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Maria Marchese

Showing results (51-60 of 64) with videos related to

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Biochemical and Biophysical Research Communications|June 14, 2016
Dolichol-phosphate mannose synthase depletion in zebrafish leads to dystrophic muscle with hypoglycosylated α-dystroglycanMaria Marchese, Andrea Pappalardo, Jacopo Baldacci, et al.
International Journal of Molecular Sciences|June 24, 2022
Trehalose Treatment in Zebrafish Model of Lafora DiseaseStefania Della Vecchia, Asahi Ogi, Rosario Licitra, et al.
Journal of Neurology|March 11, 2021
New pathogenic variants in COQ4 cause ataxia and neurodevelopmental disorder without detectable CoQ<sub>10</sub> deficiency in muscle or skin fibroblastsSerena Mero, Leonardo Salviati, Vincenzo Leuzzi, et al.
Cells|June 10, 2022
Lysosomal Proteomics Links Disturbances in Lipid Homeostasis and Sphingolipid Metabolism to CLN5 DiseaseStefano Doccini, Maria Marchese, Federica Morani, et al.
Molecular Psychiatry|May 9, 2025
CLN5 deficiency impairs glucose uptake and uncovers PHGDH as a potential biomarker in Batten diseaseMaria Marchese, Sara Bernardi, Rachele Vivarelli, et al.
Neurobiology of Disease|May 19, 2024
Targeting autophagy impairment improves the phenotype of a novel CLN8 zebrafish modelMaria Marchese, Sara Bernardi, Asahi Ogi, et al.
Scientific Reports|September 29, 2016
Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsyFederico Sicca, Elena Ambrosini, Maria Marchese, et al.
Pharmaceuticals (Basel, Switzerland)|December 28, 2021
Identification of a Thyroid Hormone Derivative as a Pleiotropic Agent for the Treatment of Alzheimer's DiseaseMassimiliano Runfola, Michele Perni, Xiaoting Yang, et al.
Neurobiology of Disease|April 29, 2020
A homozygous MRPL24 mutation causes a complex movement disorder and affects the mitoribosome assemblyMichela Di Nottia, Maria Marchese, Daniela Verrigni, et al.
Annals of Clinical and Translational Neurology|March 28, 2020
Loss of ap4s1 in zebrafish leads to neurodevelopmental defects resembling spastic paraplegia 52Angelica D'Amore, Alessandra Tessa, Valentina Naef, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
Biochemical and Biophysical Research Communications|June 14, 2016
Dolichol-phosphate mannose synthase depletion in zebrafish leads to dystrophic muscle with hypoglycosylated α-dystroglycanMaria Marchese, Andrea Pappalardo, Jacopo Baldacci, et al.
International Journal of Molecular Sciences|June 24, 2022
Trehalose Treatment in Zebrafish Model of Lafora DiseaseStefania Della Vecchia, Asahi Ogi, Rosario Licitra, et al.
Journal of Neurology|March 11, 2021
New pathogenic variants in COQ4 cause ataxia and neurodevelopmental disorder without detectable CoQ<sub>10</sub> deficiency in muscle or skin fibroblastsSerena Mero, Leonardo Salviati, Vincenzo Leuzzi, et al.
Cells|June 10, 2022
Lysosomal Proteomics Links Disturbances in Lipid Homeostasis and Sphingolipid Metabolism to CLN5 DiseaseStefano Doccini, Maria Marchese, Federica Morani, et al.
Molecular Psychiatry|May 9, 2025
CLN5 deficiency impairs glucose uptake and uncovers PHGDH as a potential biomarker in Batten diseaseMaria Marchese, Sara Bernardi, Rachele Vivarelli, et al.
Neurobiology of Disease|May 19, 2024
Targeting autophagy impairment improves the phenotype of a novel CLN8 zebrafish modelMaria Marchese, Sara Bernardi, Asahi Ogi, et al.
Scientific Reports|September 29, 2016
Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsyFederico Sicca, Elena Ambrosini, Maria Marchese, et al.
Pharmaceuticals (Basel, Switzerland)|December 28, 2021
Identification of a Thyroid Hormone Derivative as a Pleiotropic Agent for the Treatment of Alzheimer's DiseaseMassimiliano Runfola, Michele Perni, Xiaoting Yang, et al.
Neurobiology of Disease|April 29, 2020
A homozygous MRPL24 mutation causes a complex movement disorder and affects the mitoribosome assemblyMichela Di Nottia, Maria Marchese, Daniela Verrigni, et al.
Annals of Clinical and Translational Neurology|March 28, 2020
Loss of ap4s1 in zebrafish leads to neurodevelopmental defects resembling spastic paraplegia 52Angelica D'Amore, Alessandra Tessa, Valentina Naef, et al.
Pageof 7