Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Federica Giannetti"'
1
Akademický článek
PITX2 gain-of-function mutation associated with atrial fibrillation alters mitochondrial activity in human iPSC atrial-like cardiomyocytes
Autor: Patrizia Benzoni, Lorenzo Da Dalt, Noemi Elia, Vera Popolizio, Alessandro Cospito, Federica Giannetti, Patrizia Dell’Era, Morten S. Olesen, Annalisa Bucchi, Mirko Baruscotti, Giuseppe Danilo Norata, Andrea Barbuti
Publikováno v: Frontiers in Physiology, Vol 14 (2023)
Atrial fibrillation (AF) is the most common cardiac arrhythmia worldwide; however, the underlying causes of AF initiation are still poorly understood, particularly because currently available models do not allow in distinguishing the initial causes f
Externí odkaz: https://doaj.org/article/eb6bd6e9abc74426a70134e06381e27b
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2
Akademický článek
Use of hiPSC-Derived Cardiomyocytes to Rule Out Proarrhythmic Effects of Drugs: The Case of Hydroxychloroquine in COVID-19
Autor: Luca Sala, Vladislav Leonov, Manuela Mura, Federica Giannetti, Aleksandr Khudiakov, Alessandra Moretti, Lia Crotti, Massimiliano Gnecchi, Peter J. Schwartz
Publikováno v: Frontiers in Physiology, Vol 12 (2022)
In the early phases of the COVID-19 pandemic, drug repurposing was widely used to identify compounds that could improve the prognosis of symptomatic patients infected by SARS-CoV-2. Hydroxychloroquine (HCQ) was one of the first drugs used to treat CO
Externí odkaz: https://doaj.org/article/2f30eedcc12f4a179ce5aa2fa41cd5a7
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3
Akademický článek
Generation of the induced human pluripotent stem cell lines CSSi009-A from a patient with a GNB5 pathogenic variant, and CSSi010-A from a CRISPR/Cas9 engineered GNB5 knock-out human cell line
Autor: Natascia Malerba, Patrizia Benzoni, Gabriella Maria Squeo, Raffaella Milanesi, Federica Giannetti, Lynette G. Sadleir, Gemma Poke, Bartolomeo Augello, Anna Irma Croce, Andrea Barbuti, Giuseppe Merla
Publikováno v: Stem Cell Research, Vol 40, Iss , Pp - (2019)
GNB5 loss-of-function pathogenic variants cause IDDCA, a rare autosomal recessive human genetic disease characterized by infantile onset of intellectual disability, sinus bradycardia, hypotonia, visual abnormalities, and epilepsy. We generated human
Externí odkaz: https://doaj.org/article/7e6ca3fb95ff4982867323666b32b676
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6
When multiple caveolins make the difference: Cav1 partly compensates Cav3 alterations and rescues ion channels expression
Autor: A Rossini, Federica Giannetti, Annalisa Bucchi, A Cospito, Patrizia Benzoni, Mirko Baruscotti, Andrea Barbuti
Publikováno v: EP Europace. 23
Funding Acknowledgements Type of funding sources: Foundation. Main funding source(s): Fondazione Cariplo Caveolae are small-membrane invagination that contribute both to buffering excessive contraction-dependent membrane strain and to initiation of m
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e19910ec7b570f70eb97912e2ab150c5
https://doi.org/10.1093/europace/euab116.535
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9
Generation of the induced human pluripotent stem cell lines CSSi009-A from a patient with a GNB5 pathogenic variant, and CSSi010-A from a CRISPR/Cas9 engineered GNB5 knock-out human cell line
Autor: Raffaella Milanesi, Bartolomeo Augello, Lynette G. Sadleir, Giuseppe Merla, Patrizia Benzoni, Natascia Malerba, Gabriella Maria Squeo, Andrea Barbuti, Federica Giannetti, Gemma Poke, Anna Irma Croce
Publikováno v: Stem Cell Research, Vol 40, Iss, Pp-(2019)
GNB5 loss-of-function pathogenic variants cause IDDCA, a rare autosomal recessive human genetic disease characterized by infantile onset of intellectual disability, sinus bradycardia, hypotonia, visual abnormalities, and epilepsy. We generated human
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b95b19c76b4dc48eadfdf237c9c8d426
https://doi.org/10.1016/j.scr.2019.101547
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Plný text Recenzováno Digitální knihovna AV ČR
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