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Stefano Doccini

Showing results (31-40 of 50) with videos related to

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Biomolecules|August 29, 2024
Extracellular Vesicles Induce Nuclear Factor-κB Activation and Interleukin-8 Synthesis through miRNA-191-5p Contributing to Inflammatory Processes: Potential Implications in the Pathogenesis of Chronic Obstructive Pulmonary DiseaseSara Carpi, Beatrice Polini, Dario Nieri, et al.
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.
Neuropediatrics|May 12, 2020
Optic Atrophy and Generalized Chorea in a Patient Harboring an OPA10/RTN4IP1 Pathogenic VariantThea Giacomini, Alessandra Gamucci, Livia Pisciotta, et al.
Human Mutation|April 26, 2020
Bi-allelic mutations in HARS1 severely impair histidyl-tRNA synthetase expression and enzymatic activity causing a novel multisystem ataxic syndromeDaniele Galatolo, Molly E Kuo, Patrick Mullen, et al.
International Journal of Molecular Sciences|December 9, 2023
Novel <i>COX11</i> Mutations Associated with Mitochondrial Disorder: Functional Characterization in Patient Fibroblasts and <i>Saccharomyces cerevisiae</i>Chenelle A Caron-Godon, Stefania Della Vecchia, Alessandro Romano, et al.
Journal of the Neurological Sciences|March 6, 2016
Mitochondrial dysfunction in hereditary spastic paraparesis with mutations in DDHD1/SPG28Andrea Mignarri, Anna Rubegni, Alessandra Tessa, et al.
Human Molecular Genetics|August 22, 2022
Mitofusin 2 mutation drives cell proliferation in Charcot-Marie-Tooth 2A fibroblastsPaola Zanfardino, Giovanna Longo, Alessandro Amati, et al.
Human Molecular Genetics|March 5, 2015
Additive effect of nuclear and mitochondrial mutations in a patient with mitochondrial encephalomyopathyClaudia Nesti, Maria Chiara Meschini, Brigitte Meunier, et al.
Biomolecules|July 29, 2023
Tanshinone IIA and Cryptotanshinone Counteract Inflammation by Regulating Gene and miRNA Expression in Human SGBS AdipocytesSara Carpi, Stefano Quarta, Stefano Doccini, et al.
Cell Death Discovery|April 8, 2020
Proteomic and functional analyses in disease models reveal CLN5 protein involvement in mitochondrial dysfunctionStefano Doccini, Federica Morani, Claudia Nesti, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
Biomolecules|August 29, 2024
Extracellular Vesicles Induce Nuclear Factor-κB Activation and Interleukin-8 Synthesis through miRNA-191-5p Contributing to Inflammatory Processes: Potential Implications in the Pathogenesis of Chronic Obstructive Pulmonary DiseaseSara Carpi, Beatrice Polini, Dario Nieri, et al.
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.
Neuropediatrics|May 12, 2020
Optic Atrophy and Generalized Chorea in a Patient Harboring an OPA10/RTN4IP1 Pathogenic VariantThea Giacomini, Alessandra Gamucci, Livia Pisciotta, et al.
Human Mutation|April 26, 2020
Bi-allelic mutations in HARS1 severely impair histidyl-tRNA synthetase expression and enzymatic activity causing a novel multisystem ataxic syndromeDaniele Galatolo, Molly E Kuo, Patrick Mullen, et al.
International Journal of Molecular Sciences|December 9, 2023
Novel <i>COX11</i> Mutations Associated with Mitochondrial Disorder: Functional Characterization in Patient Fibroblasts and <i>Saccharomyces cerevisiae</i>Chenelle A Caron-Godon, Stefania Della Vecchia, Alessandro Romano, et al.
Journal of the Neurological Sciences|March 6, 2016
Mitochondrial dysfunction in hereditary spastic paraparesis with mutations in DDHD1/SPG28Andrea Mignarri, Anna Rubegni, Alessandra Tessa, et al.
Human Molecular Genetics|August 22, 2022
Mitofusin 2 mutation drives cell proliferation in Charcot-Marie-Tooth 2A fibroblastsPaola Zanfardino, Giovanna Longo, Alessandro Amati, et al.
Human Molecular Genetics|March 5, 2015
Additive effect of nuclear and mitochondrial mutations in a patient with mitochondrial encephalomyopathyClaudia Nesti, Maria Chiara Meschini, Brigitte Meunier, et al.
Biomolecules|July 29, 2023
Tanshinone IIA and Cryptotanshinone Counteract Inflammation by Regulating Gene and miRNA Expression in Human SGBS AdipocytesSara Carpi, Stefano Quarta, Stefano Doccini, et al.
Cell Death Discovery|April 8, 2020
Proteomic and functional analyses in disease models reveal CLN5 protein involvement in mitochondrial dysfunctionStefano Doccini, Federica Morani, Claudia Nesti, et al.
Pageof 5