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Luisa Foco

Showing results (31-40 of 51) with videos related to

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Human Molecular Genetics|December 6, 2018
Corrigendum: SLP-2 interacts with Parkin in mitochondria and prevents mitochondrial dysfunction in Parkin-deficient human iPSC-derived neurons and DrosophilaAlessandra Zanon, Sreehari Kalvakuri, Aleksandar Rakovic, et al.
Human Molecular Genetics|April 6, 2017
SLP-2 interacts with Parkin in mitochondria and prevents mitochondrial dysfunction in Parkin-deficient human iPSC-derived neurons and DrosophilaAlessandra Zanon, Sreehari Kalvakuri, Aleksandar Rakovic, et al.
Cell Reports|December 30, 2023
Genetic determinants of complement activation in the general populationDamia Noce, Luisa Foco, Dorothea Orth-Höller, et al.
Biomolecules|November 27, 2021
Genetic and Metabolic Determinants of Atrial Fibrillation in a General Population Sample: The CHRIS StudyDavid B Emmert, Vladimir Vukovic, Nikola Dordevic, et al.
Human Genetics|July 30, 2025
Genomic and molecular evidence that the LncRNA DSP-AS1 modulates desmoplakin expressionLuisa Foco, Marzia De Bortoli, Fabiola Del Greco M, et al.
Medrxiv : the Preprint Server for Health Sciences|April 16, 2025
Genomic and molecular evidence that the lncRNA <i>DSP-AS1</i> modulates Desmoplakin expressionLuisa Foco, Marzia De Bortoli, M Fabiola Del Greco, et al.
Journal of Translational Medicine|November 7, 2015
The Cooperative Health Research in South Tyrol (CHRIS) study: rationale, objectives, and preliminary resultsCristian Pattaro, Martin Gögele, Deborah Mascalzoni, et al.
Pathogens and Global Health|October 12, 2021
Prospective epidemiological, molecular, and genetic characterization of a novel coronavirus disease in the Val Venosta/Vinschgau: the CHRIS COVID-19 study protocolCristian Pattaro, Giulia Barbieri, Luisa Foco, et al.
Journal of the American College of Cardiology|July 16, 2011
Influence of 9p21.3 genetic variants on clinical and angiographic outcomes in early-onset myocardial infarctionDiego Ardissino, Carlo Berzuini, Piera Angelica Merlini, et al.
Journal of Cellular and Molecular Medicine|June 17, 2022
GCN5 contributes to intracellular lipid accumulation in human primary cardiac stromal cells from patients affected by Arrhythmogenic cardiomyopathyChiara Volani, Alessandra Pagliaro, Johannes Rainer, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|December 6, 2018
Corrigendum: SLP-2 interacts with Parkin in mitochondria and prevents mitochondrial dysfunction in Parkin-deficient human iPSC-derived neurons and DrosophilaAlessandra Zanon, Sreehari Kalvakuri, Aleksandar Rakovic, et al.
Human Molecular Genetics|April 6, 2017
SLP-2 interacts with Parkin in mitochondria and prevents mitochondrial dysfunction in Parkin-deficient human iPSC-derived neurons and DrosophilaAlessandra Zanon, Sreehari Kalvakuri, Aleksandar Rakovic, et al.
Cell Reports|December 30, 2023
Genetic determinants of complement activation in the general populationDamia Noce, Luisa Foco, Dorothea Orth-Höller, et al.
Biomolecules|November 27, 2021
Genetic and Metabolic Determinants of Atrial Fibrillation in a General Population Sample: The CHRIS StudyDavid B Emmert, Vladimir Vukovic, Nikola Dordevic, et al.
Human Genetics|July 30, 2025
Genomic and molecular evidence that the LncRNA DSP-AS1 modulates desmoplakin expressionLuisa Foco, Marzia De Bortoli, Fabiola Del Greco M, et al.
Medrxiv : the Preprint Server for Health Sciences|April 16, 2025
Genomic and molecular evidence that the lncRNA <i>DSP-AS1</i> modulates Desmoplakin expressionLuisa Foco, Marzia De Bortoli, M Fabiola Del Greco, et al.
Journal of Translational Medicine|November 7, 2015
The Cooperative Health Research in South Tyrol (CHRIS) study: rationale, objectives, and preliminary resultsCristian Pattaro, Martin Gögele, Deborah Mascalzoni, et al.
Pathogens and Global Health|October 12, 2021
Prospective epidemiological, molecular, and genetic characterization of a novel coronavirus disease in the Val Venosta/Vinschgau: the CHRIS COVID-19 study protocolCristian Pattaro, Giulia Barbieri, Luisa Foco, et al.
Journal of the American College of Cardiology|July 16, 2011
Influence of 9p21.3 genetic variants on clinical and angiographic outcomes in early-onset myocardial infarctionDiego Ardissino, Carlo Berzuini, Piera Angelica Merlini, et al.
Journal of Cellular and Molecular Medicine|June 17, 2022
GCN5 contributes to intracellular lipid accumulation in human primary cardiac stromal cells from patients affected by Arrhythmogenic cardiomyopathyChiara Volani, Alessandra Pagliaro, Johannes Rainer, et al.
Pageof 6