric Acid Derivative That Prevents Aggregation and Retention of Misfolded ProteinsSalome Azoulay-Ginsburg, Laura Trobiani, Andrea Setini, et al.
Neurobiology of Disease|February 7, 2020
UsnRNP trafficking is regulated by stress granules and compromised by mutant ALS proteinsSimona Rossi, Valentina Rompietti, Ylenia Antonucci, et al.
Human Mutation|October 30, 2018
Recessive mutations in the neuronal isoforms of DST, encoding dystonin, lead to abnormal actin cytoskeleton organization and HSAN type VIPaola Fortugno, Francesco Angelucci, Gianluca Cestra, et al.
Pageof 3