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Tito Calì

Showing results (81-90 of 93) with videos related to

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EMBO Reports|March 31, 2018
Alpha-synuclein aggregates activate calcium pump SERCA leading to calcium dysregulationCristine Betzer, Louise Berkhoudt Lassen, Anders Olsen, et al.
Cell Death & Disease|October 16, 2020
Sorcin is an early marker of neurodegeneration, Ca<sup>2+</sup> dysregulation and endoplasmic reticulum stress associated to neurodegenerative diseasesIlaria Genovese, Flavia Giamogante, Lucia Barazzuol, et al.
Cell Death & Disease|October 7, 2022
The ataxia-linked E1081Q mutation affects the sub-plasma membrane Ca<sup>2+</sup>-microdomains by tuning PMCA3 activityFrancesca Vallese, Lorenzo Maso, Flavia Giamogante, et al.
Cellular and Molecular Life Sciences : CMLS|July 13, 2023
Sorcin promotes migration in cancer and regulates the EGF-dependent EGFR signaling pathwaysClaudia Tito, Ilaria Genovese, Flavia Giamogante, et al.
Nature Cell Biology|July 3, 2026
Author Correction: Mitochondrial fission links ECM mechanotransduction to metabolic redox homeostasis and metastatic chemotherapy resistancePatrizia Romani, Nunzia Nirchio, Mattia Arboit, et al.
Nature Cell Biology|February 15, 2022
Mitochondrial fission links ECM mechanotransduction to metabolic redox homeostasis and metastatic chemotherapy resistancePatrizia Romani, Nunzia Nirchio, Mattia Arboit, et al.
Nature Metabolism|September 16, 2025
BDH2-driven lysosome-to-mitochondria iron transfer shapes ferroptosis vulnerability of the melanoma cell statesFrancesca Rizzollo, Abril Escamilla-Ayala, Nicola Fattorelli, et al.
Communications Biology|October 10, 2024
ER-mitochondria distance is a critical parameter for efficient mitochondrial Ca<sup>2+</sup> uptake and oxidative metabolismGiulia Dematteis, Laura Tapella, Claudio Casali, et al.
Cell Reports. Medicine|February 25, 2024
SEPN1-related myopathy depends on the oxidoreductase ERO1A and is druggable with the chemical chaperone TUDCASerena Germani, Andrew Tri Van Ho, Alessandro Cherubini, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 7, 2023
ATP2B2 de novo variants as a cause of variable neurodevelopmental disorders that feature dystonia, ataxia, intellectual disability, behavioral symptoms, and seizuresElena Poggio, Lucia Barazzuol, Andrea Salmaso, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
EMBO Reports|March 31, 2018
Alpha-synuclein aggregates activate calcium pump SERCA leading to calcium dysregulationCristine Betzer, Louise Berkhoudt Lassen, Anders Olsen, et al.
Cell Death & Disease|October 16, 2020
Sorcin is an early marker of neurodegeneration, Ca<sup>2+</sup> dysregulation and endoplasmic reticulum stress associated to neurodegenerative diseasesIlaria Genovese, Flavia Giamogante, Lucia Barazzuol, et al.
Cell Death & Disease|October 7, 2022
The ataxia-linked E1081Q mutation affects the sub-plasma membrane Ca<sup>2+</sup>-microdomains by tuning PMCA3 activityFrancesca Vallese, Lorenzo Maso, Flavia Giamogante, et al.
Cellular and Molecular Life Sciences : CMLS|July 13, 2023
Sorcin promotes migration in cancer and regulates the EGF-dependent EGFR signaling pathwaysClaudia Tito, Ilaria Genovese, Flavia Giamogante, et al.
Nature Cell Biology|July 3, 2026
Author Correction: Mitochondrial fission links ECM mechanotransduction to metabolic redox homeostasis and metastatic chemotherapy resistancePatrizia Romani, Nunzia Nirchio, Mattia Arboit, et al.
Nature Cell Biology|February 15, 2022
Mitochondrial fission links ECM mechanotransduction to metabolic redox homeostasis and metastatic chemotherapy resistancePatrizia Romani, Nunzia Nirchio, Mattia Arboit, et al.
Nature Metabolism|September 16, 2025
BDH2-driven lysosome-to-mitochondria iron transfer shapes ferroptosis vulnerability of the melanoma cell statesFrancesca Rizzollo, Abril Escamilla-Ayala, Nicola Fattorelli, et al.
Communications Biology|October 10, 2024
ER-mitochondria distance is a critical parameter for efficient mitochondrial Ca<sup>2+</sup> uptake and oxidative metabolismGiulia Dematteis, Laura Tapella, Claudio Casali, et al.
Cell Reports. Medicine|February 25, 2024
SEPN1-related myopathy depends on the oxidoreductase ERO1A and is druggable with the chemical chaperone TUDCASerena Germani, Andrew Tri Van Ho, Alessandro Cherubini, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 7, 2023
ATP2B2 de novo variants as a cause of variable neurodevelopmental disorders that feature dystonia, ataxia, intellectual disability, behavioral symptoms, and seizuresElena Poggio, Lucia Barazzuol, Andrea Salmaso, et al.
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