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Antonio Falace

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

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Human Mutation|March 26, 2013
Novel compound heterozygous mutations in TBC1D24 cause familial malignant migrating partial seizures of infancyMathieu Milh, Antonio Falace, Nathalie Villeneuve, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 29, 2014
TBC1D24 regulates neuronal migration and maturation through modulation of the ARF6-dependent pathwayAntonio Falace, Emmanuelle Buhler, Manuela Fadda, et al.
Scientific Reports|May 21, 2026
Optimized nuclei isolation and snRNA-seq reveal oligodendrocyte pathway dysregulation in MOGHE brain tissue from pediatric patientsClara Tuccari di San Carlo, Roberto Semeraro, Valentina Cetica, et al.
Cell Death and Differentiation|March 13, 2019
TBC1D24 regulates axonal outgrowth and membrane trafficking at the growth cone in rodent and human neuronsDavide Aprile, Floriana Fruscione, Simona Baldassari, et al.
Biochemical and Biophysical Research Communications|October 10, 2007
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changesRoberta Biancheri, Antonio Falace, Alessandra Tessa, et al.
Annals of Neurology|May 1, 2014
Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsyNicola Vanni, Floriana Fruscione, Edoardo Ferlazzo, et al.
Frontiers in Pediatrics|January 5, 2024
Case Report: Novel biallelic moderately damaging variants in <i>RTTN</i> in a patient with cerebellar dysplasiaFerruccio Romano, Elisabetta Amadori, Francesca Madia, et al.
American Journal of Human Genetics|August 24, 2010
TBC1D24, an ARF6-interacting protein, is mutated in familial infantile myoclonic epilepsyAntonio Falace, Fabia Filipello, Veronica La Padula, et al.
Archives of Neurology|October 13, 2006
POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrumRoberta Biancheri, Enrico Bertini, Antonio Falace, et al.
Neurobiology of Disease|June 9, 2024
FLNA regulates neuronal maturation by modulating RAC1-Cofilin activity in the developing cortexAntonio Falace, Lea Corbieres, Catia Palminha, et al.
Pageof 3

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

Sort By:
Pageof 3
Human Mutation|March 26, 2013
Novel compound heterozygous mutations in TBC1D24 cause familial malignant migrating partial seizures of infancyMathieu Milh, Antonio Falace, Nathalie Villeneuve, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 29, 2014
TBC1D24 regulates neuronal migration and maturation through modulation of the ARF6-dependent pathwayAntonio Falace, Emmanuelle Buhler, Manuela Fadda, et al.
Scientific Reports|May 21, 2026
Optimized nuclei isolation and snRNA-seq reveal oligodendrocyte pathway dysregulation in MOGHE brain tissue from pediatric patientsClara Tuccari di San Carlo, Roberto Semeraro, Valentina Cetica, et al.
Cell Death and Differentiation|March 13, 2019
TBC1D24 regulates axonal outgrowth and membrane trafficking at the growth cone in rodent and human neuronsDavide Aprile, Floriana Fruscione, Simona Baldassari, et al.
Biochemical and Biophysical Research Communications|October 10, 2007
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changesRoberta Biancheri, Antonio Falace, Alessandra Tessa, et al.
Annals of Neurology|May 1, 2014
Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsyNicola Vanni, Floriana Fruscione, Edoardo Ferlazzo, et al.
Frontiers in Pediatrics|January 5, 2024
Case Report: Novel biallelic moderately damaging variants in <i>RTTN</i> in a patient with cerebellar dysplasiaFerruccio Romano, Elisabetta Amadori, Francesca Madia, et al.
American Journal of Human Genetics|August 24, 2010
TBC1D24, an ARF6-interacting protein, is mutated in familial infantile myoclonic epilepsyAntonio Falace, Fabia Filipello, Veronica La Padula, et al.
Archives of Neurology|October 13, 2006
POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrumRoberta Biancheri, Enrico Bertini, Antonio Falace, et al.
Neurobiology of Disease|June 9, 2024
FLNA regulates neuronal maturation by modulating RAC1-Cofilin activity in the developing cortexAntonio Falace, Lea Corbieres, Catia Palminha, et al.
Pageof 3